ATHEROGENICS, INC.
As filed with the Securities and Exchange Commission on
June 14, 2005
Registration No. 333-123895
UNITED STATES SECURITIES AND EXCHANGE COMMISSION
Washington, D.C. 20549
Amendment No. 1
To
Form S-3
REGISTRATION STATEMENT
UNDER
THE SECURITIES ACT OF 1933
ATHEROGENICS, INC.
(Exact Name of Registrant as Specified in Its Charter)
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Georgia |
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58-2108232 |
(State or Other Jurisdiction of
Incorporation or Organization) |
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(I.R.S. Employer
Identification Number) |
8995 Westside Parkway
Alpharetta, Georgia 30004
(678) 336-2500
(Address, Including Zip Code, and Telephone Number,
Including Area Code, of Registrants Principal Executive
Offices)
Russell M. Medford, M.D., Ph.D.
President and Chief Executive Officer
AtheroGenics, Inc.
8995 Westside Parkway
Alpharetta, Georgia 30004
(678) 336-2500
(Name, Address, Including Zip Code, and Telephone Number,
Including Area Code, of Agent For Service)
Copy to:
David E. Redlick, Esq.
Peter N. Handrinos, Esq.
Wilmer Cutler Pickering Hale and Dorr LLP
60 State Street
Boston, Massachusetts 02109
(617) 526-6000
Approximate date of commencement of proposed sale to the
public: As soon as practicable after this registration
statement becomes effective.
If the only securities being registered on this form are being
offered pursuant to dividend or interest reinvestment plans,
please check the following
box. o
If any of the securities being registered on this form are to be
offered on a delayed or continuous basis pursuant to
Rule 415 under the Securities Act of 1933, other than
securities offered only in connection with dividend or interest
reinvestment plans, check the following
box. þ
If this form is filed to register additional securities for an
offering pursuant to Rule 462(b) under the Securities Act,
please check the following box and list the Securities Act
registration statement number of the earlier effective
registration statement for the same
offering. o
If this form is a post-effective amendment filed pursuant to
Rule 462(c) under the Securities Act, check the following
box and list the Securities Act registration statement number of
the earlier effective registration statement for the same
offering. o
If delivery of the prospectus is expected to be made pursuant to
Rule 434, please check the following
box. o
THE REGISTRANT HEREBY AMENDS THIS REGISTRATION STATEMENT ON
SUCH DATE OR DATES AS MAY BE NECESSARY TO DELAY ITS EFFECTIVE
DATE UNTIL THE REGISTRANT SHALL FILE A FURTHER AMENDMENT WHICH
SPECIFICALLY STATES THAT THIS REGISTRATION STATEMENT SHALL
THEREAFTER BECOME EFFECTIVE IN ACCORDANCE WITH SECTION 8(a)
OF THE SECURITIES ACT OR UNTIL THE REGISTRATION STATEMENT SHALL
BECOME EFFECTIVE ON SUCH DATE AS THE COMMISSION, ACTING PURSUANT
TO SAID SECTION 8(a), MAY DETERMINE.
The information in this prospectus is not
complete and may be changed. The selling securityholders named
in this prospectus may not sell these securities until the
registration statement filed with the Securities and Exchange
Commission is effective. This prospectus is not an offer to sell
these securities and the selling securityholders named in this
prospectus are not soliciting offers to buy these securities in
any jurisdiction where the offer or sale is not permitted.
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SUBJECT TO COMPLETION, DATED
JUNE 14, 2005
PROSPECTUS
$200,000,000
ATHEROGENICS, INC.
1.50% CONVERTIBLE NOTES DUE 2012
AND
10,416,660 SHARES OF COMMON STOCK, NO PAR VALUE PER SHARE,
ISSUABLE UPON CONVERSION OF THE NOTES
On January 12, 2005, we issued and sold $200,000,000
aggregate principal amount of our 1.50% convertible notes
due 2012, which we refer to as the notes, in a private
placement. The initial purchasers resold the notes to qualified
institutional buyers in accordance with Rule 144A under the
Securities Act of 1933, as amended. This prospectus will be used
by selling securityholders from time to time to resell their
notes and the shares of common stock issuable upon conversion of
the notes. We will not receive any proceeds from the sale of the
notes or any shares of our common stock issuable upon conversion
of the notes offered by this prospectus.
The notes bear interest at a rate of 1.50% per year. We
will pay interest on February 1 and August 1 of each year,
beginning August 1, 2005. Holders may convert the notes
into shares of our common stock at a conversion rate of
38.5802 shares per $1,000 principal amount of notes
(representing an initial conversion price of approximately
$25.92 per share), subject to adjustment, before the close
of business on February 1, 2012.
We may not redeem any of the notes at our option prior to
maturity. Subject to our rights in the event of a public
acquirer change in control, as defined in this prospectus, at
any time prior to maturity of the notes following a designated
event, as defined in this prospectus, holders may require us to
redeem all or part of the notes at a redemption price equal to
100% of the principal amount, plus accrued but unpaid interest
and liquidated damages, if any. If a holder elects to convert
its notes in connection with the occurrence of a designated
event that is also a fundamental change, in some circumstances,
subject to our rights upon a public acquirer change of control,
the holder will be entitled to receive additional shares of
common stock upon conversion. In the event of a public acquirer
change of control, in lieu of permitting a redemption at the
holders option or issuing additional shares upon
conversion, we may elect to adjust the conversion rate and
related conversion obligation so that the notes are convertible
into shares of the acquiring or surviving company, in each case,
as described in this prospectus.
The notes are general unsecured debt and are junior to any
secured debt we may incur to the extent of any assets securing
such indebtedness, on parity with our
41/2% convertible
notes due 2008 and all of our other existing and any future
senior unsecured debt and senior to all subordinated debt. The
notes are structurally subordinated to all liabilities of our
subsidiaries. As of March 31, 2005, we had no senior
secured debt and $300 million of senior unsecured debt
outstanding, including the notes. The indenture governing the
notes does not restrict the amount of debt that we or any of our
subsidiaries may incur. For a more detailed description of the
notes, see Description of Notes beginning on
page 21.
The notes are currently designated for trading on The PORTAL
Market. Our common stock is traded on the NASDAQ National Market
under the symbol AGIX. On June 10, 2005, the
reported last sale price of our common stock on the NASDAQ
National Market was $16.80 per share. We urge you to obtain
current market quotations for our common stock.
Investing in the notes or our common stock involves risks.
See Risk Factors beginning on page 6.
Neither the Securities and Exchange Commission nor any state
securities commission has approved or disapproved of these
securities or determined if this prospectus is truthful or
complete. Any representation to the contrary is a criminal
offense.
The date of this prospectus
is ,
2005.
TABLE OF CONTENTS
We use the term AtheroGenics, the
Company, we, us and
our in this prospectus to refer to the business of
AtheroGenics, Inc. and its subsidiaries.
We have not authorized anyone to provide you with information
different from that contained or incorporated by reference in
this prospectus. The selling stockholders are offering to sell,
and seeking offers to buy, shares of our common stock only in
jurisdictions where offers and sales are permitted. The
information contained in this prospectus is accurate only as of
the date of this prospectus, regardless of the time of delivery
of this prospectus or of any sale of common stock.
PROSPECTUS SUMMARY
This summary highlights important information contained
elsewhere, or incorporated by reference, in this prospectus.
This summary does not contain all of the information that you
should consider before investing in the notes or our common
stock. You should read the entire prospectus carefully,
especially the risks of investing in the notes and our common
stock discussed under Risk Factors, and the
financial statements and notes to those financial statements
incorporated by reference herein, before making an investment
decision.
AtheroGenics
AtheroGenics is a research-based pharmaceutical company focused
on the discovery, development and commercialization of novel
drugs for the treatment of chronic inflammatory diseases,
including coronary heart disease, organ transplant rejection,
rheumatoid arthritis and asthma. We have developed a proprietary
vascular protectant, or v-protectant®, technology
platform to discover drugs to treat these types of diseases.
Based on our v-protectant® platform, we have two drug
development programs in clinical trials and are pursuing a
number of other preclinical programs.
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AGI-1067 for Coronary Heart Disease |
AGI-1067 is our v-protectant® candidate that is most
advanced in clinical development. AGI-1067 is designed to
benefit patients with coronary heart disease, or CHD, which is
atherosclerosis of the blood vessels of the heart.
Atherosclerosis is a common disease that results from
inflammation and the buildup of plaque in arterial blood vessel
walls. Nearly 13 million people in the United States
currently have diagnosed CHD. There are no medications available
for physicians to treat directly the underlying chronic
inflammation associated with CHD. Instead, physicians treat risk
factors, such as high cholesterol and high blood pressure, to
slow the progression of the disease. The anti-inflammatory
mechanism of AGI-1067 represents a novel, direct therapeutic
approach that may be suitable as a chronic treatment for all
patients with CHD, including those without traditional risk
factors.
In November 2004, we completed a Phase IIb clinical trial
called CART-2, a 465-patient study that examined the effect of
12 months of AGI-1067 therapy on atherosclerosis and
post-angioplasty restenosis. Two leading cardiac intravascular
ultrasound laboratories independently analyzed the final data
from CART-2. The primary endpoint of the trial was a change in
coronary atherosclerosis, measured as total plaque volume after
a 12-month treatment period compared to baseline values.
Combined results of the final analysis from the two
laboratories, which were based on an evaluation of intravascular
ultrasounds from approximately 230 patients in the study,
indicate that AGI-1067 reduced plaque volume by an average of
2.3%, which was statistically significant. Results from the
patient group receiving both placebo and standard of
care indicated a plaque volume measure that was not
statistically different from baseline. While the plaque
regression observed in the AGI-1067 group exceeded that observed
in the standard of care group numerically, the difference did
not reach statistical significance, although a trend towards
significance was seen in one laboratorys analysis. An
important secondary endpoint from the trial, change in plaque
volume in the most severely diseased subsegment, showed
statistically significant regression from baseline by an average
of 4.8%. The results also demonstrated a significant reduction
in myeloperoxidase, an inflammatory biomarker that correlates
with future cardiovascular events. Overall adverse event rates
were similar in the AGI-1067 and standard of care groups, and
AGI-1067 was generally well tolerated.
Based on the results of an End of Phase II meeting with the
U.S. Food and Drug Administration, or FDA, we proceeded to
develop a pivotal Phase III clinical trial protocol to
evaluate AGI-1067 for the treatment of atherosclerosis. The
Phase III protocol received a Special Protocol Assessment
from the FDA in March 2003. A Special Protocol Assessment is
written confirmation from the FDA that the protocol is
adequately designed to support a New Drug Application for the
drug in the specified treatment area.
In 2003, we initiated the pivotal Phase III trial, referred
to as ARISE (Aggressive Reduction of Inflammation Stops Events),
which is being conducted in cardiac centers in the United
States, Canada, the United Kingdom and South Africa. ARISE will
evaluate the impact of AGI-1067 on important outcome measures
such as death due to coronary disease, myocardial infarction,
stroke, coronary re-vascularization and
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unstable angina in patients who have CHD. The study will assess
the incremental benefits of AGI-1067 versus the current standard
of care therapies in this patient population. As such, all
patients in the trial, including those on placebo, will be
receiving other appropriate heart disease medications, including
statins and other cholesterol-lowering therapies, high blood
pressure medications and anti-clotting agents.
We originally planned to enroll in ARISE 4,000 patients who
would be followed for an average of 18 months or until a
minimum of 1,160 primary events, or outcome measures, had
occurred. In February 2005, we announced that the FDA approved
our proposed amendment to the ARISE Phase III clinical
trial protocol. The changes to the ARISE protocol are intended
to enhance the trial as well as to accelerate its pace without
affecting the Special Protocol Assessment with the FDA. The
changes approved by the FDA include our plan to increase the
number of patients in the study to a target of 6,000, eliminate
the minimum 12 month follow-up period for patients and
decrease the minimum number of primary events to 990. With these
modifications, we would expect to complete enrollment by
mid-2005 and complete the ARISE trial by the end of the first
quarter of 2006. We plan to file a New Drug Application with the
FDA as soon as possible after we complete the trial and analyze
the results.
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AGI-1096 for Organ Transplant Rejection |
Our second v-protectant® candidate, AGI-1096, is a novel
antioxidant and selective anti-inflammatory agent which is being
developed to address the accelerated inflammation of grafted
blood vessels, known as transplant arteritis, common in chronic
organ transplant rejection. We have completed a Phase I
clinical trial of AGI-1096 in healthy volunteers that
demonstrated AGI-1096 was well-tolerated over the escalating
single oral doses studied. Adverse events were generally mild
and not considered clinically significant. Subjects reached
targeted blood levels for AGI-1096 that were equivalent to those
seen in successful preclinical models of organ transplant
rejection. In January 2004, we announced a collaboration with
Astellas Pharma (formerly Fujisawa Pharmaceutical Co., Ltd.) to
conduct preclinical and early-stage clinical trials, with
Astellas funding all development costs during the term of the
agreement. Astellas will also receive an option to negotiate for
late stage development and commercial right to AGI-1096. In
March 2005, we extended the collaboration with Astellas until
September 30, 2005 to conduct additional activities.
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Other V-Protectant® Candidates |
We previously were developing AGIX-4207, a v-protectant®
candidate for the treatment of rheumatoid arthritis. In October
2003, we initiated the enrollment in a 275-patient Phase II
clinical trial called OSCAR. In October 2004, we announced the
results of the OSCAR clinical trial, which evaluated the impact
of various doses of AGIX-4207 versus placebo on clinical
efficacy, biomarkers and safety in patients with rheumatoid
arthritis. The results indicated that none of the three dosing
arms of AGIX-4207 showed a statistically significant improvement
in ACR 20 scores, a standard measurement of response utilized to
evaluate improvement, when compared to placebo, the primary
efficacy end point of the trial. Two of the pre-specified
secondary endpoints, tender joint count and morning stiffness,
did show statistically significant improvement when compared to
placebo. Based on the aggregate findings of the study, however,
we have discontinued clinical development of AGIX-4207. We
continue to have an active program aimed at investigating other
v-protectants® in rheumatoid arthritis and have identified
other compounds with enhanced therapeutic potential within our
rheumatoid arthritis preclinical models. We are working to
select another candidate to move into formal preclinical
development.
We have also identified additional potential v-protectant®
candidates to treat other chronic inflammatory diseases,
including asthma. We are evaluating these v-protectants® to
determine lead drug candidates for clinical development. We plan
to develop these v-protectants® rapidly and may seek
regulatory fast track status, if available, to expedite
development and commercialization. We will continue to expand
upon our v-protectant® technology platform using functional
genomics to identify novel therapeutic gene targets. Functional
genomics is the process by which one uses scientific models and
techniques to discover and modify genes, measure the
consequences of the modifications, and reliably determine the
function of those genes.
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Our objective is to become a leading pharmaceutical company
focused on discovering, developing and commercializing novel
drugs for the treatment of chronic inflammatory diseases. The
key elements of our strategy include the following:
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Continue aggressive development program for AGI-1067. We
intend to rapidly develop AGI-1067 for the treatment and
prevention of atherosclerosis in patients with coronary heart
disease. We are continuing to enroll patients in the ARISE
Phase III clinical trial for the treatment of
atherosclerosis in patients with coronary heart disease. |
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Extend our v-protectant® technology platform into
additional therapeutic areas that address unmet medical needs.
We believe that our v-protectants® have the potential for
treating a wide variety of other chronic inflammatory diseases.
These indications include chronic organ transplant rejection,
rheumatoid arthritis, asthma and other diseases. We completed a
Phase I clinical trial with positive results for AGI-1096,
a v-protectant® developed for the prevention of chronic
organ transplant rejection. |
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Expand our clinical product candidate portfolio. In
addition to our existing discovery programs, we intend to
acquire rights to other product candidates and technologies that
complement our existing product candidate lines or that enable
us to capitalize on our scientific and clinical development
expertise. We plan to expand our product candidate portfolio by
in-licensing or acquiring product candidates, technologies or
companies. |
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Commercialize our products. We plan to collaborate with
large pharmaceutical companies to commercialize products that we
develop to target patient or physician populations in broad
markets, such as AGI-1067 for atherosclerosis. In contrast, we
plan to develop a sales force to commercialize those of our
products that we develop to target appropriate patient or
physician populations in narrow markets. |
We were incorporated in Georgia in 1993. Our principal executive
offices are located at 8995 Westside Parkway, Alpharetta,
Georgia 30004 and our telephone number is (678) 336-2500.
Our website is located at www.atherogenics.com. The information
contained on our website is not a part of this prospectus.
Purported securities class action lawsuits were filed against us
and some of our executive officers and directors in the United
States District Court for the Southern District of New York on
January 5, 2005 and February 8, 2005 (the SDNY
Actions) and in the United States District Court for the
Northern District of Georgia, Atlanta division on
January 7, 2005, January 10, 2005, January 11,
2005 and January 25, 2005 (the NDGA Actions).
Plaintiffs filed separate motions to consolidate these lawsuits
in both the Southern District of New York and the Northern
District of Georgia on March 7, 2005. In addition, three
class members simultaneously moved for appointment as lead
plaintiff in both districts on March 7, 2005. On
April 18, 2005, the Honorable Richard J. Howell ordered the
SDNY Actions consolidated under the caption In re
Atherogenics Securities Litigation and appointed lead
plaintiff and co-lead counsel. The motion to consolidate the
NDGA Actions is still pending, and two class members have
subsequently withdrawn their motions for appointment as lead
plaintiff in the district. We intend to seek transfer of the
SDNY Actions to Georgia to be consolidated with the existing
NDGA Actions. The allegations in these lawsuits relate to our
disclosures regarding the results of the CART-2 clinical trial
for AGI-1067. Each complaint seeks unspecified damages on behalf
of a purported class of purchasers of our securities during the
period after our disclosures regarding the CART-2 clinical trial
in September 2004 to December 31, 2004. We believe that we
have meritorious defenses to the plaintiffs allegations
and intend to defend these matters vigorously. Similar class
action lawsuits may be filed against us and our executive
officers and directors in the future.
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The Offering
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Securities Offered |
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$200,000,000 principal amount of 1.50% Convertible Notes
due 2012. |
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Maturity Date |
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February 1, 2012. |
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Interest |
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1.50% per annum on the principal amount from
January 12, 2005, payable semi-annually in arrears in cash
on February 1 and August 1 of each year, beginning
August 1, 2005. |
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Conversion |
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You may convert the notes into shares of our common stock at a
conversion rate of 38.5802 shares per $1,000 principal
amount of notes, representing a conversion price of
approximately $25.92 per share, subject to adjustment,
prior to the close of business on the final maturity date of the
notes. |
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In addition, subject to our rights described under
Description of Notes Public Acquirer Change of
Control, if you elect to convert your notes in connection
with the occurrence of a designated event that is also a
fundamental change that occurs prior to the maturity date of the
notes, you will be entitled to receive additional shares of
common stock upon conversion in some circumstances as described
under Description of Notes Conversion of
Notes Make Whole Payment Upon the Occurrence of a
Designated Event that is also a Fundamental Change. |
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Public Acquirer Change of Control |
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In the case of a fundamental change that is a public
acquirer change of control, as defined under
Description of Notes Public Acquirer Change of
Control, we may, in lieu of permitting a redemption at the
holders option, as described below, or adjusting the
conversion rate, as described in the preceding paragraph, elect
to adjust the conversion rate and the related conversion
obligation such that from and after the effective date of such
public acquirer change of control, holders of the notes will be
entitled to convert their notes into an adjusted number of
shares of public acquirer common stock. |
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Ranking |
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The notes are our general unsecured obligations, rank equally in
right of payment to our
41/2% convertible
notes due 2008 and any future senior unsecured debt, junior to
any secured indebtedness to the extent of any assets securing
such indebtedness and senior to any subordinated indebtedness.
The notes are structurally subordinated to all liabilities of
our subsidiaries. As of March 31, 2005, we had no senior
secured debt and $300 million of senior unsecured debt
outstanding, including the notes. The indenture governing the
notes does not limit the amount of indebtedness that we or any
of our subsidiaries may incur. |
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Redemption |
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We may not redeem any of the notes at our option prior to
maturity. |
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Designated Event |
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If a designated event, as described under Description of
Notes Redemption at Option of the Holder,
occurs prior to maturity, you will have the right, subject to
our rights described under Description of
Notes Public Acquirer Change of Control, to
require us to redeem all or part of your notes at a redemption
price |
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equal to 100% of their principal amount, plus accrued and unpaid
interest and liquidated damages, if any, up to, but excluding,
the redemption date. |
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Use of Proceeds |
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All of the notes and the shares of our common stock issuable
upon conversion of the notes are being sold by the selling
securityholders or by their pledgees, donees, transferees or
other successors in interest. We will not receive any proceeds
from the sale of the notes or the shares of our common stock
issuable upon conversion of the notes. |
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Trading |
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The notes are not listed on any securities exchange or included
in any automated quotation system. An active and liquid market
for the notes may not develop or be maintained. |
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NASDAQ National Market Symbol for our Common Stock |
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AGIX |
Ratio of Earnings to Fixed Charges
The following table sets forth the computation of our ratio of
earnings to fixed charges for the periods indicated:
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Years Ended December 31, | |
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Three Months Ended | |
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Ratio of earnings to fixed charges
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For the three months ended March 31, 2005 and the years
ended December 31, 2004, 2003, 2002, 2001 and 2000, our
earnings were insufficient to cover fixed charges of
($2,103,573), ($5,192,894), ($1,954,402), ($50,689), ($21,534)
and ($36,555). Fixed charges do not include estimates for
interest within rental expense, which was not considered
material for any period presented.
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RISK FACTORS
You should carefully consider the risks described below
before making an investment decision. The risks and
uncertainties we describe below are not the only ones facing our
company. Additional risks and uncertainties not presently known
to us or that we currently deem immaterial may also become
important factors that affect our company. If any of these risks
or uncertainties occur, the trading price of the notes and our
common stock could decline and you could lose all or part of
your investment.
This prospectus also contains forward-looking statements that
involve risks and uncertainties. Our actual results could differ
materially from those anticipated in these forward-looking
statements as a result of certain important factors, including
the risks faced by us described below and elsewhere in this
prospectus.
Risks Related to Our Financial Results and Need for
Additional Financing
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We have a history of operating losses, and we may not
generate revenue or achieve profitability in the future. |
Our ability to generate revenue and achieve profitability
depends on our ability, alone or with collaborators, to complete
successfully the development of our product candidates, conduct
preclinical tests in animals and clinical trials in human
beings, obtain the necessary regulatory approvals and
manufacture and market the resulting drugs. We have had no
significant revenue to date. We have experienced operating
losses since we began operations in 1994. As of March 31,
2005, we had an accumulated deficit of approximately
$230.8 million. We expect to incur additional operating
losses and expect cumulative losses to increase substantially as
our research and development, preclinical, clinical,
manufacturing and marketing efforts expand. If we are unable to
achieve and then maintain profitability, the market value of our
common stock and the notes will decline and you could lose all
or part of your investment.
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If we need additional financing and cannot obtain it, we
may not be able to develop or market our products. |
We expect our research and development expenses to increase in
connection with our ongoing activities, particularly in
connection with the ARISE trial that we initiated in June 2003.
We believe that our existing cash, cash equivalents and
short-term investments will be sufficient to enable us to fund
our operating expenses, obligations under our financing
arrangements and capital expenditure requirements for at least
the next 12 months. Our future capital requirements will
depend on many factors, including:
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the scope and results of our research, preclinical and clinical
development activities; |
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the timing of, and the costs involved in, obtaining regulatory
approvals; |
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our ability to establish and maintain collaborations and the
financial terms of any such collaborations; |
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the cost of commercialization activities, including product
marketing, sales and distribution; |
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the costs involved in preparing, filing, prosecuting,
maintaining and enforcing patent claims and other patent-related
costs; |
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the costs related to purported class action lawsuits filed
against us; and |
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the extent to which we acquire or invest in businesses, products
and technologies. |
If our future capital requirements exceed our available funds,
we will need to seek additional financing. We may be unable to
raise capital when needed or on attractive terms. If additional
funds are not available, we may need to delay clinical studies,
curtail operations or obtain funds through collaborative
arrangements that may require us to relinquish rights to some of
our products or potential markets.
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Risks Related to Development of Product Candidates
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We depend heavily on the success of our most advanced
internal product candidate, AGI-1067 for atherosclerosis, which
is in clinical development. If we are unable to commercialize
this product candidate, or experience significant delays in
doing so, our business will be materially harmed. |
AGI-1067 is our lead compound. Our ability to generate product
revenues will depend heavily on the successful development and
commercialization of this compound. The commercial success of
AGI-1067 will depend on several factors, including the following:
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successful completion of clinical trials; |
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receipt of marketing approvals from the FDA and similar foreign
regulatory authorities; |
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establishing commercial manufacturing arrangements with third
party manufacturers; |
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launching commercial sales of the product, either alone or in
collaboration with others; and |
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acceptance of the product in the medical community and with
third party payors. |
AGI-1067 could fail in clinical trials if we are unable to show
it is effective or if it causes unacceptable side effects in the
patients we treated. While the plaque regression observed in the
group treated with AGI-1067 in the CART-2 trial exceeded that
observed in the standard of care group numerically, the
difference was not statistically significant. Moreover, the
results of our Phase II clinical trials of AGI-1067 are not
necessarily indicative of the results we will obtain in our
Phase III clinical trial of AGI-1067, particularly because
the primary clinical endpoints of these trials are not the same.
Failure in clinical trials of AGI-1067 would have a material
adverse effect on our ability to generate revenue or become
profitable. If we are not successful in commercializing
AGI-1067, or are significantly delayed in doing so, our business
will be materially harmed.
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If we do not successfully develop our other product
candidates, we will have limited ability to generate
revenue. |
Other than AGI-1067, all of our other product candidates are in
early stages of development, and only one other product
candidate has undergone Phase I clinical trials. Our
product candidates are subject to the risks of failure inherent
in developing drug products based on new technologies. We do not
expect any of our potential product candidates, including
AGI-1067, to be commercially available until at least 2007. Our
drug discovery efforts may not produce any other proprietary
product candidates. Our failure to develop product candidates
will limit our ability to generate additional revenue.
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If we fail to demonstrate adequately the safety and
efficacy of a product candidate, we will not be able to
commercialize that product candidate. |
Product candidates we develop, alone or with others, may not
prove safe and effective in clinical trials and may not meet all
of the applicable regulatory requirements needed to receive
regulatory approval. If we fail to adequately demonstrate safety
and efficacy for any product candidate, we will not be able to
commercialize that product candidate. Our failure to
commercialize a product candidate will materially adversely
affect our revenue opportunities. We will need to conduct
significant research, preclinical testing and clinical trials
before we can file product approval applications with the FDA
and similar regulatory authorities in other countries.
Preclinical testing and clinical trials are long, expensive and
uncertain processes. We may spend several years completing our
testing for any particular product candidate. Failure can occur
at any stage. For example, we recently discontinued clinical
development of AGI-4207 in rheumatoid arthritis following
announcement of unsuccessful results of a Phase II clinical
trial of that product candidate.
The FDA or we may suspend our clinical trials at any time if
either of us believes that we are exposing the subjects
participating in these trials to unacceptable health risks. The
FDA or institutional review boards at the medical institutions
and healthcare facilities where we sponsor clinical trials may
suspend any trial indefinitely if they find deficiencies in the
conduct of these trials. The FDA and these institutional review
boards have authority to oversee our clinical trials, and the
FDA may require large numbers of test subjects. In
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addition, we must manufacture the product candidates that we use
in our clinical trials under the FDAs Good Manufacturing
Practices.
Even if we achieve positive results in early clinical trials,
these results do not necessarily predict final results. A number
of companies in the pharmaceutical industry have suffered
significant setbacks in advanced clinical trials, even after
achieving positive results in earlier trials. Negative or
inconclusive results or adverse medical events during a clinical
trial could cause the FDA or us to terminate a clinical trial or
require that we repeat it.
In addition, even if we receive approval for commercial sale of
any of our product candidates, after use in an increasing number
of patients, our products could show side effect profiles that
limit their usefulness or require their withdrawal although the
drugs did not show the side effect profile in Phase I
through Phase III clinical trials.
Risks Related to Our Dependence on Third Parties for
Manufacturing, Research and Development and Marketing and
Distribution Activities
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We may not be successful in establishing collaborations
for AGI-1067 and any other product candidate we may seek to
commercialize, which could adversely affect our ability to
discover, develop and commercialize products. |
A key element of our business strategy is to collaborate with
third parties, particularly leading pharmaceutical companies, to
develop and commercialize some of our product candidates,
including AGI-1067. We are currently seeking a collaborator for
development and commercialization of AGI-1067. We also expect to
seek collaborations for the development and commercialization of
other product candidates in the future. The timing and terms of
any collaboration for AGI-1067 will depend on the evaluation by
prospective collaborators of the clinical trial results of
AGI-1067 and other aspects of the drugs safety and
efficacy profile. We are currently reviewing the results of our
CART-2 trial of AGI-1067 with potential collaborators and cannot
now predict the timing and terms of such a collaboration. If we
are unable to reach agreements with suitable collaborators for
AGI-1067 or any other product candidate, we would be forced to
fund the entire development and commercialization of such
product candidates, and we may not have the resources to do so.
If resource constraints require us to enter into a collaboration
early in the development of a product candidate, we may be
forced to accept a more limited share of any revenues such
products may eventually generate. We face significant
competition in seeking appropriate collaborators. Moreover,
these collaboration arrangements are complex and time-consuming
to negotiate and document. We may not be successful in our
efforts to establish collaborations or other alternative
arrangements for AGI-1067 or any other product candidate.
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We expect to depend significantly on collaborations with
third parties to develop and commercialize some of our product
candidates. If a potential collaborator were to change its
strategy or the focus of its development and commercialization
efforts with respect to our relationship, the success of our
product candidates and our operations could be adversely
affected. |
Our collaboration with Astellas Pharma to develop AGI-1096 in
preclinical testing and early-stage clinical trials and any
other collaboration that we may establish may not be successful.
The success of any collaboration arrangement will depend heavily
on the efforts and activities of our collaborators.
Collaborators will likely have significant discretion in
determining the efforts and resources that they will apply to
these collaborations. The risks that we anticipate being subject
to in collaborations include:
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a collaborator may develop and commercialize, either alone or
with others, products and services that are similar to or
competitive with the products that are the subject of the
collaboration with us; |
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a collaborator may change the focus of its development and
commercialization efforts. Pharmaceutical and biotechnology
companies historically have re-evaluated their priorities from
time to time, including following mergers and consolidations,
which have been common in recent years in these industries; |
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the ability of our product candidates and products to reach
their potential could be limited if our collaborators decrease
or fail to increase spending relating to such products; |
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a collaborator may terminate a collaboration in the event of a
material breach by us; and |
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a collaborator may fail to maintain or defend our intellectual
property rights. |
The termination of any collaboration that we may establish might
adversely affect the development of the related product
candidates and our ability to derive revenue from them.
Collaborations with pharmaceutical companies and other third
parties often are terminated or allowed to expire by the other
party or by us. For example, in 2001, Schering-Plough and we
terminated a collaboration that we had established for AGI-1067.
Any future terminations or expirations would adversely affect us
financially and could harm our business reputation. In such
event, we might be required to devote additional resources to
the product or product candidate, seek a new collaborator or
abandon the product or product candidate, any of which could
have an adverse effect on our business.
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Third parties failure to synthesize and manufacture
our product candidates to our specifications could delay our
clinical trials or hinder our commercialization
prospects. |
We currently have no manufacturing facilities to synthesize or
manufacture our product candidates, nor do we intend to develop
these capabilities in the near future. Our reliance on third
parties for these services exposes us to various risks that
could delay our clinical trials or hinder our commercialization
prospects. These risks include the following:
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A finding that a third party did not comply with applicable
governmental regulations. Manufacturers of pharmaceutical
products are subject to continual review and periodic
inspections by regulatory agencies. Our present or future
manufacturers may not be able to comply with the FDAs
current Good Manufacturing Practices regulations and other FDA
regulatory requirements or similar regulatory requirements
outside the United States. Failure of one of our third party
manufacturers to comply with applicable regulatory requirements,
whether or not related to our product candidates, could result
in sanctions being imposed on us, including fines, injunctions,
civil penalties, failure of regulatory authorities to grant
marketing approval of our product candidates, delays, suspension
or withdrawal of approvals, license revocation, seizures or
recalls of product candidates or products, operating
restrictions and criminal prosecutions, any of which could
significantly and adversely affect supplies of our product
candidates and products. |
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A failure to synthesize and manufacture our product
candidates in accordance with our product specifications. We
need to maintain a very low maximal amount of one of the
starting materials used in the manufacture of AGI-1067. The
starting material, probucol, was prescribed by physicians as a
cholesterol-lowering agent until its manufacturer withdrew the
drug from the market for efficacy reasons. A failure by our
third party manufacturers to maintain an acceptable level of
probucol in the manufacture of AGI-1067 may result in chronic
dosing of probucol, which is associated with the occurrence of a
rare side effect. |
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A failure to deliver product candidates in sufficient
quantities or in a timely manner. Any failure by our third
party manufacturers to supply our requirements for clinical
trial materials or commercial product, or to supply these
materials in a timely manner, could jeopardize the initiation or
completion of clinical trials or could have a material adverse
effect on our ability to commercialize any approved products and
thereby generate revenue. |
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Inability to control costs. We may be subject to costs
outside of our control, which could adversely affect our future
profitability and our ability to commercialize products on a
timely and competitive basis. |
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Termination or nonrenewal of an agreement by the third party,
based on its own business priorities, at a time that is costly
or inconvenient to us. Our product candidates and any
products that we successfully develop may compete with product
candidates and products of others for access to the third
partys manufacturing facilities. |
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Risks Related to Our Intellectual Property
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Our failure to protect adequately or enforce our
intellectual property rights or secure rights to third party
patents could materially adversely affect our proprietary
position in the marketplace or prevent the commercialization of
our products. |
Our success will depend in large part on our ability to obtain
and maintain protection in the United States and other countries
for the intellectual property covering or incorporated into our
technologies and products. The patents and patent applications
in our patent portfolio are either owned by us or licensed to
us. Our ability to protect our product candidates from
unauthorized or infringing use by third parties depends
substantially on our ability to obtain and maintain valid and
enforceable patents. Due to evolving legal standards relating to
the patentability, validity and enforceability of patents
covering pharmaceutical inventions and the scope of claims made
under these patents, our ability to obtain and enforce patents
is uncertain and involves complex legal and factual questions
for which important legal principles are unresolved.
We may not be able to obtain patent rights on products,
treatment methods or manufacturing processes that we may develop
or to which we may obtain license or other rights. Even if we do
obtain patents, rights under any issued patents may not provide
us with sufficient protection for our product candidates or
provide sufficient protection to afford us a commercial
advantage against our competitors or their competitive products
or processes. It is possible that no patents will be issued from
any pending or future patent applications owned by us or
licensed to us. Others may challenge, seek to invalidate,
infringe or circumvent any patents we own or license.
Alternatively, we may in the future be required to initiate
litigation against third parties to enforce our intellectual
property rights. The cost of this litigation could be
substantial and it is possible that our efforts could be
unsuccessful. Changes in either patent laws or in
interpretations of patent laws in the United States and other
countries may diminish the value of our intellectual property or
narrow the scope of our patent protection.
Our patents also may not afford us protection against
competitors with similar technology. We may not have identified
all patents, published applications or published literature that
affect our business either by blocking our ability to
commercialize our product candidates, by preventing the
patentability of our drugs to us or our licensors or by covering
the same or similar technologies that may affect our ability to
market our product candidates. For example, patent applications
in the United States are maintained in confidence for up to
18 months after their filing. In some cases, however,
patent applications remain confidential in the United States
Patent and Trademark Office for the entire time prior to
issuance as a United States patent. Patent applications filed in
countries outside the United States are not typically published
until at least 18 months from their first filing date.
Similarly, publication of discoveries in the scientific or
patent literature often lags behind actual discoveries.
Therefore, we or our licensors might not have been the first to
invent, or the first to file, patent applications on our drug
candidates or for their use. The laws of some foreign
jurisdictions do not protect intellectual property rights to the
same extent as in the United States and many companies have
encountered significant difficulties in protecting and defending
such rights in foreign jurisdictions. If we encounter such
difficulties in protecting or are otherwise precluded from
effectively protecting our intellectual property rights in
foreign jurisdictions, our business prospects could be
substantially harmed.
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If we infringe or are alleged to infringe intellectual
property rights of third parties, it will adversely affect our
business. |
Our research, development and commercialization activities, as
well as any product candidates or products resulting from these
activities, may infringe or be claimed to infringe patents or
patent applications under which we do not hold licenses or other
rights. Third parties may own or control these patents and
patent applications in the United States and abroad. These third
parties could bring claims against us or our collaborators that
would cause us to incur substantial expenses and, if successful
against us, could cause us to pay substantial damages. Further,
if a patent infringement suit were brought against us or our
collaborators, we or they could be forced to stop or delay
research, development, manufacturing or sales of the product or
product candidate that is the subject of the suit.
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As a result of patent infringement claims, or in order to avoid
potential claims, we or our collaborators may choose or be
required to seek a license from the third party and be required
to pay license fees or royalties or both. These licenses may not
be available on acceptable terms, or at all. Even if we or our
collaborators were able to obtain a license, the rights may be
nonexclusive, which could result in our competitors gaining
access to the same intellectual property. Ultimately, we could
be prevented from commercializing a product, or be forced to
cease some aspect of our business operations, if, as a result of
actual or threatened patent infringement claims, we or our
collaborators are unable to enter into licenses on acceptable
terms. This could harm our business significantly.
There has been substantial litigation and other proceedings
regarding patent and other intellectual property rights in the
pharmaceutical and biotechnology industries. In addition to
infringement claims against us, we may become a party to other
patent litigation and other proceedings, including interference
proceedings declared by the United States Patent and Trademark
Office and opposition proceedings in the European Patent Office,
regarding intellectual property rights with respect to our
products and technology. The cost to us of any patent litigation
or other proceeding, even if resolved in our favor, could be
substantial. Some of our competitors may be able to sustain the
costs of such litigation or proceedings more effectively than we
can because of their substantially greater financial resources.
Uncertainties resulting from the initiation and continuation of
patent litigation or other proceedings could have a material
adverse effect on our ability to compete in the marketplace.
Patent litigation and other proceedings may also absorb
significant management time.
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If we fail to comply with our obligations in our
intellectual property licenses with third parties, we could lose
license rights that are important to our business. |
Our commercial success will also depend on our ability to
develop, manufacture, use, sell and offer to sell our product
candidates and proposed product candidates without breaching our
agreements with our patent licensors. We are a party to a number
of license agreements, including exclusive licenses to
technologies from Emory University, covering aspects of our
v-protectant® technology, and the National Jewish Medical
and Research Center, covering aspects of our MEKK technology
platform. We expect to enter into additional licenses in the
future. Our exclusive license with Emory University requires us
to take steps to commercialize the licensed technology in a
timely manner. If we fail to meet these obligations, Emory
University can convert our exclusive license to a non-exclusive
license, can grant others non-exclusive rights in the licensed
technology or can require us to sublicense aspects of the
licensed technology. Our license agreement with National Jewish
requires us to develop the licensed technology in a timely
manner. If we fail to meet these obligations, some or all of the
licensed technology may revert to National Jewish. Our existing
licenses impose, and we expect future licenses will impose,
various diligence, milestone payment, royalty, insurance and
other obligations on us. If we fail to comply with these
obligations, the licensor may have the right to terminate the
license, in which event we might not be able to market any
product that is covered by the licensed patents.
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If we are unable to protect the confidentiality of our
proprietary information and know-how, the value of our
technology and products could be adversely affected. |
In addition to patented technology, we rely on trade secrets,
proprietary know-how and technological advances, which we seek
to protect through agreements with our collaborators, employees
and consultants. These persons and entities could breach our
agreements, for which we may not have adequate remedies. In
addition, others could become aware of our trade secrets or
proprietary know-how through independent discovery or otherwise.
If we are unable to protect the confidentiality of our
proprietary information and know-how, competitors may be able to
use this information to develop products that compete with our
products, which could adversely impact our business.
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Risks Related to Regulatory Approval of Our Product
Candidates
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Because we cannot predict whether or when we will obtain
regulatory approval to commercialize our product candidates, we
cannot predict the timing of any future revenue from these
product candidates. |
We cannot commercialize any of our product candidates, including
AGI-1067 and AGI-1096, until the appropriate regulatory
authorities have reviewed and approved the applications for the
product candidates. The regulatory agencies may not complete
their review processes in a timely manner and we may not obtain
regulatory approval for any product candidate we or our
collaborators develop. Satisfaction of regulatory requirements
typically takes many years, if approval is obtained at all, is
dependent upon the type, complexity and novelty of the product
and requires the expenditure of substantial resources.
Regulatory approval processes outside the United States include
all of the risks associated with the FDA approval process. In
addition, we may experience delays or rejections based upon
additional government regulation from future legislation or
administrative action or changes in FDA policy during the period
of product development, clinical trials and FDA regulatory
review. The FDA has substantial discretion in the approval
process and may refuse to accept any application or may decide
that our data is insufficient for approval and require
additional preclinical, clinical or other studies. In addition,
varying interpretations of the data obtained from preclinical
and clinical testing could delay, limit or prevent regulatory
approval of a product candidate.
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We may experience delays in our clinical trials that could
adversely affect our financial results and our commercial
prospects. |
We do not know whether planned clinical trials will begin on
time or whether we will complete any of our clinical trials on
schedule or at all. We recently announced modifications of the
protocol for our ARISE trial, in part to mitigate any delay in
completing the trial. Product development costs to us and our
collaborators will increase if we have delays in testing or
approvals or if we need to perform more or larger clinical
trials than planned. Significant delays may adversely affect our
financial results and the commercial prospects for our products,
and delay our ability to become profitable.
We rely heavily on independent clinical investigators, contract
research organizations and other third party service providers
for successful execution of our clinical trials, but do not
control many aspects of their activities. We are responsible for
ensuring that each of our clinical trials is conducted in
accordance with the general investigational plan and protocols
for the trial. Moreover, the FDA requires us to comply with
standards, commonly referred to as Good Clinical Practices, for
conducting and recording and reporting the results of clinical
trials to assure that data and reported results are credible and
accurate and that the rights, integrity and confidentiality of
trial participants are protected. Our reliance on third parties
that we do not control does not relieve us of these
responsibilities and requirements. Third parties may not
complete activities on schedule, or may not conduct our clinical
trials in accordance with regulatory requirements or our stated
protocols. The failure of these third parties to carry out their
obligations could delay or prevent the development, approval and
commercialization of our product candidates.
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Failure to obtain regulatory approval in international
jurisdictions would prevent us from marketing our products
abroad. |
We intend to have our products marketed outside the United
States. In order to market our products in the European Union
and many other foreign jurisdictions, we must obtain separate
regulatory approvals and comply with numerous and varying
regulatory requirements. We expect that a collaborator may have
responsibility to obtain regulatory approvals outside the United
States with respect to some of our product candidates, and we
will depend on such collaborators to obtain these approvals. The
approval procedure varies among countries and can involve
additional testing. The time required to obtain approval may
differ from that required to obtain FDA approval. The foreign
regulatory approval process may include all of the risks
associated with obtaining FDA approval. We may not obtain
foreign regulatory approvals on a timely basis, if at all.
Approval by the FDA does not ensure approval by regulatory
authorities in other countries or jurisdictions, and approval by
one foreign regulatory authority does not ensure approval by
regulatory authorities in other foreign countries or
jurisdictions or by the FDA. We and any future collaborators may
not
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be able to file for regulatory approvals and may not receive
necessary approvals to commercialize our products in any market.
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If we do not comply with applicable regulatory
requirements in the manufacture and distribution of our
products, we may incur penalties that may inhibit our ability to
commercialize our products and adversely affect our
revenue. |
Our failure to comply with applicable FDA or other regulatory
requirements, including manufacturing, quality control,
labeling, safety surveillance, promoting and reporting, may
result in criminal prosecution, civil penalties, recall or
seizure of our products, total or partial suspension of
production or an injunction, as well as other regulatory action
against our potential products or us. Discovery of previously
unknown problems with a product, supplier, manufacturer or
facility may result in restrictions on the sale of our products,
including a withdrawal of such products from the market.
Risks Related to Commercialization
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The commercial success of any products that we may develop
will depend on the degree of market acceptance by physicians,
patients, healthcare payors and others in the medical
community. |
Any products that we bring to the market may not gain market
acceptance by physicians, patients, healthcare payors and others
in the medical community. If these products do not achieve an
adequate level of acceptance, we may not generate material
product revenues and we may not become profitable. The degree of
market acceptance of our product candidates, if approved for
commercial sale, will depend on a number of factors, including:
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the prevalence and severity of any side effects; |
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the efficacy and potential advantages over alternative
treatments; |
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the ability to offer our product candidates for sale at
competitive prices; |
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relative convenience and ease of administration; |
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the willingness of the target patient population to try new
therapies and of physicians to prescribe these therapies; |
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the strength of marketing and distribution support; and |
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sufficient third party coverage or reimbursement. |
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If our competitors develop and market products that are
more effective, have fewer side effects or are less expensive
than our current or future product candidates, we may have
limited commercial opportunities. |
The development and commercialization of new drugs is highly
competitive. Our competitors include large pharmaceutical and
more established biotechnology companies. Moreover, there are
approved products on the market for many of the diseases for
which we are developing drugs. In many cases, these products
have well known brand names, are distributed by large
pharmaceutical companies and have achieved widespread acceptance
among physicians and patients. Our competitors have significant
resources and expertise in research and development,
manufacturing, testing, obtaining regulatory approvals and
marketing. Potential competitors also include academic
institutions, government agencies, and other public and private
research organizations that conduct research, seek patent
protection and establish collaborative arrangements for
research, development, manufacturing and commercialization. It
is possible that any of these competitors could develop
technologies or products that would render our technologies or
product candidates obsolete or non-competitive, which could
adversely affect our revenue potential. These third parties also
compete with us in recruiting and retaining qualified scientific
and management personnel, establishing clinical trial sites and
patient registration for clinical trials, as well as in
acquiring technologies complementary to or necessary for our
programs or advantageous to our business.
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If we are unable to create sales, marketing and
distribution capabilities or enter into agreements with third
parties to perform these functions, we will not be able to
commercialize our product candidates. |
We currently have no sales, marketing or distribution
capabilities. In order to commercialize our product candidates,
we must either develop our own sales, marketing and distribution
capabilities or collaborate with a third party to perform these
functions. We have no experience in developing, training or
managing a sales force and will incur substantial additional
expenses in doing so. The cost of establishing and maintaining a
sales force may exceed its cost effectiveness. In addition, we
will compete with many companies that currently have extensive
and well-funded marketing and sales operations. Our marketing
and sales efforts may be unable to compete successfully against
these companies.
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If we are unable to obtain adequate reimbursement from
third party payors for any products that we may develop or
acceptable prices for those products, our revenues and prospects
for profitability will suffer. |
Most patients will rely on Medicare and Medicaid, private health
insurers and other third party payors to pay for their medical
needs, including any drugs we or any collaborators may market.
If third party payors do not provide adequate coverage or
reimbursement for any products that we may develop, our revenues
and prospects for profitability will suffer. In December 2003,
the Congress enacted a limited prescription drug benefit for
Medicare recipients in the Medicare Prescription Drug and
Modernization Act of 2003. While the program established by this
statute may increase demand for our products, if we participate
in this program, our prices will be negotiated with drug
procurement organizations for Medicare beneficiaries and are
likely to be lower than we might otherwise obtain. Non-Medicare
third party drug procurement organizations may also base the
price they are willing to pay on the rate paid by drug
procurement organizations for Medicare beneficiaries.
A primary trend in the United States healthcare industry is
toward cost containment. In addition, in some foreign countries,
particularly the countries of the European Union, the pricing of
prescription pharmaceuticals is subject to governmental control.
In these countries, pricing negotiations with governmental
authorities can take six to 12 months or longer after the
receipt of regulatory marketing approval for a product. To
obtain reimbursement or pricing approval in some countries, we
may be required to conduct a clinical trial that compares the
cost effectiveness of our product candidates or products to
other available therapies. The conduct of such a clinical trial
could be expensive and result in delays in commercialization of
our products.
Third party payors are challenging the prices charged for
medical products and services, and many third party payors limit
reimbursement for newly-approved healthcare products. In
particular, third party payors may limit the indications for
which they will reimburse patients who use any products that we
may develop. Cost control initiatives could decrease the price
we might establish for products that we may develop, which would
result in lower product revenues to us.
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If plaintiffs bring product liability lawsuits against us,
we may incur substantial financial loss or may be unable to
obtain future product liability insurance at reasonable prices,
if at all, either of which could diminish our ability to
commercialize our future products. |
The testing and marketing of medicinal products entail an
inherent risk of product liability. Clinical trial subjects,
consumers, healthcare providers, or pharmaceutical companies or
others selling our future products could bring product liability
claims against us. If we cannot successfully defend ourselves
against claims that our product candidates or products caused
injuries, we will incur substantial liabilities. Regardless of
merit or eventual outcome, liability claims may result in:
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decreased demand for any product candidates or products that we
may develop; |
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injury to our reputation; |
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withdrawal of clinical trial participants; |
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costs to defend the related litigation; |
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substantial monetary awards to trial participants or patients; |
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loss of revenue; and |
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the inability to commercialize any products that we may develop. |
We may not be able to acquire or maintain insurance coverage at
a reasonable cost or in sufficient amounts to protect us.
Risks Related to Our Operations
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Our failure to attract, retain and motivate skilled
personnel and cultivate key academic collaborations could
materially adversely affect our research and development
efforts. |
We are a small company with approximately 100 full-time
employees. If we are unable to continue to attract, retain and
motivate highly qualified management and scientific personnel
and to develop and maintain important relationships with leading
academic institutions and scientists, we may not be able to
achieve our research and development objectives. Competition for
personnel and academic collaborations is intense. We have
entered into employment agreements with each of our executive
officers. These employment agreements are terminable by the
employee on short notice. Loss of the services of any of these
officers or of our key scientific personnel could adversely
affect progress of our research and development programs. All of
our other employees are at will employees. We do not carry key
person insurance on any employee.
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The outcome of informal inquiries by the SEC and NASD
regarding our announcement of interim results from the CART-2
clinical trial for AGI-1067 and related trading in our common
stock is uncertain. |
We have been contacted by the staff of the Securities and
Exchange Commission, or SEC, and the NASD regarding informal
inquiries they are conducting related to our September 27,
2004 announcement of interim results from the CART-2 clinical
trial for AGI-1067 and trading in our common stock surrounding
that announcement. The SEC staffs notice states that its
inquiry should not be construed as an expression of opinion on
the part of the SEC or its staff that any violations of law have
occurred. The SEC and NASD staff have requested that we
voluntarily provide them with documents and other information
relating to that announcement. We are cooperating fully with
these requests. Based on our review of the facts as to the
September 27, 2004 announcement and trading in our common
stock surrounding that announcement, we do not believe that we
or any of our officers or directors have violated any laws
related to these inquiries. However, we cannot predict the
outcome of these inquiries, whether the SEC or NASD will
undertake any formal investigation or proceeding relating to us
or our officers or directors or when these matters might be
resolved.
Risks Related to the Notes and Our Common Stock
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The notes are unsecured and, therefore, are effectively
subordinated to any of our secured debt. |
The notes are not secured by any of our assets and will rank
equal in right of payment with our existing and any future
unsecured and unsubordinated indebtedness, such as our
41/2% convertible
notes due 2008. The notes are junior to any secured debt that we
may incur to the extent of the value of the assets that secure
such indebtedness. As of March 31, 2005, we had no senior
secured debt and $300 million of senior unsecured debt
outstanding, including the notes. The notes will also be
structurally subordinated to all indebtedness and
other liabilities, including trade payables and lease
obligations, of any subsidiaries. In the event of our
bankruptcy, liquidation or reorganization or upon acceleration
of the notes, payment on the notes could be less, ratably, than
on any secured indebtedness or indebtedness of any of our
subsidiaries. We may not have sufficient assets remaining to pay
amounts due on any or all of the notes then outstanding.
The indenture for the notes does not prohibit or limit us or any
subsidiary from incurring additional indebtedness and other
liabilities, or from pledging assets to secure such indebtedness
and liabilities. The incurrence of additional indebtedness and
in particular the granting of a security interest to secure the
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indebtedness, could adversely affect our ability to pay our
obligations on the notes. We anticipate that from time to time
we will incur additional indebtedness in the future.
In addition, the indenture does not contain any financial or
operating covenants or restrictions on the payment of dividends
or the issuance or repurchase of securities by us or any
subsidiary. The indenture contains no covenants or other
provisions to afford protection to holders of the notes in the
event of a fundamental change involving us except to the extent
described under Description of Notes
Redemption at the Option of the Holder and
Description of Notes Conversion of
Notes Make Whole Payment Upon the Occurrence of a
Designated Event that is also a Fundamental Change.
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We may not have the ability to raise the funds necessary
to repay the notes when due or to finance the designated event
redemption option. |
At final maturity, the entire outstanding principal amount of
the notes will become due and payable. If a designated event, as
described under the heading Description of
Notes Redemption at Option of the Holder,
occurs prior to maturity, we may be required to redeem all or
part of the notes. We may not have enough funds to pay the
redemption price for all tendered notes.
The entire principal amount of our outstanding
41/2% convertible
notes due 2008 will become due and payable prior to the final
maturity of the notes. We may not have enough funds to pay the
redemption price for those notes at such time. Even if we are
able to pay the redemption price for our
41/2% convertible
notes due 2008 at final maturity of those notes, we may not have
enough funds subsequently to pay the redemption price of our
1.50% convertible notes due 2012 at final maturity in 2012.
The
41/2% convertible
notes due 2008 also contain provisions that give the option to
those securityholders to require us to redeem those notes upon
some events, which may also constitute designated events under
the indenture for our 1.50% convertible notes due 2012. As
a result, following a designated event, we may be required to
redeem a significant amount of indebtedness along with the notes
and we may not have sufficient funds to redeem all such
indebtedness at such time. As of March 31, 2005, there was
$100 million principal amount outstanding of our
41/2% convertible
notes due 2008.
Any future credit agreements or other agreements relating to our
indebtedness may contain provisions prohibiting redemption of
the notes under some circumstances, or expressly prohibit our
redemption of the notes upon a designated event or may provide
that a designated event constitutes an event of default under
that agreement. If a designated event occurs at a time when we
are prohibited from purchasing or redeeming notes, we could seek
the consent of our lenders to redeem the notes or attempt to
refinance this debt. If we do not obtain consent, we would not
be permitted to purchase or redeem the notes. Our failure to
redeem tendered notes would constitute an event of default under
the indenture for our 1.50% convertible notes due 2012,
which might constitute a default under the terms of our other
indebtedness.
The designated event redemption rights in the notes could
discourage a potential acquirer. However, this designated event
redemption feature is not the result of managements
knowledge of any specific effort to obtain control of us by
means of a merger, tender offer or solicitation, or part of a
plan by management to adopt a series of anti-takeover
provisions. The term designated event is limited to
specified transactions and may not include other events that
might adversely affect our financial condition or business
operations. Our obligation to offer to redeem the notes upon a
designated event would not necessarily afford you protection in
the event of a highly leveraged transaction, reorganization,
merger or similar transaction involving us.
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There is no public market for the notes, which could
impair your ability to sell the notes. |
The notes are a new issue of securities for which there
currently is no public trading market. We do not intend to list
the notes on any national securities exchange or to seek the
admission of the notes for trading on the NASDAQ National
Market. A market for the notes may not develop or be maintained
and you may not be able to sell your notes. Accordingly, you may
be required to bear the financial risk of an investment in the
notes for an indefinite period of time. The notes may trade at a
discount from their initial offering price. Future trading
prices of the notes will depend on many factors, including
prevailing interest rates, the market for similar securities and
for our common stock, general economic conditions and our
financial condition,
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performance and prospects. Historically, the market for
convertible debt has been subject to disruptions that have
caused volatility in the prices of securities similar to the
notes. It is possible that the market, if any, for the notes
will be subject to disruptions that may have a negative effect
on the holders of the notes, regardless of our prospects or
financial performance.
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Our stock price has been volatile, and your investment in
our notes therefore could decline in value. |
The market price of our common stock, and the market prices for
securities of pharmaceutical and biotechnology companies in
general, have been highly volatile and may continue to be highly
volatile in the future. During the period from January 1,
2004 to June 10, 2005, the closing sale price of our common
stock on the NASDAQ National Market ranged from a low of
$10.66 per share to a high of $38.00 per share.
Because the notes are convertible into our common stock,
volatility or depressed prices for our common stock could have a
similar effect on the trading price of the notes. You must be
willing to bear the risk of fluctuations in the price of our
common stock and the risk that the value of your investment in
our securities could decline. The following factors, in addition
to other risk factors described in this prospectus, may have a
significant impact on the market price of our common stock:
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results of clinical trials of our product candidates,
particularly AGI-1067, and those of our competitors; |
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whether we enter into collaboration agreements and the timing
and accounting treatment of payments, if any, to us under those
agreements; |
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developments concerning any research and development,
manufacturing, and marketing collaborations, including whether
and when we achieve milestones; |
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announcements of technological innovations or new commercial
products by our competitors or us; |
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developments concerning proprietary rights, including patents; |
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the addition or termination of research programs or funding
support; |
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publicity regarding actual or potential results relating to
medicinal products under development by our competitors or us; |
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manufacturing and commercialization costs for any product that
receives approval for commercial sale; |
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regulatory developments in the United States and other countries; |
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litigation; |
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economic and other external factors, including disasters or
crises; and |
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period-to-period fluctuations in financial results. |
In the past, following periods of volatility in the market price
of a companys securities, securities class action
litigation has often been instituted. Purported securities class
action lawsuits were filed against us and some of our executive
officers and directors in the United States District Court for
the Southern District of New York on January 5, 2005 and
February 8, 2005 and in the United States District Court
for the Northern District of Georgia, Atlanta division on
January 7, 2005, January 10, 2005, January 11,
2005 and January 25, 2005. The class action lawsuits filed
in the United States District Court for the Southern District of
New York have been consolidated. The allegations in these
lawsuits relate to our disclosures regarding the results of the
CART-2 clinical trial for AGI-1067. The results of complex legal
proceedings, such as these purported class actions, are
difficult to predict. Each complaint seeks unspecified damages
and, therefore, we are unable to estimate the possible range of
damages that we might incur should any of these lawsuits be
resolved against us. An unfavorable outcome or settlement of
these lawsuits could harm our financial position. In addition,
similar class action lawsuits may be filed against us and our
executive officers and directors in the future. Litigation can
be costly, time consuming and disruptive to normal business
operations. The defense of these lawsuits could also result in
diversion of our managements time and attention away from
business operations, which could harm our business.
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We incurred significant additional indebtedness when we
sold the notes and we may incur additional indebtedness in the
future. Our existing indebtedness and any future indebtedness we
incur exposes us to risks that could adversely affect our
business, operating results and financial condition. |
As of March 31, 2005, we had $300 million of total
indebtedness outstanding. This includes the $200 million of
additional indebtedness we incurred on January 12, 2005
when we sold the notes. We may also incur additional long-term
indebtedness or obtain additional working capital lines of
credit to meet future financing needs. Our indebtedness could
have significant negative consequences for our business,
operating results and financial condition, including:
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increasing our vulnerability to adverse economic and industry
conditions; |
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limiting our ability to obtain additional financing; |
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requiring the dedication of a substantial portion of our cash
flow from operations to service our indebtedness, thereby
reducing the amount of our cash flow available for other
purposes; |
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limiting our flexibility in planning for, or reacting to,
changes in our business; and |
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placing us at a possible competitive disadvantage with less
leveraged competitors and competitors that may have better
access to capital resources. |
If we do not achieve a significant increase in revenues, we
could have difficulty making required payments on the notes, our
other existing indebtedness and any indebtedness that we may
incur in the future. During each of the last five years, we had
no earnings to cover our fixed charges. If we are unable to
generate sufficient cash flow or otherwise obtain funds
necessary to make required payments, or if we fail to comply
with the various requirements of the notes, our other existing
indebtedness or any indebtedness which we may incur in the
future, we would be in default, which would permit the holders
of the notes and such other indebtedness to accelerate the
maturity of the notes and such other indebtedness and could
cause defaults under the notes and such other indebtedness. Any
default under the notes, our other existing indebtedness or any
indebtedness which we may incur in the future could have a
material adverse effect on our business, operating results and
financial condition.
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Future sales or the possibility of future sales of a
substantial amount of our common stock may depress our stock
price. |
We are not restricted from issuing additional common stock
during the life of the notes. Our issuance of substantial
amounts of common stock, or the perception that we may issue
substantial amounts of common stock, may adversely affect the
price of our common stock and, in turn, the price of the notes.
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Conversion of the notes will dilute the ownership interest
of existing shareholders and could adversely affect the market
price of our common stock. |
The conversion of some or all of the notes or our
41/2% convertible
notes due 2008 will dilute the ownership interests of existing
shareholders. Any sales in the public market of the common stock
issuable upon such conversion could adversely affect prevailing
market prices of our common stock. In addition, the existence of
our convertible notes may encourage short selling by market
participants because the conversion of such notes could depress
the price of our common stock.
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The make whole payment payable upon the occurrence of a
designated event that is also a fundamental change may not
adequately compensate you for the lost option time value of your
notes as a result of such fundamental change and may not be
enforceable. |
If a fundamental change occurs at any time prior to the maturity
of the notes, we may under some circumstances increase the
conversion rate for notes converted in connection with the
designated event. The amount of such increase to the conversion
rate, if any, will be based on the average of the reported last
sale prices of our common stock over the five trading day period
ending on the trading day immediately preceding the effective
date of the transaction constituting the triggering transaction.
A description of how the make
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whole payment will be determined is described below under
Description of Notes Conversion of
Notes Make Whole Payment Upon the Occurrence of a
Designated Event that is also a Fundamental Change. While
the make whole amount is designed to compensate you for the lost
option time value of your notes as a result of a fundamental
change, the make whole amount is only an approximation of such
lost value and may not adequately compensate you for such loss.
In addition, if a fundamental change occurs after maturity of
the notes, or if the price paid per share of our common stock in
the transaction constituting the fundamental change is less than
$19.20 or greater than $115.00, there will be no such make whole
amount. Furthermore, our obligation to pay the make whole amount
could be considered a penalty, in which case the enforceability
of such obligation would be subject to general principles of
reasonableness of economic remedies.
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The conversion rate of the notes may not be adjusted for
all dilutive events. |
The conversion rate of the notes is subject to adjustment for
some events including, but not limited to, the issuance of stock
dividends on our common shares, the issuance of some rights or
warrants, subdivisions or combinations of our common shares,
some distributions of assets, debt securities, capital stock or
cash to holders of our common shares and some issuer tender or
exchange offers as described under Description of
Notes Conversion of Notes. The conversion rate
will not be adjusted for other events, such as an issuance of
common shares for cash, that may adversely affect the trading
price of the notes or the common shares. An event may occur that
adversely affects the value of the notes, but does not result in
an adjustment to the conversion rate.
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You may have to pay taxes with respect to distributions on
our common stock that you do not receive. |
The conversion rate of the notes is subject to adjustment for
some events arising from stock splits and combinations, stock
dividends, some cash dividends and some other actions by us that
modify our capital structure. See Description of
Notes Conversion of Notes. If the conversion
rate is adjusted as a result of a distribution that is taxable
to our common stockholders, such as a cash dividend, you would
be required to include an amount in income for U.S. federal
income tax purposes, notwithstanding the fact that you do not
actually receive such distribution. The amount that you would
have to include in income will generally equal the amount of the
distribution that you would have received if you had converted
your notes into our common stock. In addition,
non-U.S. holders of the notes may, in some circumstances,
be deemed to have received a distribution subject to
U.S. federal withholding tax requirements. See generally
Material U.S. Federal Income Tax Considerations.
If a fundamental change occurs on or prior to the maturity date
of the notes, under some circumstances, we will increase the
conversion rate for notes converted in connection with the
fundamental change. The receipt of additional shares in
connection with such increase may be treated as a distribution
subject to U.S. federal income tax as a dividend. See
Material U.S. Federal Income Tax
Considerations Tax Consequences to United States
Holders Possible Effect of Liquidated Damages or the
Make Whole Payment.
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If you hold notes, you will not be entitled to any rights
with respect to our common stock, but you will be subject to all
changes made with respect to our common stock. |
If you hold notes, you will not be entitled to any rights with
respect to our common stock, including voting rights and rights
to receive any dividends or other distributions on our common
stock, but you will be subject to all changes affecting the
common stock. You will have rights with respect to our common
stock only if and when we deliver shares of common stock to you
upon conversion of your notes and, to a limited extent, under
the conversion rate adjustments applicable to the notes. In the
event that an amendment is proposed to our articles of
incorporation or bylaws requiring shareholder approval and the
record date for determining the shareholders of record entitled
to vote on the amendment occurs prior to delivery of common
stock to you, you will not be entitled to vote on the amendment,
although you will nevertheless be subject to any changes in the
powers, preferences or special rights of our common stock.
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Our shareholder rights plan and anti-takeover provisions
in our charter documents may make an acquisition of us, which
may benefit our shareholders, more difficult. |
Our shareholder rights plan and provisions of our articles of
incorporation and bylaws could make it more difficult for a
third party to acquire us. These documents include provisions
that:
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allow our shareholders the right to acquire common stock from us
at discounted prices in the event a person acquires 15% or more
of our common stock or announces an attempt to do so without our
board of directors prior consent; |
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authorize the issuance of blank check preferred
stock by our board of directors without shareholder approval,
which would increase the number of outstanding shares and could
thwart a takeover attempt; |
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limit who may call a special meeting of shareholders; |
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require shareholder action without a meeting by unanimous
written consent; |
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establish advance notice requirements for nominations for
election to the board of directors or for proposing matters that
can be acted upon at shareholder meetings; |
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establish a staggered board of directors whose members can only
be dismissed for cause; |
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adopt the fair price requirements and rules regarding business
combinations with interested shareholders set forth in
Article 11, Parts 2 and 3 of the Georgia Business
Corporation Code; and |
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require approval by the holders of at least 75% of the
outstanding common stock to amend any of the foregoing
provisions. |
SPECIAL NOTE REGARDING FORWARD-LOOKING STATEMENTS
This prospectus and the documents we incorporate by reference in
this prospectus contain forward-looking statements within the
meaning of the Private Securities Litigation Reform Act of 1995
concerning our business, operations and financial condition,
including statements with respect to the expected timing of
completion of trials of our drugs under development, the safety,
efficacy and potential benefits of our product candidates under
development, expectations with respect to collaborations for
product candidates, expectations with respect to development and
commercialization of our product candidates, the timing and
success of the submission, acceptance and approval of regulatory
filings, the scope of patent protection with respect to these
product candidates and our products and information with respect
to the other plans and strategies for our business and the
business of our subsidiaries. All statements other than
statements of historical facts included or incorporated by
reference in this prospectus regarding our strategy, future
operations, timetables for product testing, regulatory approvals
and commercializations, financial position, costs, prospects,
plans and objectives of management are forward-looking
statements. We may use words such as expect,
anticipate, intend, plan,
believe, seek, estimate, and
similar expressions or the negative of such expressions that
convey uncertainty of future events or outcomes to identify
forward-looking statements, although not all forward-looking
statements contain these identifying words. Because these
forward-looking statements involve risks and uncertainties,
actual results could differ materially from those expressed or
implied by these forward-looking statements for a number of
important reasons, including those discussed under Risk
Factors and elsewhere in this prospectus.
You should read these forward-looking statements carefully
because they discuss our expectations about our future
performance, contain projections of our future operating results
or our future financial condition, or state other
forward-looking information. You should be aware
that the occurrence of any of the events described under
Risk Factors and elsewhere in this prospectus could
substantially harm our business, results of operations and
financial condition and that upon the occurrence of any of these
events, the trading price of our common stock could decline.
We cannot guarantee any future results, levels of activity,
performance or achievements. The forward-looking statements
contained in this prospectus represent our expectations as of
the date of this prospectus and
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should not be relied upon as representing our expectations as of
any other date. Subsequent events and developments will cause
our expectations to change. However, while we may elect to
update these forward-looking statements, we specifically
disclaim any obligation to do so, even if our expectations
change.
USE OF PROCEEDS
All of the notes and the shares of our common stock issuable
upon conversion of the notes are being sold by the selling
securityholders or by their pledgees, donees, transferees or
other successors in interest. We will not receive any proceeds
from the sale of the notes or the shares of our common stock
issuable upon conversion of the notes.
DESCRIPTION OF NOTES
We issued the notes under an indenture dated as of
January 12, 2005, between AtheroGenics, as issuer, and The
Bank of New York Trust Company, N.A., as trustee. We are
required under the terms of the registration rights agreement
between us and the initial purchasers to register the resale of
the notes and the shares of common stock issuable upon
conversion of the notes on a registration statement. Copies of
the indenture and the registration rights agreement are filed as
exhibits to the registration statement of which this prospectus
forms a part. You may also request a copy of the indenture and
the registration rights agreement from the trustee.
The following description is a summary of the material
provisions of the notes, the indenture and the registration
rights agreement. It does not purport to be complete. This
summary is subject to and is qualified by reference to all the
provisions of the indenture, including the definitions of some
terms used in the indenture, and to all provisions of the
registration rights agreement. Wherever particular provisions or
defined terms of the indenture or form of note are referred to,
these provisions or defined terms are incorporated in this
prospectus and any prospectus supplement by reference. We urge
you to read the indenture because it and not this description
defines your rights as a holder of notes.
General
The notes are general unsecured obligations of AtheroGenics and
rank junior to any secured debt that we may incur to the extent
of any assets securing such indebtedness, on a parity with our
41/2% convertible
notes due 2008 and any future senior unsecured debt and prior to
all subordinated debt. The notes are structurally subordinated
to all liabilities of our subsidiaries. The notes are
convertible into common stock as described under
Conversion of Notes.
The notes are limited to $200,000,000 aggregate principal
amount. The notes are issued only in denominations of $1,000 and
multiples of $1,000. The notes will mature on February 1,
2012 unless earlier converted or redeemed.
We may, without the consent of the holders, reopen
the notes and issue additional notes under the indenture with
the same terms and with the same CUSIP numbers as the notes in
an unlimited aggregate principal amount, provided that no such
additional notes may be issued unless fungible with the notes
offered hereby for U.S. federal income tax purposes. We may
also from time to time repurchase the notes in open market
purchases or negotiated transactions without prior notice to
holders.
We are not subject to any financial covenants under the
indenture. In addition, we are not restricted under the
indenture from paying dividends, incurring debt or issuing or
repurchasing our securities.
You are not afforded protection under the indenture in the event
of a highly leveraged transaction or a change in control of us
except to the extent described below under
Redemption at Option of the Holder.
The notes bear interest at a rate of 1.50% per annum.
Interest is calculated on the basis of a 360-day year consisting
of twelve 30-day months and accrues from January 12, 2005
or from the most recent date to which interest has been paid or
duly provided for. We will pay interest on February 1 and
August 1 of each year,
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beginning August 1, 2005, to record holders at the close of
business on the preceding January 15 and July 15, as the
case may be, except interest payable upon redemption upon a
designated event will be paid to the person to whom principal is
payable. Payment of cash interest on the notes will include
interest accrued through the day before the applicable interest
payment date or redemption date, as the case may be.
We maintain an office in the Borough of Manhattan, The City of
New York, where we will pay the principal and premium, if any,
on the notes and you may present the notes for conversion,
registration of transfer or exchange for other denominations,
which is initially an office or agency of the trustee. We may
pay interest by check mailed to your address as it appears in
the note register, provided that if you are a holder with an
aggregate principal amount in excess of $2.0 million, you
shall be paid, at your written election, by wire transfer in
immediately available funds.
However, payments to The Depository Trust Company, New York, New
York, which we refer to as DTC, will be made by wire transfer of
immediately available funds to the account of DTC or its nominee.
Conversion of Notes
You may convert any of your notes, in whole or in part, into
common stock prior to the close of business on the final
maturity date of the notes, subject to prior redemption of the
notes.
The number of shares of common stock you will receive upon
conversion of your notes will be determined by multiplying the
number of $1,000 principal amount notes you convert by the
conversion rate on the date of conversion. The initial
conversion rate for the notes is 38.5802 shares of common
stock per $1,000 principal amount of notes, subject to
adjustment as described below, which represents an initial
conversion price of approximately $25.92 per share. You may
convert your notes in part so long as such part is $1,000
principal amount or an integral multiple of $1,000.
If you have submitted your notes for redemption upon a
designated event, you may convert your notes only if you
withdraw your redemption notice. Upon conversion of notes, a
holder will not receive any cash payment of interest (unless
such conversion occurs between a regular record date and the
interest payment date to which it relates). We will not issue
fractional shares of common stock upon conversion of notes.
Instead, we will pay cash in lieu of fractional shares based on
the closing sale price of our common stock on the trading day
prior to the conversion date. Our delivery to the holder of the
full number of shares of our common stock into which the note is
convertible, together with any cash payment for such
holders fractional shares, will be deemed to satisfy our
obligation to pay:
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the principal amount of the note; and |
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accrued but unpaid interest attributable to the period from the
most recent interest payment date to the conversion date. |
As a result, accrued but unpaid interest to the conversion date
is deemed to be paid in full rather than cancelled, extinguished
or forfeited.
Notwithstanding the preceding paragraph, if notes are converted
after a record date but prior to the next succeeding interest
payment date, holders of such notes at the close of business on
the record date will receive the interest payable on such notes
on the corresponding interest payment date notwithstanding the
conversion. Such notes, upon surrender for conversion, must be
accompanied by funds equal to the amount of interest payable on
the notes so converted; provided that no such payment need be
made if (1) we have specified a redemption date following a
designated event that is after a record date but on or prior to
the next succeeding interest payment date or (2) to the
extent of any overdue interest at the time of conversion with
respect to such note.
To convert your note into common stock you must:
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complete and manually sign the conversion notice on the back of
the note or facsimile of the conversion notice and deliver this
notice to the conversion agent; |
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surrender the note to the conversion agent; |
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if required, furnish appropriate endorsements and transfer
documents; |
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if required, pay all transfer or similar taxes; and |
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if required, pay funds equal to interest payable on the next
interest payment date. |
The date you comply with these requirements is the conversion
date under the indenture. If you hold a beneficial interest in a
global note, to convert you must comply with the last three
requirements listed above and comply with DTCs procedures
for converting a beneficial interest in a global note.
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Conversion Rate Adjustments |
We will adjust the conversion rate if any of the following
events occurs:
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(1) we issue common stock as a dividend or distribution on
our common stock; |
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(2) we issue to all holders of common stock some rights or
warrants to purchase our common stock; |
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(3) we subdivide or combine our common stock; |
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(4) we distribute to all holders of our common stock shares
of our capital stock, evidences of indebtedness or assets,
including cash or securities but excluding: |
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rights or warrants specified above; and |
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dividends or distributions specified above. |
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If we distribute capital stock of, or similar equity interests
in, a subsidiary or other business unit of ours, the conversion
rate will be adjusted based on the market value of the
securities so distributed relative to the market value of our
common stock, in each case based on the average closing sale
prices of those securities for the 10 trading days commencing on
and including the fifth trading day after the date on which
ex-dividend trading commences for such distribution
on the NASDAQ National Market or such other national or regional
exchange or market on which the securities are then listed or
quoted. |
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If we distribute cash, then the conversion rate shall be
increased so that it equals the rate determined by multiplying
the conversion rate in effect on the record date with respect to
the cash distribution by a fraction, (a) the numerator of
which shall be the Current Market Price of a share of our common
stock on the record date, and (b) the denominator of which
shall be the same price of a share on the record date less the
amount of the distribution. Current Market Price
shall mean the average of the daily closing sale prices per
share of common stock for the ten consecutive trading days
ending on the earlier of the date of determination and the day
before the ex date with respect to the distribution
requiring such computation. For purpose of this paragraph, the
term ex date, when used with respect to any
distribution, means the first date on which the common stock
trades, regular way, on the relevant exchange or in the relevant
market from which the closing sale price was obtained without
the right to receive such distribution. |
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(5) we make a payment in respect of a tender offer or
exchange offer for our common stock to the extent that the cash
and value of any other consideration included in the payment per
share of common stock exceeds the closing sale price per share
of common stock on the trading day next succeeding the last date
on which tenders or exchanges may be made pursuant to such
tender or exchange offer; and |
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(6) someone, other than us or one of our subsidiaries,
makes a payment in respect of a tender offer or exchange offer
and, as of the closing date of the offer, our board of directors
is not recommending rejection of the offer. The adjustment
referred to in this clause (6) will only be made if: |
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the tender offer or exchange offer is for an amount that
increases the offerors ownership of common stock to more
than 25% of the total shares of common stock
outstanding; and |
23
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the cash and value of any other consideration included in the
payment per share of common stock exceeds the closing sale price
per share of common stock on the trading day next succeeding the
last date on which tenders or exchanges may be made pursuant to
the tender or exchange offer. |
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However, the adjustment referred to in this clause (6) will
generally not be made if as of the closing of the offer, the
offering documents disclose a plan or an intention to cause us
to engage in a consolidation or merger or a sale of all or
substantially all of our assets. |
To the extent that we have a rights plan in effect upon
conversion of the notes into common stock and the rights have
not separated from our common stock, you will receive, in
addition to the common stock, the rights under the rights plan.
If prior to any conversion, the rights have separated from the
common stock, the conversion rate will be adjusted at the time
of separation as if we distributed to all holders of our common
stock, shares of our capital stock, evidences of indebtedness or
assets as described in clause (4) above, subject to
readjustment in the event of the expiration, termination or
redemption of such rights.
In the event of:
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any reclassification of our common stock; |
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a consolidation, merger or combination involving us; or |
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a sale or conveyance to another person or entity of all or
substantially all of our property and assets; |
in which holders of our common stock would be entitled to
receive stock, other securities, other property, assets or cash
for their common stock, upon conversion of your notes you will
be entitled to receive the same type of consideration that you
would have been entitled to receive if you had converted the
notes into our common stock immediately prior to any of these
events.
You may in some situations be deemed to have received a
distribution subject to U.S. federal income tax as a
dividend in the event of any taxable distribution to holders of
common stock or in some other situations requiring a conversion
rate adjustment. See Material U.S. Federal Income Tax
Considerations Tax Consequences to United States
Holders Constructive Dividends.
We may, from time to time, increase the conversion rate if our
board of directors has made a determination that this increase
would be in our best interests. Any such determination by our
board will be conclusive. In addition, we may increase the
conversion rate if our board of directors deems it advisable to
avoid or diminish any income tax to holders of common stock
resulting from any stock or rights distribution. See
Material U.S. Federal Income Tax
Considerations Tax Consequences to United States
Holders Constructive Dividends.
We will not make any adjustment in the conversion rate unless
such adjustment would require a change of at least 1% in the
conversion rate in effect at such time. We will carry forward
any adjustments that are less than 1% of the conversion rate,
provided that we will make any carried forward adjustments
(a) on each anniversary of the first date of issue of the
notes, (b) five business days prior to the maturity of the
notes, whether at stated maturity or otherwise, and
(c) prior to the redemption date in connection with a
designated event. We will not make any adjustments if holders of
notes are permitted to participate in the transactions described
above in clauses (1) through (6) that would otherwise
require adjustment of the conversion rate. Except as described
above in this section, we will not adjust the conversion rate
for any issuance of our common stock or convertible or
exchangeable securities or rights to purchase our common stock
or convertible or exchangeable securities.
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Make Whole Payment Upon the Occurrence of a Designated
Event that is also a Fundamental Change |
If you elect to convert your notes upon the occurrence of a
designated event that is also a fundamental change that occurs
prior to the maturity date of the notes, subject to our rights
described below under Public Acquirer Change
of Control, in some circumstances, you will be entitled to
receive, in addition to a number of shares of common stock equal
to the applicable conversion rate, an additional number of
shares of common stock, which we refer to as the additional
shares, as described below.
24
The number of additional shares will be determined by reference
to the table below and is based on the date on which the
fundamental change becomes effective, which we refer to as the
effective date, and the average of the reported last sale prices
of our common stock over the five trading day period ending on
the trading day immediately preceding the effective date, which
we refer to as the stock price.
The stock prices set forth in the first row of the table below
will be adjusted as of any date on which the conversion rate of
the notes is adjusted. The adjusted stock prices will equal the
stock prices applicable immediately prior to such adjustment,
multiplied by a fraction, the numerator of which is the
conversion rate immediately prior to the adjustment giving rise
to the stock price adjustment and the denominator of which is
the conversion rate as so adjusted. The number of additional
shares will be adjusted in the same manner as the conversion
rate as set forth under Conversion of
Notes.
The following table sets forth the number of additional shares
per $1,000 principal amount of notes:
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Stock Price | |
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Effective Date |
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$19.20 | |
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$20.00 | |
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$22.00 | |
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$24.00 | |
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$26.00 | |
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$28.00 | |
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$30.00 | |
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$40.00 | |
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$50.00 | |
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$60.00 | |
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$70.00 | |
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$80.00 | |
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$90.00 | |
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$100.00 | |
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$115.00 | |
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January 12, 2005
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13.5 |
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12.6 |
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10.8 |
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9.3 |
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8.1 |
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7.2 |
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6.3 |
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3.8 |
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2.5 |
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1.7 |
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1.2 |
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0.9 |
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0.7 |
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0.6 |
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0.4 |
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February 1, 2006
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13.5 |
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12.6 |
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10.7 |
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9.2 |
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8.0 |
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7.0 |
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6.1 |
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3.5 |
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2.3 |
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1.5 |
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1.1 |
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0.8 |
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0.6 |
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0.5 |
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0.3 |
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February 1, 2007
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13.5 |
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12.7 |
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10.6 |
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9.1 |
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7.8 |
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6.7 |
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5.9 |
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3.3 |
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2.0 |
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1.4 |
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0.9 |
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0.7 |
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0.5 |
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0.4 |
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0.3 |
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February 1, 2008
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13.5 |
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12.7 |
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10.5 |
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8.9 |
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7.5 |
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6.4 |
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5.6 |
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2.9 |
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1.8 |
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1.1 |
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0.8 |
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0.5 |
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0.4 |
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0.3 |
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0.2 |
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February 1, 2009
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13.5 |
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12.6 |
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10.3 |
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8.5 |
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7.1 |
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6.0 |
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5.1 |
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2.5 |
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1.4 |
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0.9 |
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0.6 |
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0.4 |
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0.3 |
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0.2 |
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0.1 |
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February 1, 2010
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13.5 |
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12.4 |
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9.8 |
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7.9 |
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6.4 |
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5.3 |
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4.3 |
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1.9 |
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0.9 |
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0.5 |
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0.3 |
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0.2 |
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0.2 |
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0.1 |
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0.1 |
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February 1, 2011
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13.3 |
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11.8 |
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8.9 |
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6.7 |
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5.1 |
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3.9 |
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3.0 |
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0.9 |
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0.4 |
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0.2 |
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0.1 |
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0.1 |
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0.1 |
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0.0 |
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0.0 |
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February 1, 2012
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0.0 |
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0.0 |
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0.0 |
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0.0 |
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0.0 |
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0.0 |
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0.0 |
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0.0 |
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0.0 |
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0.0 |
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0.0 |
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0.0 |
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0.0 |
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0.0 |
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0.0 |
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The exact stock price and effective date may not be set forth on
the table, in which case:
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If the stock price is between two stock price amounts in the
table or the effective date is between two effective dates in
the table, the number of additional shares will be determined by
a straight-line interpolation between the number of additional
shares set forth for the higher and lower stock price amounts
and the two dates, as applicable, based on a 365-day year. |
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If the stock price is equal to or in excess of $115.00 per
share, subject to adjustment, we will not increase the
conversion rate by any additional shares. |
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If the stock price is less than $19.20 per share, subject
to adjustment, we will not increase the conversion rate by any
additional shares. |
Notwithstanding the foregoing, in no event will the total number
of shares issuable upon conversion of a note exceed
52.0833 per $1,000 principal amount of notes, subject to
adjustment in the same manner as the conversion rate as set
forth under Conversion of Notes.
The receipt of the make whole payment may be treated as a
distribution subject to U.S. federal income tax as a
dividend. See Material U.S. Federal Income Tax
Considerations Tax Consequences to United States
Holders Possible Effect of Liquidated Damages or the
Make Whole Payment.
Optional Redemption by AtheroGenics
We may not redeem the notes at our option in whole or in part
prior to maturity.
Redemption at Option of the Holder
If a designated event occurs at any time prior to the maturity
of the notes, you will have the right, subject to our rights
described below under Public Acquirer Change
of Control, to require us to redeem your notes, in whole
or in part, on a redemption date that is 30 days after the
date of our notice of the designated event. The notes will be
redeemable in multiples of $1,000 principal amount.
25
We will redeem the notes at a price equal to 100% of the
principal amount to be redeemed, plus accrued interest to, but
excluding, the redemption date.
We will mail to all record holders a notice of a designated
event within 10 days after it has occurred. We are also
required to deliver to the trustee a copy of the designated
event notice. If you elect to redeem your notes, you must
deliver to us or our designated agent, on or before the 30th day
after the date of our designated event notice, your redemption
notice. We will promptly pay the redemption price for notes
surrendered for redemption following the later of the redemption
date and the time of book-entry transfer or delivery of the
notes to be redeemed, duly endorsed for transfer. If the paying
agent holds money sufficient to pay the redemption price for any
note on the business day following the redemption date, then, on
and after such date, the notes will cease to be outstanding,
interest will cease to accrue and all other rights of the holder
will terminate, except the right to receive the redemption
price. This will be the case whether or not book-entry transfer
of the note has been made or the note has been delivered to the
paying agent.
You may withdraw any written redemption notice by delivering a
written notice of withdrawal to the paying agent prior to the
close of business on the redemption date. The withdrawal notice
must state:
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the principal amount of the withdrawn notes; |
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if certificated notes have been issued, the certificate numbers
of the withdrawn notes or, if your notes are not certificated,
your withdrawal notice must comply with appropriate DTC
procedures; and |
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the principal amount, if any, that remains subject to the
redemption notice. |
A designated event will be deemed to have occurred
upon a fundamental change or a termination of trading.
A fundamental change is any transaction or event,
whether by means of an exchange offer, liquidation, tender
offer, consolidation, merger, combination, reclassification,
recapitalization or otherwise, in connection with which 50% of
more of our common stock is exchanged for, converted into,
acquired for or constitutes solely the right to receive,
consideration which is not at least 90% common stock that:
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is listed on, or immediately after the transaction or event will
be listed on, a U.S. national securities exchange, or |
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is approved, or immediately after the transaction or event will
be approved, for quotation on the NASDAQ National Market or any
similar U.S. system of automated dissemination of
quotations of securities prices. |
A termination of trading will be deemed to have
occurred if our common stock, or other common stock into which
the notes are then convertible, is neither listed for trading on
a U.S. national securities exchange nor approved for
trading on the NASDAQ National Market.
We will comply with any applicable provisions of Rule 13e-4
and any other tender offer rules under the Exchange Act in the
event of a designated event.
These designated event redemption rights could discourage a
potential acquirer. However, this designated event redemption
feature is not the result of managements knowledge of any
specific effort to obtain control of us by means of a merger,
tender offer or solicitation, or part of a plan by management to
adopt a series of anti-takeover provisions. The term
fundamental change is limited to specified
transactions and may not include other events that might
adversely affect our financial condition or business operations.
Our obligation to offer to redeem the notes upon a designated
event would not necessarily afford you protection in the event
of a highly leveraged transaction, reorganization, merger or
similar transaction involving us.
We may be unable to redeem the notes in the event of a
designated event. If a designated event were to occur, we may
not have enough funds to pay the redemption price for all
tendered notes. Any future credit agreements or other agreements
relating to our indebtedness may contain provisions prohibiting
redemption of the notes under some circumstances, or expressly
prohibit our redemption of the notes upon a designated event or
may provide that a designated event constitutes an event of
default under that agreement. If a designated
26
event occurs at a time when we are prohibited from purchasing or
redeeming notes, we could seek the consent of our lenders to
redeem the notes or attempt to refinance this debt. If we do not
obtain consent, we would not be permitted to purchase or redeem
the notes. Our failure to redeem tendered notes would constitute
an event of default under the indenture, which might constitute
a default under the terms of our other indebtedness.
Public Acquirer Change of Control
In the case of a public acquirer change of control, as defined
below, we may, in lieu of permitting a redemption at the
holders option as described above under
Redemption at Option of Holder, or
adjusting the conversion rate as described above under
Conversion of Notes Make Whole
Payment Upon the Occurrence of a Designated Event that is also a
Fundamental Change, elect to adjust the conversion rate
and the related conversion obligation such that from and after
the effective date of such public acquirer change of control,
holders of the notes will be entitled to convert their notes
into shares of public acquirer common stock, as defined below.
In the event we make such election, the conversion rate will be
adjusted by multiplying the conversion rate in effect
immediately before the public acquirer change of control by a
fraction:
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the numerator of which will be (1) in the case of a merger,
consolidation or mandatory share exchange pursuant to which our
common stock is converted into cash, securities or other
property, the value of all cash and any other consideration, as
determined by our board of directors, paid or payable per share
of common stock or (2) in the case of any other public
acquirer change of control, the average of the reported last
sale prices of our common stock for the five consecutive trading
days prior to but excluding the effective date of such public
acquirer change of control, and |
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the denominator of which will be the average of the reported
last sale prices of the public acquirer common stock for the
five consecutive trading days prior to but excluding the
effective date of such public acquirer change of control. |
Within 10 trading days prior to but not including the expected
effective date of a fundamental change that is also a public
acquirer change of control, as defined below, we will provide to
all holders of the notes and the trustee and paying agent a
notification stating whether we will:
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elect to adjust the conversion rate and related conversion
obligation, in which case the holders will not have the right to
require us to redeem their notes as described above under
Redemption at Option of Holder and will
not have the right to the conversion rate adjustment described
above under Conversion of Notes
Make Whole Payment Upon the Occurrence of a Designated Event
that is also a Fundamental Change, or |
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not elect to adjust the conversion rate and related conversion
obligation, in which case the holders will have the right, if
applicable, to require us to redeem their notes as described
above under Redemption at Option of
Holder and the right, if applicable, to the conversion
rate adjustment described above under
Conversion of Notes Make Whole
Payment Upon the Occurrence of a Designated Event that is also a
Fundamental Change. |
A public acquirer change of control means any event
constituting a fundamental change that would otherwise give
holders the right to cause us to redeem the notes as described
above under Redemption at Option of the
Holder if the acquirer has a class of common stock traded
on a U.S. national securities exchange or quoted on the
NASDAQ National Market or which will be so traded or quoted when
issued or exchanged in connection with such fundamental change,
which we refer to as public acquirer common stock.
If an acquirer does not itself have a class of common stock
satisfying the foregoing requirement, it will be deemed to have
public acquirer common stock if either (1) a
direct or indirect majority-owned subsidiary of acquirer or
(2) a corporation that directly or indirectly owns at least
a majority of the acquirer, has a class of common stock
satisfying the foregoing requirement and the acquirer has
designated such common stock to serve as the public acquirer
common stock in the transaction. In such case, all references to
public acquirer common stock shall refer to such class of common
stock. Majority owned for these purposes means
having beneficial ownership, as defined in
Rule 13d-3 under the Exchange Act, of more than 50% of
27
the total voting power of all shares of the respective
entitys capital stock that are entitled to vote generally
in the election of directors.
Merger and Sale of Assets by AtheroGenics
The indenture provides that we may not consolidate with or merge
with or into any other person or convey, transfer or lease our
properties and assets substantially as an entirety to another
person, unless among other items:
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we are the surviving person, or the resulting, surviving or
transferee person, if other than us, is organized and existing
under the laws of the United States, any state of the United
States or the District of Columbia; |
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the successor person, if other than us, assumes all of our
obligations under the notes and the indenture; |
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after giving effect to such transaction, there is no event of
default, and no event that, after notice or passage of time or
both, would become an event of default; and |
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we have delivered to the trustee an officers certificate
and an opinion of counsel each stating that such consolidation,
merger, sale, conveyance, transfer or lease complies with these
requirements. |
When such a person assumes our obligations in such
circumstances, subject to some exceptions, we shall be
discharged from all obligations under the notes and the
indenture.
Events of Default; Notice and Waiver
The following will be events of default under the indenture:
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we fail to pay principal or premium, if any, when due at
maturity, upon redemption or otherwise on the notes; |
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we fail to pay any interest, including liquidated damages, if
any, on the notes, when due and such failure continues for a
period of 30 days; |
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we fail to provide notice of the occurrence of a designated
event on a timely basis; |
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we fail to perform or observe any of the covenants in the
indenture for 60 days after notice; |
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some events involving our bankruptcy, insolvency or
reorganization; or |
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default in the payment of principal when due at stated maturity
of other indebtedness or acceleration of such other indebtedness
for borrowed money where the aggregate principal amount with
respect to which the default or acceleration has occurred
exceeds $10 million, and such acceleration has not been
rescinded or annulled within a period of 30 days after
written notice as provided in the indenture. |
The trustee may withhold notice to the holders of the notes of
any default, except defaults in payment of principal, premium,
interest or liquidated damages, if any, on the notes. However,
the trustee must consider it to be in the interest of the
holders of the notes to withhold this notice.
If an event of default occurs and continues, the trustee or the
holders of at least 25% in principal amount of the outstanding
notes may declare the principal, premium, if any, and accrued
interest and liquidated damages, if any, on the outstanding
notes to be immediately due and payable. In case of some events
of bankruptcy or insolvency involving us, the principal,
premium, if any, and accrued interest and liquidated damages, if
any, on the notes will automatically become due and payable.
However, if we cure all defaults, except the nonpayment of
principal, premium, if any, interest or liquidated damages, if
any, that became due as a result of the acceleration, and meet
some other conditions, with some exceptions, this declaration
may be cancelled and the holders of a majority of the principal
amount of outstanding notes may waive these past defaults.
Payments of principal, premium, if any, or interest on the notes
that are not made when due will accrue interest at the annual
rate of 1% above the then applicable interest rate from the
required payment date.
28
The holders of a majority of outstanding notes will have the
right to direct the time, method and place of any proceedings
for any remedy available to the trustee, subject to limitations
specified in the indenture.
No holder of the notes may pursue any remedy under the
indenture, except in the case of a default in the payment of
principal, premium, if any, or interest on the notes, unless:
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the holder has given the trustee written notice of an event of
default; |
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the holders of at least 25% in principal amount of outstanding
notes make a written request, and offer reasonable indemnity, to
the trustee to pursue the remedy; |
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the trustee does not receive an inconsistent direction from the
holders of a majority in principal amount of the notes; |
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the holder or holders have offered reasonable security or
indemnity to the trustee against any costs, liability or expense
of the trustee; and |
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the trustee fails to comply with the request within 60 days
after receipt of the request and offer of indemnity. |
Modification and Waiver
The consent of the holders of a majority in principal amount of
the outstanding notes is required to modify or amend some
provisions of the indenture. However, a modification or
amendment requires the consent of the holder of each outstanding
note affected if it would:
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extend the fixed maturity of such note; |
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reduce the rate or extend the time for payment of interest,
including liquidated damages, if any, on such note; |
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reduce the principal amount or premium of such note; |
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reduce any amount payable upon redemption of such note; |
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adversely change our obligation to redeem such note upon a
designated event; |
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impair the right of a holder to institute suit for payment on
such note; |
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change the currency in which such note is payable; |
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impair the right of a holder to convert such note or reduce the
number of shares or the amount of any other property receivable
upon conversion; |
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reduce the quorum or voting requirements under the indenture; |
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change any obligation of ours to maintain an office or agency in
the places and for the purposes specified in the indenture; |
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subject to specified exceptions, modify some of the provisions
of the indenture relating to modification or waiver of
provisions of the indenture; or |
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reduce the percentage of notes required for consent to any
modification of the indenture. |
We are permitted to modify some provisions of the indenture
without the consent of the holders of the notes.
Form, Denomination and Registration
The notes are issued:
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in fully registered form; |
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without interest coupons; and |
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in denominations of $1,000 principal amount and multiples of
$1,000. |
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Global Note, Book-Entry Form |
The notes are evidenced by a global note. We have deposited the
global note with DTC and have registered the global note in the
name of Cede & Co. as DTCs nominee. Except as set
forth below, the global note may be transferred, in whole or in
part, only to another nominee of DTC or to a successor of DTC or
its nominee.
Beneficial interests in the global note may be held directly
through DTC if such holder is a participant in DTC, or
indirectly through organizations that are participants in DTC,
who we refer to as participants. Transfers between participants
will be effected in the ordinary way in accordance with DTC
rules and will be settled in clearing house funds. The laws of
some states require that some persons take physical delivery of
securities in definitive form. As a result, the ability to
transfer beneficial interests in the global note to such persons
may be limited.
Holders who are not participants may beneficially own interests
in a global note held by DTC only through participants, or some
banks, brokers, dealers, trust companies and other parties that
clear through or maintain a custodial relationship with a
participant, either directly or indirectly, who we refer to as
indirect participants. So long as Cede & Co., as the
nominee of DTC, is the registered owner of a global note,
Cede & Co. for all purposes will be considered the
sole holder of such global note. Except as provided below,
owners of beneficial interests in a global note will:
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not be entitled to have certificates registered in their names; |
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not receive physical delivery of certificates in definitive
registered form; and |
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not be considered holders of the global note. |
We will pay interest on and the redemption price of a global
note to Cede & Co., as the registered owner of the
global note, by wire transfer of immediately available funds on
each interest payment date or the redemption date, as the case
may be. Neither we, the trustee nor any paying agent will be
responsible or liable:
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for the records relating to, or payments made on account of,
beneficial ownership interests in a global note; or |
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for maintaining, supervising or reviewing any records relating
to the beneficial ownership interests. |
We have been informed that DTCs practice is to credit
participants accounts on that payment date with payments
in amounts proportionate to their respective beneficial
interests in the principal amount represented by a global note
as shown in the records of DTC, unless DTC has reason to believe
that it will not receive payment on that payment date. Payments
by participants to owners of beneficial interests in the
principal amount represented by a global note held through
participants will be the responsibility of the participants, as
is now the case with securities held for the accounts of
customers registered in street name.
Because DTC can only act on behalf of participants, who in turn
act on behalf of indirect participants, the ability of a person
having a beneficial interest in the principal amount represented
by the global note to pledge such interest to persons or
entities that do not participate in the DTC system, or otherwise
take actions in respect of such interest, may be affected by the
lack of a physical certificate evidencing its interest.
Neither we, the trustee, registrar, paying agent nor conversion
agent will have any responsibility for the performance by DTC or
its participants or indirect participants of their respective
obligations under the rules and procedures governing their
operations. DTC has advised us that it will take any action
permitted to be taken by a holder of notes, including the
presentation of notes for exchange, only at the direction of one
or more participants to whose account with DTC interests in the
global note are credited, and only in respect of the principal
amount of the notes represented by the global note as to which
the participant or participants has or have given such direction.
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DTC has advised us that it is:
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a limited purpose trust company organized under the laws of the
State of New York, and a member of the Federal Reserve System; |
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a clearing corporation within the meaning of the
Uniform Commercial Code; and |
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a clearing agency registered pursuant to the
provisions of Section 17A of the Exchange Act. |
DTC was created to hold securities for its participants and to
facilitate the clearance and settlement of securities
transactions between participants through electronic book-entry
changes to the accounts of its participants. Participants
include securities brokers, dealers, banks, trust companies and
clearing corporations and other organizations. Some of the
participants or their representatives, together with other
entities, own DTC. Indirect access to the DTC system is
available to others such as banks, brokers, dealers and trust
companies that clear through or maintain a custodial
relationship with a participant, either directly or indirectly.
DTC has agreed to the foregoing procedures to facilitate
transfers of interests in a global note among participants.
However, DTC is under no obligation to perform or continue to
perform these procedures, and may discontinue these procedures
at any time. If DTC is at any time unwilling or unable to
continue as depositary and a successor depositary is not
appointed by us within 90 days, we will issue notes in
certificated form in exchange for global notes.
Registration Rights of the Noteholders
We entered into a registration rights agreement with the initial
purchasers under which we agreed to file a shelf registration
statement, of which this prospectus forms a part, with the
Securities and Exchange Commission, covering resale of the
registrable securities by April 12, 2005. We also agreed to
use our reasonable best efforts to cause the shelf registration
statement to become effective by July 11, 2005 and to use
our reasonable best efforts to keep the shelf registration
statement effective until the earlier of:
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all of the registrable securities have been sold pursuant to the
shelf registration statement or pursuant to Rule 144 under
the Securities Act or any similar provision then in
force; or |
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the expiration of the holding period with respect to the
registrable securities under Rule 144(k) under the
Securities Act, or any successor provision. |
When we use the term registrable securities in this
section, we are referring to the notes and the common stock
issuable upon conversion of the notes until the earliest of:
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the effective registration under the Securities Act and the
resale of the registrable securities in accordance with the
registration statement; |
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the expiration of the holding period under Rule 144(k)
under the Securities Act; and |
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the sale of the registrable securities to the public pursuant to
Rule 144 under the Securities Act. |
We may suspend the use of the prospectus under some
circumstances relating to pending corporate developments, public
filings with the SEC and similar events. Any suspension period
shall not:
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exceed 30 days in any three-month period; or |
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an aggregate of 90 days for all periods in any 12-month
period. |
Notwithstanding the foregoing, we will be permitted to suspend
the use of the prospectus for up to 60 days in any 3-month
period under some circumstances, relating to possible
acquisitions, financings or other similar transactions.
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We will pay predetermined liquidated damages in the event the
shelf registration statement is not timely filed or made
effective as described above or if the prospectus included in
the registration statement is unavailable for periods in excess
of those permitted above:
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on the notes at an annual rate equal to 0.25% of the aggregate
principal amount of the notes outstanding until the registration
statement is filed or made effective or during the additional
period the prospectus is unavailable for the first 90 days
after the occurrence of the event and 0.50% thereafter; and |
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on the common stock that has been converted, at an annual rate
equal to 0.25% of an amount equal to $1,000 divided by the
conversion rate during such periods for the first 90 days
after the occurrence of the event and 0.50% thereafter. |
We will pay such liquidated damages semiannually in arrears,
with the first semiannual payment due on the first February 1 or
August 1 to occur after the date on which such liquidated
damages begin to accrue. The record dates for the payment of
liquidated damages will be the January 15 or July 15 preceding a
liquidated damages payment date, as applicable.
A holder who elects to sell registrable securities pursuant to
the shelf registration statement will be required to:
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be named as a selling stockholder in the related prospectus; |
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deliver a prospectus to purchasers; and |
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be subject to the provisions of the registration rights
agreement, including indemnification provisions. |
Rule 144A Information Request
We will furnish to the holders or beneficial holders of the
notes or the underlying common stock and prospective purchasers,
upon their request, the information required under
Rule 144A(d)(4) under the Securities Act until such time as
such securities are no longer restricted securities
within the meaning of Rule 144 under the Securities Act,
assuming these securities have not been owned by an affiliate of
ours.
Information Concerning the Trustee
We have appointed The Bank of New York Trust Company, N.A., the
trustee under the indenture, as paying agent, conversion agent,
note registrar and custodian for the notes. The trustee or its
affiliates may provide banking and other services to us in the
ordinary course of their business.
The indenture contains limitations on the rights of the trustee,
if it or any of its affiliates is then our creditor, to obtain
payment of claims in some cases or to realize on some property
received on any claim as security or otherwise. The trustee and
its affiliates will be permitted to engage in other transactions
with us. However, if the trustee or any affiliate continues to
have any conflicting interest and a default occurs with respect
to the notes, the trustee must eliminate such conflict or resign.
Governing Law
The notes and the indenture are governed by, and shall be
construed in accordance with, the laws of the State of New York.
DESCRIPTION OF CAPITAL STOCK
Our authorized capital stock consists of 100 million shares
of common stock, no par value, and five million shares of
preferred stock, no par value. As of June 10, 2005, there
were 37,750,649 shares of common stock outstanding and no
shares of preferred stock outstanding. The description set forth
below provides a summary of our capital stock and describes some
of the provisions of our articles of incorporation and bylaws,
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in addition to provisions of other agreements with our
shareholders. The following summary is qualified in its entirety
by reference to our articles of incorporation, bylaws and such
other agreements with shareholders.
Common Stock
Holders of our common stock have unlimited voting rights. Each
shareholder is entitled to one vote for each share on all
matters to be voted upon by the shareholders. There are no
cumulative voting rights and no preemptive or conversion rights.
There are no redemption or sinking fund provisions available to
the common stock. Holders of our common stock are entitled to
receive dividends share for share on a pro rata basis as may be
declared by the board of directors out of funds legally
available therefore. In the event of our liquidation,
dissolution or winding up, holders of common stock will be
entitled to share ratably in all assets remaining after payment
of our liabilities.
Preferred Stock
Our board of directors is authorized, subject to any limitations
prescribed by law, without shareholder approval, to issue from
time to time up to an aggregate of five million shares of
preferred stock, in one or more series, each series to have such
rights and preferences, including voting rights, dividend
rights, conversion rights, redemption privileges and liquidation
preferences as shall be determined by the board of directors.
The rights of the holders of common stock will be subject to,
and may be adversely affected by, the rights of holders of any
preferred stock that may be issued in the future. Issuance of
preferred stock, while providing desirable flexibility in
connection with possible acquisitions and other corporate
purposes, could have the effect of making it more difficult for
a third party to acquire, or of discouraging a third party from
attempting to acquire, a majority of our outstanding voting
stock. We have no present plans to issue any shares of preferred
stock.
Convertible Notes
On August 19, 2003, we issued $100,000,000 of
41/2% convertible
notes due 2008. The
41/2% convertible
notes are convertible into shares of common stock, at the option
of the holder, at a conversion rate of 65.189 shares per
$1,000 principal amount of notes, which represents a conversion
price of approximately $15.34, subject to adjustment, before the
close of business on September 1, 2008. Interest on the
41/2% convertible
notes is payable semi-annually in arrears on March 1 and
September 1. The
41/2% convertible
notes will mature on September 1, 2008. Each holder of the
41/2% convertible
notes has the right to require us to redeem all or part of the
41/2% convertible
notes held by it at a price equal to 100% of the principal
amount, plus accrued but unpaid interest and liquidated damages,
if any, upon the occurrence of a fundamental change or
termination of trading prior to the maturity date. A fundamental
change means, generally, the occurrence of any transaction or
event in connection with which all or substantially all of our
common stock shall be exchanged for, be converted into, be
acquired for, or constitute, in all material respects, solely
the right to receive consideration that is not all or
substantially all common stock listed on a United States
national securities exchange or approved for quotation on the
NASDAQ National Market or a similar United States system of
automated dissemination of quotations of securities prices. A
termination of trading will be deemed to have occurred if our
common stock is neither listed for trading on a United States
national securities exchange nor approved for trading on the
NASDAQ National Market. As of March 31, 2005, $100,000,000
of the
41/2% convertible
notes were outstanding.
On January 12, 2005, we issued $200,000,000 of
1.50% convertible notes due 2012. See Description of
Notes.
Shareholder Rights Agreement
On November 9, 2001, our board of directors adopted a
Shareholder Rights Plan declaring a dividend distribution of one
common stock purchase right on each outstanding share of our
common stock. Until the rights become exercisable, the rights
will trade automatically with our common stock and separate
rights certificates will not be issued. Under the rights plan,
each right consists of an initial right and subsequent
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rights. Initial rights will be exercisable only if a person or
group acquires 15% or more of our common stock, whether through
open market or private purchases or consummation of a tender or
exchange offer. Any shareholders who owned, as of
November 9, 2001, in excess of 17% of our common stock will
be permitted to acquire up to an aggregate of 20% of our
outstanding common stock without triggering the rights plan. If,
following the exercise of initial rights, a person or group
again acquires 15% or more of our common stock, or a person or
group who had previously acquired 15% or more of our common
stock acquires an additional 10% or more of the common stock,
the subsequent rights become exercisable. Each right will
initially entitle shareholders to buy eight shares of common
stock at an exercise price equal to 20% of the then current
market value of our common stock, calculated and adjusted
according to the terms of the rights plan. The number of shares
that can be purchased upon exercise will increase as the number
of shares held by the bidder increases. If we are acquired in a
merger or other business combination, each right will entitle
its holder to purchase, at the rights then-current
exercise price, a number of the acquiring companys shares
equal in value to those obtainable if the rights were
exercisable for our stock.
The rights are intended to enable all shareholders to realize
the long-term value of their investment in AtheroGenics. They
may prevent a takeover. They are intended to encourage anyone
seeking to acquire us to negotiate with our board prior to
attempting a takeover. Our board of directors may redeem any
nonexercisable rights at any time at the boards option at
a redemption price of $.0001 per right. The rights plan
expires at the close of business on November 8, 2011.
Effects of Certain Provisions of Our Articles of
Incorporation, Bylaws and Georgia Law
Classified Board and Removal of Directors. Our articles
of incorporation provide for our board of directors to be
elected initially to staggered one, two and three year terms
and, thereafter, for three year terms. In addition, members of
our board of directors may only be removed for cause. The
classification of directors, together with the limitation on the
removal of directors, has the effect of making it more difficult
for shareholders to change the composition of our board of
directors.
Shareholder Action; Special Meeting of Shareholders. Our
shareholders may not take action, outside of a duly called
annual or special meeting, by less than unanimous consent. Our
bylaws further provide that special meetings of our shareholders
may be called only upon the request of the holders of not less
than 75% of the shares then outstanding and entitled to vote.
Advance Notice Requirements for Shareholder Proposals and
Director Nominations. Our bylaws provide that any
shareholder proposals must be provided to us in writing at least
120 days before the date of our previous years proxy
statement, as provided in Rule 14a-8 under the Exchange
Act. Director nominations must be provided to us in writing
within the time period specified under Rule 14a-8 for an
annual meeting of shareholders or, in the case of a special
meeting of shareholders, at least 60 days prior to such
meeting or the tenth day following the day on which public
announcement is made of the date of the meeting. Our bylaws also
specify requirements as to form and content of a
shareholders notice. Such provisions may preclude
shareholders from bringing matters before the shareholders at an
annual or special meeting.
Anti-takeover Provisions and Georgia Law. The Georgia
Business Corporation Code, or Georgia Code, generally restricts
a corporation from entering into some business combinations with
an interested shareholder, which is defined as any person or
entity that is the beneficial owner of at least 10% of a
companys voting stock, or its affiliates, for a period of
five years after the date on which the shareholder became an
interested shareholder, unless:
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the transaction is approved by the board of directors of the
corporation prior to the date the person became an interested
shareholder; |
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the interested shareholder acquires 90% of the
corporations voting stock in the same transaction in which
it exceeds 10%; or |
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subsequent to becoming an interested shareholder, the
shareholder acquires 90% of the corporations voting stock
and the business combination is approved by the holders of a
majority of the voting stock entitled to vote on the transaction. |
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The fair price provisions of the Georgia Code further restrict
business combination transactions with 10% shareholders.
These provisions require that the consideration paid for stock
acquired in the business combination must meet specified tests
that are designed to ensure that shareholders receive at least
fair market value for their shares in the business combination.
The interested shareholder and fair price provisions of the
Georgia Code do not apply to a corporation unless the bylaws of
the corporation specifically provide that these provisions are
applicable to the corporation. We have elected to be covered by
these provisions in our bylaws, provided, however, that,
notwithstanding anything to the contrary in the provisions, the
provisions shall not apply to any business combination with
(1) any shareholder who was an interested shareholder as of
the date we adopted our bylaws or (2) any person or entity
that is at the time of that business combination wholly owned by
such interested shareholder.
Supermajority Vote Required to Amend Governing Documents.
The Georgia Code provides generally that the affirmative vote of
a majority of the shares entitled to vote on any matter is
required to amend a corporations articles of incorporation
or bylaws, unless a corporations articles of incorporation
or bylaws, as the case may be, requires a greater percentage.
Our articles of incorporation and our bylaws require the
affirmative vote of the holders of at least 75% of our
outstanding voting stock to amend or repeal any of the
provisions described above in Classified Board
and Removal of Directors, Shareholder
Action; Special Meeting of Shareholders and
Anti-takeover Provisions and Georgia
Law. Such 75% shareholder vote would be in addition to any
separate class vote that might in the future be required
pursuant to the terms of any preferred stock that might be
outstanding at the time any such changes are submitted to
shareholders.
Transfer Agent and Registrar
The transfer agent and registrar for our common stock is
American Stock Transfer & Trust Company. It is located
at 59 Maiden Lane, New York, NY 10038, and its telephone number
is (718) 921-8200.
MATERIAL U.S. FEDERAL INCOME TAX CONSIDERATIONS
The following discussion describes the material
U.S. federal income tax consequences of the purchase,
ownership and disposition of the notes and of our common stock
into which the notes may be converted. This discussion assumes
that the notes and common stock received upon the conversion of
the notes cannot be integrated with any other financial
instrument.
This summary is based on the Internal Revenue Code,
administrative pronouncements, judicial decisions and final,
temporary and proposed Treasury regulations, changes to any of
which subsequent to the date of this prospectus may affect the
tax consequences described in this prospectus, possibly with
retroactive effect. Holders are urged to consult their tax
advisers with regard to the application of the U.S. federal
income tax laws to their particular situations as well as any
tax consequences arising under the laws of any state, local or
foreign taxing jurisdiction.
This discussion applies only to holders that hold the notes and
our common stock as capital assets within the meaning of
Section 1221 of the Code, which generally is property held
for investment purposes.
This discussion does not describe all of the tax consequences
that may be relevant to a holder in light of its particular
circumstances or to holders subject to special rules, such as:
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some financial institutions; |
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insurance companies; |
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dealers and some traders in securities; |
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persons holding the notes or our common stock as part of a
straddle, hedge, conversion,
constructive sale, or similar transaction; |
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United States Holders, as defined below, whose functional
currency is not the U.S. dollar; |
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some former citizens or residents of the United States; |
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partnerships or other entities classified as partnerships for
U.S. federal income tax purposes; and |
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persons subject to the alternative minimum tax. |
Tax Consequences to United States Holders
As used in this prospectus, the term United States
Holder means a beneficial owner of a note or our common
stock that is for U.S. federal income tax purposes:
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a citizen or resident of the United States; |
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a corporation, or other entity taxable as a corporation for
U.S. federal income tax purposes, created or organized in
or under the laws of the United States or of any political
subdivision of the United States; |
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an estate the income of which is subject to U.S. federal
income taxation regardless of its source; or |
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a trust if (1) a court within the United States is able to
exercise primary supervision over the administration of the
trust and one or more U.S. persons have the authority to
control all substantial decisions of the trust, or (2) a
valid election is in place to treat the trust as a
U.S. person. |
As used in this discussion, the term Non-United States
Holder means a beneficial owner of a note or our common
stock that is not a United States Holder, and is further defined
below. Special rules apply to Non-United States Holders, as
discussed below in Tax Consequences to
Non-United States Holders.
Interest paid on the notes will be included in the income of a
United States Holder as ordinary income at the time it is
received or accrued, in accordance with the holders
regular method of tax accounting.
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Possible Effect of Liquidated Damages or the Make Whole
Payment |
If the amount or timing of any payments on a note is contingent,
the note could be subject to special rules that apply to
contingent payment debt instruments. These rules generally
require a United States Holder to accrue interest income at a
rate higher than the stated interest rate on the note and to
treat as ordinary income, rather than capital gain, any gain
recognized on a sale, exchange, repurchase or retirement of the
note before the resolution of the contingencies.
If the notes are not registered with the SEC within prescribed
time periods or in some other circumstances described above in
Description of Notes Registration Rights of
the Noteholders, holders will be entitled to liquidated
damages. Also, as described above in Description of
Notes Conversion of Notes Make Whole
Payment Upon the Occurrence of a Designated Event that is also a
Fundamental Change, holders could be entitled to receive
additional shares under some circumstances involving the
conversion of notes upon the occurrence of a designated event
that is a fundamental change. Notwithstanding the possibility of
such contingent payments, under applicable Treasury Regulations,
payments on a note that are subject to a remote or incidental
contingency may be ignored. We believe that the prospect of the
foregoing payments being made should be considered as a remote
or incidental contingency so that the payments should be ignored.
Therefore, for purposes of filing tax or information returns
with the Internal Revenue Service, we will not treat the notes
as contingent payment debt instruments. Our determination that
the notes are not contingent payment debt instruments is binding
on each holder unless the holder explicitly discloses in the
manner required by applicable Treasury Regulations that its
determination is different from ours. Our determination is not,
however, binding on the Internal Revenue Service. It is possible
that the Internal Revenue Service may make a different
determination, in which case the timing and amount of income
inclusions by a holder may be affected. This discussion assumes
that the notes are not subject to the contingent payment debt
instrument rules.
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A United States Holder that acquires a note, other than at
original issue, at a price less than the notes principal
amount may be affected by the market discount rules
of the Code. Subject to a de minimis exception, the
market discount rules generally require a United States Holder
who acquires a note at a market discount to treat any principal
payment on the note and any gain recognized on any disposition
of the note (or any appreciation in the note in the case of
certain nontaxable dispositions, such as gifts) as ordinary
income to the extent of the accrued market discount not
previously included in income at the time of such payment or
disposition. In general, the amount of market discount that has
accrued is determined on a straight-line basis over the
remaining term of the note as of the time of acquisition, or, at
the election of the holder, on a constant yield basis. Such an
election applies only to the note with respect to which it is
made and may not be revoked.
A United States Holder of a note acquired at a market discount
also may elect to include the market discount in income as it
accrues. If a United States Holder so elects, the rules
discussed above with respect to ordinary income recognition
resulting from the payment of principal on a note or the
disposition of a note would not apply, and the holders tax
basis in the note would be increased by the amount of the market
discount included in income at the time it accrues. This
election would apply to all market discount obligations acquired
by the United States Holder on or after the first day of the
first taxable year to which the election applies and may not be
revoked without the consent of the IRS.
A United States Holder may be required to defer until maturity
of the note (or, in certain circumstances, its earlier
disposition) the deduction of all or a portion of the interest
expense attributable to debt incurred or continued to purchase
or carry a note with market discount, unless the holder elects
to include market discount in income on a current basis.
Upon the conversion of a note into our common stock, any accrued
market discount on the note not included in income will be
carried over to the common stock received upon conversion of the
note, and any gain recognized upon the disposition of such
common stock will be treated as ordinary income to the extent of
such accrued market discount.
If a United States Holder purchases a note for an amount in
excess of all amounts payable on the note after the purchase
date, other than payments of qualified stated interest, the
excess will constitute bond premium. The bond premium on a note
will be the excess of the adjusted tax basis in the note upon
purchase over the notes principal amount.
A United States Holder generally may elect to amortize the bond
premium over the term of the note on a constant yield method.
The amount amortized in any year will be treated as a reduction
of interest income from the note for that year. If the
amortizable bond premium allocable to a year exceeds the amount
of interest allocable to that year, the excess would be allowed
as a deduction for that year but only to the extent of the
United States Holders prior interest inclusions with
respect to the note.
If a United States Holder does not elect to amortize bond
premium, the bond premium on a note will decrease the gain or
increase the loss that the holder otherwise recognizes on the
notes disposition. Any election to amortize bond premium
applies to all debt obligations, other than debt obligations the
interest on which is excludable from gross income, that a United
States Holder holds at the beginning of the first taxable year
to which the election applies or that the holder thereafter
acquires. A United States Holder may not revoke an election to
amortize bond premium without the consent of the IRS.
We urge holders to consult with their tax advisors regarding the
consequences of amortizable bond premium and any relevant
elections.
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Sale, Exchange, Repurchase or Retirement of Notes |
Upon a sale, exchange, repurchase or retirement of a note, other
than a conversion into our common stock, a United States Holder
will generally recognize taxable gain or loss equal to the
difference between the
37
amount realized on the sale, exchange, repurchase or retirement
and such United States Holders adjusted tax basis in the
note. A United States Holders adjusted tax basis in a note
will generally be equal to the holders purchase price for
the note, increased by the amount of any accrued but unpaid
interest and market discount previously included in the
holders taxable income.
Subject to the discussion above under Market
Discount, gain or loss recognized on the sale, exchange,
repurchase or retirement of a note, other than amounts
representing accrued but unpaid interest, generally will be
capital gain or loss and will be long-term capital gain or loss
if, at the time of the sale, exchange, repurchase or retirement,
the note has been held for more than one year. Any amounts
attributable to accrued interest, however, will be taxed as
interest income, as discussed above under
Taxation of Interest, to the extent the
holder has not previously included such amounts in the
holders taxable income. The deductibility of capital
losses is subject to limitations. A United States Holder who
sells the notes at a loss that meets certain thresholds may be
required to file a disclosure statement with the IRS.
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Conversion of Notes into Common Stock |
A United States Holders conversion of a note into our
common stock generally will not be a taxable event, except to
the extent the stock received is attributable to accrued
interest not previously included in income, in which case the
fair market value of such stock will be taxable as interest
income as discussed above under Taxation of
Interest, and except to the extent that cash is received
in lieu of a fractional share of our common stock in which case,
subject to the discussion above under Market
Discount, the holder will recognize capital gain or loss,
measured by the difference between the cash received in lieu of
the fractional share and the United States Holders tax
basis attributable to the fractional share.
A United States Holders tax basis in our common stock
received upon a conversion of a note, except for any stock
received attributable to accrued interest not previously
included in income, will be the same as the United States
Holders tax basis in the note at the time of the
conversion, reduced by any basis attributable to a fractional
share. The United States Holders holding period for the
common stock received, except for any stock received
attributable to accrued interest not previously included in
income, will include the holding period of the note converted.
A United States Holders tax basis in any stock received
attributable to accrued interest not previously included in
income will equal the fair market value of the stock at the time
of the conversion, and the United States Holders holding
period for such stock will begin on the day after the conversion.
We may adjust the conversion rate of the notes in some
circumstances, either at our discretion or pursuant to the terms
of the indenture. A change in conversion rate, including
potentially a change resulting from the make whole payment, as
described above in Description of Notes
Conversion of Notes Make Whole Payment Upon the
Occurrence of a Designated Event that is also a Fundamental
Change, which allows United States Holders of notes to
receive more shares of common stock on conversion unless we
elect to adjust the conversion rate and conversion obligation as
described above in Description of Notes Public
Acquirer Change of Control, in which case holders will not
have the right to the conversion rate adjustment of the make
whole payment, may increase those noteholders
proportionate interests in our earnings and profits or assets.
In that case, those noteholders will be treated as though they
received a dividend in the form of our stock. Any such
constructive stock dividend could be treated as a taxable
dividend to United States Holders. A taxable constructive stock
dividend would result to United States Holders of notes, for
example, if the conversion rate were adjusted to compensate
noteholders for distributions of cash or property to our
shareholders. Not all changes to the conversion rate that allow
noteholders to receive more stock on conversion, however, will
be treated as a taxable dividend to United States Holders. For
example, a change in conversion rate could simply prevent the
dilution of the noteholders interests upon a stock split
or other change in capital structure. Changes of this type, if
made under a bona fide, reasonable adjustment formula, are not
treated as taxable constructive stock dividends. On the other
hand, if an event occurs that dilutes the noteholders
interests and the conversion rate is not adjusted, the resulting
increase in the proportionate
38
interests of our shareholders could be treated as a taxable
stock dividend to the shareholders. Any taxable constructive
stock dividends resulting from a change to, or failure to
change, the conversion rate would be treated in the same manner
as dividends paid in cash or other property. Such dividends
would result in ordinary income to the recipient, to the extent
of our current or accumulated earnings and profits, with any
excess treated as a nontaxable return of capital or as capital
gain, even though the recipient did not actually receive cash,
common stock or other property.
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Taxation of Distributions on Common Stock |
Distributions, if any, paid on our common stock after a
conversion, other than some pro rata distributions of common
shares, will be treated as a dividend to the extent paid out of
current or accumulated earnings and profits, as determined under
U.S. federal income tax principles, and will be includible
in income by the United States Holder and taxable as ordinary
income when received or accrued, in accordance with such United
States Holders method of accounting. If a distribution
exceeds our current and accumulated earnings and profits, the
excess will be first treated as a tax-free return of the United
States Holders investment, up to the United States
Holders tax basis in the common stock. Any remaining
excess will be treated as capital gain. If the U.S. Holder
is a U.S. corporation, it generally would be able to claim
a deduction equal to a portion of any dividends received.
Dividends received by noncorporate United States Holders on
common stock may be subject to U.S. federal income tax at
lower rates than other types of ordinary income if certain
holding period requirements and other conditions are met. United
States Holders should consult their own tax advisers about their
particular circumstances.
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Sale or Other Disposition of Common Stock |
Unless a nonrecognition provision applies and subject to the
discussion above under Market Discount,
gain or loss realized by a United States Holder on the sale or
other disposition of our common stock received upon conversion
of a note will be recognized as capital gain or loss for
U.S. federal income tax purposes, and will be long-term
capital gain or loss if the United States Holders holding
period in the common stock is more than one year. The amount of
the United States Holders gain or loss will be equal to
the difference between the United States Holders tax basis
in the common stock disposed of and the amount realized on the
disposition. A United States Holder who sells the stock at a
loss that meets certain thresholds may be required to file a
disclosure statement with the IRS.
Tax Consequences to Non-United States Holders
As used in this prospectus, the term Non-United States
Holder means a beneficial owner of a note or our common
stock that is, for U.S. federal income tax purposes:
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an individual who is classified as a nonresident alien for
U.S. federal income tax purposes; |
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a foreign corporation; or |
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a foreign estate or trust the income of which is not subject to
U.S. federal income taxation regardless of its source. |
Subject to the discussion below regarding backup withholding in
Backup Withholding and Information
Reporting, interest income, including additional interest,
on the notes paid to a Non-United States Holder will be exempt
from U.S. federal income and withholding tax, provided that:
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the Non-United States Holder does not own, actually or
constructively, 10% or more of the total combined voting power
of all classes of our stock entitled to vote and is not a
controlled foreign corporation related, directly or indirectly,
to us through stock ownership and is not a bank receiving some
types of interest, |
39
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the certification requirement described below has been fulfilled
with respect to the Non-United States Holder, and |
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such interest is not effectively connected with the conduct by
such Non-United States Holder of a trade or business in the
United States. |
The certification requirement referred to above will be
fulfilled if the beneficial owner of a note certifies on IRS
Form W-8BEN, or an appropriate substitute form, under
penalties of perjury, that it is not a U.S. person and
provides its name and address.
Interest income, including additional interest, on the notes
that is not exempt from U.S. federal income and withholding
tax generally will be subject to U.S. withholding tax at a
30% rate, subject to reduction by an applicable treaty, unless
such income is effectively connected income as described below
in Effectively Connected Income.
Liquidated damages received by a Non-United States Holder if the
notes are not registered with the SEC within prescribed time
periods or in some other circumstances described above in
Description of Notes Registration Rights of
the Noteholders may not be exempt from
U.S. withholding tax as described above. Holders should
consult with their own tax advisers regarding such determination.
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Sale, Exchange or Other Disposition of Notes or Common
Stock |
Subject to the discussion below regarding backup withholding, a
Non-United States Holder generally will not be subject to
U.S. federal income and withholding tax on gain realized on
a sale, exchange or other disposition, other than a conversion
into our common stock, which is described below, of the notes or
of our common stock, unless:
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the gain is effectively connected with the conduct by such
Non-United States Holder of a trade or business in the United
States, |
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in the case of a Non-United States Holder who is a nonresident
alien individual, the individual is present in the United States
for 183 or more days in the taxable year of the sale, exchange
or disposition and some other conditions are met, |
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the Non-United States Holder is subject to Code provisions
applicable to some U.S. expatriates, or |
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we are or have been a U.S. real property holding
corporation for U.S. federal income tax purposes at any
time within the shorter of the five-year period preceding such
sale or other disposition, or the period such holder held the
notes or common stock; however, as long as our common stock is
regularly traded on an established securities market, only
Non-United States Holders who have held more than 5% of such
class of stock at any time during such five-year or shorter
period would be subject to taxation under this rule. We believe
that we are not, and do not anticipate becoming, a
U.S. real property holding corporation for
U.S. federal income tax purposes, although there can be no
assurance that we will not become such a corporation. |
Any gain realized on a sale, exchange or other disposition of
the notes taxed as interest income will be subject to the rules
described above regarding taxation of interest.
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Conversion of Notes into Common Stock |
Non-United States Holders generally will not be subject to
U.S. federal income and withholding tax on the conversion
of a note into shares of our common stock. However, any gain
recognized by a Non-United States Holder on the conversion of a
note into our common stock due to the receipt of cash in lieu of
a fractional share will be subject to the rules described above
regarding the sale, exchange or other disposition of a note, and
any amount of the stock taxable as interest income will be
subject to the rules described above regarding taxation of
interest.
40
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Distributions on Notes and Common Stock |
If a Non-United States Holder of a note were deemed to have
received a constructive dividend (see Tax
Consequences to United States Holders Constructive
Dividends above), the Non-United States Holder generally
will be subject to U.S. withholding tax at a 30% rate,
subject to reduction by an applicable treaty, on the taxable
amount of the dividend unless such income is effectively
connected income as described below in
Effectively Connected Income. In
addition, dividends paid to a Non-United States Holder of our
common stock generally will be subject to U.S. withholding
tax at a 30% rate, subject to reduction under an applicable
treaty, unless such income is effectively connected income as
described below in Effectively Connected
Income. In order to obtain a reduced rate of withholding,
a Non-United States Holder will be required to provide a
properly executed IRS Form W-8BEN, or an appropriate
substitute form, certifying its entitlement to benefits under a
treaty. A Non-United States Holder who is subject to withholding
tax under such circumstances should consult his own tax adviser
as to whether he can obtain a refund for all or a portion of the
withholding tax.
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Effectively Connected Income |
If a Non-United States Holder of a note or of our common stock
is engaged in a trade or business in the United States, and if
interest on the note, including additional interest, gain
realized on a sale, exchange or other disposition of the note or
of our common stock, or a dividend, including a constructive
dividend, on the note or on our common stock, is effectively
connected with the conduct of the trade or business, the
Non-United States Holder, although exempt from
U.S. withholding tax, will generally be taxed in the same
manner as a United States Holder (see Tax Consequences to
United States Holders above), except that the Non-United
States Holder will be required to provide a properly executed
IRS Form W-8ECI in order to claim an exemption from
withholding tax. If a Non-United States Holder is eligible for
the benefits of a tax treaty, any effectively connected income
or gain will generally be subject to U.S. federal income
tax only if it is also attributable to a permanent establishment
maintained by the holder in the United States. Non-United States
Holders with effectively connected income or gain should consult
their own tax advisers with respect to other tax consequences of
the ownership of the note or of our common stock, including the
possible imposition of a 30% branch profits tax.
United States Federal Estate Tax
A note held by an individual who at the time of death is not a
citizen or resident of the U.S., as specially defined for
U.S. federal estate tax purposes, will not be subject to
U.S. federal estate tax if the individual did not actually
or constructively own 10% or more of the total combined voting
power of all classes of our stock and, at the time of the
individuals death, payments with respect to such note
would not have been effectively connected with the conduct by
such individual of a trade or business in the U.S. Common
stock held by an individual who at the time of death is not a
citizen or resident of the U.S., as specially defined for
U.S. federal estate tax purposes, will be included in such
individuals estate for U.S. federal estate tax
purposes, unless an applicable U.S. estate tax treaty
otherwise applies.
Non-United States Holders should consult with their tax advisors
regarding U.S. federal, state, local and foreign tax
consequences with respect to the notes and common stock, subject
to a reduction under an applicable treaty.
Backup Withholding and Information Reporting
Information returns may be filed with the IRS in connection with
payments on the notes and the common stock and the proceeds from
a sale or other disposition of the notes or the common stock. A
United States Holder may be subject to United States backup
withholding tax on these payments if such holder fails to
provide its taxpayer identification number to the paying agent
and fails to comply with certification procedures or otherwise
establish an exemption from backup withholding. A Non-United
States Holder may be subject to United States backup withholding
tax on such payments unless the Non-United States Holder
complies with certification procedures to establish that such
holder is not a U.S. person. The amount of any backup
41
withholding from a payment will be allowed as a credit against
the holders U.S. federal income tax liability and may
entitle the holder to a refund, provided that the required
information is timely furnished to the IRS.
THE PRECEDING DISCUSSION OF MATERIAL UNITED STATES FEDERAL
TAX CONSIDERATIONS IS FOR GENERAL INFORMATION ONLY AND IS NOT
TAX ADVICE. ACCORDINGLY, EACH HOLDER SHOULD CONSULT ITS OWN TAX
ADVISOR AS TO THE PARTICULAR UNITED STATES FEDERAL, STATE, AND
LOCAL TAX CONSEQUENCES OF PURCHASING, HOLDING AND DISPOSING OF
THE NOTES AND COMMON STOCK. TAX ADVISORS SHOULD ALSO BE
CONSULTED AS TO THE UNITED STATES ESTATE AND GIFT TAX
CONSEQUENCES AND THE FOREIGN TAX CONSEQUENCES OF PURCHASING,
HOLDING AND DISPOSING OF THE NOTES AND COMMON STOCK, AS
WELL AS THE CONSEQUENCES OF ANY PROPOSED CHANGE IN APPLICABLE
LAWS.
SELLING SECURITYHOLDERS
We originally sold the notes to initial purchasers on
January 12, 2005. The initial purchasers of the notes have
advised us that the notes were resold in transactions exempt
from the registration requirements of the Securities Act to
qualified institutional buyers, as defined in
Rule 144A of the Securities Act. These subsequent
purchasers, or their transferees, pledgees, donees, assignees or
successors, may from time to time offer and sell any or all of
the notes and/or shares of the common stock issuable upon
conversion of the notes pursuant to this prospectus.
42
The following table sets forth information with respect to the
selling securityholders and the principal amount of notes and
common stock beneficially owned by each selling securityholder
that may be offered pursuant to this prospectus. The information
is based on information provided by or on behalf of the selling
securityholders. The selling securityholders may offer all, some
or none of the notes or the common stock issuable upon
conversion of the notes. Because the selling securityholders may
offer all or some portion of the notes or the common stock, we
cannot estimate the amount or percentage of the notes or the
common stock that will be held by the selling securityholders
upon termination of sales pursuant to this prospectus. In
addition, the selling securityholders identified below may have
sold, transferred or otherwise disposed of all or a portion of
their notes since the date on which they provided the
information regarding their holdings in transactions exempt from
the registration requirements of the Securities Act.
To our knowledge, no selling securityholder nor any of its
affiliates has held any position or office with, been employed
by or otherwise has had any material relationship with us or our
affiliates within the past three years.
The percentage of notes outstanding beneficially owned by each
selling securityholder is based on $200,000,000 aggregate
principal amount of notes outstanding. The number of shares of
common stock issuable upon conversion of the notes shown in the
table below assumes conversion of the full amount of notes held
by each selling securityholder at the initial conversion rate of
38.5802 shares of common stock per $1,000 principal amount
of notes.
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Principal | |
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|
Amount of | |
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|
Common | |
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|
Notes | |
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Common | |
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Stock Owned | |
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Beneficially | |
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Stock Owned | |
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After | |
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Owned and | |
|
Percentage | |
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Prior to the | |
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Completion of | |
|
|
Offered | |
|
of Notes | |
|
Offering | |
|
the Offering | |
Name |
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Hereby ($) | |
|
Outstanding | |
|
(1)(2) | |
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(2) | |
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| |
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| |
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| |
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Aristeia International Limited(3)
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9,190,000 |
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4.60 |
% |
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354,552 |
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Aristeia Trading LLC(4)
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1,810,000 |
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* |
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69,830 |
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BNP Paribas Equity Strategies, SNC(5)
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5,090,000 |
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2.55 |
% |
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202,226 |
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5,853 |
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CIBC World Markets
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500,000 |
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* |
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19,290 |
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CNH CA Master Account, L.P.(6)
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250,000 |
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* |
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368,185 |
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358,540 |
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CooperNeff Convertible Strategies (Cayman) Master Fund, LP(5)
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1,866,000 |
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* |
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71,991 |
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DKR Saturn Event Driven Holding Fund Ltd.(7)
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22,815,000 |
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11.41 |
% |
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931,707 |
(8) |
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51,500 |
(8) |
DKR Saturn Multi-Strategy Holding Fund Ltd.(9)
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22,815,000 |
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11.41 |
% |
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885,407 |
(10) |
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5,200 |
(10) |
DKR SoundShore Strategic Holding Fund Ltd.(11)
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6,000,000 |
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3.00 |
% |
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351,885 |
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120,404 |
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Drawbridge Convertible I Ltd.(12)
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64,000 |
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* |
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|
|
83,955 |
|
|
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81,486 |
|
Drawbridge Convertible II Ltd.(12)
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20,000 |
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* |
|
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26,847 |
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26,076 |
|
Drawbridge Global Macro Master Fund Ltd.(12)
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166,000 |
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* |
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224,787 |
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218,383 |
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Fore Convertible Master Fund, Ltd.(13)
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4,000,000 |
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2.00 |
% |
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154,321 |
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Fore ERISA Fund, Ltd.(13)
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2,000,000 |
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1.00 |
% |
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77,160 |
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Froley Revy Convertible Arbitrage Offshore(14)
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350,000 |
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|
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* |
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13,503 |
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FrontPoint Convertible Arbitrage Fund, L.P.(15)
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6,000,000 |
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3.00 |
% |
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|
231,481 |
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|
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GLG Market Neutral Fund(16)
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3,000,000 |
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|
1.50 |
% |
|
|
115,741 |
|
|
|
|
|
Guggenheim Portfolio Company VIII (Cayman), Ltd.(17)
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2,000,000 |
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|
|
1.00 |
% |
|
|
77,160 |
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|
|
|
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Highbridge International LLC(18)
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18,500,000 |
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|
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9.25 |
% |
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713,734 |
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|
|
|
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Jeffries & Company(19)
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250,000 |
|
|
|
* |
|
|
|
9,645 |
|
|
|
|
|
JP Morgan Securities Inc.(20)
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4,850,000 |
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|
|
2.43 |
% |
|
|
193,246 |
|
|
|
6,132 |
|
Kamunting Street Master Fund, Ltd.(21)
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7,100,000 |
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|
|
3.55 |
% |
|
|
273,919 |
|
|
|
|
|
43
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Principal | |
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Amount of | |
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Common | |
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|
Notes | |
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|
Common | |
|
Stock Owned | |
|
|
Beneficially | |
|
|
|
Stock Owned | |
|
After | |
|
|
Owned and | |
|
Percentage | |
|
Prior to the | |
|
Completion of | |
|
|
Offered | |
|
of Notes | |
|
Offering | |
|
the Offering | |
Name |
|
Hereby ($) | |
|
Outstanding | |
|
(1)(2) | |
|
(2) | |
|
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| |
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| |
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| |
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| |
KBC Financial Products USA Inc.(22)
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|
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8,600,000 |
|
|
|
4.30 |
% |
|
|
331,790 |
|
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|
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LDG Limited(23)
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71,000 |
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|
* |
|
|
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2,739 |
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Lehman Brothers Inc.
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5,100,000 |
|
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|
2.55 |
% |
|
|
196,759 |
|
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Lyxor/Convertible Arbitrage Fund Limited(5)
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|
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848,000 |
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|
|
* |
|
|
|
32,716 |
|
|
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|
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Man Convertible Bond Master Fund, Ltd.(24)
|
|
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2,936,000 |
|
|
|
1.47 |
% |
|
|
113,271 |
|
|
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|
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Man Mac I Limited
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|
3,000,000 |
|
|
|
1.50 |
% |
|
|
115,741 |
|
|
|
|
|
MSS Convertible Arbitrage I(23)
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|
|
6,000 |
|
|
|
* |
|
|
|
1,209 |
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|
|
978 |
|
Putnam Convertible Income-Growth Trust
|
|
|
3,720,000 |
|
|
|
1.86 |
% |
|
|
143,518 |
|
|
|
|
|
Saranac Capital Management L.P. (25)
|
|
|
15,000,000 |
|
|
|
7.50 |
% |
|
|
2,012,861 |
|
|
|
1,434,158 |
|
Satellite Convertible Arbitrage Master Fund, LLC(26)
|
|
|
7,000,000 |
|
|
|
3.50 |
% |
|
|
270,061 |
|
|
|
|
|
Silverback Master, Ltd.(27)
|
|
|
13,500,000 |
|
|
|
6.75 |
% |
|
|
520,833 |
|
|
|
|
|
Singlehedge US Convertible Arbitrage Fund(5)
|
|
|
745,000 |
|
|
|
* |
|
|
|
28,742 |
|
|
|
|
|
Sphinx Fund c/o TQA(23)
|
|
|
110,000 |
|
|
|
* |
|
|
|
22,236 |
|
|
|
17,992 |
|
St. Thomas Trading, Ltd.(28)
|
|
|
1,064,000 |
|
|
|
* |
|
|
|
41,049 |
|
|
|
|
|
Sturgeon Limited(5)
|
|
|
876,000 |
|
|
|
* |
|
|
|
33,796 |
|
|
|
|
|
UBS OConnor LLC F/B/O OConnor Global Convertible
Arbitrage Master Limited
|
|
|
3,000,000 |
|
|
|
1.50 |
% |
|
|
115,741 |
|
|
|
|
|
TQA Master Fund, Ltd.(23)
|
|
|
629,000 |
|
|
|
* |
|
|
|
145,062 |
|
|
|
120,795 |
|
TQA Master Plus Fund, Ltd.(23)
|
|
|
1,004,000 |
|
|
|
* |
|
|
|
234,627 |
|
|
|
195,893 |
|
TQA Special Opportunities Master Fund Ltd.(29)
|
|
|
2,000,000 |
|
|
|
1.00 |
% |
|
|
77,160 |
|
|
|
|
|
Tugar Capital, L.P.(30)
|
|
|
2,500,000 |
|
|
|
1.25 |
% |
|
|
96,451 |
|
|
|
|
|
Vicis Capital Master Fund(31)
|
|
|
4,000,000 |
|
|
|
2.00 |
% |
|
|
154,321 |
|
|
|
|
|
Wachovia Capital Markets LLC(32)
|
|
|
3,000,000 |
|
|
|
1.50 |
% |
|
|
115,741 |
|
|
|
|
|
Waterstone Market Neutral MAC51, Ltd.(33)
|
|
|
59,000 |
|
|
|
* |
|
|
|
2,276 |
|
|
|
|
|
Waterstone Market Neutral Master Fund, Ltd.(34)
|
|
|
941,000 |
|
|
|
* |
|
|
|
36,304 |
|
|
|
|
|
Xavex Convertible Arbitrage I(23)
|
|
|
26,000 |
|
|
|
* |
|
|
|
16,714 |
|
|
|
15,711 |
|
Zurich Institutional Benchmark Master c/o TQA(23)
|
|
|
154,000 |
|
|
|
* |
|
|
|
30,583 |
|
|
|
24,641 |
|
Subtotal:
|
|
|
198,525,000 |
|
|
|
99.26 |
% |
|
|
10,342,876 |
|
|
|
2,683,742 |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Any other holder of notes or future transferee, pledgee, donee,
assignee or successor of any holder(35)
|
|
|
1,475,000 |
|
|
|
* |
|
|
|
56,906 |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Total:
|
|
|
200,000,000 |
|
|
|
100.00 |
% |
|
|
10,399,782 |
|
|
|
2,683,742 |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
(1) |
Includes common stock issuable upon conversion of the notes at
the initial conversion rate of 38.5802 shares of common
stock per $1,000 principal amount of notes. However, this
conversion rate will be subject to adjustment as described under
Description of Notes Conversion of
Notes Conversion Rate Adjustments and
Description of Notes Make Whole Payment Upon
the Occurrence of a Designated Event that is also a Fundamental
Change. As a result, the amount of common stock issuable
upon conversion of the notes may increase or decrease in the
future. Selling securi- |
44
|
|
|
|
|
tyholders may have sold, transferred or otherwise disposed of
all or a portion of their notes, or acquired additional notes,
since the date on which we were provided with the information
regarding their notes in transactions exempt from the
registration requirements of the Securities Act. Accordingly,
the information provided here for any particular securityholder
may understate or overstate, as the case may be, such
securityholders current ownership. The aggregate principal
amount of notes outstanding as of the date of this registration
statement is $200,000,000, and the selling securityholders will
not sell under this registration statement more than that amount. |
|
|
(2) |
Assumes conversion of the full amount of
41/2% notes
held by the selling securityholder at the initial conversion
rate of 65.1890 shares of common stock per $1,000 principal
amount of notes. |
|
|
(3) |
Aristeia Capital LLC is the investment manager for Aristeia
International Limited. Aristeia Capital LLC is jointly owned by
Robert H. Lynch Jr., Anthony Frascella and Kevin Toner, who have
voting or investment control over these securities. |
|
|
|
(4) |
Aristeia Advisors LLC is the investment manager for Aristeia
Trading LLC. Aristeia Advisors LLC is jointly owned by Robert H.
Lynch Jr., Anthony Frascella and Kevin Toner, who have voting or
investment control over these securities. |
|
|
|
(5) |
Christian Menestrier, Chief Executive Officer of CooperNeff
Advisors, Inc., has voting or investment control over these
securities. |
|
|
|
(6) |
CNH Partners, LLC is the investment advisor of the CNH CA Master
Account, L.P. and has sole voting and dispositive power over
these securities. Robert Krail, Mark Mitchell and Todd Pulvino
exercise voting and investment control on behalf of CNH
Partners, LLC. |
|
|
|
(7) |
DKR Saturn Management Company L.P. is a registered investment
adviser with the Securities and Exchange Commission and, as
such, is the investment manager to DKR Saturn Event Driven
Holding Fund Ltd. (the Saturn Fund). Ron
Phillips, portfolio manager of the Saturn Fund, has voting or
investment control over these securities. |
|
|
|
(8) |
Includes 51,500 shares of commons stock subject to a call
option. |
|
|
|
(9) |
DKR Saturn Management L.P. is a registered investment adviser
with the Securities and Exchange Commission and, as such, is the
investment manager to DKR Saturn Multi-Strategy Fund Ltd.
(the Multi-Strategy Fund). Mike Cotton, portfolio
manager of the Multi-Strategy Fund, has voting or investment
control over these securities. |
|
|
|
|
(10) |
Includes 5,200 shares of commons stock subject to a call
option. |
|
|
|
(11) |
DKR Capital Partners L.P. (DKR LP) is a registered
investment adviser with the Securities and Exchange Commission
and, as such, is the investment manager to DKR SoundShore
Strategic Holding Fund Ltd. (the SoundShore
Fund). DKR LP has retained certain portfolio managers to
act as the portfolio manager to the SoundShore Fund managed by
DKR LP. As such, DKR LP and certain portfolio managers have
shared dispositive and voting power over securities held by the
fund. Doug Teresko has voting or investment control over these
securities. |
|
|
|
(12) |
Kevin Treacy has voting or investment control over these
securities. |
|
|
|
(13) |
David Egglishaw has voting or investment control over these
securities. |
|
|
|
(14) |
Ann Houlihan has voting or investment control over these
securities. |
|
|
|
(15) |
FrontPoint Convertible Arbitrage Fund GP LLC is the general
partner of FrontPoint Convertible Arbitrage Fund, L.P.
FrontPoint Partners LLC is the managing member of FrontPoint
Convertible Arbitrage Fund GP, LLC and as such has voting
and dispositive power over the securities held by the fund.
Philip Duff, W. Gillespie Caffray and Paul Ghaffari are members
of the board of managers of FrontPoint Partners LLC and are the
sole members of its management committee. Messrs. Duff,
Caffray and Ghaffari and FrontPoint Partners LLC and FrontPoint
Convertible Arbitrage Fund GP, LLC each disclaim beneficial
ownership of the securities held by the fund except for their
pecuniary interest therein. |
|
|
|
(16) |
GLG Market Neutral Fund (the Fund) is a publicly
owned company listed on the Irish Stock Exchange. GLG Partners
LP, an English limited partnership, acts as the investment
manager of the |
|
45
|
|
|
fund and has voting and dispositive power of the securities held
by the Fund. The general partner of GLG Partners LP is GLG
Partners Limited, an English limited company. The shareholders
of GLG Partners Limited are Noam Gottesman, Pierre Lagrange,
Jonathan Green, Philippe Jabre and Lehman (Cayman) Limited, a
subsidiary of Lehman Brothers, Inc., a publicly-held entity. GLG
Partners LP, GLG Partners Limited, Noam Gottesman, Pierre
Lagrange, Jonathan Green, Philippe Jabre and Lehman (Cayman)
Limited disclaim beneficial ownership of the securities held by
the Fund, except for their pecuniary interest therein. |
|
|
|
(17) |
Matthew Li has voting or investment control over these
securities. |
|
|
|
(18) |
Highbridge Capital Management, LLC (Highbridge) is
the trading manager of Highbridge International LLC
(HIC) and consequently has voting control and
investment discretion over securities held by HIC. Glenn Dubin
and Henry Swieca control Highbridge. Each of Highbridge, Glenn
Dubin and Henry Swieca disclaims beneficial ownership of the
securities held by HIC. |
|
|
|
(19) |
Jonathan Cunningham has voting or investment control over these
securities. |
|
|
|
(20) |
Charlotte Chui has voting or investment control over these
securities. |
|
|
|
(21) |
Allan Teh, managing member of Kamunting Street Management, LLC,
the general partner of the investment manager of Kamunting
Street Master Fund, Ltd., has voting or investment control over
these securities. |
|
|
|
(22) |
KBC Financial Products USA Inc. exercises voting and investment
control over any shares of common stock issuable upon conversion
of the notes held by the selling securityholder. Mr. Luke
Edwards, Managing Director, exercises voting and investment
control on behalf of KBC Financial Products USA Inc. |
|
|
|
(23) |
Robert Butman, George Esser, John Idone, Paul Bucci and
Bartholomew Tesoriero have voting or investment control over
these securities. |
|
|
|
(24) |
John Null and J.T. Hansen, principals of Marin Capital Partners,
LP, investment advisor to Man Convertible Bond Master Fund, Ltd.
have voting or investment control over these securities. |
|
|
|
(25) |
Ross Margolies has voting or investment control over these
securities. Saranac Capital Management L.P. acts as
discretionary investment advisor with respect to the following
accounts that hold the indicated principal amounts of these
securities: Citigroup Alternative Investments Diversified
Arbitrage Strategies Fund Ltd., 1,822,000; Citigroup
Alternative Investments Enhanced Arbitrage Strategies Fund,
539,000; Citigroup Alternative Investments QIP Multi Strategy
Arbitrage Portfolio, 8,868,000; Saranac Erisa Arbitrage LTD,
3,355,000; Saranac Erisa Arbitrage LP, 224,000; and Saranac
Arbitrage LTD, 192,000. |
|
|
|
(26) |
Leif Rosenblatt, Mark Sonnino, Gabriel Nechamkin, Christopher
Tuzzo, Brian Kriftcher, Stephen Shapiro and David Ford have
voting or investment control over these securities. Each of
these individuals disclaims beneficial ownership of the
securities. |
|
|
|
(27) |
Elliot Bossen has voting or investment control over these
securities. |
|
|
|
(28) |
John Null and J.T. Hansen, principals of Marin Capital Partners,
LP, investment advisor to St. Thomas Trading, Ltd., have voting
or investment control over these securities. |
|
|
|
(29) |
Robert Butman, George Esser, John Idone, Paul Bucci and
Bartholomew Tesoriero have voting or investment control over
these securities. |
|
|
|
(30) |
Ken Tananbaum has voting or investment control over these
securities. |
|
|
|
(31) |
Sky Lucas, John Succo and Shad Stastney have voting or
investment control over these securities. |
|
|
|
(32) |
Eric Grant has voting or investment control over these
securities. |
|
|
|
(33) |
Shawn Bergerson, Chief Executive Officer of Waterstone Market
Neutral MAC51, Ltd., has voting or investment control over these
securities. |
|
|
|
(34) |
Shawn Bergerson, Chief Executive Officer of Waterstone Market
Neutral Master Fund, Ltd., has voting or investment control over
these securities. |
|
46
|
|
(35) |
Information about other selling securityholders, except for any
future transferee, pledgee, donee, assignee or successor of
securityholders named in the table above, will be set forth in a
prospectus supplement or amendment to this registration
statement if required. For purposes of this table, we have
assumed that any other holders of notes, or any future
transferees, pledgees, donees or successors of or from any such
other holders of notes, do not beneficially own any common stock
other than the common stock issuable upon conversion of the
notes at the initial conversion rate. |
PLAN OF DISTRIBUTION
We are registering the notes and the shares of our common stock
issuable upon conversion of the notes to permit public secondary
trading of these securities by the holders from time to time
after the date of this prospectus. We have agreed, among other
things, to bear all expenses, other than selling expenses,
including any underwriting discounts and commissions,
registration expenses incurred by the selling securityholders,
and expenses and fees for all counsel and other professionals
representing the selling securityholders, in connection with the
registration and sale of the notes and the shares of our common
stock issuable upon conversion of the notes covered by this
prospectus.
We will not receive any of the proceeds from the offering of the
notes or the shares of our common stock issuable upon conversion
of the notes by the selling securityholders. The term
selling securityholders includes donees, pledges,
transferees or other successors-in-interest selling notes and
the shares of common stock issuable upon conversion of the notes
received after the date of this prospectus from a selling
securityholder as a gift, pledge, partnership distribution or
other non-sale related transfer. The selling securityholders may
pledge or grant a security interest in some or all of the notes
or shares of common stock issuable upon conversion of the notes
owned by them and, if they default in the performance of their
secured obligations, the pledges or secured parties may offer
and sell the notes or shares of common stock issuable upon
conversion of the notes from time to time pursuant to this
prospectus. The notes and shares of common stock issuable upon
conversion of the notes may be sold from time to time directly
by any selling securityholder or, alternatively, through
underwriters, broker-dealers or agents. If notes or shares of
common stock issuable upon conversion of the notes are sold
through underwriters, broker-dealers or agents, the selling
securityholder will be responsible for underwriting discounts or
commissions or agents commissions and their professional
fees.
The notes or shares of common stock issuable upon conversion of
the notes may be sold:
|
|
|
|
|
in one or more transactions at fixed prices; |
|
|
|
at prevailing market prices at the time of sale; |
|
|
|
at varying prices determined at the time of sale; or |
|
|
|
at negotiated prices. |
Such sales may be effected in transactions, which may involve
crosses or block trades or transactions in which the broker acts
as agent for the seller and the buyer:
|
|
|
|
|
on any national securities exchange or U.S. interdealer system
of a registered national securities association on which the
notes or shares of common stock issuable upon conversion of the
notes may be listed or quoted at the time of sale; |
|
|
|
in the over-the-counter market; |
|
|
|
in transactions otherwise than on a national securities exchange
or U.S. interdealer system of a registered national securities
association or in the over-the-counter market; |
|
|
|
through the settlement of short sales; or |
|
|
|
through the writing of options, whether the options are listed
on an options exchange or otherwise. |
47
In connection with sales of the notes or shares of common stock
issuable upon conversion of the notes or otherwise, any selling
securityholder may:
|
|
|
|
|
enter into hedging transactions with broker-dealers, which may
in turn engage in short sales of the notes or shares of common
stock issuable upon conversion of the notes in the course of
hedging the positions they assume; |
|
|
|
enter into option or other transactions with broker-dealers or
other financial institutions that require the delivery to the
broker-dealer or other financial institution of notes or shares
of common stock issuable upon conversion of the notes, which the
broker-dealer or other financial institutions may resell
pursuant to this prospectus; |
|
|
|
enter into transactions in which a broker-dealer makes purchases
as a principal for resale for its own account or through other
types of transactions; |
|
|
|
sell short and deliver notes or shares of common stock issuable
upon conversion of the notes to close out the short
positions; or |
|
|
|
loan or pledge notes or shares of common stock issuable upon
conversion of the notes to broker-dealers that in turn may sell
the securities. |
The outstanding common stock is publicly traded on the NASDAQ
National Market. We do not intend to apply for listing of the
notes on NASDAQ or any securities exchange. Accordingly, we
cannot assure that any trading market will develop or have any
liquidity.
The selling securityholders and any broker-dealers, agents or
underwriters that participate with the selling securityholders
in the distribution of the notes or the shares of common stock
issuable upon conversion of the notes may be deemed to be
underwriters within the meaning of the Securities
Act, in which event any commissions received by these
broker-dealers, agents or underwriters and any profits realized
by the selling securityholders on the resales of the notes or
the shares may be deemed to be underwriting commissions or
discounts under the Securities Act. Each of Aristeia Trading
LLC, CIBC World Markets, Jeffries & Co., JP Morgan
Securities Inc., KBC Financial Products USA Inc., Lehman
Brothers Inc. and Wachovia Capital Markets LLC has informed us
that it is a registered broker-dealer. As a result, each of
these selling securityholders is an underwriter in connection
with the sale of the notes or the shares of common stock
issuable upon conversion of the notes covered by this
prospectus. Each of BNP Paribas Equity Strategies, SNC,
Guggenheim Portfolio Company VIII (Cayman), Ltd. and Putnam
Convertible Income-Growth Trust has informed us that it is an
affiliate of a registered broker-dealer, that it purchased its
notes in the ordinary course of business and that at the time of
purchase of the notes it had no agreements or understandings,
directly or indirectly, with any person to distribute the notes.
The selling securityholders and any other person participating
in the sale of the notes or the shares of common stock issuable
upon conversion of the notes will be subject to the Securities
Exchange Act of 1934. The Securities Exchange Act of 1934 rules
include, without limitation, Regulation M, which may limit
the timing of purchases and sales of any of the notes and the
shares of common stock issuable upon conversion of the notes by
the selling securityholders and any other such person. In
addition, Regulation M of the Securities Exchange Act of
1934 may restrict the ability of any person engaged in the
distribution of the notes and the shares of common stock
issuable upon conversion of the notes to engage in market-making
activities with respect to the particular notes and the shares
of common stock issuable upon conversion of the notes being
distributed for a period of up to five business days before the
commencement of such distribution. This may effect the
marketability of the notes and the shares of common stock
issuable upon conversion of the notes and the ability of any
person or entity to engage in market-making activities with
respect to the notes and the shares of common stock issuable
upon conversion of the notes.
In addition, any securities covered by this prospectus which
qualify for sale pursuant to Rule 144, Rule 144A, or
any other available exemption from registration under the
Securities Act may be sold under Rule 144, Rule 144A,
or any of the other available exemptions rather than pursuant to
this prospectus.
48
There is no assurance that any selling securityholder will sell
any or all of the notes or shares of common stock issuable upon
conversion of the notes described in this prospectus, and any
selling securityholder may transfer, devise or gift the
securities by other means not described in this prospectus.
We originally sold the notes to the initial purchasers in a
private placement on January 12, 2005. We agreed to
indemnify and hold the initial purchasers of the notes harmless
against certain liabilities under the Securities Act that could
arise in connection with the sale of the notes by the initial
purchasers. The registration rights agreement provides for us
and the selling securityholders to indemnify each other against
certain liabilities arising under the Securities Act.
We agreed pursuant to the registration rights agreement to use
our best efforts to cause the registration statement to which
this prospectus relates to become effective as promptly as is
practicable and to keep the registration statement effective
until the earlier of:
|
|
|
|
|
all of the registrable securities have been sold pursuant to the
registration statement or pursuant to Rule 144 under the
Securities Act or any similar provision then in force; or |
|
|
|
the expiration of the holding period with respect to the
registrable securities under Rule 144(k) under the
Securities Act, or any successor provision. |
The registration rights agreement provides that we may suspend
the use of this prospectus in connection with sales of notes and
shares of common stock issuable upon conversion of the notes by
holders for a period not to exceed an aggregate of 30 days
in any three-month period, or not to exceed an aggregate of
90 days in any 12-month period, under certain circumstances
relating to pending corporate developments, public filings with
the SEC and similar events. Notwithstanding the foregoing, we
will be permitted to suspend the use of the prospectus for up to
60 days in any 3-month period under some circumstances,
relating to possible acquisitions, financings or other similar
transactions.
LEGAL MATTERS
The validity of the notes and the shares of common stock
issuable upon conversion of the notes offered hereby will be
passed upon for AtheroGenics by McKenna Long & Aldridge
LLP of Atlanta, Georgia.
EXPERTS
The financial statements of AtheroGenics, Inc. appearing in
AtheroGenics, Inc.s Annual Report (Form 10-K) for the
year ended December 31, 2004 and AtheroGenics, Inc.
managements assessment of the effectiveness of internal
control over financial reporting as of December 31, 2004
included therein, have been audited by Ernst & Young
LLP, independent registered public accounting firm, as set forth
in its reports thereon, included therein, and incorporated
herein by reference. Such financial statements and
managements assessment have been incorporated herein by
reference in reliance upon such reports given on the authority
of such firm as experts in accounting and auditing.
WHERE YOU CAN FIND MORE INFORMATION
We file reports, proxy statements and other documents with the
SEC. You may read and copy any document we file at the
SECs public reference room at 100 F Street, N.E.,
Room 1580, Washington, D.C. 20549. You should call
1-800-SEC-0330 for more information on the public reference
room. Our SEC filings are also available to you on the
SECs Internet site at http://www.sec.gov.
This prospectus is part of a registration statement that we
filed with the SEC. The registration statement contains more
information than this prospectus regarding us and our common
stock, including certain exhibits and schedules. You can obtain
a copy of the registration statement from the SEC at the address
listed above or from the SECs Internet site.
49
INCORPORATION OF CERTAIN INFORMATION BY REFERENCE
The SEC requires us to incorporate into this
prospectus information that we file with the SEC in other
documents. This means that we can disclose important information
to you by referring to other documents that contain that
information. The information incorporated by reference is
considered to be part of this prospectus. Information contained
in this prospectus and information that we file with the SEC in
the future and incorporate by reference in this prospectus
automatically updates and supersedes previously filed
information. We incorporate by reference the documents listed
below and any future filings we make with the SEC under
Sections 13(a), 13(c), 14 or 15(d) of the Securities
Exchange Act of 1934, prior to the termination of this offering.
|
|
|
|
|
|
Our Annual Report on Form 10-K for the fiscal year ended
December 31, 2004, as amended by an Annual Report on
Form 10-K/A filed with the SEC on April 6, 2005 and an
Annual Report on Form 10-K/A filed with the SEC on
May 6, 2005. |
|
|
|
|
|
Our Quarterly Report on Form 10-Q for the quarter ended
March 31, 2005. |
|
|
|
|
|
Our Current Reports on Form 8-K filed with the SEC on
January 4, 2005, January 5, 2005, January 6,
2005, January 7, 2005, January 11, 2005,
January 13, 2005, February 22, 2005 and April 29,
2005. |
|
|
|
|
The description of our common stock contained in our
Registration Statement on Form 8-A filed with the SEC on
August 4, 2000. |
|
|
|
The description of our common stock purchase rights contained in
our Registration Statement on Form 8-A filed with the SEC
on November 19, 2001. |
You may request a copy of these documents incorporated by
reference in this prospectus, which will be provided to you at
no cost, by writing or telephoning us using the following
contact information:
AtheroGenics, Inc.
8995 Westside Parkway
Alpharetta, Georgia 30004
Attention: Ms. Donna Glasky
Manager, Corporate Communications
Telephone: (678) 336-2500
50
PART II
INFORMATION NOT REQUIRED IN PROSPECTUS
|
|
Item 14. |
Other Expenses of Issuance and Distribution |
The following table sets forth the various expenses to be
incurred in connection with the sale and distribution of the
securities being registered hereby, all of which will be borne
by us (except selling expenses of the selling securityholders,
including any underwriting discounts and commissions,
registration expenses incurred by the selling securityholders,
and expenses and fees for all counsel and other professionals
representing the selling securityholders). All amounts shown are
estimates except the Securities and Exchange Commission
registration fee.
|
|
|
|
|
|
Securities and Exchange Commission registration fee
|
|
$ |
23,540 |
|
Legal fees and expenses of the Company
|
|
|
320,000 |
|
Trustees fees and expenses
|
|
|
8,500 |
|
Accounting fees and expenses
|
|
|
55,000 |
|
Printing and miscellaneous expenses
|
|
|
50,000 |
|
|
|
|
|
|
Total
|
|
$ |
457,040 |
|
|
|
|
|
|
|
Item 15. |
Indemnification of Directors and Officers |
Our Fourth Amended and Restated Articles of Incorporation
eliminate the personal liability of directors, as permitted by
Section 14-2-202(b)(4) of the Georgia Business Corporation
Code, and officers for monetary damages to the corporation or
its shareholders for breach of their duty of care and other
duties; provided, however, that our Articles of Incorporation
and Section 14-2-202(b)(4) of the Georgia Code do not
permit us to eliminate or limit liability for (1) a breach
of duty involving appropriation of a business opportunity of
ours; (2) an act or omission which involves intentional
misconduct or a knowing violation of law; (3) any
transaction from which an improper personal benefit is derived;
or (4) any payments of a dividend or any other type of
distribution that is illegal under Section 14-2-832 of the
Georgia Code. In addition, if at any time the Georgia Code is
amended to authorize further elimination or limitation of
personal liability, then the liability of each of our directors
and officers shall be eliminated or limited to the fullest
extent permitted by such provisions, as so amended, without
further action by the shareholders, unless the provisions of the
Georgia Code require such action.
Sections 14-2-850 to 14-2-859, inclusive, of the Georgia
Code govern the indemnification of directors, officers,
employees and agents. Section 14-2-851 of the Georgia Code
provides for indemnification of any of our directors for
liability incurred by him in connection with any threatened,
pending or completed action, suit or proceeding, whether civil,
criminal, administrative, arbitrative or investigative and
whether formal or informal, in which he may become involved by
reason of being a member of our board of directors.
Section 14-2-851 and Section 14-2-857 also provide
such indemnity for directors and officers who, at our request,
act as directors, officers, partners, trustees, employees or
agents of another foreign or domestic corporation, partnership,
joint venture, trust, employee benefit plan or another entity.
Section 14-2-851 and Section 14-2-857 permit
indemnification if (1) the director or officer conducted
himself in good faith and (2) the director or officer, in
the case of conduct in his official capacity, acted in a manner
he reasonably believed to be in our best interest, and in all
other cases acted in a manner he reasonably believed not to be
opposed to our best interest, and, in addition, in criminal
proceedings, if he had no reasonable cause to believe his
conduct was unlawful. If the required standard of conduct is
met, indemnification may include judgments, settlements,
penalties, fines or reasonable expenses, including
attorneys fees, incurred with respect to a proceeding.
However, if a director is adjudged liable to us in a derivative
action or on the basis that personal benefit was improperly
received by him, the director will only be entitled to such
indemnification for reasonable expenses as a court finds to be
proper in accordance with the provisions of
Section 14-2-854.
II-1
Section 14-2-852 of the Georgia Code provides that
directors who are wholly successful with respect to any claim
brought against them, which claim is brought because they are or
were directors, are entitled to indemnification against
reasonable expenses as of right. Conversely, if the charges made
in any action are sustained, the determination of whether the
required standard of conduct has been met will be made, in
accordance with the provisions of Section 14-2-855 of the
Georgia Code, as follows: (1) if there are two or more
disinterested members of the board of directors, by the majority
vote of the disinterested members of the board of directors,
(2) by a majority of the members of a committee of two or
more disinterested directors, (3) by special legal counsel
or (4) by the shareholders, but, in such event, the shares
owned by or voted under the control of directors who are not
disinterested may not be voted.
Section 14-2-857 of the Georgia Code provides that an
officer who is not a director has the mandatory right of
indemnification granted to directors under
Section 14-2-852, as described above. In addition, except
for liability arising out of conduct that constitutes
appropriation, in violation of his or her duties, of any
business opportunity of the corporation, acts or omissions which
involved intentional misconduct or a knowing violation of law,
liability with respect to consent to a distribution in violation
of the Georgia Code or our Fourth Amended and Restated Articles
of Incorporation or receipt of an improper personal benefit, we
may, as provided by our Articles, Bylaws, actions by our board
of directors, or by contract, indemnify and advance expenses to
an officer, employee or agent who is not a director to the
extent that such indemnification is consistent with public
policy.
Article V of our Third Amended and Restated Bylaws, as
amended, provides for indemnification of directors, officers and
in-house legal counsel acting in a legal capacity on our behalf
against third-party actions and derivative actions in which the
individual becomes involved, as a party or otherwise, arising
from their status as such. Our Bylaws provide for the same
standard of conduct for indemnification as set out above in
Section 14-2-851 of the Georgia Code. Our Bylaws prohibit
indemnification where such person is adjudged liable under
similar situations set out above in Section 14-2-854 of the
Georgia Code. Section 3 of Article V provides for
advancement of expenses as authorized by our board of directors
upon receipt of a written affirmation of such persons good
faith belief that he has met the relevant standard of conduct
and an undertaking to repay if it is determined that he is not
entitled to indemnification. Our Bylaws contain similar
requirements for determining indemnification rights that are set
out above in Section 14-2-855 of the Georgia Code. Our
Bylaws also contain a provision that allows us to purchase and
maintain insurance on behalf of an individual who is or was a
director, officer, in-house legal counsel acting in a legal
capacity, employee or agent.
Our officers and directors are presently covered by insurance
which (with certain exceptions and within certain limitations)
indemnifies them against any losses or liabilities arising from
any alleged wrongful act, including any alleged
breach of duty, neglect, error, misstatement, misleading
statement, omissions or other act done or wrongfully attempted.
We pay the cost of such insurance as permitted by our Bylaws and
the laws of the State of Georgia.
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Item 16. |
Exhibits and Financial Statement Schedules |
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Exhibit |
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Number |
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Description |
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4 |
.1(1) |
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Fourth Amended and Restated Articles of Incorporation of
AtheroGenics, Inc. |
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4 |
.2(2) |
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Third Amended and Restated Bylaws of AtheroGenics, Inc., as
amended. |
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4 |
.3(3) |
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Amended and Restated Master Rights Agreement dated
October 31, 1995, as amended by First Amendment dated
November 1, 1995; Second Amendment dated July 30,
1996; Third Amendment dated April 13, 1999; Fourth
Amendment dated May 11, 1999; and Fifth Amendment dated
August 30, 1999. |
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4 |
.4(4) |
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Rights Agreement dated as of November 9, 2001 between
AtheroGenics, Inc. and American Stock Transfer and Trust Company. |
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4 |
.5* |
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Indenture dated January 12, 2005 between AtheroGenics, Inc.
and The Bank of New York Trust Company, N.A., as Trustee. |
II-2
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Exhibit |
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Number |
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Description |
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4 |
.6(5) |
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Registration Rights Agreement dated as of January 12, 2005
among AtheroGenics, Inc., Morgan Stanley & Co.
Incorporated, Lehman Brothers Inc., J.P. Morgan Securities
Inc. and Lazard Frères & Co. LLC. |
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4 |
.7* |
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Global 1.50% Convertible Note Due 2012. |
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5 |
.1* |
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Opinion of McKenna Long & Aldridge LLP. |
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12 |
.1 |
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Statement Regarding Computation of Ratios. |
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23 |
.1 |
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Consent of Ernst & Young LLP. |
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23 |
.2* |
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Consent of McKenna Long & Aldridge LLP, included in
Exhibit 5.1. |
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24 |
.1* |
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Powers of Attorney. |
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25 |
.1* |
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Statement of Eligibility of Trustee on Form T-1. |
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(1) |
Incorporated by reference from the Registrants Annual
Report on Form 10-K/A (File No. 000-31261) filed on
April 6, 2005. |
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(2) |
Incorporated by reference from the Registrants Annual
Report on Form 10-K (File No. 000-31261) filed on
March 29, 2002. |
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(3) |
Incorporated by reference from the Registrants
Registration Statement on Form S-1 (Reg. No. 333-
31140) filed on February 25, 2000. |
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(4) |
Incorporated by reference from the Registrants Current
Report on Form 8-K (File No. 000-31261) filed on
November 19, 2001. |
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(5) |
Incorporated by reference from the Registrants Current
Report on Form 8-K (File No. 000-31261) filed on
January 13, 2005. |
The undersigned Registrant hereby undertakes:
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(1) To file, during any period in which offers or sales are
being made, a post-effective amendment to this registration
statement: |
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(i) To include any prospectus required by
Section 10(a)(3) of the Securities Act of 1933; |
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(ii) To reflect in the prospectus any facts or events
arising after the effective date of the registration statement
(or the most recent post-effective amendment thereof) which,
individually or in the aggregate, represent a fundamental change
in the information set forth in the registration statement.
Notwithstanding the foregoing, any increase or decrease in
volume of securities offered (if the total dollar value of
securities offered would not exceed that which was registered)
and any deviation from the low or high end of the estimated
maximum offering range may be reflected in the form of
prospectus filed with the SEC pursuant to Rule 424(b) if,
in the aggregate, the changes in volume and price represent no
more than 20 percent change in the maximum aggregate
offering price set forth in the Calculation of
Registration Fee table in the effective registration
statement; and |
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(iii) To include any material information with respect to
the plan of distribution not previously disclosed in the
registration statement or any material change to such
information in the registration statement; |
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provided, however, that paragraphs (1)(i) and (1)(ii) do
not apply if the registration statement is on Form S-3 or
Form S-8, and the information required to be included in
the post-effective amendment by those paragraphs is contained in
periodic reports filed by the Registrant pursuant to
Section 13 or |
II-3
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Section 15(d) of the Securities Exchange Act of 1934 that
are incorporated by reference in the registration statement. |
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(2) That, for the purpose of determining any liability
under the Securities Act, each post-effective amendment that
contains a form of prospectus shall be deemed to be a new
registration statement relating to the securities offered
therein, and the offering of such securities at that time shall
be deemed to be the initial bona fide offering thereof. |
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(3) To remove from registration by means of a
post-effective amendment any of the securities being registered
which remain unsold at the termination of the offering. |
Insofar as indemnification for liabilities arising under the
Securities Act of 1933 may be permitted to directors, officers
and controlling persons of the Registrant pursuant to the
foregoing provisions, or otherwise, the Registrant has been
advised that in the opinion of the SEC such indemnification is
against public policy as expressed in the Act and is, therefore,
unenforceable. In the event that a claim for indemnification
against such liabilities (other than the payment by the
Registrant of expenses incurred or paid by a director, officer
or controlling person of the Registrant in the successful
defense of any action, suit or proceeding) is asserted by such
director, officer or controlling person in connection with the
securities being registered, the Registrant will, unless in the
opinion of its counsel the matter has been settled by
controlling precedent, submit to a court of appropriate
jurisdiction the question whether such indemnification by it is
against public policy as expressed in the Securities Act and
will be governed by the final adjudication of such issue.
The undersigned Registrant hereby undertakes that, for purposes
of determining any liability under the Securities Act of 1933,
each filing of the Registrants annual report pursuant to
Section 13(a) or Section 15(d) of the Securities
Exchange Act of 1934 (and, where applicable, each filing of an
employee benefit plans annual report pursuant to
Section 15(d) of the Securities Exchange Act of 1934) that
is incorporated by reference in the registration statement shall
be deemed to be a new registration statement relating to the
securities offered therein, and the offering of such securities
at that time shall be deemed to be the initial bona fide
offering thereof.
II-4
SIGNATURES
Pursuant to the requirements of the Securities Act of 1933, the
Registrant certifies that it has reasonable grounds to believe
that it meets all of the requirements for filing on
Form S-3 and has duly caused this Amendment No. 1 to
registration statement to be signed on its behalf by the
undersigned, thereunto duly authorized, in the City of
Alpharetta, State of Georgia, on June 14, 2005.
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By: |
/s/ RUSSELL M. MEDFORD |
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Russell M. Medford, M.D., Ph.D. |
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President and Chief Executive Officer |
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Pursuant to the requirements of the Securities Act of 1933, this
registration statement has been signed by the following persons
in the capacities and on the dates indicated:
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Name |
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Title |
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Date |
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/s/ RUSSELL M. MEDFORD
Russell
M. Medford |
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President and Chief Executive Officer, Director (Principal
Executive Officer) |
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June 14, 2005 |
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/s/ MARK P. COLONNESE
Mark
P. Colonnese |
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Senior Vice President of Finance and Administration and Chief
Financial Officer (Principal Financial and Accounting Officer) |
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June 14, 2005 |
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*
R.
Wayne Alexander |
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Director |
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June 14, 2005 |
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David
Bearman |
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Director |
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June 14, 2005 |
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Vaughn
D. Bryson |
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Director |
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June 14, 2005 |
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T.
Forcht Dagi |
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Director |
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June 14, 2005 |
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Michael
A. Henos |
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Director |
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Arthur
M. Pappas |
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Director |
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June 14, 2005 |
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William
A. Scott |
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Director |
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June 14, 2005 |
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By: |
/s/ RUSSELL M. MEDFORD |
Name: Russell M. Medford
Title: Attorney-in-fact
II-5
EXHIBIT INDEX
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Exhibit |
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Number |
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Description |
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4 |
.1(1) |
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Fourth Amended and Restated Articles of Incorporation of
AtheroGenics, Inc. |
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4 |
.2(2) |
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Third Amended and Restated Bylaws of AtheroGenics, Inc., as
amended. |
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4 |
.3(3) |
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Amended and Restated Master Rights Agreement dated
October 31, 1995, as amended by First Amendment dated
November 1, 1995; Second Amendment dated July 30,
1996; Third Amendment dated April 13, 1999; Fourth
Amendment dated May 11, 1999; and Fifth Amendment dated
August 30, 1999. |
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4 |
.4(4) |
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Rights Agreement dated as of November 9, 2001 between
AtheroGenics, Inc. and American Stock Transfer and Trust Company. |
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4 |
.5* |
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Indenture dated January 12, 2005 between AtheroGenics, Inc.
and The Bank of New York Trust Company, N.A., as Trustee. |
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4 |
.6(5) |
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Registration Rights Agreement dated as of January 12, 2005
among AtheroGenics, Inc., Morgan Stanley & Co.
Incorporated, Lehman Brothers Inc., J.P. Morgan Securities
Inc. and Lazard Frères & Co. LLC. |
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4 |
.7* |
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Global 1.50% Convertible Note Due 2012. |
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5 |
.1* |
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Opinion of McKenna Long & Aldridge LLP. |
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12 |
.1 |
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Statement Regarding Computation of Ratios. |
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23 |
.1 |
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Consent of Ernst & Young LLP. |
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23 |
.2* |
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Consent of McKenna Long & Aldridge LLP, included in
Exhibit 5.1. |
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24 |
.1* |
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Powers of Attorney. |
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25 |
.1* |
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Statement of Eligibility of Trustee on Form T-1. |
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(1) |
Incorporated by reference from the Registrants Annual
Report on Form 10-K/A (File No. 000-31261) filed on
April 6, 2005. |
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(2) |
Incorporated by reference from the Registrants Annual
Report on Form 10-K (File No. 000-31261) filed on
March 29, 2002. |
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(3) |
Incorporated by reference from the Registrants
Registration Statement on Form S-1 (Reg. No. 333-
31140), declared effective by the SEC on August 8, 2000. |
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(4) |
Incorporated by reference from the Registrants Current
Report on Form 8-K (File No. 000-31261) filed on
November 19, 2001. |
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(5) |
Incorporated by reference from the Registrants Current
Report on Form 8-K (File No. 000-31261) filed on
January 13, 2005. |