Neurocrine Bioscience Inc.
This filing is made pursuant to Rule 424(b)(3)
under the Securities Act of 1933
in connection with Registration No. 333-147118
Dated December 3, 2007
PROSPECTUS
$150,000,000
NEUROCRINE BIOSCIENCES, INC.
Common Stock
Our common stock
is listed on the Nasdaq Global Select Market under the symbol NBIX. On
November 30, 2007, the last reported sale price of our common stock on the Nasdaq Global Select
Market was $13.02 per share.
This prospectus and the accompanying prospectus supplement will allow us to sell shares of our
common stock over time in one or more offerings, with an aggregate offering price of up to
$150,000,000. Each time we offer shares of our common stock, we will provide you with a supplement
to this prospectus. You should read this prospectus, the information incorporated by reference in
this prospectus and any prospectus supplement carefully before you invest.
Investing in our common stock involves a high degree of risk. See Risk Factors on page 2 of
this prospectus and as updated in our future filings made with the Securities and Exchange
Commission, which are incorporated by reference in this prospectus.
This prospectus may not be used to offer or sell any common stock unless accompanied by a
prospectus supplement.
The common stock may be sold by us to or through underwriters or dealers, directly to
purchasers or through agents designated from time to time. For additional information on the
methods of sale, you should refer to the section entitled Plan of Distribution in this
prospectus. If any underwriters are involved in the sale of any common stock with respect to which
this prospectus is being delivered, the names of such underwriters and any applicable discounts or
commissions and over-allotment options will be set forth in a prospectus supplement. The price to
the public of such common stock and the net proceeds we expect to receive from such sale will also
be set forth in a prospectus supplement.
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 December 3, 2007.
TABLE OF CONTENTS
You should rely only on the information contained in or incorporated by reference into this
prospectus or any applicable prospectus supplement. We have not authorized anyone to provide you
with different information. We are not making an offer to sell or seeking an offer to buy shares
of our common stock under this prospectus or any applicable prospectus supplement in any
jurisdiction where the offer or sale is not permitted. The information contained in this
prospectus, any applicable prospectus supplement and the documents incorporated by reference herein
and therein are accurate only as of their respective dates, regardless of the time of delivery of
this prospectus or any sale of a security.
ABOUT THIS PROSPECTUS
This prospectus is part of a registration statement that we filed with the Securities and
Exchange Commission (SEC) using a shelf registration process. Under this shelf registration
statement, we may sell shares of our common stock in one or more offerings up to a total dollar
amount of $150,000,000. This prospectus provides you with a general description of the common stock
we may offer. Each time we sell any of our common stock under this prospectus, we will provide a
prospectus supplement that will contain more specific information about the terms of that offering.
We may also add, update or change in a prospectus supplement any of the information contained in
this prospectus or in documents we have incorporated by reference into this prospectus. This
prospectus, together with any applicable prospectus supplement and the documents incorporated by
reference into this prospectus, include all material information relating to this offering. You
should carefully read both this prospectus and any applicable prospectus supplement together with
the additional information described under Where You Can Find More Information before buying
common stock in this offering.
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SUMMARY
The following summary does not contain all the information that may be important to purchasers of
our common stock. Prospective purchasers of our common stock should carefully review the entire
prospectus, including the financial statements and other information incorporated by reference in
this prospectus, before making an investment decision.
NEUROCRINE BIOSCIENCES, INC.
We discover, develop and intend to commercialize drugs for the treatment of neurological and
endocrine-related diseases and disorders. Our product candidates address some of the largest
pharmaceutical markets in the world, including insomnia, anxiety, depression, endometriosis,
irritable bowel syndrome, pain, diabetes and other neurological and endocrine-related diseases and
disorders. We currently have ten programs in various stages of research and development,
including six programs in clinical development. While we independently develop many of our
product candidates, we have entered into a collaboration for one of our programs. Our lead clinical
development program, indiplon, is a drug candidate for the treatment of insomnia.
The following table summarizes our most advanced products currently in clinical development
and those currently in research:
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Program |
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Target Indication |
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Status (1) |
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Commercial Rights |
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Products under clinical development: |
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Indiplon
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Insomnia
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Registration (2)
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Neurocrine |
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GnRH Antagonist
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Endometriosis
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Phase II
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Neurocrine |
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CRF R1 Antagonist (3)
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Mood Disorders,
Irritable Bowel
Syndrome
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Phase II
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GlaxoSmithKline/
Neurocrine |
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CRF R2 Peptide
Agonist Urocortin 2 (3)
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Cardiovascular
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Phase II
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Neurocrine |
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Selective norepinephrine
reuptake inhibitor (sNRI)
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Neuropathic Pain
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Phase I
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Neurocrine |
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GnRH Antagonist
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Benign Prostatic
Hyperplasia
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Phase I
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Neurocrine |
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Research: |
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Glucose Dependent Insulin
Secretagogues
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Type II Diabetes
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Research
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Neurocrine |
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GnRH Antagonist
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Endometriosis,
Benign Prostatic
Hyperplasia
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Research
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Neurocrine |
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Adenosine2A Receptor
Antagonists
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Parkinsons Disease
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Research
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Neurocrine/Almirall |
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Ion Channel Blocker
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Chronic Pain
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Research
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Neurocrine |
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Registration indicates that we or our collaborators have submitted a New Drug
Application (NDA) to the U.S. Food and Drug Administration (FDA) for regulatory approval of
the drug candidate. Phase II indicates that we or our collaborators are conducting
clinical trials on groups of patients afflicted with a specific disease in order to determine
preliminary efficacy, optimal dosages and expanded evidence of safety. Phase I indicates
that we or our collaborators are conducting clinical trials with a smaller number of patients
to determine early safety profile, maximally tolerated dose and pharmacological properties of
the product in human volunteers. Research indicates identification and evaluation of
compound(s) in laboratory and preclinical models. |
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On May 15, 2006, we received two complete responses from the FDA regarding the indiplon
capsule and tablet NDAs. These responses indicated that indiplon 5 mg and 10 mg capsules were
approvable (FDA Approvable Letter) and that the 15 mg tablets were not approvable (FDA Not
Approvable Letter). |
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The FDA Not Approvable Letter requested that we reanalyze certain safety and efficacy data
and questioned the sufficiency of the objective sleep maintenance clinical data with the 15
mg tablet in view of the fact that the majority of the indiplon tablet studies were conducted
with doses higher than 15 mg. We held an end-of-review meeting with the FDA related to the
FDA Not Approvable Letter in October 2006. This meeting was specifically focused on
determining the actions needed to bring indiplon tablets from Not Approvable to Approval in
the resubmission of the NDA for indiplon tablets. The FDA has requested additional long-term
safety and efficacy data with the 15 mg dose for the adult population and the development of
a separate dose for the elderly population. In discussions, we and the FDA noted positive
efficacy data for sleep maintenance with both indiplon capsules and tablets. On the basis of
these discussions, we are formulating a strategy to pursue a sleep maintenance claim for
indiplon. The evaluation of indiplon for sleep maintenance is ongoing and includes both
indiplon capsules and tablets. |
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The FDA Approvable Letter requested that we reanalyze data from certain preclinical and
clinical studies to support approval of indiplon 5 mg and 10 mg capsules for sleep initiation
and middle of the night dosing. The FDA Approvable Letter also requested reexamination of the
safety analyses. We held an end-of-review meeting with the FDA related to the FDA Approvable
Letter in August 2006. This meeting was specifically focused on determining the actions
needed to bring indiplon capsules from Approvable to Approval in the resubmission of the NDA
for indiplon capsules. At the meeting the FDA requested that the resubmission include further
analyses and modifications of analyses previously submitted to address questions raised by
the FDA in the initial review. This reanalysis has been completed. The FDA also requested,
and we have completed, a supplemental pharmacokinetic/food effect profile of indiplon
capsules including several meal types. |
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On June 12, 2007, we resubmitted our NDA for indiplon 5 mg and 10 mg capsules seeking
clearance to market indiplon capsules for the treatment of insomnia. The FDA accepted the NDA
resubmission and established a Prescription Drug User Fee Act (PDUFA) date of December 12,
2007. The PDUFA action date is the date by which the FDA is expected to have completed its
review of the resubmission and to document its assessment through the issuance of an action
letter. |
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R1 and R2 refer to two CRF receptor subtypes. |
We were originally incorporated in California in January 1992 and were reincorporated in the
state of Delaware in May 1996. Our corporate offices are located at 12790 El Camino Real, San
Diego, California 92130. Our telephone number is (858) 617-7600. Our website address is
www.neurocrine.com. Information contained in our website does not constitute part of this
prospectus.
Unless otherwise specified or required by context, references in this prospectus to we,
us, our and Neurocrine refer to Neurocrine Biosciences, Inc. and our subsidiaries on a
consolidated basis.
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RISK FACTORS
An investment in our common stock involves a high degree of risk. Before you make a decision
to invest in our common stock, you should consider carefully the risks described in the section
entitled Risk Factors contained in our Quarterly Report on Form 10-Q for the quarterly period
ended September 30, 2007, as filed with the SEC on November 2, 2007, which is incorporated herein
by reference in its entirety, as well as any amendment or update thereto reflected in subsequent
filings with the SEC. If any of these risks actually occur, our business, operating results,
prospects or financial condition could be materially and adversely affected. This could cause the
trading price of our common stock to decline and you may lose part or all of your investment.
FORWARD-LOOKING STATEMENTS
This prospectus, including the information incorporated by reference herein, and any
applicable prospectus supplement including the documents we incorporate by reference therein,
contain forward-looking statements that involve a number of risks and uncertainties. Although our
forward-looking statements reflect the good faith judgment of our management, these statements can
only be based on facts and factors currently known by us. Consequently, these forward-looking
statements are inherently subject to risks and uncertainties, and actual results and outcomes may
differ materially from results and outcomes discussed in the forward-looking statements.
Forward-looking statements can be identified by the use of forward-looking words such as
believes, expects, hopes, may, will, plan, intends, estimates, could, should,
would, continue, seeks, pro forma, or anticipates, or other similar words (including
their use in the negative), or by discussions of future matters such as the development of new
products, technology enhancements, possible changes in legislation and other statements that are
not historical. These statements include but are not limited to statements under the captions
Business, Risk Factors and Managements Discussion and Analysis of Financial Condition and
Results of Operations and in other sections incorporated by reference from our Annual Report on
Form 10-K and Quarterly Reports on Form 10-Q, as applicable, as well as our other filings with the
SEC. You should be aware that the occurrence of any of the events discussed under the heading Risk
Factors above and in any applicable prospectus supplement and any documents incorporated by
reference herein or therein could substantially harm our business, results of operations and
financial condition and that if any of these events occurs, the trading price of our common stock
could decline and you could lose all or a part of the value of your common stock.
The cautionary statements made in this prospectus are intended to be applicable to all related
forward-looking statements wherever they may appear in this prospectus or in any prospectus
supplement or any documents incorporated by reference herein or therein. We urge you not to place
undue reliance on these forward-looking statements, which speak only as of the date they are made.
Except as required by law, we assume no obligation to update our forward-looking statements, even
if new information becomes available in the future.
USE OF PROCEEDS
Except as described in any prospectus supplement, we currently intend to use the net proceeds
from the sale of our common stock under this prospectus for general corporate purposes, including
the clinical and preclinical development of our drug candidates, research and development expenses,
general and administrative expenses, manufacturing expenses, and potential acquisitions of
companies and technologies that complement our business. When shares of our common stock are
offered, the prospectus supplement relating thereto will set forth our intended use for the net
proceeds we receive from the sale of such shares. Pending the application of the net proceeds, we
expect to invest the proceeds in short-term, interest-bearing instruments or other investment-grade
securities.
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DESCRIPTION OF CAPITAL STOCK
As of the date of this prospectus, our restated certificate of incorporation, as amended,
authorizes us to issue 110,000,000 shares of common stock, par value $0.001 per share, and
5,000,000 shares of preferred stock, par value $0.001 per share. As
of November 28, 2007,
38,268,679 shares of common stock were outstanding and no shares of preferred stock
were outstanding.
The following summary describes the material terms of our capital stock. The description of
capital stock is qualified by reference to our restated certificate of incorporation, as amended
and our bylaws, as amended, which are incorporated by reference as exhibits into the registration
statement of which this prospectus is a part.
Common Stock
Voting. Common stockholders are entitled to one vote per share for the election of directors
and on all other matters that require stockholder approval, and do not have cumulative voting
rights.
Dividends and Other Distributions. Subject to any preferential rights of outstanding
preferred stock, if any, holders of our common stock are entitled to share ratably in any dividends
declared by our board of directors on the common stock and paid out of funds legally available for
such dividends.
Distribution on Dissolution. Subject to any preferential rights of outstanding preferred
stock, if any, in the event of our liquidation, dissolution or winding up, holders of our common
stock are entitled to share ratably in any assets remaining after payment of liabilities and the
liquidation preferences of any outstanding preferred stock.
Other Rights. Our common stock does not carry any preemptive rights enabling a holder to
subscribe for, or receive shares of, any class of our common stock or any other securities
convertible into shares of any class of our common stock. There are no redemption rights or
sinking fund provisions applicable to our common stock.
Preferred Stock
We currently have no outstanding shares of preferred stock. Under our restated certificate of
incorporation, as amended, our board of directors is authorized to issue shares of our preferred
stock from time to time, in one or more classes or series, without stockholder approval. Prior to
the issuance of shares of each series, the board of directors is required by the Delaware General
Corporation Law (DGCL), and our restated certificate of incorporation, as amended, to adopt
resolutions and file a certificate of designation with the Secretary of State of the State of
Delaware. The certificate of designation would fix for each class or series the designations,
powers, preferences, rights, qualifications, limitations and restrictions, including the following:
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the number of shares constituting each class or series; |
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voting rights; |
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rights and terms of redemption, including sinking fund provisions; |
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dividend rights and rates; |
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dissolution; |
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terms concerning the distribution of assets; |
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conversion or exchange terms; |
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redemption prices; and |
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liquidation preferences. |
Any future issuance of additional preferred stock could adversely affect the voting power of
holders of common stock and reduce the likelihood that common stockholders will receive dividend
payments and payments upon liquidation. Such an issuance could have the effect of decreasing the
market price of the common stock. Such an issuance also could have the effect of delaying,
deterring or preventing a change in control of us.
Anti-Takeover Provisions
Delaware Law. We are subject to the provisions of Section 203 of the DGCL. In general,
Section 203 prohibits a publicly held Delaware corporation from engaging in a business
combination with an interested stockholder for a period of three years after the date of the
transaction in which the person became an interested stockholder. Generally, a business
combination includes a merger, asset sale or other transaction resulting in a financial benefit to
the stockholder. An interested stockholder is a person who either owns 15% or more of our
outstanding voting stock or, together with affiliates and associates, owns or, within three prior
years, did own, 15% or more of our outstanding voting stock. These restrictions do not apply if:
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before the date that the person became an interested stockholder, our board of
directors approved either the business combination or the transaction which makes the
person an interested stockholder; |
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the interested stockholder owned at least 85% of the voting stock of the
corporation outstanding at the time the transaction commenced, excluding for purposes
of determining the number of shares outstanding (i) shares owned by persons who are
directors and also officers and (ii) shares owned by employee stock plans in which
employee participants do not have the right to determine confidentially whether shares
held subject to the plan will be tendered in a tender or exchange offer; or |
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on or after the date that the person became an interested stockholder, the
business combination is approved by (i) our board of directors and (ii) authorized at
an annual or special meeting of our stockholders by the affirmative vote of at least 66
2/3% of our outstanding voting stock that is not owned by the interested stockholder. |
The statute could have the effect of delaying, deferring, or preventing a change in control.
Bylaw and Certificate of Incorporation Provisions. Our bylaws, as amended, provide that
special meetings of our stockholders may be called by our board of directors, the chairman of our
board of directors, our President or by one or more stockholders holding 10% of the votes entitled
to be cast at that meeting. Our restated certificate of incorporation, as amended, (i) provides for
a board comprised of three classes of directors with each class serving a staggered three-year
term, (ii) authorizes our board of directors to issue preferred stock from time to time, in one or
more classes or series, without stockholder approval, (iii) requires the approval of at least
two-thirds of the outstanding voting stock to amend certain provisions of our restated certificate
of incorporation, as amended, and our bylaws, as amended and (iv) does not include a provision
for cumulative voting for directors. Under cumulative voting, a minority stockholder holding a
sufficient percentage of a class
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of shares may be able to ensure the election of one or more
directors. These and other provisions contained in our restated certificate of incorporation, as
amended, and bylaws, as amended, could delay or discourage transactions involving an actual or
potential change in control of us or our management, including transactions in which stockholders
might otherwise receive a premium for their shares over then current prices. Such provisions could
also limit the ability of stockholders to remove current management or approve transactions that
stockholders may deem to be in their best interests and could adversely affect the price of our
common stock.
Transfer Agent and Registrar
The transfer agent and registrar for our common stock is American Stock Transfer & Trust
Company. The transfer agent and registrars address is 59 Maiden Lane, New York, New York 10038.
Listing on the Nasdaq Global Select Market
Our common stock is listed on the Nasdaq Global Select Market under the symbol NBIX.
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PLAN OF DISTRIBUTION
We may sell our common stock covered by this prospectus in any of three ways (or in any
combination):
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to or through underwriters or dealers; |
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directly to one or more purchasers; or |
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through agents. |
We may distribute the common stock:
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from time to time in one or more transactions at a fixed price or prices, which may
be changed from time to time; |
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at market prices prevailing at the time of sale; |
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at prices related to the prevailing market prices; or |
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at negotiated prices. |
Each time we offer and sell common stock, we will provide a prospectus supplement or
supplements that will describe the method of distribution and set forth the terms of the offering
of our common stock covered by this prospectus, including:
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the name or names of any underwriters, dealers or agents; |
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the amounts of common stock underwritten or purchased by each of them; |
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the purchase price of the common stock and the proceeds we will receive from the
sale; |
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any over-allotment options under which underwriters may purchase additional common
stock from us; |
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any underwriting discounts or commissions or agency fees and other items
constituting underwriters or agents compensation; |
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the public offering price of the common stock; |
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any discounts, commissions or concessions allowed or reallowed or paid to dealers;
and |
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any securities exchange or market on which the common stock may be listed. |
Any public offering price and any discounts or concessions allowed or reallowed or paid to
dealers may be changed from time to time. We may determine the price or other terms of the common
stock offered under this prospectus by use of an electronic auction. We will describe how any
auction will determine the price or any other terms, how potential investors may participate in the
auction and the nature of the obligations of the underwriter, dealer or agent in the applicable
prospectus supplement.
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Underwriters or dealers may offer and sell the offered common stock from time to time in one
or more transactions, including negotiated transactions, at a fixed public offering price or at
varying prices determined at the time of sale. If underwriters or dealers are used in the sale of
any common stock, the common stock will be acquired by the underwriters or dealers for their own
account and may be resold from time to time in one or more transactions described above. The common
stock may be either offered to the public through underwriting syndicates represented by managing
underwriters, or directly by underwriters or dealers. Generally, the underwriters or dealers
obligations to purchase the common stock will be subject to certain conditions precedent. The
underwriters or dealers will be obligated to purchase all of the common stock if they purchase any
of the common stock, unless otherwise specified in the prospectus supplement. We may use
underwriters with whom we have a material relationship. We will describe the nature of any such
relationship in the prospectus supplement, naming the underwriter.
We may sell the common stock through agents from time to time. The prospectus supplement will
name any agent involved in the offer or sale of the common stock and any commissions we pay to
them. Generally, any agent will be acting on a best efforts basis for the period of its
appointment. We may authorize underwriters, dealers or agents to solicit offers by certain
purchasers to purchase the common stock from us at the public offering price set forth in the
prospectus supplement pursuant to delayed delivery contracts providing for payment and delivery on
a specified date in the future. The contracts will be subject only to those conditions set forth in
the prospectus supplement, and the prospectus supplement will set forth any commissions we pay for
solicitation of these contracts.
Agents, dealers and underwriters may be entitled to indemnification by us against certain
civil liabilities, including liabilities under the Securities Act of 1933, as amended, or to
contribution with respect to payments which the agents, dealers or underwriters may be required to
make in respect thereof. Agents, dealers and underwriters may be customers of, engage in
transactions with, or perform services for us in the ordinary course of business.
Any underwriter may engage in overallotment, stabilizing transactions, short covering
transactions and penalty bids in accordance with Regulation M under the Exchange Act of 1934.
Overallotment involves sales in excess of the offering size, which create a short position. This
short sales position may involve either covered short sales or naked short sales. Covered short
sales are short sales made in an amount not greater than the underwriters over-allotment option to
purchase additional shares in this offering described above. The underwriters may close out any
covered short position either by exercising their over-allotment option or by purchasing shares in
the open market, if possible. To determine how they will close the covered short position, the
underwriters will consider, among other things, the price of shares available for purchase in the
open market, as compared to the price at which they may purchase shares through the over-allotment
option. Naked short sales are short sales in excess of the over-allotment option. The underwriters
must close out any naked short position by purchasing shares in the open market. A naked short
position is more likely to be created if the underwriters are concerned that, in the open market
after pricing, there may be downward pressure on the price of the shares that could adversely
affect investors who purchase shares in this offering. Stabilizing transactions permit bids to
purchase the underlying security for the purpose of fixing the price of the security so long as the
stabilizing bids do not exceed a specified maximum. Penalty bids permit the underwriters to reclaim
a selling concession from a dealer when the securities originally sold by the dealer are purchased
in a covering transaction to cover short positions.
Similar to other purchase transactions, an underwriters purchase to cover the syndicate short
sales or to stabilize the market price of our common stock may have the effect of raising or
maintaining the market price of our common stock or preventing or mitigating a decline in the
market price of our common stock. As a result, the price of the shares of our common stock may be
higher than the price that might otherwise exist in the open market. The imposition of a penalty bid might
also have an effect on the price of the shares if it discourages resales of the shares.
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Neither we nor the underwriters makes any representation or prediction as to the effect that
the transactions described above may have on the price of the common stock. If such transactions
are commenced, they may be discontinued without notice at any time.
LEGAL MATTERS
The validity of the common stock being offered hereby will be passed upon by Cooley Godward
Kronish LLP, San Diego, California.
EXPERTS
Ernst & Young LLP, independent registered public accounting firm, has audited our consolidated
financial statements included in our Annual Report on Form 10-K for the year ended December 31,
2006, and managements assessment of the effectiveness of our internal control over financial
reporting as of December 31, 2006, as set forth in their reports, which are incorporated by
reference in this prospectus and elsewhere in the registration statement. Our financial statements
and managements assessment are incorporated by reference in reliance on Ernst & Young LLPs
reports, given on their authority as experts in accounting and auditing.
WHERE YOU CAN FIND MORE INFORMATION
We file annual, quarterly and special reports, proxy statements and other information with the
SEC. You may read and copy any document we file at the SECs public reference room at 450 Fifth
Street, N.W., Washington, D.C., 20549. Please call the SEC at 1-800-SEC-0330 for further
information on the operation of the public reference room. Our SEC filings are also available to
the public at the SECs website at http://www.sec.gov.
INCORPORATION OF CERTAIN INFORMATION BY REFERENCE
The SEC allows us to incorporate by reference the information we file with them, which means
that we can disclose important information to you by referring you to those documents instead of
having to repeat the information in this prospectus. The information incorporated by reference is
considered to be part of this prospectus, and later information that we file with the SEC will
automatically update and supersede this information. We incorporate by reference the documents
listed below and any future filings we will make with the SEC under Sections 13(a), 13(c), 14, or
15(d) of the Exchange Act of 1934 after the date of this prospectus until the termination of the
offering of common stock covered by this prospectus (other than information furnished under Item
2.02 or Item 7.01 of Form 8-K):
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our annual report on Form 10-K for the year ended December 31, 2006 (filed on
February 9, 2007), including all information incorporated by reference therein; |
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our quarterly reports on Form 10-Q for the quarterly periods ended March 31, 2007
(filed on May 7, 2007), June 30, 2007 (filed on August 3, 2007), and September 30, 2007
(filed on November 2, 2007); |
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our current reports on Form 8-K filed on January 16, 2007, January 23, 2007,
February 21, 2007, May 31, 2007, June 6, 2007,
June 13, 2007, August 22, 2007, October
26, 2007 and November 1, 2007; |
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the description of our common stock contained in our registration statement on
Form 8-A, filed on April 3, 1996, including any amendment or reports filed for the
purpose of updating such description; and |
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all filings we make with the SEC pursuant to Section 13(a), 13(c), 14 or 15(d) of the
Exchange Act of 1934 after the date of this prospectus and before the termination of
this offering. |
You can request a copy of these filings, at no cost, by writing or telephoning us at the
following address or telephone number:
Neurocrine Biosciences, Inc.
12790 El Camino Real
San Diego, CA 92130
(858) 617-7600
Attn: Investor Relations
This prospectus is part of a registration statement we filed with the SEC. That registration
statement and the exhibits filed along with the registration statement contain more information
about us. Because information about documents referred to in this prospectus is not always
complete, you should read the full documents which are filed as exhibits to the registration
statement. You may read and copy the full registration statement and its exhibits at the SECs
public reference rooms or its website.
10
$150,000,000
Common Stock
NEUROCRINE BIOSCIENCES, INC.
PROSPECTUS
December 3, 2007