Prepared by MerrillDirect


UNITED STATES
SECURITIES AND EXCHANGE COMMISSION
Washington, DC  20549

 

FORM 10-Q

(Mark One)

ý QUARTERLY REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934
   
For the quarterly period ended June 30, 2001
 
OR
 
o TRANSITION REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934

For the transition period from ___ to ___

Commission File Number:  0-31913

AeroGen, Inc.


(Exact name of Registrant as specified in its charter)

 

Delaware 33-0488580
(State or other jurisdiction of incorporation or organization) (I.R.S. Employer Identification No.)
   
1310 Orleans Drive, Sunnyvale, CA 94089
(Address of principal executive offices) (zip code)
   
(408) 543-2400
Registrant’s telephone number, including area code

Indicate by check mark whether the Registrant (1) has filed all reports required to be filed by Section 13 or 15(d) of the Securities Exchange Act of 1934 during the preceding 12 months (or for such shorter period that the Registrant was required to file such reports), and (2) has been subject to such filing requirements for the past 90 days.

Yes  ý   No  o

As of July 31, 2001 there were 20,005,425 shares of the Registrant’s Common Stock, par value $0.001 per share, outstanding.



 

AeroGen, Inc.
(a company in the development stage)
Form 10-Q
Table of Contents

Part  I. Financial Information   
     
  Item 1. Consolidated Financial Statements (unaudited)  
       
    Condensed Consolidated Balance Sheets as of June 30, 2001 and December 31, 2000 3
       
    Condensed Consolidated Statements of Operations for the three and six months ended June 30, 2001 and 2000 4
       
    Condensed Consolidated Statements of Cash Flows for the six months ended June 30, 2001 and 2000 and 1997 5
       
    Notes to Condensed Consolidated Financial Statements 6
       
  Item 2. Management’s Discussion and Analysis of Financial Condition and Results of Operations 8
       
  Item 3. Quantitative and Qualitative Disclosures About Market Risk and Factors that May Affect Future Operating Results 12
       
       
Part  II. Other Information  
       
  Item 1. Legal Proceedings 12
       
  Item 2. Changes in Securities and Use of Proceeds 12
       
  Item 3. Defaults Upon Senior Securities 13
       
  Item 4. Submission of Matters to a Vote of Security Holders 13
       
  Item 5. Other information 13
       
  Item 6. Exhibits and Reports on Form 8-K 13
       
  Signatures 14

 

Part    I.  Financial Information

Item   1.  Consolidated Financial Statements

AeroGen, Inc.
(a development stage company)
Condensed Consolidated Balance Sheets
(unaudited; in thousands)

 

        June 30,
2001
  December 31,
2000
 
           
       
 
 
               
ASSETS        
  Current assets:        
    Cash and cash equivalents $ 39,945   $ 48,810  
    Available-for-sale securities 11,996   12,166  
    Accounts receivable 721   762  
    Inventory 233   ––  
    Prepaid expenses and other current assets 884   1,201  
     
 
 
      Total current assets 53,779   62,939  
  Property and equipment, net 1,918   1,905  
  Goodwill and other intangible assets, net 1,475   1,823  
  Other assets 23   45  
   
 
 
      Total assets $ 57,195   $ 66,712  
       
 
 
               
LIABILITIES AND STOCKHOLDERS’ EQUITY        
  Current liabilities:        
    Accounts payable $ 760   $ 915  
    Accrued liabilities 2,375   1,135  
    Deferred revenues 211   250  
     
 
 
      Total current liabilities 3,346   2,300  
               
  Other long-term liabilities 209   184  
   
 
 
      Total liabilities 3,555   2,484  
       
 
 
               
  Stockholders’ equity:        
    Common stock 20   20  
    Additional paid-in capital 110,675   110,692  
    Notes receivable from stockholders (679 ) (665 )
    Deferred stock-based compensation, net (5,195 ) (6,095 )
    Accumulated other comprehensive income (loss) (78 ) 15  
    Deficit accumulated during the development stage (51,103 ) (39,739 )
     
 
 
      Total stockholders’ equity 53,640   64,228  
       
 
 
         Total liabilities and stockholders’ equity $ 57,195   $ 66,712  
       
 
 

 

The accompanying notes are an integral part of these condensed consolidated financial statements.

3


AeroGen, Inc.
(a development stage company)
Condensed Consolidated Statements of Operations
(unaudited; in thousands, except per share data)

 

      Three Months Ended
June 30,
  Six Months Ended
June 30,
 
 
 
 
      2001   2000   2001   2000  
     
 
 
 
 
                     
Revenues:                
  Research and development $ 889   $ 2,429   $ 1,501   $ 3,568  
  Royalty, fee and other 62   ––   125   ––  
   
 
 
 
 
    Total revenues 951   2,429   1,626   3,568  
     
 
 
 
 
                     
Operating expenses:                
  Research and development 5,701   4,568   10,712   7,514  
  Selling, general and administrative 2,209   870   3,729   1,793  
  Purchased in-process research and development ––   3,500   ––   3,500  
   
 
 
 
 
    Total operating expenses 7,910   8,938   14,441   12,807  
     
 
 
 
 
Loss from operations (6,959 ) (6,509 ) (12,815 ) (9,239 )
Interest income, net 643   83   1,451   184  
 
 
 
 
 
                 
Net loss (6,316 ) (6,426 ) (11,364 ) (9,055 )
Dividend related to beneficial conversion feature of preferred stock ––   (202 ) ––   (202 )
 
 
 
 
 
Net loss available to common stockholders (6,316 ) (6,628 ) (11,364 ) (9,257 )
     
 
 
 
 
Net loss per common share, basic and diluted $ (0.32 ) $ (2.93 ) $ (0.58 ) $ (4.28 )
 
 
 
 
 
Shares used in computing net loss per common share, basic and diluted 19,628   2,263   19,543   2,163  
 
 
 
 
 

 

The accompanying notes are an integral part of these condensed consolidated financial statements.

4


 

AeroGen, Inc.
(a development stage company)
Condensed Consolidated Statements of Cash Flows
(unaudited; in thousands)

 

            Six Months Ended
June 30,
 
             
 
            2001   2000  
           
 
 
                   
Cash flows from operating activities:        
  Net loss $ (11,364)   $ (9,055 )
  Adjustments to reconcile net loss to net cash used in operating activities:        
    Depreciation and amortization 742   381  
    Purchased in-process research and development ––   3,500  
    Amortization of deferred stock-based compensation 667   178  
    Accrued interest on notes receivable from stockholders (14)   (10 )
    Amortization of investment discount (premium) (85)   ––  
    Changes in operating assets and liabilities:        
      Accounts receivable 41   (1,007 )
      Inventory (233)   ––  
      Prepaid expenses and other current assets 317   (133 )
      Other assets 22   28  
      Accounts payable (155)   503  
      Accrued liabilities 1,240   567  
      Deferred revenue (39)   ––  
      Other liabilities 43   ––  
       
 
 
        Net cash used in operating activities (8,818)   (5,048 )
           
 
 
                   
Cash flows from investing activities:        
  Acquisition of property and equipment (408)   (914 )
  Purchases of available-for-sale securities (12,011)   ––  
  Proceeds from maturities of available-for- sale investments 12,358   6,020  
  Cash acquired, net ––   392  
   
 
 
        Net cash provided by (used in) investing activities (61)   5,498  
         
 
 
                   
Cash flows from financing activities:        
  Proceeds from issuance of common stock 224   115  
  Proceeds from issuance of convertible preferred stock, net ––   4,988  
  Repayment of note payable ––   (157 )
  Repurchase of common stock (8)   ––  
   
 
 
        Net cash provided by financing activities 216   4,946  
         
 
 
Effect of exchange rate changes on cash (202)   27  
Net increase (decrease) in cash and cash equivalents (8,865)   5,423  
Cash and cash equivalents, beginning of period 48,810   1,822  
 
 
 
Cash and cash equivalents, end of period $ 39,945   $ 7,245  
 
 
 

 

The accompanying notes are an integral part of these condensed consolidated financial statements.

5


AeroGen, Inc.
(a development stage company)
NOTES TO CONDENSED CONSOLIDATED FINANCIAL STATEMENTS

Note 1 – SUMMARY OF SIGNIFICANT ACCOUNTING POLICIES

Organization and business of the company

             AeroGen, Inc., formerly Fluid Propulsion Technologies, Inc. (the “Company” or “Aerogen”), was incorporated in November 1991 to develop products using a proprietary aerosol generator.

             The Company is in the development stage and since inception has devoted substantially all of its efforts to developing products, including engaging in research and development activities with and without partners, raising capital, and recruiting personnel.  The Company has incurred net losses since inception and expects to incur substantial losses for the next several years.  To date, the Company has funded its operations primarily through the sale of equity securities, payments from partners, and interest income.

Basis of  presentation

             The accompanying unaudited condensed consolidated financial statements have been prepared in accordance with accounting principles generally accepted in the United States for interim financial information and with the instructions to Form 10-Q and Article 10-01 of Securities and Exchange Commission Regulation S-X.  Accordingly, they do not contain all of the information and footnotes required by generally accepted accounting principles for complete financial statements.  In the opinion of management, the accompanying unaudited, condensed consolidated financial statements reflect all adjustments (consisting of normal, recurring adjustments) considered necessary for a fair presentation of the Company's interim financial information.  These financial statements and notes should be read in conjunction with the audited financial statements and notes thereto of the Company included in the Company's Annual Report on Form 10-K for the year ended December 31, 2000.

             The results of operations for the three and six months ended June 30, 2001 are not necessarily indicative of the operating results that may be reported for the fiscal year ending December 31, 2001 or for any other future period.

Basis of consolidation

             In May 2000, the Company acquired Cerus Limited, which is now Aerogen (Ireland) Limited, a wholly owned subsidiary of the Company.  The consolidated financial statements include the accounts of the Company and its subsidiary.  All intercompany balances and transactions have been eliminated in consolidation.

Cash and cash equivalents

             Cash and cash equivalents include money market and deposit accounts and all highly liquid investments purchased with original maturities of three months or less.

Available–for–sale securities

             All investments are classified as available–for–sale and therefore are carried at fair market value.  Unrealized gains and losses on such investments are reported as a component of stockholders’ equity.  Realized gains and losses on sales of all such investments are reported in earnings and computed using the specific identification cost method.

Inventory

             Inventories are stated at the lower of cost (principally standard cost, which approximates actual cost on a first-in, first-out basis) or market value.  At June 30, 2001, inventory is comprised of $98,000 of raw materials, $116,000 of work in process and $19,000 of finished goods.  There was no inventory as of December 31, 2000.

6


 

Revenue recognition

             Research and development revenues are earned under agreements with third parties for contract research and development activities and are recorded as the related expenses are incurred.  Charges to these third parties are based upon negotiated rates for full time equivalent employees of the Company, and actual out-of-pocket costs.  Rates for full time equivalent employees are intended to approximate the Company’s costs.  Payments received that are related to future performance are recorded as deferred revenue and recognized as revenues as they are earned. None of the revenues recognized to date are refundable if the relevant research effort is not successful.

             Revenue from product sales and sales to distributors will be recognized at the time of product shipment, provided any significant rights to return products have expired, and collection of the receivable is probable.

             Royalty revenues are recorded as earned.  Fee and other revenues are recorded in accordance with Staff Accounting Bulletin No. 101 (“SAB  No. 101”), “Revenue Recognition in Financial Statements”.

Research and development expenses

             Research and development costs are charged to operations as incurred.  Certain research and development projects are funded under agreements with third parties, and the costs related to these activities are included in research and development expenses.

Foreign currency translation

             The Company’s Irish subsidiary uses its local currency as its functional currency.  Assets and liabilities are translated at exchange rates in effect at the balance sheet date and income and expense amounts at the average exchange rates during the period.  Resulting translation adjustments are recorded directly to a component of stockholders’ equity.

Comprehensive income (loss)

             Comprehensive income (loss) generally represents all changes in stockholders’ equity except those resulting from investments or contributions by stockholders.  The Company’s unrealized gains and losses on available-for-sale securities and foreign currency translation gains and losses represent the only components of comprehensive income (loss) that are excluded from the Company’s net loss.

Net loss per common share

             Basic net loss per share is computed by dividing net loss available to common stockholders by the weighted average number of vested common shares outstanding for the period.  Diluted net loss per share is computed giving effect to all potential dilutive common shares, including options, warrants and convertible preferred stock.  Options, warrants, common stock subject to possible repurchase by the Company and convertible preferred stock were not included in the diluted net loss per share calculations because the effect would be antidilutive.  Options, warrants, and common stock subject to possible repurchase were 2,767,000 and 2,118,000 shares as of June 30, 2001 and 2000, respectively.  Convertible preferred stock was none and 10,504,000 shares as of June 30, 2001 and 2000, respectively.

7


Note 2 – RECENT ACCOUNTING PRONOUNCEMENTS

             Effective January 1, 2001 the Company adopted Statement of Financial Accounting Standards No. 133 (“SFAS No. 133”), as amended, “Accounting for Derivative Instruments and Hedging Activities.”  SFAS No. 133 requires that all derivatives be recognized at fair value in the statement of financial position, and that the corresponding gains or losses be reported either in the statement of operations or as a component of comprehensive income, depending on the type of relationship that exists. The Company has not engaged in derivative or hedging activities and the adoption of SFAS No. 133 did not have a significant impact on its financial position or results of operations.

             In July 2001, the Financial Accounting Standards Board (“FASB”) issued SFAS No. 141"Business Combinations" which establishes financial accounting and reporting for business combinations and supersedes APB Opinion No. 16, Business Combinations, and FASB Statement No. 38, Accounting for Preacquisition Contingencies of Purchased Enterprises.  SFAS No. 141 requires that all business combinations be accounted for using one method, the purchase method. The provisions apply to all business combinations initiated after June 30, 2001.  The adoption of SFAS No. 141 is expected to have no material impact on financial reporting and related disclosures of the Company.

             In July 2001, the FASB issued SFAS No. 142 "Goodwill and Other Intangible Assets," (“SFAS No. 142”) which establishes financial accounting and reporting for acquired goodwill and other intangible assets and supersedes APB Opinion No. 17, Intangible Assets.  SFAS No. 142 addresses how intangible assets that are acquired individually or with a group of other assets (but not those acquired in a business combination) should be accounted for in financial statements upon their acquisition, and after they have been initially recognized in the financial statements. The provisions of SFAS No. 142 are effective for fiscal years beginning after December 15, 2001.  The Company will adopt SFAS No. 142 during the first quarter of fiscal 2002, and is in the process of evaluating the impact of implementation on the financial position of the Company.

Item     2.          Management’s Discussion and Analysis of Financial Condition and Results of Operations

             In addition to historical information, this report contains estimates and other forward-looking statements within the meaning of Section 27A of the Securities Act of 1933, as amended, and Section 21E of the Securities Exchange Act of 1934, as amended.  Actual results could differ materially from any future performance suggested in this report as a result of many factors, including those referred to in “Factors That May Affect Future Operating Results,” elsewhere in this report and in the Company's Annual Report on Form 10-K for the year ended December 31, 2000 (the “Form 10-K”).  The following discussion should be read in conjunction with the unaudited condensed consolidated financial statements and notes included elsewhere in this report and the information included in the Form 10-K.

Overview

             Aerogen was incorporated in November 1991.  We specialize in the controlled delivery of drugs to the lungs.  We are using our technology to develop respiratory products for marketing by us, and we are developing products in collaboration with pharmaceutical and biotechnology companies for both respiratory therapy and for the delivery of drugs via the lungs to the bloodstream.

             We are in the development stage and since inception have devoted substantially all of our efforts to the development of products.  We have an accumulated deficit of approximately $51.1 million as of June 30, 2001.  We expect to incur significant additional operating losses over the next several years and expect cumulative losses to increase, primarily due to the expansion of our research and development activities, an increase in the number and size of clinical trials, the costs associated with the marketing and manufacturing of our initial products, and the general expansion of our business activities.  We anticipate that our quarterly financial results will fluctuate for the foreseeable future.  Therefore, period to period comparisons should not be relied upon as predictive of the results in future periods.  Our sources of working capital have been equity financings, research and development revenues, interest earned on investments and, to a lesser extent, equipment lease financings and royalties.

8


Results of Operations

Revenues

             Research and development revenues for the three and six months ended June 30, 2001 were $0.9 million, and $1.5 million, respectively, compared with $2.4 million and $3.6 million for the same periods of 2000.  The decreases in revenues resulted primarily from a lower level of product development activities performed for partner companies other than PathoGenesis Corporation (now a wholly-owned subsidiary of Chiron Corporation).

             Research and development revenues can be expected to vary from period to period based on the activities requested by partner companies in any particular period, and therefore are not predictable.  Based on agreements we currently have in place, we expect research and development revenues for 2001 to be lower than those for 2000.

             We shipped initial units of our Aeroneb ™ Portable Nebulizer System to a distributor during the quarter ended June 30, 2001; revenues and the related product costs have been deferred until the rights to return these products, applicable only to the initial units, have expired.

             Royalty, fee and other revenues for the three and six months ended June 30, 2001 were $0.1 million and $0.1 million, respectively, compared with none for the same periods of 2000.  The increases resulted primarily from minimum royalties earned from a consumer products company.

Research and development expenses

             Research and development expenses for the three and six months ended June 30, 2001 were $5.7 million and $10.7 million, respectively, compared with $4.6 million and $7.5 million for same periods of 2000.  The increase in research and development expenses resulted primarily from the expansion of development and clinical activities for the respiratory products we plan to market ourselves and our Aerodose ™ insulin inhaler product.  The increases are primarily attributable to increased salary and benefit costs ($0.8 million and $1.4 million), increased costs incurred by our Irish subsidiary ($0.5 million and $0.9 million including Irish payroll related costs), increased clinical costs ($0.1 million and $0.5 million) and increased amortization of deferred stock-based compensation ($0.2 million and $0.2 million), partially offset by decreased professional services ($0.3 million and $0.4 million), as well as fluctuations in other categories of research and development spending.

             Research and development expenses represent expenses related to our own research and development projects, as well as the costs related to research and development activities for our partners.  Research and development expenses for partner activities approximate our revenues from those partners.  Research and development expenses include salaries and benefits for scientific and development personnel, laboratory supplies, consulting services, clinical expenses, and the expenses associated with the development of manufacturing processes, including related overhead.  We expect research and development spending to increase significantly over the next several years as we increase clinical trials, expand our research and development activities to support our products and those which we develop in our collaborations, and increase commercial manufacturing.  Future research and development and clinical expenditures cannot be predicted reliably, as they depend in part upon our success in continuing existing development collaborations, entering into new partnering agreements, and the level of internally funded research and development efforts.

Selling, general and administrative expenses.

             Selling, general and administrative expenses for the three and six months ended June 30, 2001 were $2.2 million and $3.7 million, respectively, compared with $0.9 million and $1.8 million for the same periods of 2000.  The increases for both periods were primarily due to increased personnel and other marketing costs associated with product launch preparations ($0.6 million and $0.9 million), other costs associated with operating as a public company ($0.6 million and $ 0.7 million) and amortization of goodwill and stock-based compensation ($0.2 million and $0.3 million).  We expect that selling, general and administrative expenses will increase as our business expands and as we increase our sales efforts in the second half of 2001 and launch new products.

9


 

Purchased in-process research and development

             Purchased in-process research and development expenses of $3.5 million were recorded for the three and six months ended June 30, 2000 in conjunction with our acquisition of Aerogen (Ireland) Limited in May 2000.  There were no corresponding expenses in 2001.

 

Interest income, net

             Interest income, net for the three and six months ended June 30, 2001 was $0.6 million and $1.5 million, respectively, compared with $ 0.1 million and $0.2 million for the same periods of 2000.  The increase in interest income, net was primarily due to higher average cash, cash equivalents and investment balances resulting from the completion of equity placements of our common stock in our IPO and convertible preferred stock.  We sold convertible preferred stock in July, May and March of 2000 for total net proceeds of approximately $21.3 million.  Sales of common stock in our IPO resulted in approximately $44.5 million of net proceeds, including $6.0 million from exercise of the underwriters’ over-allotment option.

 

Liquidity and Capital Resources

             Since inception, we have financed our operations primarily through equity financings, research and development revenues and the interest earned on these funds.  We have received approximately $97.8 million aggregate net proceeds from sales of our common and preferred stock through June 30, 2001, including approximately $44.5 million of net proceeds from our IPO.

             As of June 30, 2001, we had cash, cash equivalents and available–for–sale securities of approximately $51.9 million.  Net cash used in operating activities of $8.8 million during the six months ended June 30, 2001 resulted primarily from the net loss for the period, partially reduced by non-cash related charges of approximately $1.4 million and an increase in accrued liabilities of $1.2 million.  Net cash used in operating activities of $5.0 million during the six months ended June 30, 2000 resulted primarily from the net loss for the period, partially reduced by non-cash charges of approximately $4.1 million, $3.5 million of which were recorded in conjunction with the acquisition of Aerogen (Ireland) Limited.

             Net cash used in investing activities of $0.1 million for the six months ended June 30, 2001 consisted primarily of acquisition of $0.4 million of property and equipment.  Net cash provided by investing activities of $5.5 million for the six months ended June 30, 2000 consisted primarily of proceeds from maturities of securities of $6.0 million, partially offset by acquisitions of property and equipment of $0.9 million.

             Net cash provided by financing activities of $4.9 million for the six months ended June 30, 2000 primarily consisted of proceeds from the sale of convertible preferred stock.

             The development of our technology and products will require a commitment of substantial funds to conduct the costly and time-consuming product development and clinical trials required to develop and expand our technology and products and to bring any such products to market.  Our future capital requirements and operating expenses will depend on many factors including, but not limited to, research and development activities, the timing, cost, extent and results of clinical trials, our success in licensing drugs for use in our products, regulatory approvals, the status of competitive products, marketing and manufacturing costs associated with commercialization of products, costs involved in obtaining and maintaining patents, and our ability to enter into collaborative agreements.

             Based upon our current plans, we believe that our cash, cash equivalents and available–for–sale securities will be sufficient to meet our capital requirements through calendar year 2002.  Our forecast of the period of time through which our financial resources will be adequate to support our operations is a forward–looking statement that involves risks and uncertainties, and actual results could vary materially.  The factors described above, as well as the risk factors discussed in the Form 10-K, will impact our future capital requirements and the adequacy of our available funds.

10


 

Recent Accounting Pronouncements

             Effective January 1, 2001 the Company adopted Statement of Financial Accounting Standards No. 133 (“SFAS No. 133”), as amended, “Accounting for Derivative Instruments and Hedging Activities.”  SFAS No. 133 requires that all derivatives be recognized at fair value in the statement of financial position, and that the corresponding gains or losses be reported either in the statement of operations or as a component of comprehensive income, depending on the type of relationship that exists.  We have not engaged in derivative or hedging activities and the adoption of SFAS No. 133 did not have any significant impact on our financial position or results of operations.

             In July 2001, the Financial Accounting Standards Board (“FASB”) issued SFAS No. 141"Business Combinations"" which establishes financial accounting and reporting for business combinations and supersedes APB Opinion No. 16, Business Combinations, and FASB Statement No. 38, Accounting for Preacquisition Contingencies of Purchased Enterprises.  SFAS No. 141 requires that all business combinations be accounted for using one method, the purchase method. The provisions apply to all business combinations initiated after June 30, 2001.  We expect the adoption of SFAS No. 141 will have no material impact on our financial reporting and related disclosures.

             In July 2001, the FASB issued SFAS No. 142"Goodwill and Other Intangible Assets," (“SFAS No. 142”) which establishes financial accounting and reporting for acquired goodwill and other intangible assets and supersedes APB Opinion No. 17, Intangible Assets.  SFAS No. 142 addresses how intangible assets that are acquired individually or with a group of other assets (but not those acquired in a business combination) should be accounted for in financial statements upon their acquisition, and after they have been initially recognized in the financial statements. The provisions of SFAS No. 142 are effective starting with fiscal years beginning after December 15, 2001.  We will adopt SFAS No. 142 during the first quarter of fiscal 2002, and are in the process of evaluating the impact of implementation on our financial position.

11


Item 3.  Quantitative and Qualitative Disclosure About Market Risk

Interest rate risk

             Interest rate risk represents the risk of loss that may impact our financial position, operating results, or cash flows due to changes in interest rates.  This exposure is directly related to our normal operating activities.  Our cash, cash equivalents, and short-term investments are invested with high quality issuers and are generally of a short-term nature.  As a result, we do not believe that near-term changes in interest rates will have a material effect on our future results of operations.  As of June 30, 2001 there had been no material change in our interest rate exposure from that described in our Form 10-K.

Exchange rate risk

             Due to our Irish operations, we have market risk exposure to adverse changes in foreign currency exchange rates.  The revenues and expenses of our subsidiary, Aerogen (Ireland) Limited, are denominated in Irish currency.  At the end of each quarter, the revenues and expenses of our subsidiary are translated into U.S. dollars using the average currency exchange rate in effect for that quarter, and assets and liabilities are translated into U.S. dollars using the exchange rate in effect at the end of that quarter.  Fluctuations in exchange rates therefore impact our financial condition and results of operations, as reported in U.S. dollars.  To date, we have not experienced any significant negative impact as a result of fluctuations in foreign currency markets.  As a policy, we do not engage in speculative or leveraged transactions, nor do we hold financial instruments for trading purposes.

             We plan to expand our overseas operations.  As a result, our operating results may become subject to more significant fluctuations based on changes in exchange rates of foreign currencies in relation to the U.S. dollar.  We will periodically analyze our exposure to currency fluctuations and we may adjust our policies to allow for financial hedging techniques to minimize exchange rate risk.

 

Factors That May Affect Future Operating Results

             Risk factors that may affect future operating results are described in Part I of our Form 10-K and have not changed materially since such date.  Please also see “Liquidity and Capital Resources” above.

 

Part   II.     Other Information

Item 1. Legal Proceedings
None
   
Item 2. Changes in Securities and Use of Proceeds

             In November 2000, the Securities Exchange Commission declared our Registration Statement on Form S-1 effective. We completed our initial public offering, including exercise of the underwriters’ over-allotment option, of 4,140,000 shares at an initial public offering price of $12.00 per share, for aggregate cash proceeds of approximately $49.7 million.  The managing underwriters of the offering were Chase Securities Inc., CIBC World Markets Corp., and SG Cowen Securities Corporation.

             In connection with the offering, we paid a total of approximately $3.5 million in underwriting discounts and commissions and $1.7 million in other offering costs and expenses. After deducting the underwriting discounts and commissions and the offering costs and expenses, our net proceeds from the offering, including the over-allotment option were approximately $44.5 million.

             From January 1, 2001 through June 30, 2001 the proceeds from the offering were used for research and development and clinical activities, marketing and manufacturing expenditures for existing and future products, capital expenditures, and general corporate purposes.  In the future we intend to use the net proceeds in a similar manner.

12


 

             As of June 30, 2001, $35.3 million of the proceeds from our IPO remained available and were primarily invested in cash equivalents and short-term available-for-sale securities.

 

Item 3. Defaults Upon Senior Securities
None
 
           
Item 4. Submission of Matters to a Vote of Security Holders  
     
  On May 8, 2001, at the Company’s annual meeting of stockholders, the following votes were cast:
           
  To elect as Class I Directors for a three year term ending in 2004:  
           
      For Withheld    
     

   
    Dr. Phyllis I. Gardner 12,428,384 400    
    Mr. Philips M. Young 12,428,384 400    
           
  To ratify the appointment of PricewaterhouseCoopers LLC as the Company’s independent accountants:
           
      For Against Abstain  
     


 
      12,386,559 40,350 1,875  
           
Item 5. Other Information
None
 
           
Item 6. Exhibits and Reports on Form 8-K  
    a.   Exhibits:  
      3.2 Certificate of Incorporation  (including Certificate of Designation of Series A Junior Participating Preferred Stock)1
           
      10.14 Restated Executive Severance Agreement
         
      10.15 Rights Agreement dated as of June 5, 2001 between AeroGen, Inc. and Mellon Investor Services LLC, as Rights Agent.1
           
    b.   Reports on Form 8-K:  
       
    The Company filed a Report on Form 8-K on June 30, 2001 (File Number 0-31913) concerning the adoption by the Company's Board of Directors of a stockholder rights plan.

 


1  Incorporated by reference to the Company’s Report on Form 8-K filed with the Securities and Exchange Commission on June 13, 2001 ( File Number 0-31913)


 

Signatures

 

             Pursuant to the requirements of the Securities Exchange Act of 1934, as amended, (the “Exchange Act”) the registrant has duly caused this report to be signed on its behalf by the undersigned, thereunto duly authorized.

  AeroGen, Inc.
  (Registrant)
     
     
Dated: August 14, 2001 By: /s/  JANE E. SHAW
   
    Jane E. Shaw, Phd.
    Chairman and Chief Executive Officer
     
Dated:  August 14, 2001 By: /s/  DEBORAH K. KARLSON
   
    Deborah K. Karlson
    Vice President, Finance and
    Chief Financial Officer