FORM 10-Q SECURITIES AND EXCHANGE COMMISSION Washington, DC 20549 (Mark one) [x] QUARTERLY REPORT UNDER SECTION 13 OR 15 (d) OF THE SECURITIES EXCHANGE ACT OF 1934 For the quarterly period ended September 30, 1997 OR [_] 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 0-16132 CELGENE CORPORATION ------------------------------------------------------ (Exact name of registrant as specified in its charter) Delaware 22-2711928 --------------------------------------- ---------------------- (State or other jurisdiction of (I.R.S. Employer incorporation or organization) Identification Number) 7 Powder Horn Drive, Warren, NJ 07059 --------------------------------------- ---------------------- (Address of principal executive offices) (Zip Code) Registrant's telephone number, including area code: 732-271-1001. 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 _x__ No ___ At November 12, 1997, 13,189,596 shares of Common Stock and 76 shares of Series A Convertible Preferred Stock, par value $.01 per share, were outstanding. 1 CELGENE CORPORATION INDEX TO FORM 10-Q Page No. PART I FINANCIAL INFORMATION Item I Unaudited Condensed Financial Statements Condensed Balance Sheets as of September 30, 1997 (unaudited) and December 31, 1996 3 Condensed Statement of 4 Operations - Nine-Month Periods Ended September 30, 1997 and 1996 (unaudited) Condensed Statements of Operations - Three-Month Periods Ended September 30, 1997 and 1996 (unaudited) 5 Condensed Statements of Cash Flows - Nine-Month Periods Ended September 30, 1997 and 1996 (unaudited) 6 Notes to Unaudited Condensed Financial Statements 8 Item 2 Management's Discussion and Analysis of Financial Condition and Results of Operations 11 PART II OTHER INFORMATION 17 Signatures 18 2 PART I - FINANCIAL INFORMATION Item 1 - Condensed Financial Statements CELGENE CORPORATION CONDENSED BALANCE SHEETS ASSETS Sept 30, 1997 Dec 31, 1996 ------------- ------------ (Unaudited) Current assets: Cash and cash equivalents $ 475,638 $ 922,961 Marketable securities available for sale 4,527,139 16,892,023 Accounts receivable 168,426 378,595 Other current assets 638,017 635,841 ------------- ------------ Total current assets 5,809,220 18,829,420 Plant and equipment, net 2,521,901 1,940,615 Deferred costs -- 126,577 Other assets 79,167 41,250 ------------- ------------ $ 8,410,288 $ 20,937,862 ============= ============ LIABILITIES AND STOCKHOLDERS' EQUITY Current liabilities: Accounts payable $ 1,308,110 $ 1,552,674 Accrued expenses 1,367,327 881,604 Capital lease obligation 210,499 -- ------------- ------------ Total current liabilities 2,885,936 2,434,278 ------------- ------------ Capitalized lease obligation-net of current portion 420,997 -- Convertible debentures -- 2,026,043 Convertible debentures - accrued interest -- 412,532 ------------- ------------ Total liabilities 3,306,933 4,872,853 ------------- ------------ Stockholders' equity: Preferred stock, $.01 par value; 5,000,000 shares authorized Series A convertible, redeemable 4.9% cumulative preferred; 80 shares and 267 shares issued and outstanding at September 30, 1997 and December 31, 1996 respectively; includes $306,633 and $533,416 accretion at September 30, 1997 and December 31, 1996, respectively 4,306,633 13,883,416 Series B Convertible, redeemable, 9 % cumulative preferred, par value $.01 per share. Authorized 20,000 shares; issued 5,000 shares 0 shares outstanding at September 30, 1997 -- -- Common stock, par value $.01 per share Authorized 20,000,000 shares; issued 13,191,278 and 10,611,422 shares at September 30, 1997 and December 31, 1996, respectively 131,913 106,114 Additional paid-in capital 112,322,889 94,770,176 Unamortized deferred compensation - restricted stock -- (1,133) Accumulated deficit (111,581,674) (92,599,039) Net unrealized gain on marketable securities available for sale 128 5,714 Common stock in treasury, at cost, 22,888 shares at September 30,1997 and 29,985 shares at December 31, 1996 respectively (76,534) (100,239) ------------- ------------ Total stockholders' equity 5,103,355 16,065,009 ------------- ------------ $ 8,410,288 $ 20,937,862 ============= ============ See accompanying notes to financial statements. 3 CELGENE CORPORATION CONDENSED STATEMENTS OF OPERATIONS (Unaudited) Nine Month Period Ended September 30, ------------------------------------- 1997 1996 ------------ ------------ Revenues: Chirally pure intermediates $ 896,870 $ 1,096,605 Research contracts 919,068 711,666 ------------ ------------ Total revenues 1,815,938 1,808,271 Expenses: Cost of goods sold 641,862 683,005 Research and development 13,285,060 10,981,813 Selling, general and administrative 5,780,827 2,738,528 ------------ ------------ Total expenses 19,707,749 14,403,346 ------------ ------------ Operating loss ($17,891,811) ($12,595,075) Interest income 441,436 989,751 Interest expense 104,866 255,535 ------------ ------------ Net loss ($17,555,241) ($11,860,859) Accretion of premium payable on Preferred Stock Series A and B 474,317 764,138 Deemed dividend and fair value of warrants on Series B Preferred Stock 953,077 2,777,777 ------------ ------------ Net loss applicable to common shareholders ($18,982,635) ($15,402,774) ============ ============ Net loss applicable to common shareholders per share of common stock ($ 1.63) ($ 1.67) ============ ============ Weighted average number of shares of common stock outstanding 11,647,000 9,227,000 ============ ============ See accompanying notes to financial statements. 4 CELGENE CORPORATION CONDENSED STATEMENTS OF OPERATIONS (Unaudited) Three-Month Period Ended September 30, -------------------------------------- 1997 1996 ------------ ----------- Revenues: Chirally pure intermediates $ 137,130 $ 77,800 Research contracts 283,986 376,666 ------------ ----------- Total revenues 421,116 454,466 Expenses: Cost of goods sold 179,593 234,390 Research and development 4,175,469 4,661,390 Selling, general and administrative 2,253,621 1,274,289 ------------ ----------- Total expenses 6,608,683 6,170,069 ------------ ----------- Operating loss ($ 6,187,567) ($5,715,603) Interest income 99,034 359,086 Interest expense 10,377 68,379 ------------ ----------- Net loss ($ 6,098,910) ($5,424,896) Accretion of premium payable on Preferred Stock Series A and B 158,675 381,938 Deemed dividend and fair value of warrants on Series B Preferred stock 893,510 2,777,777 ------------ ----------- Net loss applicable to common shareholders ($ 7,151,095) ($8,584,611) ============ =========== Net loss applicable to common shareholders per share of common stock ($ .58) ($ .90) ============ =========== Weighted average number of shares of common stock outstanding 12,362,000 9,520,000 ============ =========== See accompanying notes to financial statements. 5 CELGENE CORPORATION CONDENSED STATEMENTS OF CASH FLOW (unaudited) Nine Month Period Ended September 30, 1997 1996 ------------ ------------- Cash flows from operating activities: - ------------------------------------- Net loss ($17,555,241) ($ 11,860,859) Depreciation 747,096 684,983 Amortization of deferred compensation 1,133 4,818 Interest on convertible debentures 68,736 255,535 Issuance of stock for employee benefits 78,955 -- Issuance of stock award 55,625 -- Change in current assets and liabilities: Increase in accounts payable and accrued expenses 65,152 187,199 Decrease in accounts receivable 210,169 146,969 (Increase) in other assets (40,093) (317,570) ------------ ------------- Net cash used in operating activities (16,368,468) (10,898,925) Cash flows from investing activities: - ------------------------------------- Capital expenditures (1,201,805) (1,186,284) Proceeds from sales and maturities of marketable securities available for sale 41,750,254 117,485,212 Purchases of marketable securities available for sale (29,390,956) (126,698,269) ------------ ------------- Net cash provided by (used in) investing activities 11,157,493 (10,399,341) ------------ ------------- Cash flows from financing activities: - ------------------------------------- Net proceeds from exercise of common stock options 12,695 237,946 Capital lease funding 631,496 -- Redemption of preferred shares (721,287) -- Net proceeds from issuance of preferred stock 4,840,748 23,829,625 ------------ ------------- Net cash provided by financing activities 4,763,652 24,067,571 ------------ ------------- Net increase (decrease) in cash and cash equivalents (447,323) 2,769,305 Cash and cash equivalents at beginning of period 922,961 337,165 ------------ ------------- Cash and cash equivalents at end of period $ 475,638 $ 3,106,470 ============ ============= (continued) See accompanying notes to financial statements. 6 CELGENE CORPORATION CONDENSED STATEMENTS OF CASH FLOW, continued (unaudited) Nine Month Period Ended September 30, ------------------------------------- 1997 1996 ----------- ---------- Non-cash investing activity: Change in net unrealized gain (loss) on marketable securities available for sale $ (5,586) $ 13,791 =========== ========== Non-cash financing activities: Issuance of common stock upon the conversion of convertible debentures and accrued interest thereon, net $ 2,331,304 $2,649,115 =========== ========== Accretion of premium payable on preferred stock and warrants $ 474,317 $ 764,138 =========== ========== Deemed dividend for preferred stock conversion discount $ 953,077 $2,777,777 =========== ========== Issuance of common stock upon the conversion of convertible preferred stock and accretion thereon, net $14,329,813 $3,818,627 =========== ========== Issuance of common stock upon exercise of options through the return of common stock previously outstanding $ -- $ 99,996 =========== ========== See Accompanying Notes to Financial Statements. 7 CELGENE CORPORATION Notes to Unaudited Condensed Financial Statements September 30, 1997 1. Basis of Presentation --------------------- The unaudited condensed financial statements have been prepared from the books and records of Celgene Corporation (the "Company") in accordance with generally accepted accounting principles for interim financial information pursuant to Rule 10-01 of Regulation S-X. Accordingly, they do not include all of the information and footnotes required by generally accepted accounting principles for complete financial statements. In the opinion of management, all adjustments (consisting only of normal recurring accruals) considered necessary for a fair presentation have been included. Interim results may not be indicative of the results that may be expected for the year. The interim condensed financial statements should be read in conjunction with the financial statements and notes thereto included in the Company's latest annual report on Form 10K. 2. Series A Convertible Preferred Stock ------------------------------------ On March 13, 1996, in a private placement, the Company completed the sale of 503 shares of Series A Convertible Preferred Stock, par value $.01 per share (the "Preferred Stock"), at an issue price of $50,000 per share. The Company received net proceeds, after offering costs, of $23,829,625. The Preferred Stock, plus accretion at a rate of 4.9% per year, is convertible into common stock of the Company at the option of the holders thereof at a conversion price per share of common stock equal, generally, to the lesser of (i) $18.81 or (ii) 90% of the average closing price per share of the common stock for the seven trading days immediately prior to the date of conversion. The average closing price per share of common stock for the seven trading days immediately prior to September 30, 1997 was $10.75. The Company may redeem the shares in increments of not less than $1.5 million plus accretion commencing December 13, 1996, on thirty business days written notice to the preferred stock holders, at a price that equals a specified premium, ranging from 120% to 130%, of the purchase price plus accretion premium. Under certain conditions, upon receipt of a conversion notice from the holder, the Company has the right (i) to redeem shares presented for conversion, or (ii) to defer conversion for 90 days in exchange for warrants to purchase additional shares of common stock as specified in the Certificate of Designation of Series A Convertible Preferred Stock. Any shares of Series A Convertible Preferred Stock outstanding on March 13, 1998 shall be converted automatically into common stock on such date at the conversion price then in effect. The holders of Preferred Stock have no voting rights. As of September 30, 1997, 423 shares of the Series A preferred Stock, with their respective accretion, had been converted or redeemed into 2,731,915 shares of common stock. Through September 30, 1997 the Company had accrued $1,349,042 representing accretion of the premium on the Preferred Stock of which $306,633 relates to preferred shares not yet tendered for conversion. The Company agreed to reduce the maximum conversion price of 58 shares to $8.50 per share of common stock from 8 $18.81 for holders who agreed to a lock-up through December 1, 1997. As of September 30, 1997 the Company had also issued warrants valued at $138,156, that entitle certain stockholders of the Series A Preferred Stock to purchase 162,203 shares of common stock at an exercise price of $11.50. The warrants were issued in exchange for the deferral of conversion for 90 days. These warrants are exercisable for a period of two years from the date of issuance. The warrants are still outstanding at September 30, 1997. 3. Series B Convertible Preferred Stock ------------------------------------ On June 9, 1997, in a private placement with Chancellor LGT Asset Management, Inc. ("Chancellor") on behalf of certain Chancellor clients, the Company completed the sale of 5,000 shares of Series B Convertible Preferred Stock (the "Series B Preferred"), par value $.01 per share, at an issue price of $1,000 per share. A shelf registration statement with respect to holders' resales of Common Stock issuable upon conversion of Series B Preferred was filed and declared effective on August 6, 1997. The Company received net proceeds of $4,840,748, after offering costs. Subject to the satisfaction of certain conditions, the Company may, at its option, during specified periods ending June 9, 1998, issue and sell to such purchasers up to an additional 15,000 shares of Series B preferred Stock, at an aggregate purchase price of $15 million, in increments of $5 million (5,000 shares). With respect to the third and fourth increments ($10 million) certain FDA approvals are necessary before Chancellor is obligated to buy the additional Series B Preferred Stock. As of September 30, 1997, all shares of Series B Preferred had been converted into Common Stock. Upon request of the purchasers of the Series B Preferred (but no later than June 1, 1998)(in either case, the "Issuance Date"), the Company will issue warrants to acquire a number of shares of Common Stock equal to (i) 1,500,000 divided by the Conversion Price in effect on the Issuance Date (230,769 warrants as of September 30, 1997) plus (ii) 37.5% of the conversion Shares issuable on such Issuance Date upon conversion of all shares of Series B Preferred Stock issued through the Issuance Date (288,461 warrants as of September 30, 1997). All such warrants will have a term of four years from the Issuance Date and an exercise price equal to 115% of the Conversion Price in effect on the Issuance Date. The fair value of warrants at the issuance date was $1.28 per warrant. Through September 30, 1997, the Company had recorded $953,077 representing accretion of the deemed dividend on the Series B Preferred Stock. The deemed dividend represents the difference between the Series B Preferred Stock conversion price and the Company's Common Stock fair market value at the date of issuance. The deemed dividend and the fair value of the warrants was accreted over the lock-up period subject to acceleration contingencies. Such contingencies were met and the full deemed dividend was recognized at that time. 4. Convertible Debentures ---------------------- During 1995, the Company sold in a private placement offering, 8% convertible debentures due July 31, 1997 in the aggregate principal amount of $12,000,000, and received net proceeds, after offering costs, of $11,022,570. The recorded value of the debentures at the date of issuance was discounted to produce a market interest rate approximating 13.5%. Such debentures are convertible into common stock of the Company at the option of either the holders thereof or the Company. 9 The holders of the convertible debentures may convert the debentures into common stock of the Company at a conversion price that varies and is based upon the market price (as defined) of the common stock on the date of conversion. During the quarter ended June 30, 1997, the convertible debenture fully converted. As of September 30, 1997, convertible debentures in the aggregate principal amount of $12,000,000, plus accrued interest, had been converted into a total of 1,709,845 shares of common stock. No interest was paid in cash. 5. Marketable Securities Available for Sale ---------------------------------------- Marketable securities available for sale at September 30, 1997 include debt securities with maturities ranging from October, 1997 to April, 1998. A summary of marketable securities at September 30, 1997 is as follows: Gross Gross Estimated Unrealized Unrealized Fair Cost Gain Loss Value ---------- ---------- ---------- ---------- Commercial Paper $ 733,793 $ -- $ -- $ 733,793 Corporate Bonds 999,790 210 -- 1,000,000 US Government & agency obligations 2,793,428 -- (82) 2,793,346 ---------- ---- ---- ---------- Total $4,527,011 $210 $(82) $4,527,139 ========== ==== ==== ========== 10 PART I - FINANCIAL INFORMATION ITEM 2.- MANAGEMENT'S DISCUSSION AND ANALYSIS OF FINANCIAL CONDITION AND RESULTS OF OPERATIONS. Results of Operations - --------------------- Nine-month period ended September 30, 1997 vs. Nine-month period ended September 30, 1996 - ------------------------------------------ Total revenues; Revenue Backlog. Revenues for the nine months ended September 30, 1997 were $1,816,000, which was an increase of $8,000, or less than 1%, as compared to the same period in 1996. The Company's order backlog for chirally pure intermediates and research contracts at September 30, 1997 was approximately $797,000. Sales of Chirally Pure Intermediates. Sales of chirally pure intermediates for the nine months ended September 30, 1997 were $897,000, which was a decrease of $200,000, or 18%, as compared to the same period in 1996. The decrease in revenues for chirally pure intermediates was due primarily to the variant nature of orders resulting from the cyclicality of customer research programs. Research Contracts. Chiral research contract revenues for the nine months ended September 30, 1997 were $919,000, which was an increase of $207,000, or 29%, as compared to the same period in 1996. The increase in research contract revenues was due to the Company entering into research contracts to expand development of existing compounds. During the 1997 period, the Company received increased research and development support payments from BASF, a major multinational agrochemical customer. Cost of Goods Sold. Costs of goods sold (which includes certain fixed manufacturing costs) for the nine months ended September 30, 1997 were $642,000, which was a decrease of $41,000, or 6%, as compared to the same period in 1996, due to decreased sales of chirally pure intermediates. Research and Development Expenses. Research and development expenses for the nine months ended September 30, 1997 were $13,300,000, which was an increase of $2,300,000 or 21%, as compared to the same period in 1996. This increase was due to an increase in expense of $787,000 associated with the Company's immunotherapeutic and Thalomid programs, $1,100,000 of expenses associated with the new Celgro(TM) subsidiary and $687,000 of expenses associated with the chiral pharmaceutical development program. The increased cost of the Company's immunotherapeutic and Thalomid programs included increases in manufacturing costs for developmental quantities of Thalomid of $990,000 and personnel related expenses of $625,000. These expenses were partially offset by the absence of expenses associated with preparing the NDA filed in 1996 and by lower preclinical and clinical 11 trial expenses ($828,00). Major components contributing to the increased costs of the new Celgro subsidiary are personnel related expenses of $464,000; facilities-related spending of $303,000; and other ongoing research expenses of $333,000. The higher costs associated with the Company's chiral pharmaceutical program are due primarily to higher preclinical and clinical trial expenses of $282,000; personnel related costs of $148,000 and other ongoing research expenses of $257,000. Selling, General and Administrative Expenses. Selling, general and administrative expenses for the nine months ended September 30, 1997 were $5,800,000, which was an increase of $3,100,000, or 115%, as compared to the same period in 1996, due to the formation of a small sales and marketing group and associated expenses for market research and the development of a launch program and materials, all in anticipation of approval of thalidomide by the FDA, of approximately $1,600,000; development of a Medical Affairs Department costing $230,000 (in anticipation of the Thalomid launch upon approval by the FDA); higher legal fees of $269,000; costs associated with the formation of the Celgro subsidiary of approximately $374,000; and higher personnel related expenses of $676,000. Interest Income and Interest Expense. Interest income for the nine months ended September 30, 1997 was $441,000, which was a decrease of $549,000, or 55%, as compared to the same period in 1996. This decrease was attributable to lower average cash balances in 1997. Interest expense for the nine months ended September 30, 1997 was $105,000, which was a decrease of $151,000, or 59%, as compared to the same period in 1996. This decrease was due to the conversion to equity of the remaining 8% Convertible Debentures. Net Loss. The net loss for the nine months ended September 30, 1997 was $17,600,000, which was an increase of $5,700,000, or 48%, as compared to the same period in 1996. This increase was due primarily to higher spending on Thalomid and the immunotherapeutics program, the creation of the Celgro subsidiary, and the continued development of the chiral pharmaceutical programs. Three-month period ended September 30, 1997 vs. Three-month period ended September 30, 1996 - ------------------------------------------- Total revenues. The Company's total revenues for the three months ended September 30, 1997 decreased by 7% to approximately $421,000 from approximately $454,000 in the same period of 1996. Chirally pure intermediate revenues. Chirally pure intermediate revenues for the three months ended September 30, 1997 increased by 76% to approximately $137,000 from approximately $78,000 in the same period of 1996. The increase in chirally pure intermediate revenues was due primarily to the sporadic nature of orders. 12 Research contract revenues. Research contract revenues for the three months ended September 30, 1997 decreased by 25% to approximately $284,000 from $377,000 for the same period of 1996. This decrease was primarily due to higher sales in 1996 to Sandoz, a multinational agrochemical customer. Cost of goods sold. Cost of goods sold in the three months ended September 30, 1997 decreased by 23% to approximately $180,000 from approximately $234,000 in the same period of 1996. This decrease in cost of goods sold was due primarily to the decrease in revenues. Research and development expenses. Research and development expenses for the three months ended September 30, 1997 decreased by 10% to approximately $4.2 million from approximately $4.7 million in the same period in 1996. This decrease was due to lower expenses of approximately ($781,000) associated with the Company's immunotherapeutic and Thalomid(TM) program, lower expenses of ($155,000) associated with the chiral intermediates program, offset by increased expenses of $252,000 associated with the new Celgro(TM) subsidiary and $160,000 of expenses associated with the chiral pharmaceutical development program. The decrease in expenses in the Company's immunotherapeutic and Thalomid(TM) programs resulted from lower spending in clinical and pre-clinical toxicology ($1.2 million), offset by higher manufacturing costs for developmental quantities of Thalomid(TM), approximately $390,000. All other expenses were higher by $29,000. The major components contributing to the increased costs of the new Celgro(TM) division are personnel related expenses, approximately $77,000 and facilities related spending, approximately $190,000. The higher costs associated with the Company's chiral pharmaceutical program are due primarily to higher preclinical and clinical trial expenses, approximately $43,000; personnel related costs, approximately $25,000; higher legal and consulting fees $58,000; and other on-going research expenses, approximately $34,000. Selling, general and administrative expenses. Selling, general and administrative expenses for the three months ended September 30, 1997 increased by 77% to approximately $2.3 million from approximately $1.3 million in the three month period ended September 30, 1996. This increase was primarily due to the formation of a small sales and marketing group and associated expenses for market research and the development of a launch program and materials, approximately $738,000; a Medical Affairs department, approximately $94,000 (both in anticipation of the Thalomid(TM) launch upon approval by the FDA); higher personnel related expenses, approximately $285,000. All other expenses were lower by ($117,000). Interest income and interest expense. Interest income for the three month period ended September 30, 1997 decreased by 72% to approximately $99,000 from approximately $359,000 in the same period of 13 1996. This decrease was attributable to lower average cash balances in 1997. Interest expense for three month period ended September 30, 1997 decreased by 85% to approximately $10,000 from approximately $68,000. This decrease was due to the conversion to equity of the remaining portion of the 8% Convertible Debentures. Net loss. The net loss for the three month period ended September 30, 1997 increased by 11% to approximately $6.1 million from approximately $5.5 million in the same period of 1996. This increase was due primarily to higher spending in the sales and marketing area for Thalomid(TM) pre-launch programs, the creation of the Celgro(TM) subsidiary, and the continued development of the chiral pharmaceutical programs. Liquidity and Capital Resources - ------------------------------- Since inception, the Company has financed its working capital requirements primarily through private and public sales of its debt and equity securities, income earned on the investment of the proceeds from the sale of such securities, and revenues from product sales. The Company has raised approximately $81.0 million in net proceeds from two public and three private offerings, including its initial public offering in July 1987. In July 1995, the Company issued and sold in a private placement offering $12.0 million aggregate principal amount of 8% Convertible Debentures due July 31, 1997 for total net proceeds, after offering costs, of approximately $11.0 million. As of September 30, 1997, the entire $12.0 million principal amount of the 8% Convertible Debentures had been converted into Common Stock. In March 1996, the Company issued and sold in a private placement offering 503 shares of Series A Convertible Preferred Stock at $50,000 per share, for total gross proceeds of $25.2 million. The Company received net proceeds, after offering costs, of approximately $23.8 million. In June, 1997 the Company issued and sold in a private placement offering 5,000 shares of Series B Convertible Preferred Stock at $1,000 per share, for total gross proceeds of $5.0 million and net proceeds, after offering costs, of approximately $4.8 million. On September 18,1997 all 5,000 shares were converted to 788,469 common shares. The Company's Series B Preferred Stock purchase agreement provides for the sale of an additional $15 million of Series B Preferred Stock in $5 million increments through June 2, 1998, at the Company's option. The third and fourth increments ($10 million) are subject to certain FDA approvals. The second $5 million is available to the Company after October 1, 1997. See Notes 2, 3 and 4 to the unaudited condensed Financial Statements. 14 On September 30, 1997, the Company had available cash, cash equivalents and marketable securities of approximately $5,000,000. In the nine months ended September 30, 1997, working capital decreased approximately $13,500,000, or 82%, from December 31, 1996, which was attributable to the cash used in operations which more than offset receipt of funds from the sale of Series B Convertible Preferred Stock. During the nine months ended September 30, 1997, capital expenditures totaled approximately $1,200,000, primarily for equipment and leasehold improvements to expand its research development and manufacturing capabilities. In September 1997, the Company received from the FDA an approvable letter for its NDA for Thalomid for the treatment of ENL, a disease state associated with leprosy. At present, the Company cannot estimate the impact of potential sales of Thalomid on future revenues. The Company expects to make substantial expenditures to further its immunotherapeutic program, to commercialize Thalomid and to expand its chiral business and, based on these expenditures, it is probable that losses will continue for at least the next 18 to 24 months. The Company is currently utilizing its cash resources at a rate of approximately $2,000,000 per month. The Company expects that its rate of spending will remain high as the result of increased clinical trial costs and expenses associated with the regulatory approval process and commercialization of products now in development. In order to assure funding for the Company's future operations the Company is seeking additional capital resources. These may include the sale of additional securities under appropriate market conditions, alliances or other partnership agreements with entities interested in and possessing resources to support the Company's immunotherapeutic or chiral programs, or other business transactions which would generate sufficient resources to assure continuation of the Company's operations and research programs in the long-term. In particular, each of the persons who purchased Series B Preferred also agreed to purchase, at the option of the Company and subject to the satisfaction of certain conditions, an aggregate of up to 15,000 additional shares of Series B Preferred Stock for an aggregate purchase price of $15 million at subsequent closings. However, no assurances can be given that the Company will be successful in raising such additional capital or entering into a business alliance. Further, there can be no assurance, assuming the Company successfully raises additional funds or enters into a business alliance, that the Company will achieve profitability or positive cash flow. If the Company is unable to raise additional funds, the Company believes that its current financial resources, including its option to 15 issue and sell an additional $5,000,000 of Series B Preferred Stock (which is subject to the satisfaction of certain customary conditions), could fund operations through early 1998. The Company's actual cash requirements may vary materially from those now planned and will depend upon numerous factors, including the results of the Company's development and commercialization programs, the timing and results of preclinical and clinical trials, the timing and costs of obtaining regulatory approvals, the level of resources that the Company commits to the development of manufacturing, marketing and sales capabilities, the ability of the Company to license its biocatalytic chiral process technology to agrochemical companies, the technological advances and activities of competitors, and other factors. As of September 30, 1997, the Company had for Federal income tax purposes a net operating loss carryforward of approximately $104,000,000. If not utilized to offset future taxable income, such loss carryforward will expire between 2001 and 2012. Certain events, including any sales by the Company of shares of its stock, including pursuant to this Offering, and/or transfers of a substantial number of shares of Common Stock by the current stockholders, may partially restrict the ability of the Company to utilize its net operating loss carryforward. Recently Issued Accounting Standards - ------------------------------------ In February 1997, the Financial Accounting Standards Board issued Statement of Financial Accounting Standards No. 128, Earnings Per Share ("EPS"), which is effective as of December 31, 1997. This standard changes the way companies compute EPS to require all companies to show "basic" and "dilutive" EPS and is to be retroactively applied, including each 1997 interim quarter. The statement is not expected to have a material effect on the Company's calculation of EPS. Cautionary Statements For Forward Looking Information - ----------------------------------------------------- The Management Discussion and Analysis of Financial Condition and Results of Operations provided above contains certain forward-looking statements which involve known and unknown risks, delays, uncertainties and other factors not under the Company's control which may cause actual results, performance or achievements of the Company to be materially different from the results, performance or other expectations implied by these forward looking statements. These factors include results of current or pending clinical trials, actions by the FDA and those factors detailed in the company's filings with the Securities and Exchange Commission. 16 PART II - OTHER INFORMATION Item 1. - None Item 2. - None Item 3. - None Item 4. - None Item 5. - None Item 6. - Exhibits 27 Financial Data Schedule - Article 5 for third quarter Form 10-Q. 17 SIGNATURES Pursuant to the requirements of the Securities Exchange Act of 1934, the registrant has duly caused this report to be signed on its behalf by the undersigned thereunto duly authorized. CELGENE CORPORATION DATE November 14, 1997 BY /s/ John W. Jackson --------------------------- ----------------------------------- John W. Jackson Chairman of the Board Chief Executive Officer DATE November 14, 1997 BY /s/ James R. Swenson --------------------------- ----------------------------------- James R. Swenson Controller (Chief Accounting Officer) 18