1 WASHINGTON, D.C. 20549 FORM 10-Q (Mark One) /X/ QUARTERLY REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934 For the quarterly period ended December 31, 1995 ------------------------------------------------- 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 0-15190 ---------------------------------------------------------- ONCOGENE SCIENCE, INC. - -------------------------------------------------------------------------------- (Exact name of registrant as specified in its charter) DELAWARE 13-3159796 - -------------------------------------------------------------------------------- (State or other jurisdiction of (I.R.S. Employer incorporation or organization) Identification No.) 106 Charles Lindbergh Blvd., Uniondale, New York 11553 - -------------------------------------------------------------------------------- (Address of principal executive offices) (Zip Code) 516-222-0023 - -------------------------------------------------------------------------------- (Registrant's telephone number, including area code) - -------------------------------------------------------------------------------- (Former name, former address and former fiscal year, if changed since last report.) 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 --- --- APPLICABLE ONLY TO CORPORATE ISSUERS: At January 31, 1996 the registrant had outstanding 17,541,034 shares of common stock .$01 par value. Total Pages: 10 2 ONCOGENE SCIENCE, INC. AND SUBSIDIARIES INDEX Page No. -------- PART I - FINANCIAL INFORMATION - UNAUDITED Consolidated Balance Sheets - December 31, 1995 and September 30, 1995 3 Consolidated Statements of Operations - Three months ended December 31, 1995 and 1994 4 Consolidated Statements of Cash Flows - Three months ended December 31, 1995 and 1994 5 Note to Consolidated Financial Statements 6 Management's Discussion and Analysis of Financial 7 Condition and Results of Operations PART II - OTHER INFORMATION 9 SIGNATURES 10 * * * * 3 ITEM 1. FINANCIAL STATEMENTS ONCOGENE SCIENCE, INC. AND SUBSIDIARIES CONSOLIDATED BALANCE SHEETS December 31, September 30, Assets 1995 1995 ----------- ----------- Current assets: Cash and cash equivalents $ 1,787,990 $17,919,609 Short-term investments 22,296,727 8,866,957 Receivables, including trade receivables of $88,371 and $163,132 at December 31 and September 30, 1995, respectively 2,253,533 1,320,015 Interest receivable 67,769 45,263 Grants receivable 209,748 433,530 Prepaid expenses and other 652,024 518,150 ----------- ----------- Total current assets 27,267,791 29,103,524 ----------- ----------- Property, equipment and leasehold improvements - net 5,445,005 5,709,515 Other receivable 408,659 262,703 Loans to officers and employees 25,464 25,516 Other assets 324,500 325,582 Intangible assets - net 8,267,392 8,630,581 ----------- ----------- $41,738,811 $44,057,421 =========== =========== Liabilities and Stockholders' Equity Current liabilities: Account payable and accrued expenses $ 1,806,902 $ 2,825,702 Current portion of unearned revenue 193,166 150,041 ----------- ----------- Total current liabilities 2,000,068 2,975,743 ----------- ----------- Other Liabilities: Long-term portion of unearned revenue 151,509 165,839 Accrued postretirement benefits cost 399,329 366,203 ----------- ----------- Total liabilities 2,550,906 3,507,785 ----------- ----------- Stockholders' equity: Common stock, $.01 par value; 50,000,000 shares authorized, 17,750,310 and 17,683,047 issued at December 31 and September 30, 1995, respectively 177,503 176,830 Additional paid-in capital 66,998,116 66,735,375 Accumulated deficit (27,899,935) (26,129,341) Cumulative foreign currency translation adjustment (40,220) (55,669) Unrealized holding gain (loss) on short-term investments 95,000 (35,000) ----------- ----------- 39,330,454 40,692,195 Less: treasury stock, at cost 222,521 shares at December 31 and September 30, 1995 (142,559) (142,559) ----------- ----------- Total stockholders' equity 39,187,905 40,549,636 ----------- ----------- Commitments and contingencies $41,738,811 $44,057,421 =========== =========== See accompanying notes to consolidated financial statements. 4 ONCOGENE SCIENCE, INC. AND SUBSIDIARIES CONSOLIDATED STATEMENTS OF OPERATIONS (UNAUDITED) Three Months Ended December 31, --------------------------------------- 1995 1994 ------------ ----------- Revenues: Collaborative program revenues, principally from related parties $ 1,987,458 $ 2,318,374 Sales 29,042 1,313,689 Other research revenue 259,748 575,918 ------------ ----------- 2,276,248 4,207,981 ------------ ----------- Expenses: Research and development 2,683,262 3,076,965 Production 21,863 405,278 Selling, general and administrative 1,331,539 1,874,429 Amortization of intangibles 363,189 436,334 ------------ ----------- 4,399,853 5,793,006 Loss from operations (2,123,605) (1,585,025) ------------ ----------- Other income (expense): Net investment income 364,524 220,672 Other expense (11,513) (26,634) ------------ ----------- Net loss (1,770,594) (1,390,987) ============ =========== Weighted average number of shares of common stock outstanding 17,476,343 16,342,604 ============ =========== Net loss per weighted average share of common stock outstanding $ (.10) $ (.09) ============ =========== See accompanying notes to consolidated financial statements. 5 ONCOGENE SCIENCE, INC. AND SUBSIDIARIES CONSOLIDATED STATEMENTS OF CASH FLOWS Three Months Ended December 31, -------------------------------- 1995 1994 ---- ---- Cash flow from operating activities: Net loss $(1,770,594) $(1,390,987) Adjustments to reconcile net loss to net cash used by operating activities: Gain on sale of investments (27,608) - Depreciation and amortization 341,240 323,233 Amortization of intangibles 363,189 436,334 Foreign exchange loss 15,449 11,474 Changes in assets and liabilities: Receivables (933,518) 460,588 Inventory - 111,282 Interest receivable (22,506) (117,109) Grants receivable 223,782 134,997 Prepaid expenses and other (133,874) 46,322 Other receivable (145,956) (279,584) Other assets 1,082 4,392 Accounts payable and accrued expenses (1,018,800) (375,977) Unearned revenue 28,795 459,676 Accrued postretirement benefit cost 33,126 34,689 ----------- ----------- Net cash used by operating activities $(3,046,193) $(140,670) ----------- ----------- Continued 6 ONCOGENE SCIENCE, INC. AND SUBSIDIARIES CONSOLIDATED STATEMENTS OF CASH FLOWS (CONTINUED) Three Months Ended December 31, ------------------------------- 1995 1994 ---- ---- Cash flows from investing activities: Additions to short-term investments (15,772,162) (499,687) Maturities and sales of short-term investments 2,500,000 1,756,725 Additions to property, equipment and leasehold improvements (76,730) (428,460) Net change in loans to officers and employees 52 - Other - (7,900) ------------ ----------- Net cash provided by (used in) investing activities (13,348,840) 820,678 ------------ ----------- Cash flows from financing activities: Proceeds from exercise of stock options, employee stock purchase plan and other 263,414 1,956 ------------ ----------- Net cash provided by financing activities 263,414 1,956 ------------ ----------- Net increase (decrease) in cash and cash equivalents (16,131,619) 681,964 Cash and cash equivalents at beginning of year 17,919,609 322,308 ------------ ----------- Cash and cash equivalents at end of year $ 1,787,990 $ 1,004,272 ============ =========== See accompanying notes to consolidated financial statements. 7 ONCOGENE SCIENCE, INC. AND SUBSIDIARIES NOTES TO CONSOLIDATED FINANCIAL STATEMENTS (UNAUDITED) (1) Opinion of Management In the opinion of Management, the accompanying unaudited consolidated financial statements contain all adjustments (consisting of only normal recurring accruals) necessary to present fairly the Company's financial position as of December 31, 1995 and September 30, 1995, its results of operations and its cash flows for the three months ended December 31, 1995 and 1994. Certain reclassifications have been made to the prior financial statements to conform them to the current presentation. It is recommended that these consolidated financial statements be read in conjunction with the consolidated financial statements and notes thereto in the Company's 1995 Annual Report on Form 10-K. Results for interim periods are not necessarily indicative of results for the entire year. Net loss per share of common stock outstanding is based on the weighted average number of shares outstanding. Common share equivalents (stock options) are not included in the computation for the three months ended December 31, 1995 and 1994 since their inclusion would be anti-dilutive. (2) Use of Estimates Management of the Company has made a number of estimates and assumptions relative to the reporting of assets and liabilities and the disclosure of contingent assets and liabilities to prepare these financial statements in conformity with generally accepted accounting principles. Actual results could differ from those estimates. (3) Dependence on Collaborative Relationships The Company does not intend to conduct late-stage clinical trials, manufacturing or marketing activities with respect to any of its product candidates in the foreseeable future. The Company has collaborations with Ciba-Geigy, Ltd., Pfizer Inc., Hoechst Marion Roussel, Inc. and Wyeth-Ayerst Laboratories for the development of potential drug candidates, and with Becton Dickinson and Co. for the development of cancer diagnostics. The Company is dependent on the companies with which it collaborates for the preclinical testing, clinical development, regulatory approval, manufacturing and marketing of potential products developed under its collaborative research programs. The Company's collaborative agreements allow its collaborative partners significant discretion in electing to pursue or not to pursue any of these activities. The Company cannot control the amount and timing of resources its collaborative partners devote to the Company's programs or potential products. If any of the Company's collaborative partners were to breach or terminate its agreements with the Company or otherwise fail to conduct its collaborative activities successfully in a timely manner, the preclinical or clinical development or commercialization of product candidates or research programs could be delayed or terminated. Any such delay or termination could have a material adverse effect on the Company's business, financial condition and results of operations. 8 ITEM 2.MANAGEMENT'S DISCUSSION AND ANALYSIS OF FINANCIAL CONDITION THREE MONTHS ENDED DECEMBER 31, 1995 COMPARED TO THE THREE MONTHS ENDED DECEMBER 31, 1994. Revenues Revenues for the quarter ended December 31, 1995 were approximately $2.3 million, a decrease of $1.9 million, or 46% when compared to revenues of $4.2 million reported for the quarter ended December 31, 1994. The decrease was due to lower sales of research products which accounted for approximately $1.3 million of the decrease in revenues. The Company sold its Research Products Business for $6.0 million in cash plus other considerations on August 2, 1995, and accordingly there were no significant sales of research products recorded after this date. In the purchase agreement, the Company agreed to indemnify the purchaser for a period of two years for certain breaches of the agreement. Collaborative program revenue decreased approximately $331,000 or 14%. This was largely due to a reduction in collaborative revenue under the collaborative arrangement with Hoechst Marion Roussel, Inc. ("HMRI") as compared to the total revenue in the prior year's quarter from Marion Merrell Dow Inc. ("MMDI"), Hoechst Roussel Pharmaceuticals, Inc. and Hoechst AG. Other research revenues representing primarily government grants have decreased approximately $316,000 in the quarter ended December 31, 1995 compared to the quarter ended December 31, 1994 due in part to the expiration of a U.S. government grant. The balance of the decrease represents changes in the timing and amount of grant awards. The Company expects that grant revenue will be somewhat lower in the current fiscal year. Expenses The Company's operating expenses decreased by approximately $1.4 million or 24% for the quarter ended December 31, 1995 compared to the quarter ended December 31, 1994. Research and development expenses decreased approximately $394,000, or 13% due to reductions in expenses in the HMRI and Becton Dickinson and Co. ("Becton") collaborations commensurate with the reduced funding in these programs. This was offset in part by increased expenditures in the Company's proprietary research programs. Production expenses and selling, general and administrative expenses decreased approximately $926,000. These reductions were directly related to expenses which were associated with the Company's Research Products Business in the quarter ended December 31, 1994. The reduction of approximately $73,000 of amortization of intangibles is due to a portion of goodwill relating to the Research Products Business which was expensed when the business was sold in August 1995. Other Income and Expense Investment income increased approximately $144,000, or 65% for the quarter ended December 31, 1995 as compared to the quarter ended December 31, 1994. This increase was largely due to the increase in funds invested as a result of the 9 THREE MONTHS ENDED DECEMBER 31, 1995 COMPARED TO THE THREE MONTHS ENDED DECEMBER 31, 1994. proceeds from the sale of the Research Products Business and the sale of stock to Ciba-Geigy, Ltd. ("Ciba") in April 1995. New Accounting Pronouncements In March 1995, Statement of Financial Accounting Standards (SFAS) No. 121, "Accounting for the Impairment of Long-Lived Assets and for Long-Lived Assets to Be Disposed Of" was issued which establishes accounting standards for the impairment of long-lived assets, certain identifiable intangibles, and goodwill related to those assets to be held and used and for long-lived assets and certain intangibles to be disposed of. SFAS No. 121 requires that long-lived assets and certain intangibles to be held and used by an entity be reviewed for impairment whenever events or changes in circumstances indicate that the carrying amount of the asset may not be recoverable. SFAS No. 121 must be implemented no later than fiscal 1997. The adoption of SFAS No. 121 is not expected to have material impact on the Company's consolidated financial position or operating results. In October 1995, SFAS No. 123, "Accounting for Stock-Based Compensation", was issued which establishes financial accounting and reporting standards for stock-based employee compensation plans. SFAS No. 123 defines a fair value based method of accounting for an employee stock option or similar equity instrument and encourages all entities to adopt that method of accounting for all of their employee stock compensation plans. However, SFAS No. 123 would permit the Company to continue to measure compensation costs for its stock option plans using the intrinsic value based method of accounting prescribed by APB Opinion No. 25, "Accounting for Stock Issued to Employees". If the Company elected to remain with its current accounting, the Company must make pro forma disclosures of net income and earnings (loss) per share as if the fair value based method of accounting had been applied. SFAS No. 123 must be implemented no later than fiscal 1997. The Company has not yet determined the valuation method it will employ or the effect on operating results of implementing SFAS No. 123. Liquidity and Capital Resources At December 31, 1995, working capital (representing primarily cash, cash equivalents and short-term investments) aggregated approximately $25.3 million. The Company has been, and will continue to be, dependent upon collaborative research revenues, government research grants, interest income and cash balances until products developed from its technology are commercially marketed. On April 19, 1995, Ciba purchased 909,091 shares of the Company's common stock for an aggregate purchase price of $5.0 million. 10 THREE MONTHS ENDED DECEMBER 31, 1995 COMPARED TO THE THREE MONTHS ENDED DECEMBER 31, 1994. During 1995, MMDI was acquired by HMRI as part of a transaction in which the pharmaceutical operations of Hoechst AG, Hoechst Roussel Pharmaceuticals, Inc. and MMDI were consolidated. The Company is aware that HMRI is conducting a review of all its research and development programs. Based on discussions with HMRI, the Company expects its programs with HMRI to continue under one overall agreement in the future, although there can be no assurance that the Company and HMRI will enter into such an overall agreement, or if such an agreement is entered into, that it will not be on terms less favorable than the existing agreements. The Company anticipates that the total funding under the consolidated agreement will be somewhat lower than the aggregate level of funding under the three previously separate agreements. Since its commencement in 1991 and until the second quarter of fiscal 1995, the cancer diagnostics collaborative program with Becton has focused on both serum-based and histochemical immunoassays. During the second quarter of fiscal 1995, Becton decided to focus exclusively on cellular cancer diagnostics including histochemical immunoassays. Becton has reduced its funding under this program in fiscal 1996, and the Company is uncertain as to Becton's ongoing support for this program thereafter. The Company is continuing the development of serum-based cancer diagnostic products and is in discussions with possible new collaborative partners in this area. However, there can be no assurance that the development of these tests will not be terminated. The Company believes that with the funding from its collaborative research programs, government research grants, interest income, and cash balances, the Company's financial resources are adequate for its operations through fiscal 1999. However, the Company's capital requirements may vary as a result of a number of factors, including, competitive and technological developments, funds required for expansion of the Company's technology platform, including possible joint ventures, collaborations, and acquisitions, the time and expense required to obtain governmental approval of products, and any potential indemnification payments to the purchaser of the Research Products Business, some of which factors are beyond the Company's control. The Company intends to increase substantially its expenditures and capital investment over the next several years in enhancing its drug discovery technologies and pursuing proprietary drug discovery programs. There can be no assurance that scheduled payments will be made by third parties, that current agreements will not be cancelled, that government research grants will continue to be received at current levels or that unanticipated events requiring the expenditure of funds will not occur. Further, there can be no assurance that the Company will be able to obtain any additional required funds, or, if such funds are available, that such funds will be available on favorable terms. Failure to obtain additional funds when required would have a material adverse effect on the Company's business, financial condition and results of operations. 11 ITEM 6. EXHIBITS The following is a list of exhibits filed as part of this Report: 10.1* Amendatory Agreement dated as of December 31, 1993 between the Company and American Home Products Corporation 10.2* Collaborative Research Agreement dated as of December 31, 1991 between the Company and American Home Products Corporation 10.3* Collaborative Research Agreement dated as of January 4, 1993 between the Company and Hoechst AG 10.4* Collaborative Research Agreement dated as of October 1, 1993 between the Company and Hoechst Roussel Pharmaceuticals, Inc. 27 Financial Data Schedule - ------------- * Portions of this exhibit have been redacted and are the subject of a confidential treatment request filed with the Secretary of the Securities and Exchange Commission pursuant to rule 24b-2 under the Securities Exchange Act of 1934, as amended. 12 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. ONCOGENE SCIENCE, INC. ---------------------------- (Registrant) Date 2 / 14 / 96 /s/ Gary E. Frashier ------------------ ---------------------------- Gary E.Frashier Chief Executive Officer Date 2 / 14 / 96 /s/ Robert L. Van Nostrand ------------------ ---------------------------- Robert L. Van Nostrand Vice President Finance & Administration 13 INDEX TO EXHIBITS Exhibits Page No. - -------- -------- 10.1* Amendatory Agreement dated as of December 31, 1993 between the Company and American Home Products Corporation 10.2* Collaborative Research Agreement dated as of December 31, 1991 between the Company and American Home Products Corporation 10.3* Collaborative Research Agreement dated as of January 4, 1993 between the Company and Hoechst AG 10.4* Collaborative Research Agreement dated as of October 1, 1993 between the Company and Hoechst Roussel Pharmaceuticals, Inc. 27 Financial Data Schedule - -------------- * Portions of this exhibit have been redacted and are the subject of a confidential treatment request filed with the Secretary of the Securities and Exchange Commission pursuant to rule 24b-2 under the Securities Exchange Act of 1934, as amended.