0000950109-95-003123.txt : 19950815 0000950109-95-003123.hdr.sgml : 19950815 ACCESSION NUMBER: 0000950109-95-003123 CONFORMED SUBMISSION TYPE: 10-Q PUBLIC DOCUMENT COUNT: 2 CONFORMED PERIOD OF REPORT: 19950630 FILED AS OF DATE: 19950811 SROS: NASD FILER: COMPANY DATA: COMPANY CONFORMED NAME: CENTOCOR INC CENTRAL INDEX KEY: 0000708823 STANDARD INDUSTRIAL CLASSIFICATION: IN VITRO & IN VIVO DIAGNOSTIC SUBSTANCES [2835] IRS NUMBER: 232117202 STATE OF INCORPORATION: PA FISCAL YEAR END: 1231 FILING VALUES: FORM TYPE: 10-Q SEC ACT: 1934 Act SEC FILE NUMBER: 000-11103 FILM NUMBER: 95562089 BUSINESS ADDRESS: STREET 1: 200 GREAT VALLEY PKWY CITY: MALVERN STATE: PA ZIP: 19355 BUSINESS PHONE: 6106516000 MAIL ADDRESS: STREET 1: 200 GREAT VALLEY PARKWAY CITY: MALVERN STATE: PA ZIP: 19355 10-Q 1 FORM 10-Q UNITED STATES SECURITIES AND EXCHANGE COMMISSION 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 June 30, 1995 ------------- [_] 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 0-11103 ------- CENTOCOR, INC. -------------------------------------------------------------------------------- (Exact name of registrant as specified in its charter) Pennsylvania 23-2117202 ---------------------------------------- ----------------------------- (State or other jurisdiction of (IRS Employer incorporation or organization) Identification No.) 200 Great Valley Parkway Malvern, Pennsylvania 19355-1307 -------------------------------------------------------------------------------- (Address of principal executive offices) (Zip Code) 610-651-6000 -------------------------------------------------------------------------------- (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 X No _______ ------- Shares of Common Stock outstanding at August 1, 1995 were 58,321,353. Part I: Financial Information ----------------------------- Item 1: Financial Statements CENTOCOR, INC. AND SUBSIDIARIES CONSOLIDATED BALANCE SHEETS (In thousands)
(Unaudited) June 30, December 31, 1995 1994 --------------------------------------------- --------------- --------------- ASSETS Current assets: Cash and cash equivalents (Notes 4 and 6) $44,587 $78,925 Short-term investments (Notes 4 and 6) 109,691 102,663 Accounts and contracts receivable 19,424 11,842 Interest receivable 1,973 1,082 Inventory (Note 5) 22,152 16,682 Prepaid expenses 2,141 2,722 Other current assets 608 1,041 --------------- --------------- 200,576 214,957 Fixed assets (Note 6): Land and buildings 73,325 71,137 Equipment, furniture, fixtures and improvements 68,441 60,671 --------------- --------------- 141,766 131,808 Less accumulated depreciation (71,226) (61,768) --------------- --------------- 70,540 70,040 Long-term investments (Note 4) 8,743 2,919 Intangible and other assets 18,269 17,999 --------------- --------------- Total assets $298,128 $305,915 =============== ===============
See accompanying Notes to Consolidated Financial Statements. 2 CENTOCOR, INC. AND SUBSIDIARIES CONSOLIDATED BALANCE SHEETS (CONT'D.) (In thousands)
(Unaudited) June 30, December 31, 1995 1994 -------------------------------------- --------------- ------------ LIABILITIES AND SHAREHOLDERS' EQUITY Current liabilities: Accounts payable $4,807 $6,383 Accrued expenses 32,445 26,378 Unearned revenues 383 1,407 Notes payable (Note 6) 7,792 6,897 Current portion of long-term debt (Note 6) 20,547 26,182 --------------- ------------ 65,974 67,247 Long-term debt (Note 6) 231,640 231,640 Other liabilities 1,363 1,240 Minority interest 849 510 Shareholders' equity (Note 2): Preferred Stock, $.01 par value, 10,000 shares authorized, none issued - - Common Stock, $.01 par value, 100,000 shares authorized and 58,283 and 57,081 issued and outstanding at June 30, 1995 and December 31, 1994, respectively 583 571 Additional paid-in capital 767,460 750,175 Deficit (777,257) (751,707) Unrealized gain on marketable securities 251 - Cumulative foreign currency translation adjustments 7,265 6,239 --------------- ------------ (1,698) 5,278 --------------- ------------ Total liabilities and shareholders' equity $298,128 $305,915 =============== ============
See accompanying Notes to Consolidated Financial Statements. 3 CENTOCOR, INC. AND SUBSIDIARIES CONSOLIDATED STATEMENTS OF OPERATIONS (In thousands except per share data) (Unaudited)
========================================================================== For the three months ended June 30, 1995 1994 ========================================================================== REVENUES Sales $17,754 $12,114 Contracts 3,000 4,270 -------- -------- 20,754 16,384 COST AND EXPENSES Cost of sales 8,071 4,471 Research and development 17,008 16,666 Marketing, general and administrative 7,120 6,809 -------- -------- 32,199 27,946 OTHER INCOME (EXPENSE) Interest income 2,798 1,561 Interest expense (4,868) (4,933) Litigation settlement (Note 2) (3,750) - Other (44) (484) --------- --------- (5,864) (3,856) NET LOSS ($17,309) ($15,418) ========= ========= NET LOSS PER SHARE ($0.30) ($0.30) ========= ========= Weighted number of shares outstanding 58,258 50,835 ========= =========
See accompanying Notes to Consolidated Financial Statements. 4 CENTOCOR, INC. AND SUBSIDIARIES CONSOLIDATED STATEMENTS OF OPERATIONS (IN THOUSANDS EXCEPT PER SHARE DATA) (UNAUDITED)
------------------------------------------------------------------------------------------ For the six months ended June 30, 1995 1994 ------------------------------------------------------------------------------------------ Revenues: Sales $37,073 $21,943 Contracts (including related party revenues of $1,652 in 1994) (Note 7) 7,676 9,714 -------------- -------------- 44,749 31,657 Costs and expenses: Cost of sales 16,696 8,101 Research and development (including contract revenue-related expenses of $1,572 in 1994) 30,509 31,055 Marketing, general and administrative (including contract revenue-related expenses of $343 in 1994) 14,614 13,627 Charge for acquired research and development (Note 8) - 36,966 -------------- -------------- 61,819 89,749 Other Income (expense): Interest income 5,583 2,669 Interest expense (9,832) (9,893) Litigation settlement (Note 2) (3,750) - Other (482) (739) -------------- -------------- (8,481) (7,963) Net loss ($25,551) ($66,055) ============== ============== Net loss per share ($0.44) ($1.38) ============== ============== Weighted average number of shares outstanding 58,014 47,813 ============== ==============
See accompanying Notes to Consolidated Financial Statements. 5 CENTOCOR, INC. AND SUBSIDIARIES CONSOLIDATED STATEMENTS OF CASH FLOWS (IN THOUSANDS) (UNAUDITED)
================================================================================== For the six months ended June 30, 1995 1994 ================================================================================== Cash flows used for operating activities: Net loss ($25,551) ($66,055) Adjustments to reconcile net loss to net cash used for operating activities: Charge for acquired research and development - 36,966 Litigation reserve 3,750 - Net loss on long-term investments 1,039 1,091 Depreciation and amortization 8,663 8,963 Amortization of deferred income (1,657) (1,930) Other 338 1 Changes in assets and liabilities: Accounts and contracts receivable (7,253) 1,825 Interest receivable (859) (728) Inventory (4,265) (1,484) Prepaid expenses (1,057) (648) Other current assets 228 (146) Intangible and other assets (1,185) (665) Accounts payable (1,827) (2,988) Unearned revenue 123 1,000 Accrued expenses and other liabilities 988 (4,407) Other long-term liabilities 508 855 ----------- ----------- Net cash used for operating activities (28,017) 28,350 Cash flows from (used for) investing activities: Net (purchases) sales of investments (12,662) 18,777 Net purchases of fixed assets (2,968) (2,039) Acquisition of Tocor II - 3,991 ----------- ----------- Net cash from (used for) investing activities (15,630) 20,729 Cash flows from (used for) financing activities: Net proceeds from issuance of Common Stock 16,682 3,113 Reduction of long-term debt and notes payable (7,977) (1,344) ----------- ----------- Net cash from financing activities 8,705 1,769 Effect of foreign currency translation 604 874 ----------- ----------- Net decrease in cash and cash equivalents (34,338) (4,978) Beginning cash and cash equivalents 78,925 46,210 ----------- ----------- Ending cash and cash equivalents $44,587 $41,232 =========== ===========
See accompanying Notes to Consolidated Financial Statements. 6 Centocor, Inc. And Subsidiaries Notes to Consolidated Financial Statements (Unaudited) -------------------------------------------------------------------------- Note 1 BASIS OF PRESENTATION The accompanying consolidated financial statements have been prepared in accordance with generally accepted accounting principles applicable to interim periods. These financial statements do not include all disclosures required for annual financial statements and should be read in conjunction with the more complete disclosures contained in Centocor, Inc.'s ("Centocor" or "the Company") audited financial statements in the Company's Annual Report on Form 10-K for the year ended December 31, 1994. The statements reflect, in the opinion of management, all adjustments of a normal and recurring nature necessary to present fairly the Company's consolidated financial position at June 30, 1995 and December 31, 1994 and the consolidated results of operations for the three and six months ended June 30, 1995 and 1994 and consolidated cash flows for the six months ended June 30, 1995 and 1994. The results of operations and the cash flows are not necessarily indicative of the results to be expected for the entire year. Note 2 COMMITMENTS AND CONTINGENCIES Liquidity and Capital Resources ------------------------------- The Company has incurred significant operating expenses attempting to develop pharmaceutical products. The Company's product sales through 1994 were almost exclusively generated by in-vitro diagnostic products. Consequently, excluding the impact of significant contract revenues through collaborative alliances with pharmaceutical companies and financing activities, the Company has experienced substantial net cash outflows. The Company's future financial condition is highly dependent upon the reduction of the Company's rate of net cash outflows and, ultimately, upon the achievement of significant and sustained levels of pharmaceutical product sales. The Company commenced the commercial sale of two pharmaceutical products -ReoPro (TM) in January 1995 and Panorex(R) in February 1995. During the year ending December 31, 1995, sales of those two products alone are not expected to generate sufficient revenue to enable the Company to avoid a net cash outflow for the year. Under the Company's collaborative strategy of entering into alliances with established pharmaceutical companies, the Company generally shares sales revenues from products covered by such arrangements with its partners. There can be no assurance that those products, in conjunction with the Company's pharmaceutical product candidates under development and in-vitro diagnostic products, will achieve a level of sales sufficient to generate positive cash flow from operations for 7 Centocor, Inc. And Subsidiaries Notes to Consolidated Financial Statements (Unaudited) -------------------------------------------------------------------------- the Company, given the current and currently anticipated future scope of the Company's operations. The level of future sales of both diagnostic and pharmaceutical products will be dependent upon several factors including, but not limited to, the timing and extent of future regulatory approvals of the Company's products, approval and commercialization of competitive products and the degree of acceptance of the Company's products in the marketplace. There can be no assurance that the U.S. Food and Drug Administration ("FDA") or other regulatory approvals expanding the authorized use of ReoPro(TM) and Panorex(R) or permitting the commercial sale of any of the Company's product candidates under development will be obtained. Failure to obtain additional timely FDA or other regulatory approvals for the use of ReoPro(TM) and Panorex(R) or other product candidates will have a material adverse effect on the Company. The Company expects that it will need to secure significant additional funding in the future from collaborative arrangements with pharmaceutical companies or from the capital markets until significant and sustained levels of pharmaceutical sales are achieved. There can be no assurance that significant additional funding will be available to the Company or that the Company can obtain additional collaborations with established pharmaceutical companies and receive payments for product rights and/or the achievement of milestones under such collaborative agreements. Even if the Company obtains such funding, there can be no assurance that such funding will be sufficient to produce positive cash flows from operations. Legal Proceedings ----------------- On December 23, 1993, a purported class action captioned Peter Cordaro v. Hubert J.P. Schoemaker, Stelios Papadopoulos, Marc Feldmann, David Golden, Centocor, Inc., and Tocor II, Inc. ("Tocor II") was filed in the Court of Common Pleas of the Commonwealth of Pennsylvania, in and for Chester County. The complaint alleges that the defendants breached their fiduciary duties to Tocor II Unitholders by, among other things, making an offer to exchange shares of the Company's Common Stock for Tocor II Units, recommending acceptance of the exchange offer, and failing to maximize shareholder value. The complaint sought, among other relief, an injunction against consummation of the exchange offer, the establishment of a "truly independent" special committee and the retention of a financial advisor to consider the exchange offer, and an award of damages (including rescissionary damages), costs and plaintiff's counsel fees. No injunction was, in fact, sought, and the exchange offer was made and consummated. The defendants filed a motion to dismiss the complaint on the ground that the Pennsylvania court should not exercise jurisdiction over a matter relating to the internal affairs of a foreign corporation. On February 27, 1995, this motion was denied without prejudice to its subsequent renewal. The Company believes that the allegations set forth in the complaint are without merit and intends to vigorously defend the suit. In January 1993, following suspension of the Company's CHESS trial of Centoxin(TM) ("HA- 8 Centocor, Inc. And Subsidiaries Notes to Consolidated Financial Statements (Unaudited) -------------------------------------------------------------------------- 1A(R)"), purported security holders of the Company and/or Tocor II filed complaints in the United States District Court for the Eastern District of Pennsylvania against the Company, Tocor II, and certain present and former directors and/or officers of the Company and/or Tocor II, and Eli Lilly and Company ("Lilly"). The cases were consolidated pursuant to an order, and a Consolidated Class Action Complaint captioned In Re Centocor Securities Litigation II, No. 93-CV-0236 was filed in May 1993, based on alleged violations of securities laws and alleged breaches of common law duties. All claims against all defendants, except the Company and two of its officers/directors and a former director, were voluntarily dismissed when that Complaint was filed. In November 1994, a Corrected Consolidated Amended Class Action complaint was filed in which a number of the original plaintiffs were dropped ("the Complaint"). The Complaint alleges that defendants knowingly or recklessly omitted certain material facts and made false and misleading statements of material facts about Centoxin(TM) and the CHESS trial in violation of Sections 10(b) and 20 of the Securities Exchange Act of 1934 and Rule 10b-5 thereunder, and also alleges violations of the common law of negligent misrepresentation. The action has been conditionally certified as a class action on behalf of persons who purchased common stock and convertible subordinated debentures of the Company from April 21, 1992 through January 15, 1993 and who were allegedly damaged thereby. An agreement has been reached by all parties which, if approved by the Court, would lead to a settlement and dismissal of this action. If the settlement is approved, all claims will be dismissed with prejudice pursuant to the appropriate order of the court. In connection with the proposed settlement, the Company recorded a charge to operations of $3,750,000 for the three and six months ended June 30, 1995. In May 1993, the Company was served with a complaint filed earlier in the United States District Court for the Southern District of California at San Diego. The plaintiff, who allegedly had purchased shares of Corvas International, Inc. ("Corvas") in its initial public offering on January 30, 1992, brought suit against Corvas and certain of its directors, the Company, and one of the Company's directors and a former director (the "Centocor defendants"), on behalf of similarly situated investors. The complaint alleges the defendants violated the federal securities laws by disclosing to Corvas' investors that Centocor and Corvas had entered into a "strategic alliance" to develop one of Corvas' products, but failing to disclose that the Company allegedly would not be able to perform on that agreement because of events relating to Centoxin(TM) (HA-1A(R)). The Complaint sought to proceed as a class action on behalf of all those who purchased Corvas common stock during the period from January 30, 1992 through January 15, 1993. A motion to dismiss the complaint in its entirety as to the Centocor defendants was filed in early June 1993. Corvas and its directors had also filed a motion to dismiss. In September 1993, the Court dismissed a number of plaintiff's claims including claims relating to the period after April 14, 1992 and, in effect, the claim brought against the Company under Section 10(b) of the Securities Exchange Act of 1934. As to the remaining claims, the Court conditionally certified a class of all purchasers of Corvas common stock during the period January 30, 1992 through April 14, 1992. An agreement has been 9 Centocor, Inc. And Subsidiaries Notes to Consolidated Financial Statements (Unaudited) -------------------------------------------------------------------------- reached by all parties which, if approved by the Court, would lead to the settlement and dismissal of this action. The Company would contribute to the settlement 600,000 shares of the stock of Corvas which it holds. In October 1992, the Company was served with a complaint filed by the Velos Group, a Maryland partnership ("Velos"), in the United States District Court for the District of Maryland. The complaint alleges, principally, that the Company breached certain provisions of a license agreement between Velos and the Company pursuant to which the Company has exclusive rights to U.S. Patent No. 5,057,598, which includes claims relating to monoclonal antibodies used in treating manifestations of Gram-negative bacterial infections. The complaint seeks declaratory relief, monetary relief in excess of $100,000,000, and requests that the Company place in escrow one-half of the amounts received by the Company pursuant to its agreements with Lilly. The complaint does not seek to terminate or rescind any of the Company's rights under the license agreement. The Company answered the complaint and asserted affirmative defenses and counterclaims on January 7, 1993, but the counterclaims and certain affirmative defenses were dismissed with leave to replead on June 22, 1993. On July 28, 1993, the Court permitted plaintiff to file an amended complaint that updated some of the claims in the original complaint but otherwise reasserted the basic factual allegations and, with one minor exception, relied upon the same legal theories. On August 27, 1993, the Company filed its Answer, Affirmative Defenses and Counterclaim for Damages and Equitable Relief, to the amended complaint (the "Amended Answer"). In the Amended Answer, the Company again denied all of the allegations made by Velos and stated certain affirmative defenses and counterclaims against Velos with respect to the license agreement, based on theories of (I) failure of consideration, (ii) fraud in the inducement, and (iii) unilateral mistake as to facts, which mistake was induced by the fraudulent misrepresentation of Velos. On September 22, 1993, plaintiff moved to dismiss the Company's counterclaims and to strike certain of the Company's affirmative defenses. On February 6, 1995, the motion was denied. Discovery has now been resumed and trial is fixed for January 1996. The Company believes that the allegations of Velos are without merit and intends vigorously to defend the suit and to pursue its counter claims. In July 1995, PaineWebber Development Corporation ("PaineWebber"), a wholly-owned subsidiary of PaineWebber Group, Inc., caused suits to be filed against the Company by two research and development partnerships formed in the mid-1980s by PaineWebber and managed by it since then. The two PaineWebber partnerships (PaineWebber R&D Partners, L.P. and PaineWebber R&D Partners II, L.P.) were, respectively, investors in Centocor Partners II, L.P. ("CPII"), and Centocor Partners III, L.P. ("CPIII"), research partnerships for which PaineWebber acted as the Sales Agent. The Company purchased the limited partners' interests in CPII in February 1992 and that partnership was then dissolved. The suit by PaineWebber R&D Partners, L.P., was filed in the Supreme Court of the State of New York, County of New York, and purports to be a class action on behalf of all former limited partners of CPII. The complaint charges that some portion of the 10 Centocor, Inc. And Subsidiaries Notes to Consolidated Financial Statements (Unaudited) -------------------------------------------------------------------------- $100 million paid by Lilly to the Company in July 1992 constituted revenues to the Company for the licensing, sublicensing or sale of Centoxin and that the Company is obligated to pay a percentage thereof to the former limited partners of CPII, in addition to amounts already paid. The theories of recovery are similar to those asserted by Velos in 1992, as described above. The suit by PaineWebber R&D II, L.P., was filed in the Court of Chancery of the State of Delaware. In the complaint in this action, the plaintiff seeks to sue derivatively on behalf of CPIII. CPIII is named as a nominal defendant and the Company and a wholly owned subsidiary of the Company which acts as the general partner of CPIII are named as defendants against whom relief is sought. The claim in this case is that at least $25 million of the money paid by Lilly to the Company in 1992 represented profits from the marketing of ReoPro, obligating the Company to pay a portion thereof to CPIII, and that the Company is obligated to pay an increased percentage of the profits from ReoPro to CPIII going forward. The Company believes that these suits are without merit and intends to defend them vigorously. While it is not possible to predict with certainty the eventual outcome of these matters, the Company believes that the foregoing proceedings will not have a material adverse effect on the financial position of the Company. Partnerships ------------ The Company has licensed certain technology related to ReoPro(TM) and a certain cardiovascular imaging product to CPIII and performs research and development with respect to such technology on CPIII's behalf. CPIII holds the rights to the licensed technology and results of the research and development efforts related thereto. The Company has the option to acquire such rights through its option to purchase the limited partnership interests in CPIII. The Company's option to purchase the limited partnership interests in CPIII is exercisable upon the earlier of (a) each limited partner having received distributions related to sales of the CPIII products equal to $15,000 per full limited partnership interest and the expiration of at least 24 months after the first commercial sale of a CPIII product or (b) the expiration of at least 48 months after the first commercial sale of a CPIII product; but, in any event, not prior to the expiration of the then applicable long-term capital gains holding period after the expenditure by the Company of all funds paid to it pursuant to the Development Agreement with CPIII. The Company commenced commercial sales of ReoPro(TM) in January 1995. If the Company elects to exercise its option to purchase the limited partnership interests in CPIII, the Company must make an advance payment of approximately $13,598,000 in cash or, at the Company's election, approximately $15,229,000 in the Company's Common Stock, and future payments generally of six percent of sales of products developed by CPIII. The Company and CPIII have formed a joint venture for the purpose of commercializing ReoPro(TM). Joint venture profits, if any, are allocated 75 percent to the Company and 25 percent to CPIII. The Company consolidates the results of the joint venture's operations and 11 Centocor, Inc. And Subsidiaries Notes to Consolidated Financial Statements (Unaudited) -------------------------------------------------------------------------- records the profits allocable to CPIII as a royalty expense, a component of cost of sales. The joint venture will terminate upon the occurrence of certain events including the exercise or expiration of the purchase option. The Company has entered into indemnity agreements with CPIII and the former limited partners of Centocor Cardiovascular Imaging Partners, L.P. ("CCIP"), and CPII pursuant to which the Company would be obligated, under certain circumstances, to compensate these parties for the fair market value of their respective interests under any license agreements with the Company relating to their respective products which are lost through the exercise by the United States Government of any of its rights relating to the licensed technology. The amount of any such loss would be determined annually by independent appraisal. Royalties --------- The Company is required to make certain future payments to the former limited partners of CCIP and CPII based on sales of products developed by each of the respective partnerships. Upon any exercise by the Company of its option to acquire the limited partnership interests in CPIII, the Company would be required to make future payments to the former limited partners of CPIII, including payments based on any sales of ReoPro(TM). As discussed above, until such option is exercised, CPIII's allocable profits are reported as royalty expense. Additionally, pursuant to its agreements with Lilly, the Company may be required to make royalty payments on sales of ReoPro. The Company has entered into agreements to support research at certain research institutions. These agreements, which grant the Company licenses and/or options to license certain technology resulting from the research, generally require the Company to pay royalties to such institutions on the sales of any products that utilize the licensed technology. Further, the Company has licenses under certain patents, patent applications and technology and pays the licensors or their licensees royalties under such agreements. All royalties are reflected in cost of sales as incurred. Royalty costs represent a significant percentage of sales. Product Liability ----------------- The testing and marketing of medical products entails an inherent risk of product liability. The Company maintains limited product liability insurance coverage. Such insurance is difficult and expensive to obtain. The Company's business may be adversely affected by a successful product liability claim in excess of its insurance coverage. 12 Centocor, Inc. And Subsidiaries Notes to Consolidated Financial Statements (Unaudited) --------------------------------------------------------------------------- Under various contractual agreements, the Company has agreed to indemnify third parties against certain losses, including losses arising from product liability and patent infringement claims pertaining to the Company's products. Note 3 COLLABORATIVE ARRANGEMENTS Relationship with Lilly ----------------------- Under a Sales and Distribution Agreement, the Company is principally responsible for developing and manufacturing HA-1A(R) and ReoPro(TM). Lilly is principally responsible for the marketing, sale and distribution of HA-1A(R) and ReoPro(TM). Under agreements with Lilly, the Company and Lilly share equally in the profits from ReoPro(TM) and the Company may be required to pay Lilly royalties on sales of ReoPro(TM). The Company may be required to make a payment to Lilly of $50 million through December 31, 1995, or decreasing amounts through December 31, 1999, in the event of any change in control of the Company or in the event of any governmental action or determination which results in the Sales and Distribution Agreement not being in full force and effect in all material respects in major jurisdictions, excluding the United States, and the subsequent termination of the Sales and Distribution Agreement by Lilly based solely on such events. Relationship with Glaxo/Wellcome plc. ------------------------------------- The Company entered into an alliance agreement with Glaxo/Wellcome plc. (previously Wellcome plc.) for the development and marketing of certain of the Company's monoclonal antibody-based cancer therapeutic products, including Panorex(R). Under the alliance agreement, the Company and Glaxo/Wellcome share revenues from the sale of the products, including Panorex(R). Centocor is principally responsible for the manufacture of Panorex(R) and for securing regulatory approvals for Panorex(R). Glaxo/Wellcome is principally responsible for the clinical development, marketing, sale and distribution of such drugs, including Panorex(R), on a worldwide basis. Note 4 CASH EQUIVALENTS AND INVESTMENTS The Company's equity investments classified as available for sale are carried at estimated fair value with unrealized gains and losses recorded as a special component of stockholders' equity. The Company's investments in U.S. treasury securities and corporate bonds which the Company has the ability and intent to hold to maturity are carried at amortized cost. 13 Centocor, Inc. And Subsidiaries Notes to Consolidated Financial Statements (Unaudited) --------------------------------------------------------------------------- At June 30, 1995, securities classified as available for sale and held to maturity are summarized below (in thousands):
Estimated Estimated Adjusted Unrealized Unrealized Carrying Cost Gains Losses Value ---- ----- ------ ----- Investments available for sale: Equity securities $ 2,936 $ 251 $ - $ 3,187 ===== ===== ===== ======
Estimated Estimated Carrying Unrealized Unrealized Fair Value Gains Losses Value ----- ----- ------ ----- Investments held to maturity: Securities and obligations of the U.S. Treasury and other U.S. government agencies $87,955 $ 164 $(263) $87,856 Certificates of deposit 29,015 - - 29,015 Corporate bonds and commercial paper 31,763 88 (11) 31,840 ------ -- ---- ------ $148,733 $ 252 $(274) $148,711 ======= ==== ===== ======= At June 30, 1995, these securities were classified as follows (in thousands): Cash equivalents $ 33,486 Short-term investments 109,691 Long-term investments 8,743 ------ $151,920 ========
The Company has agreed to maintain investments of $27,700,000 as of June 30, 1995 at certain banks as collateral for loans from those banks. See Note 6. 14 Centocor, Inc. And Subsidiaries Notes to Consolidated Financial Statements (Unaudited) --------------------------------------------------------------------------- NOTE 5 INVENTORY Inventory consists of the following (in thousands):
June 30, December 31, 1995 1994 -------- ---------- Raw materials $ 6,593 $ 3,564 Work in process 8,302 8,973 Finished goods 7,257 4,145 ------ ----- $22,152 $16,682 ======= =======
Inventories have various expiration dates. The Company continually evaluates the extent of inventory reserves considered necessary based upon the future regulatory and commercial status of such products. There can be no assurance that reserves for inventories will not be required in the future. Note 6 DEBT Notes Payable Notes payable at June 30, 1995 and December 31, 1994 consists of $7,792,000 and $6,897,000, respectively, of borrowings under short-term notes at an interest rate of 5.57 percent per annum at June 30, 1995, payable in Dutch guilders no later than September 28, 1995. These borrowings are secured by investments at the lending bank of $7,700,000 (see "Loan Covenants"). 15 Centocor, Inc. And Subsidiaries Notes to Consolidated Financial Statements (Unaudited) ---------------------------------------------------------------------------- Long-term debt Long-term debt consists of the following (in thousands):
June 30, December 31, 1995 1994 -------- ------------ 7-1/4 percent Notes $106,640 $106,640 6-3/4 percent Debentures 125,000 125,000 Mortgage Debt 9,989 15,941 Long-term Note 10,558 10,241 ------ -------- 252,187 257,822 Current Portion (20,547) (26,182) ------- -------- $231,640 $231,640 ======= =======
7-1/4 Percent Notes On January 28, 1991, the Company issued $106,645,000 principal amount of 7- 1/4 percent Convertible Subordinated Notes (the "7-1/4 percent Notes") due February 1, 2001. The 7-1/4 percent Notes are convertible by the holders into approximately 3,843,000 shares of the Company's Common Stock at a conversion price of $27.75 per share at any time prior to redemption or maturity. The 7- 1/4 percent Notes are subordinated in right of payment to senior indebtedness at June 30, 1995 of $28,339,000 and all future senior indebtedness of the Company, and rank pari passu with the 6-3/4 percent Debentures described below. The 7- 1/4 percent Notes are redeemable by the Company for cash in whole or in part until February 1, 2001 at amounts ranging up to 104 percent of the principal amount of the 7-1/4 percent Notes. The Company may be required to redeem the 7- 1/4 percent Notes at their principal amount at the option of the holders of the 7-1/4 percent Notes under certain limited circumstances, including a change in control of the Company. 6-3/4 Percent Debentures On October 16, 1991, the Company issued $125,000,000 principal amount of 6- 3/4 percent Convertible Subordinated Debentures (the "6-3/4 percent Debentures") due October 16, 2001. The 6-3/4 percent Debentures are convertible by the holders into approximately 2,049,000 shares of the Company's Common Stock at a conversion price of $61.00 per share at any time prior to redemption or maturity. The 6-3/4 percent Debentures are subordinated in right of payment to senior indebtedness at June 30, 1995 of $28,339,000 and all future senior indebtedness of the Company, and rank pari passu with the 7-1/4 percent Notes. The 6-3/4 percent Debentures are redeemable by the Company for cash in whole or in part until October 16, 2001 at amounts ranging 16 Centocor, Inc. And Subsidiaries Notes to Consolidated Financial Statements (Unaudited) --------------------------------------------------------------------------- up to 104 percent of the principal amount of the 6-3/4 percent Debentures. The Company may be required to redeem the 6-3/4 percent Debentures at their principal amount at the option of the holders of the 6-3/4 percent Debentures under certain limited circumstances, including a change in control of the Company. Mortgage Debt Mortgage loans have been used to finance a portion of the acquisition and expansion of certain of the Company's facilities in the United States and The Netherlands. These loans are generally secured by the related land and buildings. In the United States, the Company had such a loan which was repaid on its maturity date of May 1, 1995 in the amount of $6,442,000. A Netherlands loan, with an outstanding balance of approximately $6,510,000 at June 30, 1995, is payable in Dutch guilders, bears interest at an annual rate of 8-1/4 percent through its final maturity date of September 30, 2011, and is secured by certain equipment, inventories, and accounts receivable. At June 30, 1995, this loan is classified as short-term (see "Loan Covenants"). Long-term Note The Company borrowed $10,558,000 under a 9-1/2 percent long-term note which is payable in Dutch guilders. This loan is secured by the same assets as the Netherlands loan discussed above. At June 30, 1995, this loan is classified as short-term (see "Loan Covenants"). Loan Covenants Agreements covering $20,547,000 of the Company's outstanding debt balances contain certain financial and non-financial covenants, including the maintenance of minimum equity and cash balances and compliance with certain financial ratios. The Company has obtained waivers of certain of such covenants on the condition that it maintains certain investments at the lending bank, which at June 30, 1995 totaled $20,000,000. There can be no assurance that the Company will be able to continue to collateralize such loans and, accordingly, the Company has classified $20,547,000 of debt as short-term. Additionally, $7,792,000 of the Company's short-term debt is secured by investments at the lending bank of $7,700,000. If cash flows continue to be negative, the Company's ability to service its debt may be impaired. 17 Centocor, Inc. And Subsidiaries Notes to Consolidated Financial Statements (Unaudited) --------------------------------------------------------------------------- Note 7 CONTRACT REVENUES Lilly Related ------------- Pursuant to the Company's agreements with Lilly, the Company recognized revenues of $3,000,000 and $6,000,000 for the three and six months ended June 30, 1995 and $3,000,000 and $6,500,000 for the three and six months ended June 30, 1994, respectively, related to ReoPro(TM) milestones. Lilly may make certain future payments based on the achievement of certain milestones related to ReoPro(TM). Related Party Research & Development ------------------------------------ In 1994, the Company conducted research and development under a contract with Tocor II. Under the contract, the Company received reimbursement of its costs plus a management fee. Such revenues were recorded net of amortization of deferred costs resulting from the issuance of warrants to Tocor II Unitholders. See Note 8 for a discussion of an exchange offer which resulted in the termination of the research and development contract and services agreement. For the six months ended June 30, 1994, revenues related to the Tocor II research program were $1,652,000. Expenses incurred, including general and administrative expenses for the six months ended June 30, 1994 were $1,915,000. Note 8 CHARGE FOR ACQUIRED RESEARCH AND DEVELOPMENT In February 1994, the Company initiated the exchange offer pursuant to which the Company offered to exchange 3.2 shares of its Common Stock for each of the 2,250,000 outstanding Tocor II Units tendered. Each Unit consisted of one share of callable common stock of Tocor II, one callable warrant to purchase one share of Centocor Common Stock and one Series T warrant to purchase one share of Centocor Common Stock (the "Warrants"). The exchange offer expired at the close of business on March 11, 1994, at which time the Company accepted all of the 94 percent of the Tocor II Units tendered in exchange for approximately 6,793,000 shares of its Common Stock, thereby increasing shareholders equity by $81,607,000. The transaction was accounted for as a purchase and the Company allocated the excess of the consideration paid over the net assets of Tocor II to the value of the acquired research and development. The Company recorded a charge to earnings in the first quarter of 1994 of $36,966,000 representing principally the cost allocated to the acquired research and development. In connection with the transaction, the Company acquired $50,124,000 of cash and short-term investments and warrants with a value of $8,492,000 which 18 Centocor, Inc. And Subsidiaries Notes to Consolidated Financial Statements (Unaudited) --------------------------------------------------------------------------- were retired. The unaudited comparative statement of operations data excluding the charge for acquired research and development, assuming the exchange offer was consummated as of January 1, 1993, would have been as follows (in thousands except per share amounts):
Statements of For the three months ended For the six months ended Operations Data June 30, 1994 June 30, 1994 --------------- ------------- ------------- Revenues $ 16,384 $ 30,005 Loss $(15,418) $(30,360) Loss per share $ (.30) $ (0.59)
Effective March 30, 1994, each remaining share of Tocor II callable Common Stock ("Tocor II Shares") was converted into 2.88 shares of the Company's Common Stock through a merger of Tocor II into a wholly-owned subsidiary of the Company. Pursuant to the terms of the merger, holders of Tocor II Shares at the time of the merger were required to surrender the certificates representing Tocor II Shares to an exchange agent in exchange for certificates representing Common Stock of the Company. Through June 30, 1995, stock certificates representing 221,000 shares of the Company's Common Stock had been delivered by the exchange agent in connection with the merger. If all of the remaining Tocor II Shares are surrendered to the exchange agent, stock certificates representing an additional 146,000 shares of the Company's Common Stock will be delivered. Shares of the Company's Common Stock into which the Tocor II Shares were converted by the merger are not classified as issued and outstanding until the delivery by the exchange agent of the stock certificate representing such shares. Warrants not tendered as part of Units in the exchange offer remain outstanding. Note 9 INCOME TAXES The Company recorded a charge for acquired research and development of $36,966,000 in 1994, which was not deductible for U.S. tax purposes. At June 30, 1995, the tax effect of the Company's net tax loss carryforward was $182,535,000 with expiration dates ranging from 2005 to 2010. Additionally, at June 30, 1995, the Company had research and development tax credits and other tax credits of $5,424,000 substantially all with expiration dates ranging from 1999 to 2008. Realization of net deferred tax assets related to these items is dependent on future earnings, which are uncertain. Accordingly, a valuation reserve was recorded by the Company and, therefore, the Company had no net deferred tax assets at June 30, 1995. Note 10 SUPPLEMENTAL INFORMATION ON CASH FLOWS Interest paid for the six months ended June 30, 1995 and 1994 was $9,365,000 and $9,545,000, respectively. Income tax payments for the six months ended June 30, 1995 were $9,000. No income tax payments were made for the six months ended June 30, 1994. 19 Centocor, Inc. And Subsidiaries Notes to Consolidated Financial Statements (Unaudited) --------------------------------------------------------------------------- Cash used for the purchases of investments as well as the cash received upon the maturities and sales of investments were as follows (in thousands):
Six months ended June 30, 1995 1994 --------- --------- Purchases $(78,962) $(44,590) Maturities and sales 66,300 63,367 ------ -------- $(12,662) $ 18,777
During the first quarter of 1994, the Company acquired cash and short-term investments of $50,124,000 in connection with an exchange offer more fully described in Note 8. 20 Item 2: Management's Discussion and Analysis of Financial Condition and Results of Operations -------------------------------------------------------------------------------- FINANCIAL CONDITION LIQUIDITY AND CAPITAL RESOURCES The Company has incurred significant operating expenses attempting to develop pharmaceutical products. The Company's product sales through 1994 were almost exclusively generated by in-vitro diagnostic products. Consequently, excluding the impact of significant contract revenues through collaborative alliances with pharmaceutical companies and financing activities, the Company has experienced substantial net cash outflows. The Company's future financial condition is highly dependent upon the reduction of the Company's rate of net cash outflows and, ultimately, upon the achievement of significant and sustained levels of pharmaceutical product sales. The Company commenced the commercial sale of two pharmaceutical products - ReoPro(TM) in January 1995 and Panorex(R) in February 1995. During the year ending December 31, 1995, sales of those two products alone are not expected to generate sufficient revenue to enable the Company to avoid a net cash outflow for the year. Under the Company's collaborative strategy of entering into alliances with established pharmaceutical companies, the Company generally shares sales revenues from products covered by such arrangements with its partners. There can be no assurance that those products, in conjunction with the Company's pharmaceutical product candidates under development and in-vitro diagnostic products, will achieve a level of sales sufficient to generate positive cash flow from operations for the Company, given the current and currently anticipated future scope of the Company's operations. The level of future sales of both diagnostic and pharmaceutical products will be dependent upon several factors including, but not limited to, the timing and extent of future regulatory approvals of the Company's products, approval and commercialization of competitive products and the degree of acceptance of the Company's products in the marketplace. There can be no assurance that the U.S. Food and Drug Administration ("FDA") or other regulatory approvals expanding the authorized use of ReoPro(TM) and Panorex(R) or permitting the commercial sale of any of the Company's product candidates under development will be obtained. Failure to obtain additional timely FDA or other regulatory approvals for the use of ReoPro(TM) and Panorex(R) or other product candidates will have a material adverse effect on the Company. The Company expects that it will need to secure significant additional funding in the future from collaborative arrangements with pharmaceutical companies or from the capital markets until significant and sustained levels of pharmaceutical sales are achieved. There can be no assurance that significant additional funding will be available to the Company or that the Company can obtain additional collaborations with established pharmaceutical companies and receive payments for product rights and/or the achievement of milestones under such collaborative agreements. Even if the Company obtains such funding, there can be no assurance that such funding will be sufficient to produce positive cash flows from operations. At June 30, 1995, the Company had cash, cash equivalents, and investments of $163,021,000 including equity investments of $3,187,000. For the six months ended June 30, 1995, the Company had negative cash flows from operations of $28,017,000. The Company's total cash flows for the six months ended June 30, 1995 included the receipt of $12,100,000 from the exercise of warrants to purchase shares of the Company's Common Stock. The extent and timing of future warrant 21 Item 2: Management's Discussion and Analysis of Financial Condition and Results of Operations -------------------------------------------------------------------------------- exercises, if any, are primarily dependent upon the market price of the Company's Common Stock and general financial market conditions, as well as the exercise prices and expiration dates of the warrants. The Company's total cash, cash equivalents and investments decreased by $21,486,000 from December 31, 1994 principally as a result of cash used for operations and purchases of fixed assets partially offset by cash received from the exercise of warrants as discussed above. Agreements covering $20,547,000 of the Company's outstanding debt balances contain certain financial and non-financial covenants, including the maintenance of minimum equity and cash balances and compliance with certain financial ratios. The Company has obtained waivers of certain of such covenants on the condition that it maintain certain investments at the lending bank, which at June 30, 1995 totaled $20,000,000. There can be no assurance that the Company will be able to continue to collateralize such loans and, accordingly, the Company has classified $20,547,000 of debt as short-term. Additionally, $7,792,000 of the Company's short-term debt is secured by investments at the lending bank of $7,700,000. If cash flows continue to be negative, the Company's ability to service its debt may be impaired. See Note 2 to the Company's Consolidated Financial Statements for a discussion of litigation and other factors that may affect the Company's future liquidity and capital resources. ASSETS The decrease in the aggregate amount of cash and investments at June 30, 1995 as compared to December 31, 1994 is discussed under Liquidity and Capital Resources. Accounts and contracts receivable at June 30, 1995 increased as compared to December 31, 1994 principally as a result of commercial sales of ReoPro(TM) to Lilly and sales of Panorex(R) to Glaxo/Wellcome. Inventory at June 30, 1995 increased as compared to December 31, 1994 due primarily to the production of ReoPro(TM), Panorex(R) and certain infectious disease diagnostic products. The Company continually evaluates the realizability of its inventories. There can be no assurance that reserves to reduce the carrying value of inventory will not be required in the future. Gross fixed assets at June 30, 1995 increased as compared to December 31, 1994 principally due to the investment of $2,968,000 for the purchase of fixed assets, in addition to the impact of foreign exchange rates on fixed assets denominated in foreign currencies. At the Company's present level of operations, the Company currently maintains idle facilities and equipment in Malvern. The Company continually evaluates the future needs for its facilities and equipment. There can be no assurance that reserves to further reduce the carrying value of certain fixed assets will not be required in the future. LIABILITIES AND SHAREHOLDERS' EQUITY Shareholders' equity at June 30, 1995 decreased as compared to December 31, 1994 principally as a result of the Company's loss for the six months ended June 30, 1995 partially offset by the proceeds from the exercise of options and warrants. The extent and timing of future warrant 22 Item 2: Management's Discussion and Analysis of Financial Condition and Results of Operations -------------------------------------------------------------------------------- and option exercises, if any, are primarily dependent upon the market price of the Company's Common Stock and general financial market conditions, as well as the exercise prices and expiration dates of the warrants and options. Shareholders' equity at June 30, 1995 was negative. The Company expects that shareholders' equity will decrease in future periods unless and until the Company is successful in securing additional capital from collaborative arrangements with pharmaceutical companies or the capital markets, or significant and sustained levels of pharmaceutical product sales are achieved. There can be no assurance that significant and sustained levels of pharmaceutical product sales will be achieved or that any additional capital will be available to the Company. RESULTS OF OPERATIONS GENERAL Product sales have not produced sufficient revenues to cover the Company's operating expenses. The Company has incurred significant operating expenses attempting to develop products and has incurred significant special charges. Consequently, the Company has experienced substantial operating losses. The Company established a goal of achieving profitability in 1995. To achieve profitability, the Company established the following objectives: early and strong market acceptance for both ReoPro (TM) and Panorex(R); growth in the Company's diagnostic product sales; establishment of a long-term strategic alliance for CenTNF; and management of the Company's internal cost structure. Although the Company is implementing plans to address each of these areas, it is unlikely that the Company will be profitable in 1995. REVENUES The increase in sales for the three and six months ended June 30, 1995 as compared to the three and six months ended June 30, 1994 is principally due to the commencement of commercial sales of two pharmaceutical products - ReoPro (TM) in January 1995 and Panorex(R) in February 1995. The Company is highly dependent upon the ability of its marketing partners to develop and expand markets for both ReoPro (TM) and Panorex(R). ReoPro sales to Lilly for the three and six months ended June 30, 1995 were $7,900,000 and $12,400,000, respectively. The Company expects that ReoPro sales to Lilly in the second half of 1995 will be lower than the level of sales in the first half of 1995 primarily due to the levels of inventories maintained by Lilly. Panorex(R) sales to Glaxo/Wellcome for the three and six months ended June 30, 1995 were $1,300,000 and $3,000,000, respectively. The Company expects that Panorex(R) sales to Glaxo/Wellcome in the second half of 1995 will be at about the same level as the level of sales in the first half of 1995. Diagnostic product sales for the three and six months ended June 30, 1995 were $10,100,000 and $21,500,000 as compared to $9,800,000 and $21,900,000 for the three and six months ended June 30, 1994, respectively. The decrease in sales for the six months ended June 30, 1995 as compared to the same period in 1994 is primarily related to reduced imaging and infectious disease product sales partially offset by an increase in sales within the oncology product line. The Company expects that Diagnostic product sales in the second half of 1995 will be at about the same level as the level of sales for the first half of 1995. 23 Item 2: Management's Discussion and Analysis of Financial Condition and Results of Operations -------------------------------------------------------------------------------- The level of future sales of both diagnostic and pharmaceutical products will be dependent upon several factors, including but not limited to the timing and extent of future regulatory approvals of the Company's products, approval and commercialization of competitive products and ultimately the degree of acceptance of the Company's products in the marketplace. Contract revenues for the three and six months ended June 30, 1995 include $3,000,000 and $6,000,000 recognized pursuant to the Company's agreements with Lilly, as compared to $3,000,000 and $6,500,000 for the three and six months ended June 30, 1994. Contract revenues for the three and six months ended June 30, 1994 include $1,652,000 recognized pursuant to the Company's agreement with Tocor II. As a result of the exchange offer which is more fully described in Note 8 to the Company's Consolidated Financial Statements, the revenues under the Tocor II research program terminated in 1994. Contract revenues for the three and six months ended June 30, 1995 include government subsidy revenue of $1,600,000 which relates to the completion of certain manufacturing requirements. The level of contract revenues in future periods will depend primarily upon the extent to which the Company enters into other collaborative contractual arrangements, if any, and the achievement of milestones under current arrangements. COSTS AND EXPENSES Cost of sales increased for the three and six months ended June 30, 1995 as compared to the corresponding periods of 1994 due to the initiation of sales of ReoPro (TM) and Panorex(R) in the first quarter of 1995. As further described in Note 2 to the Company's Consolidated Financial Statements, the Company is required to make certain royalty payments based on sales of products, which payments are reflected in cost of sales. Royalty costs represent a significant percentage of sales. The Company expects an increase in cost of sales in 1995 as compared to 1994, dependent upon the level of sales increase in 1995. Research and development expenses for the three and six months ended June 30, 1995 were $17,008,000 and $30,509,000 as compared to $16,666,000 and $31,055,000 for the three and six months ended June 30, 1994, respectively. Research and development expenses decreased for the six months ended June 30, 1995 as compared to the corresponding period of 1994 due principally to a higher allocation of costs to manufacturing activities related to ReoPro (TM) and Panorex(R) production. The Company expects an increased level of clinical trial expenses in 1995 as compared to 1994, although the level of total research and development expenses in 1995 is expected to be lower than in 1994. This decrease is expected to occur as a result of a higher allocation of costs to manufacturing activities related to ReoPro (TM) and Panorex(R) production. These costs were previously charged to research and development expenses in prior periods. The increase in clinical trial expenses expected in 1995 relate to obtaining regulatory approvals for additional indications of pharmaceutical products and further develop other pharmaceutical and diagnostic product opportunities. Marketing, general and administrative expenses for the three and six months ended June 30, 1995 increased as compared to the corresponding period of 1994 due principally to increases in facilities, insurance and market development expenses. The Company expects the levels of marketing, general and administrative expenses to increase in 1995 as compared to 1994. 24 Item 2: Management's Discussion and Analysis of Financial Condition and Results of Operations -------------------------------------------------------------------------------- OTHER INCOME AND EXPENSES Interest income increased for the six months ended June 30, 1995 as compared to the year earlier period due principally to an increase in interest rates on investments and an increase in the Company's average cash and investment balances. Interest income in future periods will depend primarily on the level of the Company's investments and the interest rates obtained on such investments. The Company recorded a charge to operations of $3,750,000 for the three and six months ended June 30, 1995 relating to litigation. See Note 2 to the Company's Consolidated Financial Statements for a discussion of commitments and contingencies. PER SHARE CALCULATIONS At June 30, 1995, approximately 5,964,312 shares of the Company's Common Stock were issuable upon exercise of outstanding options and warrants and upon vesting of restricted stock awards. Options, warrants, and stock awards are considered Common Stock equivalents for purposes of per share data. The Company uses the weighted average number of shares outstanding in calculating per share data. The effect of Common Stock issuable upon the exercise of Common Stock equivalents is reflected in the per share data calculation only if the effect would be dilutive. The 3,843,000 shares issuable upon conversion of the 7-1/4 percent Convertible Subordinated Notes and the 2,049,000 shares issuable upon conversion of the 6-3/4 percent Convertible Subordinated Debentures are not considered Common Stock equivalents and are not included in the calculation of primary per share data but are included in the calculation of fully diluted per share data if their effect is dilutive. No Common Stock equivalents or shares issuable upon conversion of the 7-1/4 percent Notes and 6-3/4 percent Debentures were included in the per share calculations for any periods presented since to do so would have been antidilutive as the Company has recorded net losses in all periods presented. In future periods, depending upon the market value of the Company's Common Stock and its results of operations for such periods, the Company may be required to include its then outstanding Common Stock equivalents as well as shares issuable upon the conversion of the 7-1/4 percent Notes and the 6-3/4 percent Debentures in its calculations of per share data for such periods if the effect would be dilutive. 25 Part II OTHER INFORMATION Item 1: Legal Proceedings See Note 2 to the Company's Consolidated Financial Statements, which is incorporated herein by reference. Item 4: Submission of Matters to a Vote of Security Holders. (a) The Annual Meeting of Shareholders was held on May 17, 1995 at the Company's principal office at 200 Great Valley Parkway, Malvern, Pennsylvania. (b) Two matters were voted upon at the meeting. With respect to the election of directors for a term of one year expiring on the date of the 1996 annual meeting of shareholders, each nominee was elected with the following vote:
Total Vote for Total Vote Withheld Each Director From Each Director ------------- ------------------ Anthony B. Evnin 45,686,297 722,425 William F. Hamilton 45,688,796 719,926 David P. Holveck 45,602,604 806,118 Antonie T. Knoppers 45,676,867 731,855 Ronald A. Matricaria 45,647,732 760,990 Hubert J.P. Schoemaker 45,598,763 809,959 Richard D. Spizzirri 45,637,406 771,316 Lawrence Steinman 45,594,280 814,442 Jean C. Tempel 45,688,600 720,122
A proposal to amend the Company's 1989 Non-Employee Directors' Non-Qualified Stock Option Plan to increase by 400,000 the number of shares for which options may be granted pursuant to the plan passed with the following vote: For: 37,346,366 Against: 8,006,814 Abstain: 281,703 Broker Non-Votes: 773,839
Item 6: Exhibits and Reports on Form 8-K (a) Exhibits -------- None. (b) Reports on Form 8-K ------------------- The Registrant has filed the following reports on Form 8-K since the beginning of the quarter ended June 30, 1995: Date of Report Item Covered -------------- ------------ July 12, 1995 5, 7 26 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. Centocor, Inc. (Registrant) Date: August 11, 1995 /s/David P. Holveck --------------- ------------------------------ David P. Holveck President and Chief Executive Officer (Principal Executive Officer) Date: August 11, 1995 /s/Dominic J. Caruso --------------- ------------------------------ Dominic J. Caruso Vice President, Finance and Chief Financial Officer (Principal Financial and Accounting Officer) EX-27 2 FINANCIAL DATA SCHEDULE
5 THIS SCHEDULE CONTAINS SUMMARY FINANCIAL INFORMATION EXTRACTED FROM CENTOCOR INC. CONSOLIDATED BALANCE SHEETS AND CONSOLIDATED STATEMENTS OF OPERATIONS AND IS QUALIFIED IN ITS ENTIRETY BY REFERENCE TO SUCH FINANCIAL STATEMENTS. 1,000 U.S. DOLLARS 6-MOS DEC-31-1995 JAN-01-1995 JUN-30-1995 1 44,587 109,691 21,397 0 22,152 200,576 141,766 71,226 298,128 65,912 231,640 583 0 0 (2,281) 298,128 37,073 44,749 16,696 16,696 45,123 0 9,832 (25,551) 0 (25,551) 0 0 0 (25,551) (.44) (.44)