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Medarex Announces 2008 First Quarter Financial Results
PRINCETON, N.J. (Map) - Including a gain of Total revenues for the quarter ended Research and development (R&D) expenses for the quarter ended Medarex ended the first quarter of 2008 with approximately Non-GAAP Financial Measurements This press release and the accompanying tables include non-GAAP financial measures. Please see the section of the accompanying tables titled "Reconciliation of GAAP Net Income to Non-GAAP Net Loss" for a description of these non-GAAP financial measures, including reasons for Medarex management's decision to use each measure, and reconciliations of these non-GAAP financial measures to the most directly comparable financial measures prepared in accordance with Generally Accepted Accounting Principles. Medarex's product development and business activities during the first quarter of 2008 include the following: -- Announcing the receipt of a milestone payment from our licensing partner, Centocor, Inc., in connection with Centocor's submission of a regulatory application to the European Medicines Agency requesting marketing approval of golimumab (CNTO 148), a human anti-TNF antibody for the treatment of rheumatoid arthritis, psoriatic arthritis and ankylosing spondylitis, that was generated using Medarex's UltiMAb(R) technology; -- Announcing the receipt of a milestone payment from our licensing partner, Novo Nordisk A/S, for the filing of an Investigational New Drug application for an antibody generated by Medarex's UltiMAb(R) technology; and -- Adding approximately $152 million to our cash resources through the sale of Genmab A/S common stock, reducing our ownership in Genmab to approximately 5.1% of the total outstanding shares. "This is an exciting time for Medarex, and we begin the year with
continued focus on laying the groundwork for sustained growth and value by
investing in and making positive advances with products in our pipeline," said
As previously announced, 17 presentations for ipilimumab and antibodies targeting PD-1 and CD70 are expected at the upcoming annual meeting of the American Society of Clinical Oncology (ASCO) in May. About Medarex Medarex is a biopharmaceutical company focused on the discovery, development and potential commercialization of fully human antibody-based therapeutics to treat life-threatening and debilitating diseases, including cancer, inflammation, autoimmune disorders and infectious diseases. Medarex applies its UltiMAb(R) technology and product development and clinical manufacturing experience to generate, support and potentially commercialize a broad range of fully human antibody product candidates for itself and its partners. Over forty of these therapeutic product candidates derived from Medarex technology are in human clinical testing or have had INDs submitted for such trials, with seven of the most advanced product candidates currently in Phase 3 clinical trials or the subject of regulatory applications for marketing authorization. Medarex is committed to building value by developing a diverse pipeline of antibody products to address the world's unmet healthcare needs. For more information about Medarex, visit its website at www.medarex.com. Statement on Cautionary Factors Except for the historical information presented herein, the statements
relating to Medarex's investments and advances related to its products in this
press release may constitute forward-looking statements, as defined in the
Private Securities Litigation Reform Act of 1995, that are subject to certain
risks and uncertainties that could cause actual results to differ materially
from any future results, performance or achievements expressed or implied by
such statements. Medarex disclaims, however, any intent or obligation to
update these forward-looking statements. Risks and uncertainties include risks
associated with product discovery and development, uncertainties related to
the outcome of clinical trials, slower than expected rates of patient
recruitment, unforeseen safety issues resulting from the administration of
antibody products in patients, uncertainties related to product manufacturing,
the need for additional capital, compliance with regulatory requirements,
risks associated with the use of hazardous substances and risks associated
with the enforceability of our patents as well as risks detailed from time to
time in Medarex's public disclosure filings with the U.S. Securities and
Exchange Commission (SEC), including its Annual Report on Form 10-K for the
fiscal year ended Medarex(R), the Medarex logo and UltiMAb(R) are registered trademarks of Medarex, Inc. All rights are reserved. MEDAREX, INC. Condensed Consolidated Statements of Operations (In thousands, except per share data) Three Months Ended March 31, (unaudited) 2008 2007 Contract and license revenues $7,984 $6,998 Reimbursement of development costs 4,019 4,541 Total revenues 12,003 11,539 Costs and expenses: Research and development 49,292 47,022 General and administrative 12,409 11,302 Operating loss (49,698) (46,785) Equity in net loss of affiliate (1,785) - Investment and interest income, net 154,818 155,401 Minority interest - Celldex - 1,651 Income before provision for income taxes 103,335 110,267 Provision for income taxes 23 2 Net income $103,312 $110,265 Basic net income per share $0.81 $0.88 Diluted net income per share $0.76 $0.80 Weighted average number of common shares outstanding during the year - basic 127,643 124,690 - diluted 138,580 140,144 Condensed Consolidated Balance Sheets (In thousands) March 31, December 31, 2008 2007 (unaudited) (1) Cash, cash equivalents and marketable securities - Medarex $464,477 $486,772 Cash and cash equivalents - Celldex - 14,000 Other current assets 15,818 29,013 Property, buildings and equipment, net 75,966 79,925 Marketable securities - Genmab 115,587 139,165 Investments in Avant Immunotherapeutics 9,381 - Investments in, and advances to affiliate and partners 6,040 6,040 Segregated cash - non current 1,300 1,530 Other assets 2,206 3,415 $690,775 $759,860 Current liabilities $64,319 $81,645 Other liabilities 86,170 89,454 Convertible notes 143,986 143,505 Shareholders' equity 396,300 445,256 $690,775 $759,860 (1) Derived from the December 31, 2007 audited financial statements. For further information, refer to the consolidated financial statements and footnotes thereto included in Medarex's Annual Report on Form 10-K for the year ended December 31, 2007. This press release dated The following reconciliation of GAAP net income to non-GAAP net loss and GAAP net income per share to non-GAAP net loss per share is provided as a complement to results presented in accordance with GAAP because Medarex's management believes these non-GAAP financial measures provide better insight into Medarex's performance by focusing on results generated by its ongoing operations and are important in comparing current results with prior period results. Non-GAAP net loss and non-GAAP net loss per share are intended to illustrate Medarex's results of operations for the periods presented excluding the items discuss below. Medarex's management believes investors' understanding of Medarex's financial performance is enhanced as a result of our disclosing these non-GAAP financial measures. Non-GAAP net loss and non- GAAP net income per share should not be viewed in isolation or as a substitute for GAAP net loss or GAAP net income per share. MEDAREX, INC. Reconciliation of GAAP Net Income to Non-GAAP Net Loss (In thousands, except per share data) (unaudited) Three Months Ended March 31, 2008 2007 GAAP net income $103,312 $110,265 Celldex net loss (1) 2,924 4,128 Minority interest - Celldex (1) - (1,651) Stock-Based compensation expense (2) 5,291 3,498 Equity in net loss of affiliate 1,785 - Gain on sale of Genmab stock (151,834) (152,143) Non-GAAP Net loss $(38,522) $(35,903) GAAP Net income (loss) per share, basic $0.81 $0.88 diluted $0.76 $0.80 Non-GAAP Net loss per share, basic and diluted $(0.30) $(0.29) Shares used in computing basic and diluted Non-GAAP net loss per share 127,643 124,690 (1) In management's view, the operations of Celldex prior to its merger with AVANT Immunotherapeutics, Inc. (effective March 7, 2008) are not necessarily indicative of, or directly attributable to, Medarex's continuing operations. Celldex's operations relate primarily to the research, development and commercialization of therapeutic vaccines, which is outside the scope of Medarex's core business operations. (2) For the three months ended March 31, 2008, Medarex incurred $5.3 million in non-cash stock compensation expense, of which $2.0 million is included in research and development expenses and $3.3 million is included in general and administrative expenses. Stock compensation expense includes costs associated with stock awards, including stock options which were recorded in accordance with the provisions of FAS 123(R). FAS 123(R) requires companies to record stock-based payments in the financial statements using a fair value method. Medarex adopted FAS 123(R) on a modified prospective basis beginning on January 1, 2006. In addition to excluding the items described in footnotes 1 and 2 above, items have been excluded based upon management's evaluation (on an individual basis) of both quantitative and qualitative aspects of the item, including, (i) size and nature, (ii) whether it relates to our ongoing business operations, and (iii) whether management expects it to occur as part of our normal business on a regular basis. Those additional items excluded for purposes of determining non-GAAP net loss and non-GAAP net loss per share are gain on sales of Genmab stock and equity in net loss of affiliate.
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