OSI Pharmaceuticals, Inc. (NASDAQ: OSIP) announced today its financial results for the Company's second quarter ended June 30, 2007. The Company reported net income from continuing operations of $29.3 million (or $0.48 per share) for the three months ended June 30, 2007, compared with net loss from continuing operations of $2.4 million (or $0.04 loss per share) for the second quarter of 2006.

The Company reported total revenues from continuing operations of $79 million for the second quarter of 2007 compared to revenues of $56 million for the second quarter of 2006, an increase of 42%. The increase is primarily due to the growth in revenues arising from worldwide Tarceva® (erlotinib) sales. Total worldwide net sales of Tarceva for the second quarter of 2007, as reported by the Company's collaborators for Tarceva, Genentech, Inc. and Roche, were approximately $212 million representing a 35% growth in global sales compared to the same period last year. For the six months ended June 30, 2007 worldwide Tarceva net sales were approximately $409 million, a 41% increase over the same period last year.

Total revenues from continuing operations for the second quarter of 2007 were comprised of the following key items:

  • Net revenues from the unconsolidated joint business for Tarceva of $43 million, compared to $39 million in the second quarter of 2006, arising from the Company's co-promotion arrangement with Genentech. The net revenues are based on total U.S. Tarceva sales of $102 million, compared to $103 million in the second quarter of 2006. Sales for the second quarter of 2007 were negatively impacted by approximately $9 million of reserve adjustments due to unusually high product returns related to expiring inventory returned to Genentech. Excluding this adjustment, U.S. net sales for Tarceva in the second quarter of 2007 were up 7% versus the prior year quarter;
  • Royalties of $23 million compared to $11 million in the second quarter of 2006 from Roche, the Company's international partner for Tarceva. The royalty revenues are based on total rest of world sales of approximately $110 million which increased 103%, compared to the $54 million reported in the second quarter of 2006;
  • License, milestone and other revenues of $13 million compared with $6 million in the second quarter of 2006. The increase is comprised primarily of royalty income related to worldwide non-exclusive licensing agreements under the Company's DP-IV patent portfolio covering the use of DP-IV inhibitors for treatment of type 2 diabetes, and the amortization of an upfront license fee related to a licensing agreement granted to Eli Lilly and Company, in January 2007, for our Glucokinase Activator program. Offsetting these increases was a decline in DP-IV related milestone income, and commissions related to sales of Novantrone® (mitoxantrone for injection concentrate) which lost patent exclusivity in April 2006.

Operating expenses from continuing operations for the second quarter of 2007 were $53.8 million, compared to $57.6 million for last year's second quarter. Cost of goods sold of $2.0 million was relatively unchanged from the prior year period, and represents costs associated with the U.S. manufacturing and supply of Tarceva. Research and development expense for the second quarter of 2007 decreased $2.1 million to $27.3 million compared to $29.4 million for last year's second quarter. Selling, general and administrative expenses for the second quarter of 2007 decreased $1.7 million to $24.0 million compared to $25.7 million for the second quarter of 2006. Operating expenses include $3.9 million (or $0.06 per share) of equity based compensation expense for the second quarter of 2007, compared to $2.9 million (or $0.05 per share) for the second quarter of 2006.

Included in other income (expense) - net for the second quarter of 2007 was a $4.1 million gain recognized as a result of the Company's decision to curtail its post retirement medical plan.

On November 6, 2006, we announced our intention to divest our eye disease business, a process which we expect to complete in 2007. Our eye disease business consists principally of Macugen® (pegaptanib sodium injection), our marketed product for the treatment of wet AMD, as well as research assets in the eye disease area. As a result of our decision to divest the eye disease business, or Eyetech, the operating results for Eyetech, for all periods presented, is shown as discontinued operations in the accompanying consolidated statement of operations.

The Company's net income, including results from discontinued operations, was $19.6 million (or $0.33 per share) for the three months ended June 30, 2007, compared with a net loss of $319.9 million (or $5.62 per share) reported for the second quarter of 2006.

Conference Call

OSI will host a conference call reviewing the Company's financial results, product portfolio and business developments on July 30, 2007 at 5:00PM (Eastern Time). To access the live webcast or the fourteen-day archive via the Internet, log on to www.osip.com. Please connect to the Company's website at least 15 minutes prior to the conference call to ensure adequate time for any software download that may be needed to access the webcast. Alternatively, please call 1-888-802-2268 (U.S.) or 1-913-312-1271 (international) to listen to the call. The conference ID number for the live call is 4897707. Telephone replay is available approximately two hours after the call through August 13, 2007. To access the replay, please call 1-888-203-1112 (U.S.) or 1-719-457-0820 (international). The conference ID number is 4897707.

About OSI Pharmaceuticals

OSI Pharmaceuticals is committed to "shaping medicine and changing lives" by discovering, developing and commercializing high-quality and novel pharmaceutical products designed to extend life and/or improve the quality of life for patients with cancer and diabetes/obesity. The Company's oncology programs are focused on developing molecular targeted therapies designed to change the paradigm of cancer care. OSI's diabetes/obesity efforts are committed to the generation of novel, targeted therapies for the treatment of type 2 diabetes and obesity. OSI's flagship product, Tarceva® (erlotinib), is the first drug discovered and developed by OSI to obtain FDA approval and the only EGFR inhibitor to have demonstrated the ability to improve survival in both non-small cell lung cancer and pancreatic cancer patients in certain settings. OSI markets Tarceva through partnerships with Genentech, Inc. in the United States and with Roche throughout the rest of the world. For additional information about OSI, please visit http://www.osip.com.

This news release contains forward-looking statements. These statements are subject to known and unknown risks and uncertainties that may cause actual future experience and results to differ materially from the statements made. Factors that might cause such a difference include, among others, the completion of clinical trials, the FDA review process and other governmental regulation, OSI's and its collaborators' abilities to successfully develop and commercialize drug candidates, competition from other pharmaceutical companies, the ability to effectively market products, and other factors described in OSI Pharmaceuticals' filings with the Securities and Exchange Commission.

OSI Pharmaceuticals, Inc. and Subsidiaries
Selected Financial Information
 
Consolidated Statements of Operations  
(In thousands, except per share data) Three Months Ended June 30,Six Months Ended June 30,
  2007     2006     2007     2006  
UnauditedUnauditedUnauditedUnaudited
Revenues:
Net revenue from unconsolidated joint business $ 42,999 $ 39,211 $ 82,121 $ 74,866
Royalties on product licenses 22,546 10,912 41,839 18,926
License, milestone, and other revenues   13,338     5,529     32,392     21,115  
Total revenues   78,883     55,652     156,352     114,907  
 
Expenses:
Cost of goods sold 2,047 1,999 3,951 4,221
Research and development 27,269 29,421 57,895 56,499
Selling, general and administrative 24,038 25,702 49,167 53,510
Amortization of intangibles   459     451     917     899  
Total expenses   53,813     57,573     111,930     115,129  
 
Income (loss) from continuing operations 25,070 (1,921 ) 44,422 (222 )
 
Other income (expense):
Investment income - net 2,995 1,873 6,090 3,240
Interest expense (1,809 ) (1,857 ) (3,612 ) (3,655 )
Other income (expense) - net 3,020 (535 ) 2,071 (1,427 )
       
Net income (loss) from continuing operations 29,276 (2,440 ) 48,971 (2,064 )
Loss from discontinued operations   (9,654 )   (339,535 )   (22,708 )   (357,766 )
Net income (loss) before extraordinary gain 19,622 (341,975 ) 26,263 (359,830 )
Extraordinary Gain   -     22,046     -     22,046  
Net income (loss) $ 19,622   $ (319,929 ) $ 26,263   $ (337,784 )
 
Basic and diluted income (loss) per common share:
Basic earnings (loss)
Continuing operations $0.51 ($0.04 ) $0.85 ($0.04 )
Discontinued operations ($0.17 ) ($5.96 ) ($0.40 ) ($6.29 )
Net income (loss) before extraordinary gain $0.34 ($6.00 ) $0.46 ($6.33 )
Extraordinary gain $0.00 $0.39 $0.00 $0.39
Net income (loss) $0.34 ($5.62 ) $0.46 ($5.94 )
Diluted earnings (loss)
Continuing operations $0.48 ($0.04 ) $0.82 ($0.04 )
Discontinued operations ($0.16 ) ($5.96 ) ($0.37 ) ($6.29 )
Net income (loss) before extraordinary gain $0.33 ($6.00 ) $0.45 ($6.33 )
Extraordinary gain $0.00 $0.39 $0.00 $0.39
Net income (loss) $0.33 ($5.62 ) $0.45 ($5.94 )
 
Weighted average shares of common stock outstanding:
Basic shares 57,545 56,962 57,424 56,889
Diluted shares 62,182 56,962 61,958 56,889
 
 
June 30, December 31,
  2007     2006  
Unaudited

© Business Wire - 2007
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