CV Therapeutics Reports 2006 Second Quarter Financial Results
Thursday August 3, 4:05 pm ET
PALO ALTO, Calif., Aug. 3 /PRNewswire-FirstCall/ -- CV Therapeutics, Inc. (Nasdaq: CVTX - News) today reported financial results for the three and six months ended June 30, 2006.
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For the quarter ended June 30, 2006, the Company reported a net loss of $73.1 million, or $1.59 per share. This compares to a net loss of $51.6 million, or $1.43 per share, for the same quarter in 2005 and to a net loss of $70.5 million or $1.57 per share, for the prior quarter ended March 31, 2006. For the six months ended June 30, 2006, the Company reported a net loss of $143.6 million, or $3.16 per share, compared to a net loss of $98.0 million, or $2.74 per share, for the six months ended June 30, 2005. At June 30, 2006, the Company had cash, cash equivalents, marketable securities and restricted cash of approximately $330.6 million, compared to $481.8 million at December 31, 2005.
Operating expenses were $80.6 million for the quarter ended June 30, 2006. This compares to operating expenses of $56.7 million for the same quarter in 2005 and $76.3 million for the prior quarter ended March 31, 2006. For the six months ended June 30, 2006, operating expenses were $156.9 million compared to $108.2 million for the same period in the prior year.
The increase in operating expenses for the quarter ended June 30, 2006 compared to the same period in the prior year was primarily due to higher selling, general and administrative expenses associated with the Company's marketing of Ranexa® (ranolazine extended-release tablets) subsequent to the product's launch in the first quarter of 2006, expenses associated with the Company's national cardiovascular specialty sales force that was recruited in the second and third quarters of 2005 and higher headcount related expenses including stock-based compensation in other areas to support the Company's increased commercialization and business activities. These increases were partially offset by lower outside contract expenses for the regadenoson development program and lower marketing expenses related to the co-promotion of ACEON® (perindopril erbumine) Tablets.
The small increase in operating expenses for the quarter ended June 30, 2006 compared to the prior quarter ended March 31, 2006 was primarily due to higher outside contract services expense for research and development activities related primarily to Ranexa and to a lesser extent higher external general and administrative expenses, offset by lower compensation expense for personnel for the quarter ended June 30, 2006.
The increase in operating expenses for the six months ended June 30, 2006 compared to the same period in the prior year was primarily due to higher selling, general and administrative expenses associated with the Company's national cardiovascular specialty sales force that was recruited in the second and third quarters of 2005, expenses incurred to market Ranexa and higher headcount related expenses, including stock-based compensation, in other areas to support the Company's increased commercialization and business activities. These increases were partially offset by lower outside contract expenses for Phase 3 regadenoson development.
The Company recognized collaborative research revenue of $4.9 million for the quarter ended June 30, 2006, compared to $5.7 million for the same quarter in 2005. Collaborative research revenue recognized primarily relates to the reimbursement of certain regadenoson development costs from a collaborative partner and amortization of up-front payments earned. For the quarter ended June 30, 2006, the Company also recorded $1.2 million of net product revenue for sales of Ranexa and $0.8 million of co-promotion revenue due to sales of ACEON®, which amount represents the Company's share of product revenues that exceeded the baseline specified in the amended co-promotion agreement with Solvay Pharmaceuticals, Inc. The Company received FDA approval for Ranexa on January 27, 2006 and commenced commercial product sales of Ranexa in March 2006.
Company management will webcast a conference call on August 3, 2006 at 5:00 p.m. EDT, 2:00 p.m. PDT, on the Company's website. To access the live webcast, please log on to the Company's website at www.cvt.com and go to the Investor Information section. Alternatively, domestic callers may participate in the conference call by dialing (888) 370-6121, and international callers may participate in the conference call by dialing (706) 679-7163. Webcast and telephone replays of the conference call will be available approximately two hours after the completion of the call through Thursday, August 10, 2006. Domestic callers can access the replay by dialing (800) 642-1687, and international callers can access the replay by dialing (706) 645-9291; the PIN access number is 3317478.
About CV Therapeutics
CV Therapeutics, Inc., headquartered in Palo Alto, California, is a biopharmaceutical company focused on applying molecular cardiology to the discovery, development and commercialization of novel, small molecule drugs for the treatment of cardiovascular diseases.
CV Therapeutics' approved products include Ranexa® (ranolazine extended- release tablets) and ACEON® (perindopril erbumine) Tablets. Ranexa is indicated for the treatment of chronic angina in patients who have not achieved an adequate response with other antianginal drugs, and should be used in combination with amlodipine, beta-blockers or nitrates. In addition, CV Therapeutics co-promotes ACEON®, an ACE inhibitor, for reduction of the risk of cardiovascular mortality or nonfatal myocardial infarction in patients with stable coronary artery disease and treatment of essential hypertension.
CV Therapeutics also has other clinical and preclinical drug development candidates and programs, including regadenoson, which is being developed for potential use as a pharmacologic stress agent in myocardial perfusion imaging studies. Regadenoson has not been approved for marketing by any regulatory authorities. |
