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Amylin Pharmaceuticals Reports Second Quarter Financial Results
Monday, July 21, 2008 4:05 PM


Product sales increased 20% over second quarter 2007 to $200 million

SAN DIEGO, July 21 /PRNewswire-FirstCall/ -- Amylin Pharmaceuticals, Inc. (Nasdaq: AMLN) today reported financial results for the quarter ended June 30, 2008. The Company reported total revenue of $222.0 million for the second quarter, including net product sales of $200.3 million. Net loss for the quarter ended June 30, 2008 was $64.8 million, or $0.47 per share. At June 30, 2008, the Company held cash, cash equivalents and short-term investments of approximately $891.0 million.

'In the second quarter we continued to make substantial progress against our goals, with a focus on improving BYETTA and SYMLIN sales and supporting the exenatide once weekly regulatory submission,' said Daniel M. Bradbury, President and Chief Executive Officer of Amylin Pharmaceuticals. 'SYMLIN sales continued to increase steadily and we implemented a number of important changes in our sales and marketing approach for BYETTA to drive growth in prescriptions with primary care physicians.'

Bradbury continued, 'We are encouraged by the scientific community's strong interest in BYETTA and exenatide once weekly (investigational therapy), as demonstrated by the many prominent discussions that centered on both therapies at the American Diabetes Association's 2008 annual meeting. It was apparent that not only is glucose control important in managing diabetes; but how glucose control is achieved is being recognized as an important consideration. A medicine such as BYETTA, which provides powerful, durable glucose control with progressive weight loss and other potential benefits, is uniquely poised to take advantage of the market's growing appreciation for the benefits of our novel therapies.'

Quarter ended June 30, 2008

Net product sales of $200.3 million for the quarter ended June 30, 2008 include $177.5 million for BYETTA(R) (exenatide) injection and $22.8 million for SYMLIN(R) (pramlintide acetate) injection. This compares to net product sales of $167.3 million, consisting of $152.1 million for BYETTA and $15.2 million for SYMLIN for the same period in 2007.

Revenues under collaborative agreements were $21.7 million for the quarter ended June 30, 2008, compared to $29.6 million for the same period in 2007. Collaborative revenues for the quarter ended June 30, 2008 consist primarily of cost sharing payments from Eli Lilly and Company, or Lilly, for development expenses associated with exenatide once weekly and BYETTA. Collaborative revenues for the quarter ended June 30, 2007 included $15.0 million in milestones, earned upon Lilly's launch of BYETTA in the European Union.

Selling, general and administrative expenses were $111.1 million for the quarter ended June 30, 2008, compared to $93.1 million for the same period in 2007. The increase reflects expenses associated with the recent expansion of the Company's field force, increased promotional expenses for BYETTA and SYMLIN, expenses associated with exenatide once weekly market development and increases in business infrastructure to support the Company's growth.

Research and development expenses were $75.4 million for the quarter ended June 30, 2008, compared to $71.7 million for the same period in 2007. The increase primarily reflects development expenses for exenatide once weekly and growth in the Company's research capabilities. Research and development expenses for the quarter ended June 30, 2007 included a development milestone associated with leptin.



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