Wednesday, 16 January 2008

More profit for Forest Lab due to Escitalopram and Memantine hydrochloride

Forest Lab (In a press release) said third- quarter profit rose 21 percent on higher sales of its top- selling drugs, the antidepressant Lexapro (Escitalopram) and Namenda (Memantine hydrochloride) for Alzheimer's disease, products nearing generic competition.
Net income in the fiscal quarter ended Dec. 31 climbed to $301.8 million, or 96 cents a share, from $250.3 million, or 78 cents, a year earlier, the New York-based drugmaker said today in a statement. Earnings beat analysts' estimates, and the company raised its forecast for the year.
Revenue in the quarter rose 12 percent to $998.2 million. The company was expected to bring in $944.1 million, according to the average estimate of 24 analysts surveyed. Research and development spending fell 3 percent to $108.2 million, partly because Forest disbursed less in milestone payments to partners.
``We find it extremely encouraging that Forest can hold down costs and still generate upside to revenue -- demonstrating high profitability and lots of flexibility for future investment in its pipeline,'' said Corey Davis, an analyst at Natixis Bleichroeder in New York, in a note to clients today. He recommends buying Forest shares.
Lexapro sales rose 11 percent to $603.5 million, largely because wholesalers held more inventory at the end of the quarter. Sales of Namenda climbed 26 percent to $218.7 million. Revenue from the blood-pressure drug Benicar, which Forest co- promotes with Japan's Daiichi Sankyo Co., increased 34 percent to $51.8 million.
Higher-than-expected drug sales prompted Forest to boost its forecast for earnings in the fiscal year ending March 31. The company now expects profit in the range of $3.35 to $3.45 a share, excluding 15 cents a share in licensing costs from the second quarter, Forest said today. That's 25 cents higher than the company's Oct. 16 forecast.
The company plans to introduce Bystolic, a new blood- pressure medicine, this month. Forest and partner Cypress BioScience Inc. applied in December to U.S. regulators for approval of the experimental fibromyalgia treatment milnacipran.

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