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All three drug candidates are being developed by small companies and are under review by the U.S. Food and Drug Administration. Qnexa will be the first to be reviewed by an FDA panel of experts, at a meeting scheduled for July 15. Lorcaserin is set for review by an FDA panel on Sept. 16, with a tentative deadline of Oct. 22 for the FDA to rule on approval. Contrave is scheduled for a panel review on Dec. 7, and the agency is set to make a ruling on that drug by Jan. 31, 2011. Finding a successful obesity treatment has been difficult, with numerous past drugs failing because of limited effectiveness, safety problems or unpleasant side effects such as loose stool. But with Americans and people in many other countries getting fatter and fatter, any treatment that works well would be a blockbuster. The market for obesity drugs alone is likely to be worth billions a year, and the new drugs might also turn out to help in treating diseases related to obesity, such as Type 2 diabetes and sleep apnea. Qnexa, the Vivus drug, has been tested in multiple studies of patients with either diabetes or sleep apnea. Multiple studies on research by the companies, including the latest on lorcaserin, were presented during the American Diabetes Association medical conference in Orlando, Fla., that wrapped up at the beginning of this week.
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