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Sanofi-aventis Receives Complete Response Letter from the FDA for Eplivanserin Submission
Sanofi-aventis, 09/17/09
Sanofi–aventis announced that the U.S. Food and Drug Administration has issued a complete response letter regarding the company's New Drug Application for eplivanserin. Eplivanserin was reviewed as a potential treatment for patients with chronic insomnia characterized by difficulties with sleep maintenance.
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