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See Latest ArticlesSanofi-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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Cell Therapeutics Announces FDAs Oncologic Drugs Advisory Committee to Review Pixantrone for the Treatment of Relapsed/Refractory Aggressive Non-Hodgkins Lymphoma, February 2010
Cell Therapeutics, 12/18/09
Sanofi Pasteur obtains license from Syntiron to develop & commercialize vaccine to prevent Staphylococcus infections
Sanofi-aventis, 12/17/09
Telmisartan/amlodipine: approved for high blood pressure
Formulary , 12/16/09
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