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POZEN Inc.

POZEN IND and NDA for Treximet Sumatriptan/Naproxen Sodium Transferred to GlaxoSmithKline

Published in Medical Letter on the CDC and FDA, June 8th, 2008

POZEN Inc. (NASDAQ: POZN), announced that the U.S. Food and Drug Administration has been notified that ownership of the IND (Investigational New Drug application) and NDA (New Drug Application) for Treximet has been officially transferred to GlaxoSmithKline.

The FDA approved Treximet for the acute treatment of migraine attacks, with or without aura, in adults on April 15, 2008. Treximet will be commercialized by GlaxoSmithKline.

Keywords: Biotechnology, Drug Development, Drugs, GlaxoSmithKline, Naproxen Sodium, Pharmaceutical Business, Pharmaceutical Company, Pharmaceuticals, Regulatory Actions, Selective Serotonin Agonist, Sumatriptan, Therapy,...

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