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Pozen transfers Treximet IND and NDA to GSK

Pozen has notified the FDA that ownership of the investigational new drug application and 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.