Baxter International, Inc. Submits Application For FDA Approval Of OBI-1 For Patients With Acquired Hemophilia A

Published: Dec 10, 2013

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DEERFIELD, Ill.--(BUSINESS WIRE)--Baxter International Inc. (NYSE:BAX) today announced that the company has submitted a biologics license application (BLA) to the U.S. Food and Drug Administration (FDA) for the approval of OBI-1, a recombinant antihemophilic porcine sequence factor VIII, in patients with acquired hemophilia A. Phase 2/3 data supporting the submission were presented at the American Society of Hematology’s (ASH) 55th Annual Meeting in New Orleans, LA.

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