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Ipilimumab Receives FDA Priority Review Designation

Bristol-Myers Squibb Company (NYSE: BMY) has announced that the U.S. Food and Drug Administration (FDA) has accepted, for filing and review, the Biologics License Application (BLA) for ipilimumab for the treatment of adult patients with advanced melanoma who have been previously treated.

Original Source of Ipilimumab Receives FDA Priority Review Designation

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