FDA Approves RiaSTAP for Treatment of Bleeding in Patients with Rare Genetic Defect
Fri, 16 Jan 2009 14:25:00 -0600
The U.S. Food and Drug Administration today licensed RiaSTAP, an orphan drug for the treatment of bleeding in patients with a rare genetic defect known as congenital fibrinogen deficiency. Without treatment, these patients are at risk of potentially life-threatening bleeding.
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