Six months after scoring FDA approval for hemophilia B gene therapy Beqvez, Pfizer has earned a nod from the U.S. regulator for another of its products in the indication.
On Friday, the FDA signed off on Hympavzi (marstacimab-hncq), an anti-tissue factor pathway inhibitor for patients age 12 and older with hemophilia A or B who have not developed antibodies to previous inhibitor treatments.
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