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U.S. Food and Drug Administr...
FDA Approves Pfizer's Hympavzi as First Once-Weekly Subcutaneous Treatment for Hemophilia A and B
The U.S. Food and Drug Administration approved Pfizer's Hympavzi (marstacimab-hncq) for routine prophylaxis in patients aged 12 and older with hemophilia A or B without inhibitors, delivered via a once-weekly auto-injector pen.