Pfizer PFE announced that the FDA has approved its subcutaneously administered drug marstacimab for treating certain hemophilia patients. The drug will be marketed under the trade name Hympavzi.
Earlier this year, FDA approved Pfizer’s Beqvez (fidanacogene elaparvovec-dzkt) for moderate to severe hemophilia B in adult patients who currently use factor IX (FIX) prophylaxis therapy or ...
Pfizer Inc. has won regulatory approval for its hympavzi drug ... from hemophilia B, as they have fewer options than are available for hemophilia A. Ciara Linnane is MarketWatch's investing ...
(RTTNews) - Pfizer Inc. (PFE) announced Friday that the U.S. Food and Drug Administration has approved ... patients 12 years of age and older with hemophilia A (congenital factor VIII deficiency ...
FDA approves Pfizer’s Hympavzi for routine prophylaxis in hemophilia A and B patients, offering a once-weekly dosing via auto-injector pen. Phase 3 trial showed Hympavzi reduced bleeding rates ...
Pfizer Inc. has won regulatory approval for its hympavzi drug as a treatment ... for people living with hemophilia. In April, the FDA approved Pfizer's Beqvez, a one-time gene therapy for patients ...
On Friday, the FDA approved Pfizer Inc’s (NYSE:PFE) Hympavzi (marstacimab-hncq) for routine prophylaxis to prevent or reduce the frequency of bleeding episodes in adults and pediatric patients with ...