Pfizer's HYMPAVZI Receives FDA Priority Review for Blood Cancer Treatment
Pfizer Inc. (NYSE:PFE) is one of top healthcare stocks priced under $50 for investment. Pfizer Inc. (NYSE:PFE) stated on February 6 that the U.S. Food and Drug Administration has accepted and provided Priority Review for its supplemental Biologics License Application for HYMPAVZI® to broaden the approved indication to cover the treatment of hemophilia A or B patients aged 6 years and older with inhibitors, as well as pediatric patients with hemophilia A or B who do not have inhibitors. HYMPAVZI is currently approved in the United States for treating patients 12 years of age and older with hemophilia A who do not have factor VIII inhibitors, or hemophilia B who do not have factor IX inhibitors.

Pfizer Inc. (NYSE:PFE) also stated that the FDA has established a Prescription Drug User Fee Act action date for the second quarter of 2026. Should it be approved, HYMPAVZI would offer a blend of bleeding protection along with a simple, once-weekly subcutaneous injection method that involves little preparation and eliminates the necessity for regular treatment-related laboratory monitoring in these challenging patient groups.
In a separate update, Pfizer Inc. (NYSE:PFE) revealed on February 5 that it has initiated its TrumpRx program, aiming to increase access to and reduce the cost of innovative medications for U.S. residents. The program offers significant discounts on more than 30 medicines compared to their list prices. According to management, this effort is included in Pfizer Inc.'s (NYSE:PFE) larger landmark Most Favored Nation deal with the U.S. government.
Pfizer Inc. (NYSE:PFE) is a worldwide biopharmaceutical corporation engaged in the production, research, promotion, and distribution of biopharmaceutical products across the globe. It promotes health, prevention, therapy, and solutions in developing and emerging markets.
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