Pfizer (PFE) Announces EU Approval of DURVEQTIX
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European Commission Approves Pfizer’s DURVEQTIX® (fidanacogene elaparvovec), a One-Time Gene Therapy for Adults with Hemophilia B
July 25, 2024 10:48 AM EDTA one-time dose of DURVEQTIX has reduced bleeds post-treatment compared to standard of care with a median annualized bleed rate (ABR) of zero bleeds (range 0 to 9.9) after up to four years of follow-up, providing sustained bleed protection and potentially avoiding years of treatment burden with prophylaxis for many patients.
NEW YORK--(BUSINESS WIRE)-- Pfizer Inc. (NYSE:... More
