US FDA approves Pfizer's drug for rare bleeding disorder
Oct 11 (Reuters) - The U.S. Food and Drug Administration
approved Pfizer's PFE.N once-a-week injection for the two main
types of a rare bleeding disorder called hemophilia, the company
said on Friday.
(Reporting by Sruthi Narasimha Chari and Christy Santhosh in
Bengaluru; Editing by Vijay Kishore)
((SruthiNarasimha.Chari@thomsonreuters.com))
Recent news on BioMarin Pharmaceutical
See all newsUS RESEARCH ROUNDUP-Analog Devices, IBM, Qualcomm
Brief: Biomarin Pharmaceutical Expects Q3 2026 Pre-Tax Charges Of $283 Million For Bought Ipr&D Expense
Brief: Biomarin Appoints Cara Bauer As Chief People Officer
Brief: Biomarin Pharmaceutical Enters Settlement And License Agreement With Ascendis Pharma On Sept 24, 2026
U.S. STOCKS ON THE MOVE-GitLab, California utilities, Herbalife