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Beqvez is currently under review with the european medicines agency (ema), and the treatment recently received regulatory approval in canada. Food and drug administration (fda) has approved beqvez™ (pfizer, inc.), a new hemophilia b gene therapy product Beqvez fda approval history last updated by judith stewart, bpharm on may 21, 2024
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Yes (first approved april 26, 2024) brand name May 21, 2024 fda approves second hemophilia b gene therapy product the u.s Developed by pfizer, beqvez was approved by the us food and drug administration (fda) on april 26, 2024, for adult patients with moderate to severe hemophilia b, defined as circulating factor ix activity of 2% or less.
