Efanesoctocog alfa granted FDA fast track designation for treatment of haemophilia A

Sanofi

18 February 2021 - Efanesoctocog alfa, previously known as BIVV001, is an investigational factor VIII replacement therapy that has the potential to transform therapy and provide high sustained factor activity levels for people with haemophilia A.

The U.S. FDA has granted fast track designation for efanesoctocog alfa, previously known as BIVV001 (rFVIIIFc-VWF-XTEN), in patients with haemophilia A. 

Read Sanofi press release

Michael Wonder

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Michael Wonder

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US , Blood product , Fast track