LFB announces the approval of Cevenfacta (eptacog beta) in the European Union

LFB-Biomedicaments

25 July 2022 - The first new bypassing agent approved in the European Union for the treatment and control of bleeding episodes in haemophilia A and B patients with inhibitors in over 2 decades.

LFB today announced that the EMA has granted on 15 July a Marketing Authorisation for Cevenfacta (eptacog beta), as the first new bypassing agent in over 20 years.

Read LFB-Biomedicaments press release

Michael Wonder

Posted by:

Michael Wonder

Posted in:

Outcome , Europe , Blood product