European Commission grants Sobi® Marketing Authorisation for ALTUVOCT™ for treatment of haemophilia A

June 19, 2024

https://www.prnewswire.com/news-releases/european-commission-grants-sobi-marketing-authorisation-for-altuvoct-for-treatment-of-haemophilia-a-302176511.html

STOCKHOLM, June 19, 2024 /PRNewswire/ — Sobi® today announced the European Commission has granted Marketing Authorisation for ALTUVOCT™ (efanesoctocog alfa), for the treatment and prevention of bleeds and perioperative prophylaxis in haemophilia A. ALTUVOCT is a high-sustained factor VIII replacement therapy for all ages and any disease severity. Children, adolescents, and adults can experience non-haemophilia factor VIII activity levels (above 40%) for a significant part of the week with once-weekly prophylaxis, reaching trough levels of 15% in adults and adolescents before the next dose. This results in significantly improved protection from bleeds compared to prior factor VIII prophylaxis.

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