European Union marketing authorization recommended for Altuvoct for hemophilia A caused by factor VIII deficiency.
The Europe an Medicines Agency this week recommended granting a marketing authorization for Altuvoct for the treatment and prophylaxis of bleeding in patients with
The active substance of Altuvoct is efanesoctocog alfa, a recombinant human factor VIII, which replaces the missing coagulation factor VIII needed for effective hemostasis., the EMA's Committee for Medicinal Products for Human Use accepted evidence from clinical trials that Altuvoct could prevent and control bleeding when used on demand and during surgical procedures in adults and children with hemophilia A.
The full indication for Altuvoct is treatment and prophylaxis of bleeding in patients with hemophilia A of all age groups.
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