Biogen Idec and SOBI's Elocta MAA validated in Europe

1 November 2014

Biotechnology companies Biogen Idec (Nasdaq: BIIB) of the USA and Swedish Orphan Biovitrum (STO: SOBI) said on Friday that the European Medicines Agency has validated the Marketing Authorization Application (MAA) of Elocta (rFVIIIFc), a recombinant factor VIII Fc fusion protein product candidate for the treatment of hemophilia A.

Eloctate/Elocta is the first recombinant clotting factor VIII therapy with prolonged circulation to provide protection from bleeding episodes with the potential for an extended interval between prophylactic injections.

Sales projections

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