EC approves marketing authorization switch of Elocta from Biogen to SOBI

24 March 2016

Swedish Orphan Biovitrum (STO: SOBI) now owns marketing authorization rights to hemophilia A treatment Elocta (efmoroctocog alfa) in the European Union

The transfer of marketing authorization rights from US biotech major Biogen (Nasdaq: BIIB) to the Stockholm-based biopharmaceutical firm has been approved by the European Commission.

Elocta is a recombinant factor VIII Fc fusion protein with an extended half-life and is the first hemophilia A treatment in the EU to offer prolonged protection against bleeding episodes with prophylactic injections every three to five days.

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