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Europe approves first gene therapy for treatment of haemophilia A

Europe approves first gene therapy for treatment of haemophilia A
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First Gene Therapy for Adults with Severe Hemophilia A, BioMarin s ROCTAVIAN™ (valoctocogene roxaparvovec), Approved by European Commission (EC)

BioMarin Pharmaceutical Inc. (NASDAQ: BMRN) today announced that the European Commission (EC) has granted conditional marketing authorization (CMA) to ROCTAVIAN™ (valoctocogene roxaparvovec) gene therapy for the treatment of severe hemophilia A (congenital Factor VIII deficiency) in adult patients without a .

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