4.6 Article

Valoctocogene Roxaparvovec: First Approval

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DRUGS
卷 82, 期 14, 页码 1505-1510

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ADIS INT LTD
DOI: 10.1007/s40265-022-01788-y

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This article provides an overview of the development milestones of Valoctocogene roxaparvovec, a gene therapy for the treatment of hemophilia A, which has recently received conditional marketing authorization in the EU.
Valoctocogene roxaparvovec (ROCTAVIAN((TM))) is a gene therapy being developed by BioMarin Pharmaceutical Inc. for the treatment of haemophilia A. In August 2022, valoctocogene roxaparvovec was granted conditional marketing authorization in the EU for the treatment of severe haemophilia A [congenital factor VIII (FVIII) deficiency] in adults without a history of FVIII inhibitors and without detectable antibodies to adeno-associated virus serotype 5 (AAV5). This article summarizes the milestones in the development of valoctocogene roxaparvovec leading to this first approval for severe haemophilia A.

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