Biomarin gets ready for launch in second half-year of 2021

Biomarin's revenue retreated in Q1 but the company will receive news on several applications in the following months.

Photo: Rob Acket/EMA

June will be a significant month for Biomarin on several accounts.

Firstly, the firm will soon find out whether the European Medicine Agency's (EMA) Committee for Medicinal Products for Human Use (CHMP) can recommend the drug vosoritide for treating achondroplasia, and secondly, the company plans to resubmit an application for approval for the gene therapy valoctocogene roxaparvovec against hemophilia A. Last year, the EMA rejected this application.

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