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Biomarin is still expecting an EMA decision on hemophilia drug in H1 2022

The international pharmaceutical giant Biomarin is anticipating a decision in the first half of 2022 from the EMA about its candidate, Valoctocogene, meant to treat severe hemophilia. More information about the ongoing phase III trial with the drug will come in the New Year, says CEO.

Biomarin hopes to have a European approval of its potential new drug for the treatment of severe hemophilia A before summer 2022, the company reports in a press release in connection with its third quarter results.

Biomarin Chair and Chief Executive Jean-Jacques Bienaimé also promises to present data from the company's ongoing phase III trial with Valoctocogene Roxaparvovec in the beginning of 2022.

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