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Roctavian Receives Approval by the FDA for Severe Hemophilia A - Vimarsana News

Roctavian Receives Approval by the FDA for Severe Hemophilia A

The approval is supported by positive results from the largest and longest phase 3 study for gene therapy in hemophilia, showing a 52% reduction in annualized bleeding rate compared with baseline rates on routine prophylaxis.

BBCNEWS BBC News September 22, 2021 09:38:00 - Vimarsana News

BBCNEWS BBC News September 22, 2021 09:38:00

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