European Medicines Agency validates Bristol Myers Squibb’s application for mavacamten for the treatment of obstructive hypertrophic cardiomyopathy

BMS

1 October 2021 - Application based on positive results from Phase 3 EXPLORER-HCM trial.

Bristol Myers Squibb today announced that the EMA has validated its marketing authorisation application for mavacamten, an investigational, first-in-class cardiac myosin inhibitor, for the treatment of patients with obstructive hypertrophic cardiomyopathy.

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Michael Wonder

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Michael Wonder

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Medicine , Europe , Dossier