FDA approves expanded use of BMS’ Camzyos

2 October 2026

The US Food and Drug Administration (FDA) approved Camzyos (mavacamten), from Bristol Myers Squibb (NYSE: BMY) for the treatment of symptomatic obstructive hypertrophic cardiomyopathy (oHCM) to improve functional capacity and symptoms in adults and pediatric patients weighing 30 kg (66 lbs) or more.

According to the US pharma major, Camzyos now has the broadest indication of any cardiac myosin inhibitor (CMI). This expanded indication offers a new treatment option for patients with significant unmet need.1

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