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June 2, 2026

BMS secures FDA acceptance for Camzyos sNDA

The US Food and Drug Administration (FDA) has accepted Bristol Myers Squibb’s (BMS) supplemental new drug application (sNDA) for Camzyos (mavacamten) to treat adolescents aged 12 to under 18 years with symptomatic obstructive hypertrophic cardiomyopathy (oHCM).

BMS secures FDA acceptance for Camzyos sNDA