The US Food and Drug Administration's requirement for frequent echocardiogram monitoring of patients receiving Bristol Myers Squibb Company’s Camzyos (mavacamten) for obstructive hypertrophic cardiomyopathy (oHCM) should not be a barrier to the product’s commercial use, according to BMS executives.
The company spoke extensively with physicians and patients about the monthly monitoring required initially to establish appropriate Camzyos dosing, and...
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