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BioWorld - Friday, March 27, 2026
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Home » BMS wins FDA approval for chronic HCM drug mavacamten
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BMS wins FDA approval for chronic HCM drug mavacamten

April 29, 2022
By Lee Landenberger and Richard Staines
Bristol Myers Squibb Co.’s audacious $13.1 billion 2020 takeover of Myokardia Inc. appears to have paid off with U.S. FDA approval of the drug at the heart of the deal, mavacamten. The medicine, a cardiac myosin inhibitor for treating adults with obstructive hypertrophic cardiomyopathy (HCM), will be marketed under the brand name Camzyos.
BioWorld Regulatory Cardiovascular U.S. FDA

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