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Hypertrophic cardiomyopathy (HCM) is phenotypically heterogeneous, including the extent to which dynamic left ventricular outflow tract (LVOT) obstruction is present. Some individuals with HCM do not have significant LVOT obstruction but are symptomatic — in some cases, severely so. The cardiac myosin inhibitor mavacamten, when used to treat the obstructive phenotype, reduces LVOT gradient and improves symptoms, functional capacity, and quality of life; however, its efficacy in individuals with nonobstructive HCM is unclear.
In a manufacturer-funded trial, investigators randomized 580 adults with symptomatic nonobstructive HCM and preserved left ventricular ejection fraction to receive either mavacamten (initially 5 mg daily, titrated…