Mavacamten is a myosin inhibitor indicated for the treatment of adults with symptomatic New York Heart Association (NYHA) class II-III obstructive hypertrophic cardiomyopathy (HCM). It received initial US FDA approval in 2022, and it is one of the first myosin inhibitors to be used in humans. Mavacamten was also approved by Health Canada in October 2022 and by EMA in July 2023 for the same indication.
Mavacamten is indicated for the treatment of adults with symptomatic New York Heart Association (NYHA) class II-III obstructive hypertrophic cardiomyopathy (HCM) to improve functional capacity and symptoms by the FDA, Health Canada, and the EMA.
Shanghai Chest Hospital, Shanghai, China
Analysis Group Inc., Boston, Massachusetts, United States
St. Paul's Hospital, Vancouver, British Columbia, Canada
IQVIA, Durham, North Carolina, United States
London Health Science Centre (LHSC), London, Ontario, Canada
Rady Children's Hospital-San Diego, San Diego, California, United States
Children's Hospital of Philadelphia-Center for Childhood Cancer Research, Philadelphia, Pennsylvania, United States
The Hospital for Sick Children (SickKids), Toronto, Ontario, Canada
Local Institution - 0001, Seoul, Korea, Republic of
Novotech Laboratory Korea Co., Ltd., Seoul, Korea, Republic of
Local Institution - 0056, Pavia, Lombardia, Italy
Cedars Sinai Medical Center - 1207 San Vicente Blvd, Los Angeles, California, United States
Piedmont Hospital, Atlanta, Georgia, United States
University of Virginia, Charlottesville, Virginia, United States
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