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A Study to Assess the Safety of Mavacamten in Korean Patients With Symptomatic Obstructive Hypertrophic Cardiomyopathy

A Study to Assess the Safety of Mavacamten in Korean Patients With Symptomatic Obstructive Hypertrophic Cardiomyopathy

Recruiting
19 years and older
All
Phase N/A
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Overview

The purpose of this observational post-marketing surveillance study is to assess the real-world safety of mavacamten for the treatment of symptomatic obstructive hypertrophic cardiomyopathy (oHCM) in adult participants in Korea. Participants who will receive at least 1 dose of mavacamten will be enrolled.

Eligibility

Inclusion Criteria:

  • Adult participants 19 years of age or older
  • Participants who receive mavacamten according to the approved product label
  • Participants who sign the informed consent form

Exclusion Criteria:

  • Participants who are prescribed mavacamten for therapeutic indications not approved in Korea
  • Participants for whom mavacamten is contraindicated as clarified in Korean prescribing information approved by the Ministry of Food and Drug Safety

Study details
    Obstructive Hypertrophic Cardiomyopathy

NCT06146660

Bristol-Myers Squibb

16 October 2025

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