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Clinical Trial Summary

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.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT06146660
Study type Observational
Source Bristol-Myers Squibb
Contact BMS Study Connect Contact Center www.BMSStudyConnect.com
Phone 855-907-3286
Email Clinical.Trials@bms.com
Status Not yet recruiting
Phase
Start date June 30, 2024
Completion date November 30, 2026

See also
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