Mavacamten Outcomes in Hypertrophic Cardiomyopathy (HCM) and the Associated Patient and Physician Experiences in the US
- Sponsor
- Bristol-Myers Squibb
- Study ID
- NCT07557498
- Status
- Recruiting
Conditions
- Obstructive Hypertrophic Cardiomyopathy (oHCM)
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Mavacamten — DRUGAccording to the product label
Study Details
The purpose of this study is to understand the real-world clinical outcomes and treatment patterns of adults with obstructive hypertrophic cardiomyopathy (HCM) treated with mavacamten, and to understand patient and physician experiences with mavacamten treatment, in the US community-based practice
Key Dates
- Start date
- Jan 15, 2026
- Status verified
- Apr 2026
- Primary completion
- Dec 14, 2026
- Completion
- Jun 17, 2027
Study Design
- Enrollment
- 362 participants (estimated)
Arms
- Arm: Group 1Participants with obstructive hypertrophic cardiomyopathy (oHCM) receiving mavacamten
- Arm: Group 2Physicians treating patients diagnosed with obstructive hypertrophic cardiomyopathy (oHCM)
Primary Outcome Measure
Participant blood pressure (both systolic and diastolic) [ Time Frame: Baseline ]
Central Contacts
- BMS Clinical Trials Contact Center www.BMSClinicalTrials.com855-907-3286
- First line of the email MUST contain NCT # and Site #.