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Recruiting NCT06551129

Real-world Patient Reported Outcomes Among Patients Treated With Camzyos

Trial Parameters

Condition Obstructive Hypertrophic Cardiomyopathy
Sponsor Bristol-Myers Squibb
Study Type OBSERVATIONAL
Phase N/A
Enrollment 118
Sex ALL
Min Age 18 Years
Max Age N/A
Start Date 2024-05-10
Completion 2026-12-31
Interventions
Mavacamten

Brief Summary

This real-world study will assess changes in health status among participants with symptomatic obstructive hypertrophic cardiomyopathy who are treated with mavacamten in the real world.

Eligibility Criteria

Inclusion Criteria: * Participants ≥18 years of age. * Participants who are prescribed mavacamten for obstructive hypertrophic cardiomyopathy * Provided informed consent to participate in the study Exclusion Criteria: * Previously or currently enrolled in clinical trials for any cardiac myosin inhibitors * Treated for \>7 days with mavacamten by the day of completing the baseline survey * Enrolled in any clinical trials at the time of or within the six-month period prior to the screening * Had heart attack requiring coronary artery bypass grafting within the three-month period prior to the screening * Had stroke or transient ischemic attack within the six-month period prior to the screening * Had moderate-to-severe lung disease which impacted the ability to perform daily activities of living and ability to breathe * Had major lung (thoracic) or heart (cardiac) surgery within the six-month period prior to the screening * Scheduled for a major surgery for the next three months, such as j

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