Home › Hypertrophic Cardiomyopathy › NCT06551129
Real-world Patient Reported Outcomes Among Patients Treated With Camzyos
RecruitingObservational study
Real-World Camzyos Patient Reported OutcoMes Through PAtient SurveyS in Hypertrophic CardioMyopathy (COMPASS-HCM): A Prospective Longitudinal Study
Who can join
Ages 18 and older · All sexes
Full 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 joint surgeries including hip replacement, abdominal surgeries, lung surgeries, heart surgeries, eye surgeries, brain surgeries, and any other major surgeries that require general anesthesia and at least an overnight hospital stay * Hospitalized requiring an overnight stay at the time of or within the two-week period prior to the screening
About the study
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.
What is being tested
- Mavacamten (drug)
Sponsor: Bristol-Myers Squibb · Participants: 118 · Started: May 10, 2024
Contact the study team
- BMS Study Connect Contact Center www.BMSStudyConnect.com · Phone: 855-907-3286
Official record on ClinicalTrials.gov — NCT06551129
Locations in the U.S.
| Massachusetts | Analysis Group Inc., Boston |
Conditions
From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.