Real-world Patient Reported Outcomes Among Patients Treated With Camzyos
Part of paid clinical trials in Boston, Massachusetts.
- Sponsor
- Bristol-Myers Squibb
- Study ID
- NCT06551129
- Status
- Recruiting
Conditions
- Obstructive Hypertrophic Cardiomyopathy
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Mavacamten — DRUGAs prescribed by treating physician
Study Details
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.
Key Dates
- Start date
- May 10, 2024
- Status verified
- Nov 2024
- Primary completion
- Dec 31, 2026
- Completion
- Jun 30, 2027
Study Design
- Enrollment
- 118 participants (estimated)
Arms
- Arm: MavacamtenAdult participants with symptomatic obstructive hypertrophic cardiomyopathy treated with mavacamten
Primary Outcome Measure
Participant Hypertrophic Cardiomyopathy symptoms as assessed by Hypertrophic Cardiomyopathy Symptom Questionnaire (HCMSQ v2,0 - 7-day recall version) [ Time Frame: Baseline and weeks 2, 4, 8, 12, 24, 30, 48, 60, 72, 84 and 96 ]
Central Contacts
- BMS Study Connect Contact Center www.BMSStudyConnect.com855-907-3286
- First line of the email MUST contain NCT # and Site #.
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| Analysis Group Inc. | Boston | Massachusetts | 02199 | Min Yang, Site 0001 |
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