Mavacamten to Aficamten Transition in Patients With Obstructive Hypertrophic Cardiomyopathy
Part of paid clinical trials in Kansas City, Missouri.
- Sponsor
- Oregon Health and Science University
- Study ID
- NCT07600177
- Phase
- PHASE4
- Status
- Recruiting
Conditions
- Hypertrophic Cardiomyopathy (HCM)
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - 90 Years
- Healthy Volunteers
- Not accepted
Interventions
- Aficamten — DRUGPatients will be switched from mavacamten to aficamten. Mavacamten will be stopped at enrollment, and aficamten started 2 weeks later.
Study Details
This is an investigator-initiated two-center study. The goal of this study is to investigate the feasibility, safety and efficacy outcomes of a seamless transition from mavacamten to aficamten in patients with obstructive hypertrophic cardiomyopathy (oHCM).
Key Dates
- Start date
- May 5, 2026
- Status verified
- May 2026
- Primary completion
- Dec 31, 2026
- Completion
- Mar 15, 2027
Study Design
- Enrollment
- 40 participants (estimated)
- Allocation
- NA
- Intervention model
- SINGLE_GROUP
- Primary purpose
- TREATMENT
Arms
- Experimental: CMISwitching from mavacamten on day 1 to aficamten starting at week 2.
Primary Outcome Measure
Safety Endpoints [ Time Frame: Up to 16 weeks ]
Central Contacts
- Ahmad Masri503-494-7551
Locations (2)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| St. Luke's Hospital - Mid America Heart Institute | Kansas City | Missouri | 64111 | Michael Nassif, MD (PRINCIPAL_INVESTIGATOR) |
| Oregon Health & Science University | Portland | Oregon | 97239 |
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