Home › Hypertrophic Cardiomyopathy › NCT07600177
Mavacamten to Aficamten Transition in Patients With Obstructive Hypertrophic Cardiomyopathy
RecruitingPhase 4
Who can join
Ages 18 to 90 · All sexes
Full eligibility criteria
Inclusion Criteria: * Documented history of oHCM with documented resting and/or Valsalva LVOT obstruction ≥ 50 mmHg who are currently receiving mavacamten commercially. * Echo-derived LVEF ≥55% on mavacamten at the time of enrollment. * Patient willing to consent for the study and undergo the study procedures. Exclusion Criteria: * Severe aortic stenosis or sub-aortic obstruction * Known infiltrative or storage disorder causing cardiac hypertrophy that mimics HCM (eg, Noonan syndrome, Fabry disease, amyloidosis). * History of LVEF \<30%. * Paroxysmal atrial fibrillation (AF) with documented episode within 3 months. * Atrial fibrillation (paroxysmal or permanent) not on systemic anticoagulation. * Documented history of current obstructive coronary artery disease (\> 70% stenosis in one or more epicardial coronary arteries) or documented history of myocardial infarction.
About the study
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).
What is being tested
- Aficamten (drug)
Sponsor: Oregon Health and Science University · Participants: 40 · Started: May 5, 2026
Contact the study team
- Ahmad Masri · Phone: 503-494-7551
Official record on ClinicalTrials.gov — NCT07600177
Locations in the U.S.
| Missouri | St. Luke's Hospital - Mid America Heart Institute, Kansas City (Not yet recruiting) |
| Oregon | Oregon Health & Science University, Portland |
Conditions
From ClinicalTrials.gov, data retrieved Oct 2, 2026. Each study sets its own eligibility; the study team decides who can join.