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MEMENTO - A Phase 4, Single-arm, Open-label Clinical Study to Evaluate Mavacamten in Adults With Symptomatic Obstructive Hypertrophic Cardiomyopathy to Assess the Impact on Myocardial Structure With Cardiac Magnetic Resonance Imaging (CMR)
The purpose of this study is to evaluate the mavacamten impact on myocardial structure with cardiac magnetic resonance imaging (CMR) in adult participants with symptomatic obstructive hypertrophic cardiomyopathy (oHCM) \[New York Heart Association (NYHA) Functional Class II or III\].
Age
18 - No limit years
Sex
ALL
Healthy Volunteers
No
Local Institution - 0087
West Hollywood, California, United States
Local Institution - 0003
Atlanta, Georgia, United States
Local Institution - 0093
Boston, Massachusetts, United States
Local Institution - 0090
Cleveland, Ohio, United States
Local Institution - 0086
Pittsburgh, Pennsylvania, United States
Local Institution - 0017
Houston, Texas, United States
Local Institution - 0035
Murray, Utah, United States
Local Institution - 0076
Ciudad Autónoma de Buenos Aires, Buenos Aires, Argentina
Local Institution - 0075
Ciudad Autónoma de Buenos Aires, Buenos Aires, Argentina
Local Institution - 0079
Pilar, Buenos Aires, Argentina
Start Date
January 24, 2024
Primary Completion Date
July 9, 2026
Completion Date
July 9, 2026
Last Updated
September 22, 2025
63
ACTUAL participants
Mavacamten
DRUG
Lead Sponsor
Bristol-Myers Squibb
NCT06253221
NCT04418297
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.
View ClinicalTrials.gov Terms and ConditionsNCT03450252