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Completed Phase 3 Interventional Results available

A Study to Evaluate Mavacamten in Adults With Symptomatic Obstructive HCM Who Are Eligible for Septal Reduction Therapy

ClinicalTrials.gov ID: NCT04349072

Public ClinicalTrials.gov record NCT04349072. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Jul 21, 2026, 10:15 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Randomized, Double-blind, Placebo-controlled Study to Evaluate Mavacamten in Adults With Symptomatic Obstructive Hypertrophic Cardiomyopathy Who Are Eligible for Septal Reduction Therapy

Study identification

NCT ID
NCT04349072
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Bristol-Myers Squibb
Industry
Enrollment
112 participants

Conditions and interventions

Interventions

  • Mavacamten Drug
  • Placebo Drug

Drug

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jul 5, 2020
Primary completion
Feb 6, 2022
Completion
May 19, 2024
Last update posted
May 22, 2025

2020 – 2024

United States locations

U.S. sites
21
U.S. states
15
U.S. cities
19
Facility City State ZIP Site status
Local Institution - 0009 Los Angeles California 90027
Local Institution - 0011 Stanford California 94305 5406
Local Institution - 0001 New Haven Connecticut 06520
Local Institution - 0021 Weston Florida 33331
Local Institution - 0016 Boston Massachusetts 02114-2696
Local Institution - 0007 Boston Massachusetts 02115
Local Institution - 0006 Ann Arbor Michigan 48109
Local Institution - 0013 Grand Rapids Michigan 49503
Local Institution - 0015 Rochester Minnesota 55905
Local Institution - 0005 St Louis Missouri 63110
Local Institution - 0010 New York New York 10016
Local Institution - 0017 Valhalla New York 10595
Local Institution - 0004 Durham North Carolina 27710
Local Institution - 0020 Cleveland Ohio 44195
Local Institution - 0002 Portland Oregon 97239
Local Institution - 0003 Philadelphia Pennsylvania 19104
Local Institution - 0019 Pittsburgh Pennsylvania 15212
Local Institution - 0014 Nashville Tennessee 37205
Local Institution - 0018 Nashville Tennessee 37235
Local Institution Houston Texas 77030
Local Institution - 0012 Murray Utah 84107-5701

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT04349072, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted May 22, 2025 · Synced Jul 21, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT04349072 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →