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Terminated Phase 2 Interventional Results available

Exploratory Study of Danicamtiv in Patients With Primary Dilated Cardiomyopathy (DCM) Due to Genetic Variants or Other Causalities

ClinicalTrials.gov ID: NCT04572893

Public ClinicalTrials.gov record NCT04572893. 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 Oct 27, 2026, 6:26 AM EDT

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

Official title

An Open-Label, Exploratory Study of the Safety and Preliminary Efficacy of Danicamtiv in Stable Ambulatory Participants With Primary Dilated Cardiomyopathy Due to Either MYH7 or TTN Variants or Other Causalities

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The purpose of this Phase 2a study is to establish safety and preliminary efficacy of treatment with danicamtiv in patients with primary dilated cardiomyopathy (DCM) due to MYH7 or TTN variants or other causalities.

Study identification

NCT ID
NCT04572893
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 2
Lead sponsor
Bristol-Myers Squibb
Industry
Enrollment
41 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years to 80 Years
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
Aug 4, 2020 (Actual)
Primary completion
Feb 22, 2024 (Actual)
Completion
Feb 22, 2024 (Actual)
Last update posted
May 21, 2025

2020 – 2024

United States locations

U.S. sites
12
U.S. states
11
U.S. cities
12
Facility City State ZIP Site status
Local Institution - 0007 La Jolla California 92037 —
Local Institution - 0010 Washington D.C. District of Columbia 20007 —
Local Institution - 0009 Tampa Florida 33612 —
Local Institution - 0002 Chicago Illinois 60611-5966 —
Local Institution - 0003 Boston Massachusetts 02115 —
Local Institution - 0005 Rochester Minnesota 55905 —
Local Institution - 0006 Cleveland Ohio 44195-0001 —
Local Institution - 0019 Columbus Ohio 43210 —
Local Institution - 0001 Philadelphia Pennsylvania 19104 —
Local Institution - 0004 Charleston South Carolina 29425 —
Local Institution - 0008 Germantown Tennessee 38138 —
Local Institution - 0018 Austin Texas 78705 —

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

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 7 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT04572893, 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 21, 2025 · Synced Oct 27, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT04572893 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →