A Study About the Natural History in Adults With BAG3 Dilated Cardiomyopathy (a Type of Heart Disease) (BAG3 DCM)
NCT ID: NCT05981092
Last Updated: 2025-12-11
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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ACTIVE_NOT_RECRUITING
35 participants
OBSERVATIONAL
2022-10-14
2027-08-12
Brief Summary
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The study is seeking up to about 35 participants who have:
* BAG3 mutation (change in the gene) that causes or is likely to cause dilated cardiomyopathy
* NYHA (New York Heart Association) Class I-IV at screening (Stage B-D)
* Left Ventricular Ejection Fraction less than or equal to 50% (meaning reduced heart function)
All participants in this study will receive their usual treatment. The investigators will observe the natural progression of people who have BAG3 DCM. This will help the investigators better understand the disease and aid in future research.
Participants will take part in this study for three years. During this time, participants will visit the site at least 8 times (about every 3 months for the first year and annually during year 2 and three). Participants will undergo study procedures and give information about their health. These procedures will include a physical exam, cardiac magnetic resonance imaging, echocardiography, ECG monitoring, activity monitoring, cardiopulmonary exercise testing, and blood tests. Participants will answer questions about health and quality of life. The study team will also call participants about 1 time over the phone.
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Detailed Description
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Conditions
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Study Groups
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BAG3 DCM
A single arm observational trial where all participants will undergo the same schedule of assessments.
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
* Heart failure Stage B-D, New York Heart Association (NYHA) Class I-IV
* Left Ventricular Ejection Fraction ≤50% (i.e., Reduced Heart Function)
Exclusion Criteria
* Any of the following within 3 months prior to screening: myocardial infarction (MI), cardiac surgical procedures (other than for pacemaker/ICD/CRT-defibrillator \[CRT-D\] implantation), acute coronary syndrome, or hospitalization for cardiac arrhythmia.
* History of heart transplantation
* eGFR \<30 mL/min/1.73 m2 (significantly impaired kidney function)
* Noncardiac condition that limits lifespan to \<1 year.
* Presence of other form(s) of cardiomyopathy contributing to heart failure
* Previous administration with an investigational drug within 30 days (or as determined by the local requirement).
* No more than 3 first-degree members of the same family who are already participating in the study
18 Years
ALL
No
Sponsors
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Alexion Pharmaceuticals, Inc.
INDUSTRY
Responsible Party
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Locations
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Research Site
Palo Alto, California, United States
Research Site
Aurora, Colorado, United States
Research Site
Boston, Massachusetts, United States
Research Site
Rochester, Minnesota, United States
Research Site
The Bronx, New York, United States
Research Site
Philadelphia, Pennsylvania, United States
Research Site
Amsterdam, , Netherlands
Research Site
Maastricht, , Netherlands
Research Site
Warsaw, , Poland
Research Site
Majadahonda, Madrid, Spain
Research Site
El Palmar, Murcia, Spain
Research Site
A Coruña, , Spain
Research Site
Madrid, , Spain
Research Site
Harefield, London, United Kingdom
Research Site
London, , United Kingdom
Countries
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Other Identifiers
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C4981001
Identifier Type: OTHER
Identifier Source: secondary_id
ALXN2350-DCM-501
Identifier Type: OTHER
Identifier Source: secondary_id
R0765C00001
Identifier Type: -
Identifier Source: org_study_id
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