Phosphatase Inhibition by Intracoronary Gene Therapy in Subjects With Non-Ischemic NYHA Class III Heart Failure (NCT05598333)
A Phase 2, Adaptive, Double-blinded, Placebo Controlled, Randomized, Multi-center Trial to Evaluate the Efficacy, Safety and Tolerability of Intracoronary Infusion of AB-1002 in Adult Subjects With New York Heart Association (NYHA) Class III Heart Failure and Non-ischemic Cardiomyopathy
๐ฉบ Plain-English Summary (8th-Grade Level)
This is a Phase 2 adaptive, double-blinded, placebo-controlled, randomized, multi-center trial study to evaluate the safety and efficacy of a single dose of AB-1002, administered via antegrade intracoronary artery infusion, in males and females age \>18 years with non-ischemic cardiomyopathy and NYHA Class III symptoms of HF. Subjects will be randomized into one of three treatment groups in a 1:1:1
Who can join: Review the eligibility criteria below.
Location: Cardiology P.C. Birmingham โ Birmingham, Alabama
Age range: 18 Years
๐งช Interventions in This Study
๐ "Do I Qualify?" โ 1-Minute Self Screener
Instant ChecklistFull eligibility criteria are available on the official NIH protocol. View the criteria โ
๐ All Participating Trial Locations (96 Sites)
Showing the first 25 of 96 sites.
- Cardiology P.C. Birmingham โ Birmingham, Alabama
- University of Arizona Sarvor Heart Center โ Tucson, Arizona
- University of California Irvine Medical Center โ Irvine, California
- University of California San Diego โ La Jolla, California
- University of California San Francisco โ San Francisco, California
- Baycare Medical Group โ Clearwater, Florida
- University of Miami โ Coral Gables, Florida
- University of Florida โ Gainesville, Florida
- Augusta University โ Augusta, Georgia
- Loyola Medicine Burr Ridge โ Oakbrook Terrace, Illinois
- University of Iowa โ Iowa City, Iowa
- University of Kansas Medical Center (KUMC) โ Kansas City, Kansas
- Massachusetts General Hospital โ Boston, Massachusetts
- Brigham and Women's Hospital โ Boston, Massachusetts
- Minneapolis Heart Institute Foundation โ Minneapolis, Minnesota
- Mayo Clinic - Minnesota โ Rochester, Minnesota
- Aurora Saint Luke's Health System โ Kansas City, Missouri
- St. Louis University โ St Louis, Missouri
- Renown Health โ Reno, Nevada
- Morristown Medical Center - Cardiology โ Morristown, New Jersey
- Mt. Sinai New York โ New York, New York
- Stony Brook โ Stony Brook, New York
- Montefiore Medical Center โ The Bronx, New York
- Duke University โ Durham, North Carolina
- The Christ Hospital / The Linder Center for Research โ Cincinnati, Ohio
๐ฐ Cost, Insurance & Patient Rights
- 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
- Routine Patient Care: Under federal law (ACA ยง 2709) and many state statutes, routine care costs are covered during participation.
- Voluntary Participation: You may withdraw at any time without affecting your standard medical care.
More studies in Congestive Heart Failure
- SyncAV Post-Market Trial โ Huntsville, Alabama
- Plasma ExtrAcellular RNAs and Biomarkers of Heart FaiLure During Decongestion: PEARL-HF Study โ Boston, Massachusetts
- Boston Medical Center Ultrasound Decongestion Study in Heart Failure โ Boston, Massachusetts
- Palliative Care for People With HF โ Indianapolis, Indiana
- Assessing Changes in Myocardial Tissue and Blood in Patients With Advanced Heart Disease โ Murray, Utah
Explore by condition: All Congestive Heart Failure clinical trials
๐ก How to Participate
- Check the checklist above to see if you may qualify.
- Review the official NIH record below to find the coordinating site.
- Ask about the visit schedule, what is covered at no cost, and any travel support.
- Confirm with your own doctor before making a decision.