NIH-funded research R01 grant

Repairing damaged heart tissue to stop dangerous ventricular rhythms after ischemic heart damage

Official title: Biological substrate modification to suppress ventricular arrhythmias in a porcine model of chronic ischemic cardiomyopathy

Funded at Cedars-Sinai Medical Center · NIH-11168680 · Data updated 2026-11-12

The team is testing whether tiny particles from heart-derived cells can repair scarred heart tissue and stop life-threatening ventricular rhythms in people with ischemic cardiomyopathy.

More Cardiomyopathy research and trials

Quick facts

Grant typeR01 grant
Study typeNIH-funded research
Funding institutionCedars-Sinai Medical Center
NIH-funded
Lab location1 site (Los Angeles, United States)
Project startSeptember 1, 2022
Project endAugust 31, 2027
Funding year2025
Award (this year)$730,577
NIH project number5R01HL164896-04
Project IDNIH-11168680 on NIH RePORTER

Who could benefit from this research

Could help

People with ischemic cardiomyopathy and a history of ventricular arrhythmias or scars from prior heart attacks would be the most likely candidates for future versions of this therapy.

Less likely to help

Patients whose arrhythmias stem from inherited electrical disorders, non-ischemic cardiomyopathy, or who cannot undergo intracoronary procedures may not benefit from this specific approach.

What this research studies

Researchers are using a pig model that mimics human ischemic cardiomyopathy to map areas of slow electrical conduction that can trigger dangerous ventricular arrhythmias. They deliver exosomes released by cardiosphere-derived human heart cells into those mapped areas and compare effects to a control treatment. The project compares direct heart injections and new intracoronary delivery methods, and uses MRI-based electrical models and programmed stimulation to check for scar reduction and arrhythmia suppression. If these preclinical methods reduce slow conduction and arrhythmias in pigs, they could be adapted into clinical trials for patients.

Why it matters

Potential benefit: If successful, this approach could shrink scarred heart tissue, eliminate slow-conduction pathways, and reduce the risk of recurrent ventricular arrhythmias and sudden cardiac death.

How similar studies have gone: Prior preclinical work, including pig studies, showed that CDC-derived exosomes can reduce scar and suppress arrhythmias, but clinical testing in people remains limited and the intracoronary delivery approach is new.

Where this research is happening

  • Cedars-Sinai Medical Center
    Los Angeles, United States
    Active

Researchers

  • Principal investigator: Dawkins, James F. — Cedars-Sinai Medical Center
  • Study coordinator: Dawkins, James F.

Related research

Other NIH-funded projects on the same topics.

About this research

  1. This is an active NIH-funded research project — typically early-stage science, not a clinical trial accepting patient enrollment.
  2. Some NIH-funded labs run parallel clinical studies or seek volunteers for related work. To check, contact the principal investigator or institution listed above.
  3. For full project details, budget, and progress reports, visit the official NIH RePORTER page.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.