AAV gene therapy and a catheter device to stop ventricular tachycardia after a heart attack

Novel Gene Therapy, Techniques, and Devices to Prevent Ventricular Tachycardia

NIH-funded research Rithim Biologics, INC. · NIH-11165093

Uses AAV gene delivery and a minimally invasive catheter technique to fix dangerous heart electrical problems in people who have had a heart attack and are at risk for ventricular tachycardia.

Quick facts

Grant typeSbir 2 grant
Study typeNIH-funded research
Funding institutionRithim Biologics, INC. NIH-funded
Lab location1 site (Woodbine, United States)
Project IDNIH-11165093 on NIH RePORTER

What this research studies

This project develops a way to ‘paint’ gene therapy onto the outer surface of the heart with a small catheter so therapeutic AAV vectors reach the scar border zone left after a heart attack. It targets KCNE3 and KCNE4 proteins that create uneven repolarization and can trigger reentrant ventricular tachycardia. The team is finalizing a prototype catheter that can deliver the therapy without open‑chest surgery and will test safety and effect in laboratory and animal experiments as a step toward human use. The work aims to turn these preclinical methods into a practical treatment pathway for patients with scar‑related VT.

Who could benefit from this research

Good fit: Ideal candidates would be people who have had a prior myocardial infarction and have scar‑related ventricular tachycardia or are judged at high risk for scar‑related VT.

Not a fit: People whose arrhythmias are not caused by post‑MI scar (for example primary electrical disorders or atrial arrhythmias) or who cannot receive gene therapy or invasive catheter procedures would likely not benefit.

Why it matters

Potential benefit: If successful, this approach could reduce or prevent life‑threatening post‑infarct ventricular tachycardia and lower sudden cardiac death risk.

How similar studies have performed: Prior work shows epicardial gene painting can deliver genes to heart tissue and that KCNE3/4 are linked to VT in preclinical models, but applying AAV epicardial delivery to prevent post‑MI ventricular tachycardia in patients is largely new.

Where this research is happening

Woodbine, United States

Researchers

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 below.
Last reviewed 2026-06-13 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.