Study of YAP101 for Heart Failure with Reduced Ejection Fraction
This study is testing a new gene therapy called YAP101 for adults with heart failure caused by a previous heart attack (ischemic heart failure) and a weakened pumping ability (reduced ejection fraction). YAP101 aims to help the heart repair itself by delivering a special gene therapy directly to heart cells. Researchers want to see if YAP101 is safe and how well it's tolerated, as well as its early effects on heart function. You might be able to join if you are between 18 and 79 years old, have stable heart failure from a heart attack, and your heart's pumping ability (ejection fraction) is between 20% and 40%. This study is currently recruiting about 24 participants.
- Study design
- This is a Phase I, single-center, open-label study, meaning everyone knows what treatment is being given. It will enroll about 24 participants to test different doses of YAP101.
- What's involved
- You would receive a one-time injection of YAP101 into your heart. After that, you would have outpatient visits for monitoring over 12 months.
- Compensation
- Not stated in the trial record.
- Follow-up
- Participants will be monitored for safety and other outcomes for 12 months after receiving the treatment.
AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.
Study Assessing Left Ventricular Administration of a Genetic Medicine Directing Organ Regeneration in Heart Failure
At a glance
Conditions
NCT06831825
Where you'd take part
This study runs at 1 site. They're the same protocol — you choose where, and that choice sets who your contact draft is addressed to.
Texas Heart Institute
Houston, Texasstudy coordinator listed
Recruiting
Sites open and close at different times, so the status above is per site — it can differ from the study's overall status.
Study leadership
- Alexander Postalian, MD · PRINCIPAL_INVESTIGATOR · Texas Heart Institute
Who to contact
Opens a ready-to-send draft in your own email app — review before sending.
What this trial measures
- Incidence of the following: DLTs and AEs12 months
Incidence of dose limiting toxicities and adverse events
- Maximum tolerated dose12 months
Maximum tolerated dose