Mesenchymal Stem Cells for Heart Failure Caused by Chemotherapy

This study is looking at how safe and effective donor bone marrow derived mesenchymal stem cells are for people with heart failure. This heart failure is caused by a type of chemotherapy called anthracyclines, which can damage the heart. Researchers want to see if these stem cells, given either through a vein (intravenously) or directly into the heart muscle (transendocardially), can help control heart failure symptoms and improve heart function. You might be able to join if you are between 18 and 80 years old, have reduced heart pumping ability (left ventricular ejection fraction or LVEF of 40% or less), and heart failure symptoms (NYHA class I, II, or III) due to anthracycline treatment. The study aims to enroll 72 participants and is currently unclear on its recruitment status.

Study design
This is a randomized pilot study, meaning participants are assigned by chance to one of three groups. It aims to enroll 72 participants.
What's involved
Participants will receive either mesenchymal stem cells intravenously, mesenchymal stem cells directly into the heart, or standard heart failure care. The intravenous stem cells are given on four specific days within a month.
Compensation
Not stated in the trial record.
Follow-up
Participants will be followed up periodically after their study treatment, with safety and heart function measured up to 6 months.

AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.

NCT02962661

Donor Bone Marrow Derived Mesenchymal Stem Cells in Controlling Heart Failure in Patients With Cardiomyopathy Caused by Anthracyclines

Suspended
PHASE1Ages 18–80InterventionalTreatment
M.D. Anderson Cancer Center
~72 participants
Updated 2026-08-03 on ClinicalTrials.gov
What's tested:Best PracticeLaboratory Biomarker AnalysisMesenchymal Stem Cell Transplantation

At a glance

Recruiting sites
0 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Incidence of adverse events
Measured over Up to 6 months
+1 more outcome measured
Cardiomyopathy
Heart Failure
Hematopoietic and Lymphoid Cell Neoplasm
Malignant Solid Neoplasm
1 sites across 1 states
Texas1
  • Paul Lin, MD · PRINCIPAL_INVESTIGATOR · M.D. Anderson Cancer Center

This trial hasn't published a contact. View it on ClinicalTrials.gov

  • Incidence of adverse eventsUp to 6 months

    Statistical analyses of safety will be descriptive.

  • Change in left ventricular ejection fraction (LVEF)Baseline to 6 months

    The comparison will be between the two groups of patients.