Trial ID or NCT#

NCT02501811

Status

recruiting iconRECRUITING

Purpose

This is a phase II, randomized, placebo-controlled clinical trial designed to assess feasibility, safety, and effect of autologous bone marrow-derived mesenchymal stem cells (MSCs) and c-kit+ cells both alone and in combination (Combo), compared to placebo (cell-free Plasmalyte-A medium) as well as each other, administered by transendocardial injection in subjects with ischemic cardiomyopathy.

Official Title

A Phase II, Randomized, Placebo-Controlled Study of the Safety, Feasibility, & Efficacy of Autologous Mesenchymal Stem Cells & C-kit+ Cardiac Stem Cells, Alone or in Combination, Administered Transendocardially in Subjects With Ischemic HF

Eligibility Criteria

Ages Eligible for Study: 21 Years to 79 Years
Sexes Eligible for Study: All
Accepts Healthy Volunteers: No

Investigator(s)

Phillip C. Yang, MD
Phillip C. Yang, MD
Cardiologist
Professor of Medicine (Cardiovascular Medicine)

Contact us to find out if this trial is right for you.

CONTACT

Fouzia Khan
(650) 736-1410