drugset / Trial / NCT00721045

A Phase II Dose-escalation Study to Assess the Feasibility and Safety of Transendocardial Delivery of Three Different Doses of Allogeneic Mesenchymal Precursor Cells (MPCs)in Subjects With Heart Failure

NCT00721045 ↗

Phase 2 Completed 60 enrolled Mesoblast, Inc.
RandomizedFactorialSingle-blindTreatment

Summary

This is a dose-ranging clinical study to evaluate the feasibility, safety, and tolerability of 3 different doses of immunoselected, culture expanded, nucleated, allogeneic MPCs in subjects who have cardiomyopathy of both ischemic and idiopathic etiology.

Timeline

Start
2008-08
Primary completion
2011-06
Completion
2013-07

Drugs

EvaluationDrugModalityDoseRoute
Comparator Mesenchymal Precursor Cells (MPCs) Cell therapy 2.5e+07 cells Other
Comparator Mesenchymal Precursor Cells (MPCs) Cell therapy 7.5e+07 cells Other
Comparator Mesenchymal Precursor Cells (MPCs) Cell therapy 1.5e+08 cells Other

Indications