Clinical trial
A 12-Month Follow-Up Study to Protocol 24779 (A Double-blind, Prospective, Randomized, Placebo-controlled Study to Determine the Tolerability, Efficacy, Safety, and Dose Range of Intramyocardial Injections of G-CSF Mobilized Auto CD34+ Cells for Reduction of Angina Episodes in Patients With Refractory Chronic Myocardial Ischemia [ACT34-CMI])
NCT00545610 is registered in ClinicalTrials.gov with Lisata Therapeutics, Inc. as lead sponsor.
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Registry record
As filed in ClinicalTrials.gov.
- Title
- A 12-Month Follow-Up Study to Protocol 24779 (A Double-blind, Prospective, Randomized, Placebo-controlled Study to Determine the Tolerability, Efficacy, Safety, and Dose Range of Intramyocardial Injections of G-CSF Mobilized Auto CD34+ Cells for Reduction of Angina Episodes in Patients With Refractory Chronic Myocardial Ischemia [ACT34-CMI])
- Lead sponsor
- Lisata Therapeutics, Inc.
- Phase
- Observational
- Overall status
- Completed
- Start date
- October 31, 2007
- Completion date
- June 30, 2010
- Enrollment
- 150 (estimated)
- Sites
- 23
Conditions
As the registry lists them; a condition with its own page is linked.