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. Author manuscript; available in PMC: 2009 Apr 1.
Published in final edited form as: Drug Discov Today Ther Strateg. 2008;5(1):73–78. doi: 10.1016/j.ddstr.2008.05.001

Table 1.

Major clinical trials of stem cell therapy in acute myocardial infarction (MI)

Study Number of patients Treated / control Time of delivery post-MI (days) Treatment, route of administration and cell type Results
Strauer et al 2002 [46] 10/10 5 to 9 IC, BM-MNC Decreased infarct size, improved regional wall motion and perfusion. No change in EF or LVEDV
TOPCARE-AMI [33,34,47] 29 MNC 30 CPC 11 control 3 to 7 IC, CPC or BM-MNC Significant increase in EF, improved regional wall motion, reduced infarct size, no change in LVEDV
BOOST [31,32] 30/30 6 IC, BM-MNC Improved EF at 6 months, No difference at 18 months
FIRST-LINE-AMI [40] 25/25 0 to 6 Mobilization by G-CSF Improved EF and remodeling at 4 months
REPAIR-AMI [36] 102/102 4 IC, BM-MNC Improved EF and reduced infarct size at 4 months
ASTAMI [38] 100 5 to 8 IC, BM-MNC No difference at 6 months
Chen et al 2004 [37] 34/35 18 IC, MSC Improved and perfusion at 6 months
JANSSENS et al 2006 [39] 33/34 1 IC, BM-MNC No effect
REVIVAL [41] 56/58 0 to 5 Mobilization by G-CSF No difference at 6 months
STEMMI [42] 39/39 0 to 6 Mobilization by G-CSF No difference at 6 months

IC: intra-coronary, BM-MNC: Bone marrow-derived mononuclear cells, CPC: circulating blood-derived progenitor cells EF: ejection fraction, LVEDV: left ventricular end-diastolic volume