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A confirmatory study of CL2020 in patients with ST-elevation myocardial infarctio

Phase 2
Completed
Conditions
ST-elevation myocardial infarction
Registration Number
JPRN-jRCT1080224979
Lead Sponsor
ife Science Institute Inc.
Brief Summary

Following a single intravenous administration of CL2020 or placebo to patients with ST elevation acute myocardial infarction, the change from baseline in LVEF at Week 24 on echocardiography was not statistically significantly different between the CL2020 group and the placebo group, failing to meet the primary endpoint. There were no safety concerns with administration of CL2020.

Detailed Description

Not available

Recruitment & Eligibility

Status
completed
Sex
All
Target Recruitment
86
Inclusion Criteria

Patients diagnosed ST-elevation myocardial infarction
-Patients with cardiac dysfunction in spite of successful reperfusion by PCI

Exclusion Criteria

-Patients with any existing or previous malignant tumor
-Pregnant or nursing women, or women of child-bearing potential

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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