Clinical Trials Directory

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UnknownNCT03087539

Exploratory P2 Trial to Evaluate Efficacy and Safety of Clotinab® (Abciximab) in Acute MI Patients

Exploratory Phase II Clinical Trial to Evaluate the Efficacy and Safety of Clotinab® (Abciximab) in Acute Myocardial Infarction Patients: Multicenter, Randomized, Double Blind, Placebo-controlled and Parallel Group Trial

Status
Unknown
Phase
Phase 2
Study type
Interventional
Enrollment
146 (estimated)
Sponsor
ISU Abxis Co., Ltd. · Industry
Sex
All
Age
20 Years – 80 Years
Healthy volunteers
Not accepted

Summary

Exploratory Phase II Clinical Trial to Evaluate the Efficacy and Safety of Clotinab® (Abciximab) in Acute Myocardial Infarction Patients: Multicenter, Randomized, Double-Blind, Placebo-controlled and Parallel Group Trial

Detailed description

This study was an exploratory phase 2 of Clinical Trial to evaluate the efficacy and safety of Clotinab® (Abciximab) in the acute myocardial infarction patients and was designed as a multicenter, randomized, double-blinded, placebo-controlled and parallel group study. The objective of this phase 2 clinical trial is to evaluate correlation between infarct size and major adverse cardiac event (MACE) of acute myocardial infarction patient, prearranged for percutaneous coronary intervention(PCI), to measure possibility to use infarct size as a primary efficacy test variable in phase 3 for final confirmation of safety and efficacy. Also to determine exploratively an average variance estimation of infarct size between study drug and placebo to confirm safety and efficacy of study drug, compared to placebo and to use the estimation for calculating sample size for phase III clinical trial.

Conditions

Interventions

TypeNameDescription
BIOLOGICALAbciximab
BIOLOGICALPlacebo

Timeline

Start date
2013-05-01
Primary completion
2016-12-14
Completion
2017-06-01
First posted
2017-03-22
Last updated
2017-03-22

Locations

1 site across 1 country: South Korea

Source: ClinicalTrials.gov record NCT03087539. Inclusion in this directory is not an endorsement.