drugset / Trial / NCT01015287

A Comparison of Prasugrel at PCI or Time of Diagnosis of Non-ST Elevation Myocardial Infarction

NCT01015287 ↗

Phase 3 Completed 4033 enrolled Eli Lilly and Company Daiichi Sankyo · collab
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The purpose of this trial is to investigate the potential benefits/risks regarding pretreatment with prasugrel in non-ST-elevation myocardial infarction (NSTEMI) participants with elevated troponin scheduled for coronary angiography/percutaneous coronary intervention (PCI).

Timeline

Start
2009-12
Primary completion
2013-01
Completion
2013-02

Outcome

Missed primary endpoint

paper primary endpoint through 7 days from randomization in the pre-treatment group versus the no pre-treatment group was 13.1% versus 13.1% (p = 0.93). PMID 25524333 ↗

paper did not differ significantly between the two groups (hazard ratio with pretreatment, 1.02; 95% confidence interval [CI], 0.84 to 1.25; P=0.81). PMID 23991622 ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Prasugrel Small molecule 5 mg Oral
Subject Prasugrel Small molecule 10 mg Oral