drugset / Trial / NCT00526474

Trial to Assess the Effects of Vorapaxar (SCH 530348; MK-5348) in Preventing Heart Attack and Stroke in Patients With Atherosclerosis (TRA 2°P - TIMI 50) (P04737)

NCT00526474 ↗

Phase 3 Completed 26449 enrolled Merck Sharp & Dohme LLC The TIMI Study Group · collab
RandomizedParallel-groupTriple-blindPrevention

Summary

The study is designed to determine whether vorapaxar, when added to the existing standard of care (SOC) for preventing heart attack and stroke (eg, aspirin, clopidogrel) in participants with a known history of atherosclerosis, will yield additional benefit over the existing standard of care without vorapaxar in preventing heart attack and stroke. The study is also designed to assess risk of bleeding with vorapaxar added to the standard of care versus the standard of care alone.

Timeline

Start
2007-09-01
Primary completion
2011-12-01
Completion
2011-12-01

Outcome

Met primary endpoint

registry NUMBER Placebo: 12.4 Percentage of Participants NUMBER Vorapaxar: 11.2 Percentage of Participants analysis (superiority or other test); Placebo vs Vorapaxar; p = 0.001; NCT00526474 ↗

release “TRA-2P showed that the addition of vorapaxar to standard of care significantly reduced the risk of the protocol-specified primary” merck.com ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Vorapaxar Small molecule 2.5 mg Oral