CI

At a glance

ClinicalIndex Comparison Record
Phase 3Completed· 26,449 enrolled
Drug / intervention
Vorapaxar +1 moredrug
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT00526474
NCT00526474Phase 3Completed

A Multicenter, Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Safety and Efficacy of SCH 530348 in Addition to Standard of Care in Subjects With a History of Atherosclerotic Disease: Thrombin Receptor Antagonist in Secondary Prevention of Atherothrombotic Ischemic Events (TRA 2°P - TIMI 50)

Merck Sharp & Dohme LLC·interventional·Posted Sep 10, 2007·Updated Sep 21, 2018

In Brief

A Phase 3 clinical trial evaluating Vorapaxar and Placebo for Atherosclerosis and 4 related conditions. Completed, enrolled 26,449 participants.

Detailed 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.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
Countries--

Timeline

Phase 3CompletedFinished
20082009201020112012201320142015201620172018201920202021202220232024202520262027
First PostedSep 10, 2007
Enrollment StartSep 1, 2007
Primary CompletionDec 1, 2011
TodayJul 2, 2026
Enrollment to primary: 4.3 yearsPosted 18.8 years ago

Interventions

Vorapaxardrug

2.5-mg tablet daily for at least 1 year

Placebodrug

matching tablet daily for at least 1 year