drugset / Trial / NCT00684203

Trial to Assess the Safety and Effects of Vorapaxar in Japanese Subjects With Acute Coronary Syndrome (P04772; MK-5348-016)

NCT00684203

Phase 2 Completed 120 enrolled Merck Sharp & Dohme LLC
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The study is designed to assess safety and effects of vorapaxar, when added to standard of care (aspirin and clopidigrel), in Japanese subjects with acute coronary syndrome. The study may also provide information about the effect of vorapaxar on preventing heart attack and stroke in this subject population.

Timeline

Start
2006-12-01
Primary completion
2007-10-01
Completion
2007-10-01

Drugs

EvaluationDrugModalityDoseRoute
Subject Vorapaxar Small molecule 1 mg Oral
Subject Vorapaxar Small molecule 2.5 mg Oral
Background Aspirin Small molecule 75 mg
Background Aspirin Small molecule 100 mg
Background Clopidogrel Small molecule 100 mg