drugset / Trial / NCT00684203
Trial to Assess the Safety and Effects of Vorapaxar in Japanese Subjects With Acute Coronary Syndrome (P04772; MK-5348-016)
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| 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 | — |