drugset / Trial / NCT00684515
Trial to Assess the Safety of Vorapaxar in Japanese Subjects With Cerebral Infarction (P05005; MK-5348-017)
RandomizedParallel-groupQuadruple-blindTreatment
Summary
The study is designed to assess safety of Vorapaxar when added to standard of care (aspirin) in Japanese subjects with cerebral infarction. The study will assess incidence and tolerability of bleeding, major adverse cardiac events, all adverse events, and effect on expression of markers of inflammation.
Timeline
- Start
- 2006-09-21
- Primary completion
- 2007-11-08
- Completion
- 2007-11-08
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 | Oral |
| Background | Aspirin | Small molecule | 150 mg | Oral |