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Clinical Trial 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.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT00684515
Study type Interventional
Source Merck Sharp & Dohme Corp.
Contact
Status Completed
Phase Phase 2
Start date September 21, 2006
Completion date November 8, 2007

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