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Clinical Trial Summary

There are two separate objectives in this study:

1. To demonstrate the pharmacodynamic (PD) profile when participants treated with cangrelor are switched to oral prasugrel 60 mg administered 30 minutes (min) after cangrelor infusion is discontinued

2. To demonstrate the PD profile when participants treated with cangrelor are switched to oral clopidogrel 600 mg administered during or immediately after cangrelor infusion.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT01979445
Study type Interventional
Source The Medicines Company
Contact
Status Completed
Phase Phase 2
Start date December 2, 2013
Completion date January 20, 2014

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