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Clinical Trial Summary

The primary purpose of this study is to evaluate the efficacy of rimegepant (BMS-927711) compared with placebo in the acute treatment of migraine as measured by Pain Freedom (headache pain intensity level reported as "no pain") at 2 hours post dose using a four point numeric rating scale (no pain, mild pain, moderate pain, severe pain) while identifying an optimal dose to support the Phase 3 clinical trials.


Clinical Trial Description

Intervention Model: Parallel Versus Comparator + Placebo ;


Study Design


Related Conditions & MeSH terms


NCT number NCT01430442
Study type Interventional
Source Pfizer
Contact
Status Completed
Phase Phase 2
Start date October 2011
Completion date May 2012

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