Efficacy, Safety, and Tolerability of Oral Ubrogepant in the Acute Treatment of Migraine

Study Identifier
UBR-MD-02
CT.gov Identifier
EudraCT Identifier
Not available
EUCTIS ID
Not available
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Study Complete

Results Available

Protocol
Available Language(s): English
Statistical Analysis Plan
Available Language(s): English

Study Details

Medical Condition
  • Migraine - General
  • Study Drug
  • Ubrogepant
  • Placebo-matching Ubrogepant
  • Phase
    Phase 3
    Sex
    Female & Male
    Age
    18 - 75 Years

    Protocol Summary

    This study will evaluate the efficacy, safety, and tolerability of 2 doses of ubrogepant (25 and 50 mg) compared to placebo for the acute treatment of a single migraine attack.

    Study Locations

    Location
    Status
    Location
    Clinical Research Advantage, Inc./Simon Williamson Clinic
    Birmingham, Alabama, United States, 35211
    Status
    Not applicable
    Location
    Clinical Research Advantage, Inc./East Valley Family Physicians, PLC
    Chandler, Arizona, United States, 85224
    Status
    Not applicable
    Location
    St. Joseph's Hospital & Medical Center - Barrow Neurologic Institute (BNI)
    Phoenix, Arizona, United States, 85013
    Status
    Not applicable
    Location
    Clinical Research Advantage, Inc./Central Phoenix Medical Clinic, LLC
    Phoenix, Arizona, United States, 85020
    Status
    Not applicable
    Location
    Mayo Clinic Arizona, May Clinic Scottsdale
    Scottsdale, Arizona, United States, 85259
    Status
    Not applicable
    Location
    Radiant Research Inc.
    Tucson, Arizona, United States, 85712
    Status
    Not applicable
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