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

Study Identifier
UBR-MD-01
CT.gov Identifier
EudraCT Identifier
Not available
EUCTIS ID
Not available
For general inquiries, please contact
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 (50 and 100 mg) compared to placebo for the acute treatment of a single migraine attack.

    Study Locations

    Location
    Status
    Location
    Clinical Research Advantage, Inc./Desert Clinical Research, LLC.
    Mesa, Arizona, United States, 85213
    Status
    Not applicable
    Location
    Xenoscience, Inc.
    Phoenix, Arizona, United States, 85004
    Status
    Not applicable
    Location
    Clinical Research Advantage, Inc./Orange Grove Family Practice
    Tucson, Arizona, United States, 85741
    Status
    Not applicable
    Location
    Principals Research Group, Inc.
    Hot Springs, Arkansas, United States, 71901
    Status
    Not applicable
    Location
    KLR Business Group, Inc. dba Arkansas Clinical Research
    Little Rock, Arkansas, United States, 72205
    Status
    Not applicable
    Location
    The Research Center of Southern California, LLC
    Carlsbad, California, United States, 92011
    Status
    Not applicable
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