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
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
Study Drug
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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