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
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 (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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