Efficacy, Safety, and Tolerability Study of Oral Ubrogepant in the Acute Treatment of Migraine
Status: | Completed |
---|---|
Conditions: | Migraine Headaches |
Therapuetic Areas: | Neurology |
Healthy: | No |
Age Range: | 18 - 75 |
Updated: | 1/5/2019 |
Start Date: | July 22, 2016 |
End Date: | December 14, 2017 |
A Phase 3, Multicenter, Randomized, Double-Blind, Placebo-Controlled Single Attack Study to Evaluate the Efficacy, Safety, and Tolerability of Oral Ubrogepant in the Acute Treatment of Migraine
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.
and 100 mg) compared to placebo for the acute treatment of a single migraine attack.
Inclusion Criteria:
- At least a 1-year history of migraine with or without aura consistent with a diagnosis
according to the International Classification of Headache Disorders, 3rd edition, beta
version
- Migraine onset before age 50
- History of migraines typically lasting between 4 and 72 hours if untreated or treated
unsuccessfully and migraine episodes are separated by at least 48 hours of headache
pain freedom
- History of 2 to 8 migraine attacks per month with moderate to severe headache pain in
each of the previous 3 months.
Exclusion Criteria:
- Difficulty distinguishing migraine headache from other headaches
- Has taken medication for acute treatment of headache (including acetaminophen,
nonsteroidal anti-inflammatory drugs [NSAIDs], triptans, ergotamine, opioids, or
combination analgesics) on 10 or more days per month in the previous 3 months
- Has a history of migraine aura with diplopia or impairment of level of consciousness,
hemiplegic migraine, or retinal migraine
- Has a current diagnosis of new persistent daily headache, trigeminal autonomic
cephalgia (eg, cluster headache), or painful cranial neuropathy
- Required hospital treatment of a migraine attack 3 or more times in the previous 6
months
- Has a chronic non-headache pain condition requiring daily pain medication
- Has a history of malignancy in the prior 5 years, except for adequately treated basal
cell or squamous cell skin cancer, or in situ cervical cancer
- Has a history of any prior gastrointestinal conditions (eg, diarrhea syndromes,
inflammatory bowel disease) that may affect the absorption or metabolism of
investigational product; participants with prior gastric bariatric interventions which
have been reversed are not excluded
- Has a history of hepatitis within previous 6 months.
We found this trial at
90
sites
Wake Research Associates, LLC Wake Research is an Organization of Unified Investigational Sites working closely...
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University of South Florida The University of South Florida is a high-impact, global research university...
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Lynn Health Science Institute Our mission is to provide clinical trials research and health services...
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Quality Clinical Research, Inc. Welcome to Quality Clinical Research. We originated here in Omaha, NE...
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Overland Park, Kansas 66212
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1901 S Hawthorne Rd #306
Winston-Salem, North Carolina 27103
Winston-Salem, North Carolina 27103
(336) 768-8062
PMG Research of Winston-Salem PMG Research of Winston-Salem, founded in 1979, occupies a 10,000 square...
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