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Study to Assess the Real-World Effectiveness of Ubrogepant in Adult Participants When Treating During the Prodrome Phase of Migraine Attacks
Sponsor: AbbVie
Summary
Migraine is a neurological disease characterized by moderate or severe headaches, associated with nausea, vomiting, and/or sensitivity to light and sound. This study will assess changes in migraine attack severity for adult participants treating with oral ubrogepant across migraine attacks. Ubrogepant is a drug that is approved for the acute treatment of migraine in adults. Approximately 189 participants will be enrolled in approximately 15 sites across the US. Participants will receive ubrogepant as prescribed by their physician according to their routine clinical practice and local label. Participants will be followed for up to 13 weeks. There is expected to be no additional burden for participants in this trial. Participants will attend regular visits during the study at a hospital or clinic according to their routine clinical practice.
Official title: PHASES: Prodrome in tHe reAl World: aSsESsing Ubrogepant Acute Use
Key Details
Gender
All
Age Range
18 Years - Any
Study Type
OBSERVATIONAL
Enrollment
189
Start Date
2026-01-27
Completion Date
2027-03
Last Updated
2026-02-10
Healthy Volunteers
No
Conditions
Locations (3)
Neurology and Pain Specialty Center /ID# 278508
Aliso Viejo, California, United States
Chicago Headache Center & Research Inst /ID# 272345
Naperville, Illinois, United States
Tri City Research Center, LLC /ID# 278800
Grand Island, Nebraska, United States