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RECRUITING
NCT07310290

Study to Assess the Real-World Effectiveness of Ubrogepant in Adult Participants When Treating During the Prodrome Phase of Migraine Attacks

Sponsor: AbbVie

View on ClinicalTrials.gov

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