Study to Assess the Real-World Effectiveness of Ubrogepant in Adult Participants When Treating During the Prodrome Phase of Migraine Attacks
Recruiting now
Conditions studied: Migraine
In brief
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.
Key facts
- Study ID
- NCT07310290
- Run by
- AbbVie
- People needed
- 189
- Starts
- 2026-01-27
- Expected to finish
- 2027-03-01
- Last updated by the study team
- 2026-02-10
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- History of 4 to 10 migraine days per month with moderate to severe headache pain in each month of the 3 months prior to Visit 1
- -a. Participants with a diagnosis of chronic migraine who report having 4 to 10 migraine days per month with moderate to severe headache pain in each month of the 3 months prior to Visit 1 due to concomitant preventive treatment are allowed in the study
- Participant is currently prescribed ubrogepant and has been using ubrogepant for at least 3 months for the acute treatment of migraine in adults, according to the US Food and Drug Administration (FDA)-approved indication
- Adult participants with current clinical diagnosis of migraine or chronic migraine according to International Classification of Headache Disorders (ICHD)-3
You may not qualify if…
- Currently participating in a concurrent clinical or non-interventional study.
- Concomitant use with a strong Cytochrome P450 3A4 (CYP3A4 ) inhibitor.
- Current diagnosis of new persistent daily headache, trigeminal autonomic cephalgia, status migrainosus or painful cranial neuropathy as defined by ICHD-3
Where it is running
- Neurology and Pain Specialty Center /ID# 278508 — Aliso Viejo, California, United States (enrolling)
- Chicago Headache Center & Research Inst /ID# 272345 — Naperville, Illinois, United States (enrolling)
- Tri City Research Center, LLC /ID# 278800 — Grand Island, Nebraska, United States (enrolling)
Full record on ClinicalTrials.gov
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