Trials / Completed
CompletedNCT05827887
An Observational Study to Assess Ubrogepant Tablets and Atogepant Tablets to Treat Migraine in Adult Participants
ProspeCtive Observational Real-world Study of uBRogepant and Atogepant in Israel (COBRA)
- Status
- Completed
- Phase
- —
- Study type
- Observational
- Enrollment
- 226 (actual)
- Sponsor
- AbbVie · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
Migraine is a neurological disease characterized by moderate or severe headache, associated with nausea, vomiting, and/or sensitivity to light and sound. This study will evaluate how effective the use of ubrogepant and atogepant is in treating adult participants with migraine. Urogepant (Ubrelvy) and Atogepant (Qulipta) are approved drugs for treatment of migraine in adults in the US. Approximately 200 adult participants who are prescribed Ubrogepant or atogepant by their doctors will be enrolled in this study in Israel. Participants will receive ubrogepant oral tablets or atogepant oral tablets as prescribed by their physician. Participants will be followed for 90 days. 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.
Conditions
Timeline
- Start date
- 2023-06-25
- Primary completion
- 2026-01-28
- Completion
- 2026-01-28
- First posted
- 2023-04-25
- Last updated
- 2026-04-03
Locations
11 sites across 1 country: Israel
Source: ClinicalTrials.gov record NCT05827887. Inclusion in this directory is not an endorsement.