A Long-Term Safety and Tolerability Extension Study Evaluating Atogepant for the Prevention of Chronic or Episodic Migraine
Part of paid clinical trials in Phoenix, Arizona.
- Sponsor
- AbbVie
- Study ID
- NCT04686136
- Phase
- PHASE3
- Status
- Completed
Conditions
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - 80 Years
- Healthy Volunteers
- Not accepted
Interventions
- Atogepant 60 mg — DRUGTablets containing 60 mg of Atogepant
Study Details
This study will evaluate the Long-Term Safety and Tolerability of Atogepant 60 mg daily for the Prevention of Migraine in Participants with Chronic or Episodic Migraine
Key Dates
- Start date
- Feb 19, 2021
- Status verified
- Dec 2025
- Primary completion
- Oct 20, 2025
- Completion
- Oct 20, 2025
Study Design
- Enrollment
- 596 participants (actual)
- Allocation
- NA
- Intervention model
- SINGLE_GROUP
- Primary purpose
- TREATMENT
Arms
- Experimental: Atogepant 60 mgTaken once daily
Primary Outcome Measure
Percentage of Participants with at Least 1 Treatment Emergent Adverse Event [ Time Frame: 156 weeks ]
Locations (42)
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