Atogepant for Prophylaxis of Migraine in Participants Who Failed Previous Oral Prophylactic Treatments.
Part of paid clinical trials in Colton, California.
- Sponsor
- Allergan
- Study ID
- NCT04740827
- Phase
- PHASE3
- Status
- Completed
Conditions
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - 80 Years
- Healthy Volunteers
- Not accepted
Interventions
- Atogepant 60 mg — DRUGAtogepant tablets.
- Placebo — DRUGAtogepant matching placebo tablets.
Study Details
This study will assess the safety, tolerability, and efficacy of Atogepant 60 mg compared with placebo in participants with episodic migraine and who have previously failed 2 to 4 classes of oral prophylactic treatments.
Key Dates
- Start date
- Mar 5, 2021
- Status verified
- Sep 2023
- Primary completion
- Aug 4, 2022
- Completion
- Aug 4, 2022
Study Design
- Enrollment
- 315 participants (actual)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- TREATMENT
Arms
- Placebo Comparator: PlaceboParticipants received atogepant-matching placebo tablets, orally, once daily (QD) for up to 12 weeks in a double-blind (DB) treatment period.
- Active Comparator: Atogepant 60 mgParticipants received atogepant 60 mg, orally, QD for up to 12 weeks in a DB treatment period.
Primary Outcome Measure
Change From Baseline in Mean Monthly Migraine Days Across 12-Week Treatment Period in mITT Population [ Time Frame: Baseline to Week 12 ]
Locations (26)
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