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Study of Oral Atogepant Tablets to Assess Change in Disease Activity in Adult Japanese Participants With Episodic Migraine

← catalyst calendar

NCT05861427 · results posted

Sponsored by AbbVie (industry) · ABBV — their whole pipeline →.

Phase
Phase 3
Status
Completed
Study type
Interventional
Design
Randomized · Quadruple · Treatment
Enrollment
524actual
Sites
48
Country
Japan

Every value on this page is a field the sponsor filed with ClinicalTrials.gov, reproduced. Dates are their own estimates, revised as a study runs, unless the registry marks them actual. sources →

Source: ClinicalTrials.gov, retrieved 2026-08-19

Dates

each axis at the precision it was filed, with the registry's own basis
DateFiledBasisWhat it is
Start2023-07-12actualWhen the study began enrolling
Primary completion2025-03-01actualThe date the last participant is measured for the primary outcome — the readout window
Study completion2025-03-01actualThe whole study's end, after follow-up
First posted2023-05-16actualWhen this record first appeared on the registry
Results posted2026-06-11actualWhen the sponsor posted results to the registry
Record updated2026-06-11actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Condition

  • Migraine

Interventions

  • Drug: Atogepant — also filed as Qulipta
  • Drug: Placebo for Atogepant

Primary outcomes

what the primary-completion date above is the date OF
Change From Baseline in Mean Monthly Migraine Days
measured Up to Week 12
Number of Participants Experiencing With Adverse Events (AEs)
measured Up to Week 12

Posted documents

hosted by the registry — we link, never re-serve
Study Protocolposted 2024-07-18 · 2.8 MB · Prot_000.pdf
Statistical Analysis Planposted 2024-10-22 · 587 KB · SAP_001.pdf

Publications

Linked on the registry record. A “linked by the registry” entry is NLM's own automated PubMed match, not a claim by the sponsor that the paper reports this study.

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