A Trial Investigating Lu AG09222 With Ubrogepant in Participants With Migraine
← catalyst calendarSponsored by H. Lundbeck A/S (industry) · HLUN-B.CO — their whole pipeline →.
Phase
Phase 1
Status
Completed
Study type
Interventional
Design
Randomized · Double · Treatment
Enrollment
43actual
Sites
4
Country
United States
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| Date | Filed | Basis | What it is |
|---|---|---|---|
| Start | 2024-09-13 | actual | When the study began enrolling |
| Primary completion | 2025-07-11 | actual | The date the last participant is measured for the primary outcome — the readout window |
| Study completion | 2025-07-11 | actual | The whole study's end, after follow-up |
| First posted | 2024-08-29 | actual | When this record first appeared on the registry |
| Results posted | — | When the sponsor posted results to the registry | |
| Record updated | 2025-10-14 | actual | The sponsor's own last edit to this record — every projection above is as current as this date |
What it studies
Condition
- Migraine
Interventions
- Drug: Ubrogepant
- Drug: Lu AG09222
- Drug: Placebo
Primary outcome
what the primary-completion date above is the date OFNumber of participants with treatment-emergent adverse events (TEAEs)
measured Up to 92 Days
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