drugset / Trial / NCT02828020

Efficacy, Safety, and Tolerability Study of Oral Ubrogepant in the Acute Treatment of Migraine

NCT02828020 ↗

Phase 3 Completed 1672 enrolled Allergan
RandomizedParallel-groupDouble-blindTreatment

Summary

This study will evaluate the efficacy, safety, and tolerability of 2 doses of ubrogepant (50 and 100 mg) compared to placebo for the acute treatment of a single migraine attack.

Timeline

Start
2016-07-22
Primary completion
2017-12-13
Completion
2017-12-14

Outcome

Met primary endpoint

registry analysis (superiority test); Placebo vs Ubrogepant 50 mg; p = 0.0023; Odds Ratio (OR) 1.83 (95% CI 1.25 to 2.66); NCT02828020 ↗

registry analysis (superiority test); Placebo vs Ubrogepant 50 mg; p = 0.0023; Odds Ratio (OR) 1.70 (95% CI 1.27 to 2.28); NCT02828020 ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Ubrogepant Small molecule 50 mg Oral
Subject Ubrogepant Small molecule 100 mg Oral

Indications