drugset / Trial / NCT02867709

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

NCT02867709 ↗

Phase 3 Completed 1686 enrolled Allergan
RandomizedParallel-groupDouble-blindTreatment

Summary

This study will evaluate the efficacy, safety, and tolerability of 2 doses of ubrogepant (25 and 50 mg) compared to placebo for the acute treatment of a single migraine attack.

Timeline

Start
2016-08-26
Primary completion
2018-01-25
Completion
2018-02-26

Outcome

Mixed primary results

registry analysis (superiority test); Placebo vs Ubrogepant 50 mg; p = 0.0129; Odds Ratio (OR) 1.62 (95% CI 1.14 to 2.29); NCT02867709 ↗

registry analysis (superiority test); Placebo vs Ubrogepant 25 mg; p = 0.0711; Odds Ratio (OR) 1.37 (95% CI 1.02 to 1.83); NCT02867709 ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Ubrogepant Small molecule 25 mg Oral
Subject Ubrogepant Small molecule 50 mg Oral

Indications