drugset / Trial / NCT05518123

Efficacy and Tolerability of Rimegepant for the Prevention of Migraine in Adults With History of Inadequate Response to Oral Preventive Medications

NCT05518123 ↗

Phase 4 Completed 962 enrolled Pfizer
RandomizedParallel-groupQuadruple-blindPrevention

Summary

This study is being conducted to evaluate the efficacy and tolerability of rimegepant for migraine prophylaxis in adults with a history of inadequate response to oral preventive medications

Timeline

Start
2022-11-07
Primary completion
2025-03-31
Completion
2025-07-08

Outcome

Met primary endpoint

registry analysis (superiority test); DB Rimegepant vs DB Placebo; p <0.0001; Least square mean (LSM) Difference -1.6 (95% CI -2.13 to -1.15); Mixed Models Analysis NCT05518123 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Rimegepant Small molecule 75 mg Oral

Indications