Rimegepant in Women When Used for Intermittent Prevention of Menstrual Migraine
Research type
Research Study
Full title
An Interventional Efficacy And Safety, Phase 3, Double-Blind, Parallel Group Study To Investigate Intermittent Prevention Of Menstrual Migraine With Rimegepant Compared With Placebo In Women Participants 18 To 45 Years Of Age
IRAS ID
1011792
Contact name
Alissa Carmona
Contact email
Sponsor organisation
Pfizer Inc.
Clinicaltrials.gov Identifier
Research summary
This study will explore Rimegepant administered during the peri-menstrual period (PMP) in women for intermittent prevention of menstrual migraine. The purpose of research is to gather information to advance science and medicine. The study duration will be 10 months. Approximately 470 participants will be randomized in the study.
REC name
East of England - Essex Research Ethics Committee
REC reference
25/EE/0145
Date of REC Opinion
26 Aug 2025
REC opinion
Further Information Favourable Opinion