Fremanezumab for Menstrual Migraine
What You Need to Know Before You Apply
What is the purpose of this trial?
This trial aims to determine if fremanezumab, an injectable medicine, can reduce migraines associated with menstrual periods. Participants will receive either the active medicine or a placebo (inactive substitute) and will record their migraine experiences in diaries. The trial targets women aged 18 to 45 who have migraines linked to their menstrual cycle and have experienced these migraines for at least six months. As a Phase 4 trial, this research seeks to understand how the already FDA-approved and effective treatment benefits a broader range of patients.
Will I have to stop taking my current medications?
The trial requires that you do not start any new migraine preventive medications during the study. However, it does not specify if you need to stop taking your current medications, so it's best to discuss this with the study team.
What is the safety track record for fremanezumab?
Studies have shown that fremanezumab is generally well-tolerated by patients. Research involving over 2,800 people with occasional or frequent migraines found fremanezumab to be safe, as it did not cause major heart or brain problems. Reports confirmed its safety over a 12-week period compared to a placebo, a substance with no active medicine. While no treatment is entirely risk-free, fremanezumab's history suggests it is safe for most people. Prospective trial participants can find reassurance in this information regarding the treatment's safety.12345
Why are researchers enthusiastic about this study treatment?
Fremanezumab is unique because it targets the calcitonin gene-related peptide (CGRP) pathway, which is a key player in the development of migraines. Unlike standard treatments for menstrual migraines, such as NSAIDs and hormonal therapies, fremanezumab directly interrupts the migraine process by blocking CGRP, a protein that spikes during migraines and contributes to pain and inflammation. Researchers are excited about fremanezumab because it offers a targeted approach that could potentially provide relief for those who haven't responded well to existing treatments. Plus, its dosing schedule—just once every three months—could make it a convenient option for patients seeking long-lasting migraine control.
What is the effectiveness track record for fremanezumab in treating menstrual migraines?
Research has shown that fremanezumab, which participants in this trial may receive, effectively reduces the number of migraine days. This treatment targets a specific pathway in the body. Studies found that over 66% of people with occasional migraines and about 51.6% with frequent migraines experienced a significant reduction—at least 50%—in their monthly migraine days. In simpler terms, more than half of the patients had fewer migraines after using fremanezumab. This is promising for those who suffer from migraines, especially those linked to menstruation. The evidence suggests that this treatment can provide meaningful relief for many people.36789
Who Is on the Research Team?
Carolyn A Bernstein, MD
Principal Investigator
Brigham and Women's
Are You a Good Fit for This Trial?
This trial is for women aged 18-45 who suffer from migraines during their menstrual period. Participants should have a diagnosis of migraine, which can also occur at other times of the month. They must be willing to receive injections, keep a diary on their headaches, and provide saliva samples.Inclusion Criteria
Exclusion Criteria
Timeline for a Trial Participant
Screening
Participants are screened for eligibility to participate in the trial
Treatment
Participants receive fremanezumab or placebo injections every three months for two treatments, with monitoring through diaries and hormone level tests
Follow-up
Participants are monitored for safety and effectiveness after treatment, including assessment of migraine days, severity, and quality of life
What Are the Treatments Tested in This Trial?
Interventions
- Fremanezumab
Fremanezumab is already approved in United States, European Union, United Kingdom for the following indications:
- Prevention of migraines in adults
- Prevention of migraines in adults
- Prevention of migraines in adults
Find a Clinic Near You
Who Is Running the Clinical Trial?
Brigham and Women's Hospital
Lead Sponsor
Teva Pharmaceuticals USA
Industry Sponsor
Dr. Eric A. Hughes
Teva Pharmaceuticals USA
Chief Medical Officer since 2022
MD and PhD from Yale School of Medicine
Richard Francis
Teva Pharmaceuticals USA
Chief Executive Officer since 2023
BSc in Biochemistry from Imperial College London