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RECRUITING Phase 3

A Study to Learn About the Study Medicine Called Rimegepant in Women When Used for Intermittent Prevention of Menstrual Migraine

NCT06641466 · View on ClinicalTrials.gov ↗

Study Summary

The purpose of this study is to evaluate the efficacy and safety of rimegepant when administered during the peri-menstrual period (PMP) for intermittent prevention of migraine in women who experience menstrual migraine attacks.

Conditions Studied

Interventions

  • DRUG Standard of Care
  • DRUG Placebo Comparator
  • DRUG Rimegepant

Study Locations (20)

Arizona

  • Mayo Clinic Hospital — Phoenix
  • Mayo Clinic Specialty Building — Phoenix
  • Mayo Clinic Arizona — Scottsdale

California

  • Hope Clinical Research, Inc. — Canoga Park
  • Axiom Research — Colton
  • Diablo Clinical Research, Inc. — Walnut Creek

Florida

  • VIN - Aventura — Aventura
  • Velocity Clinical Research, Hallandale Beach — Hallandale
  • Jacksonville Center for Clinical Research — Jacksonville

Georgia

  • Urban Family Practice Associates — Marietta
  • Clinical Research Atlanta — Stockbridge

Missouri

  • Clinvest Headlands Llc — Springfield
  • St. Charles Clinical Research — Weldon Spring

New York

  • Rochester Clinical Research, LLC — Rochester
  • Montefiore Medical Center — The Bronx

Idaho

  • St Luke's Clinic - Neurology — Meridian

Indiana

  • Alliance for Multispecialty Research - Medisphere Medical Research Center — Evansville

Trial Details

FieldValue
Enrollment Target 723 participants
Start Date 2025-03-11
Est. Completion 2027-03-30
Phase Phase 3

Sponsor

Pfizer

769 total trials

Interested in This Trial?

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT06641466

The ClinicalTrials.gov registry entry for NCT06641466 describes a study currently listed as recruiting. It is categorized as Phase 3, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 723 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Pfizer, which has 769 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Menstrual Migraine appearing as the primary indexed condition, and to 3 interventions — of which Standard of Care is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT06641466 reports 20 study locations spanning 11 distinct geographic areas — top geographies include Arizona, California, Florida. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT06641466 about?

NCT06641466 is a clinical study titled "A Study to Learn About the Study Medicine Called Rimegepant in Women When Used for Intermittent Prevention of Menstrual Migraine". The purpose of this study is to evaluate the efficacy and safety of rimegepant when administered during the peri-menstrual period (PMP) for intermittent prevention of migraine in women who experience menstrual migraine attacks.

What is the current status of trial NCT06641466?

This trial is currently recruiting. It is a Phase 3 study. The enrollment target is 723 participants. The study started on 2025-03-11. Estimated completion is 2027-03-30.

What conditions does trial NCT06641466 study?

This clinical trial studies the following conditions: Menstrual Migraine. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT06641466?

The interventions under investigation include: Standard of Care (DRUG), Placebo Comparator (DRUG), Rimegepant (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT06641466?

This trial is sponsored by Pfizer, which has 769 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT06641466 being conducted?

This trial has 20 study locations across Arizona, California, Florida, Georgia, Idaho. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial