Migraine

Last updated: December 12, 2022
Sponsor: Eli Lilly and Company
Overall Status: Active - Recruiting

Phase

4

Condition

Migraine (Adult)

Treatment

N/A

Clinical Study ID

TX291178
I5Q-MC-CGBD_
  • Ages 18-65
  • All Genders

Study Summary

A Study to Investigate the Efficacy and Safety of Galcanezumab Versus Rimegepant in Adult Participants with Episodic Migraine

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • Age 18 to 65 Years
  • Have a diagnosis of migraine, with or without aura, as determined by the study investigator and in consideration of International Headache Society International Classification of Headache Disorders - 3rd edition guidelines (ICHD-3 2018)

Exclusion

Exclusion Criteria:

  • Have a known hypersensitivity to rimegepant or galcanezumab, and their excipients, or to multiple drugs, monoclonal antibodies or other therapeutic proteins
  • Have acute cardiovascular events and/or serious cardiovascular risk, or have had myocardial infarction, unstable angina, percutaneous coronary intervention, coronary artery bypass graft, or stroke within 6 months of screening, or have planned cardiovascular surgery or percutaneous coronary angioplasty.
  • Evidence of significant active or unstable psychiatric disease by medical history, such as bipolar disorder, schizophrenia, personality disorders, or other serious mood or anxiety disorders.
  • Women who are pregnant or nursing

Study Design

Study Start date:
Estimated Completion Date:

Study Description

  • Condition: Migraine

  • Clinical Trial Identifier: NCT05127486

  • Sponsor: Eli Lilly and Company

Connect with a study center

  • AMR Lexington

    Lexington, Kentucky 40509
    United States

    Active - Recruiting

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