Phase
Condition
Migraine (Adult)
Pain (Pediatric)
Pain
Treatment
Zavegepant
Clinical Study ID
Ages > 18 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria
Meets International Classification of Headache Disorders 3 (ICHD-3) diagnostic criteria for migraine with or without aura
At least 18 years of age
2- 8 migraine attacks per month
Participants should be on a calcitonin gene-related peptide (CGRP)-targeting preventive migraine medication on a stable dose for a) ≥2 months prior to zavegepant treatment if an oral gepant or a monoclonal antibody (mAb) injected monthly, or b) at least two treatments if a mAb injected each 3 months.
Atogepant
Eptinezumab
Erenumab
Fremanezumab
Galcanezumab
Rimegepant
Exclusion Criteria
Primary headache disorders other than migraine (tension-type headache days are allowed)
History of hypersensitivity reaction to zavegepant or to any of the components of zavegepant
Eligibility Notes
Participants may have either episodic or chronic migraine.
Prior use of zavegepant and other gepants is permitted.
Participants can be using migraine preventive medications/treatments in addition to the CGRP-targeting preventive treatment, as long as those treatments have been stable for at least two months at the time of enrollment.
Additional Eligibility Criteria for Participants to Start on Rimegepant for Migraine Prevention
Inclusion Criteria:
• Must have 4 or more migraine days per month, on average, during the 2 months prior to the Screening Visit, according to participant self-report.
Exclusion Criteria
• History of hypersensitivity reaction to rimegepant or to any of the components of rimegepant.
Study Design
Study Description
Connect with a study center
Mayo Clinic in Arizona
Phoenix, Arizona 85254
United StatesActive - Recruiting
Mayo Clinic in Arizona
Scottsdale, Arizona 85259
United StatesSite Not Available
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