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Observational Study to Assess Maternal, Fetal and Infant Outcomes Following Exposure to Rimegepant

Observational Study to Assess Maternal, Fetal and Infant Outcomes Following Exposure to Rimegepant

Recruiting
18 years and older
Female
Phase N/A
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Overview

The purpose of the study is to evaluate fetal, maternal, and infant outcomes through 12 months of age.

Eligibility

Inclusion Criteria:

  • Pregnant women with migraine exposed to rimegepant: a diagnosis of migraine and at least 1 dose of rimegepant during pregnancy or just prior to pregnancy (up to 3 days prior to conception)
  • Pregnant women with migraine unexposed to rimegepant: a diagnosis of migraine and no exposure to Rimegepant before or during pregnancy

Exclusion Criteria: 

        • Women exposed to other calcitonin gene-related peptide (CGRP)antagonists (e.g.,
        ubrogepant), CGRP monoclonal antibodies, or ditans (e.g., lasmiditan) at any time during
        pregnancy or just prior to pregnancy

Study details
    Migraine

NCT05046613

Pfizer

30 January 2026

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