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

NCT05046613 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 780

Last updated 2026-05-05

No results posted yet for this study

Summary

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

Conditions

Interventions

OTHER

Rimegepant

75mg

OTHER

Not taking Rimegepant

No rimegepant

Sponsors & Collaborators

  • PPD, Part of Thermo Fisher Scientific

    collaborator INDUSTRY
  • Pfizer

    lead INDUSTRY

Principal Investigators

  • Pfizer CT.gov Call Center · Pfizer

Eligibility

Min Age
0 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2021-09-23
Primary Completion
2029-11-04
Completion
2034-04-30

Countries

  • United States

Study Locations

More Related Trials

Entities

Diseases
Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05046613 on ClinicalTrials.gov