Migraine Trial, Recruiting NCT05158894 Sponsor: AbbVie Condition: Migraine
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Migraine Trial, Recruiting

NCT05158894
Recruiting Not Applicable

Who may be able to join

AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI

Who might be able to join this trial:

  • You must be located in the United States or Canada.
  • You must currently be pregnant at the time of signing up.
  • You must have been diagnosed with migraines by your doctor or healthcare provider.
  • You must be willing to provide contact details for yourself, your doctor, and your baby's doctor (if applicable).
  • You must give permission for your doctor(s) to share your medical information and your baby's medical information with the research team, if asked.
  • You must fall into one of these three groups:
    • You have taken at least one dose of Ubrelvy during your pregnancy, and can provide details about how often you took it each trimester.
    • You have taken at least one dose of Qulipta during your pregnancy, and can provide the dates you started and stopped taking it.
    • You have never taken Ubrelvy or Qulipta, or you stopped taking Ubrelvy at least 2 days before becoming pregnant, or stopped Qulipta at least 5 days before becoming pregnant.

Who may not be able to join:

  • You have taken any other migraine medications in the same drug family as Ubrelvy or Qulipta (called gepants), or certain migraine-prevention injections (called CGRP monoclonal antibodies), either shortly before conception or at any point during your pregnancy before enrolling (confirm with trial site).
  • Your pregnancy has already ended and the outcome is already known — this study only accepts people who are currently pregnant.

Important: Always verify eligibility with the trial site directly before applying.

Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 28 July 2026
This study is not part of the standard drug-approval phase pathway (for example an observational, device, behavioural, or registry study), so a phase success rate does not apply.

Contact this trial

Principal Investigator: ABBVIE INC., AbbVie

Phone: 833-782-7241

Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.

GP referral letter

Print a one-page summary to share with your doctor.

Trial details

Status
Recruiting
Phase
Not Applicable
Sponsor
Registry
ClinicalTrials.gov
Start date
10 January 2023
Est. completion
1 January 2036

Where this trial is recruiting

🇨🇦 Canada 🇺🇸 United States

Primary endpoints

Major Congenital Malformations (MCMs)

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 28 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov