Migraine Trial, Recruiting
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:
- People who are female and between 18 and 45 years of age
- People who have an established diagnosis of migraine
- People who had a straightforward delivery without lasting health complications for themselves
- People whose baby did not stay in a neonatal intensive care unit (NICU) for more than 3 nights
- People who are between 14 days and 9 months after giving birth, and are still breastfeeding, at the time of joining the trial
- People for whom a prescribing doctor has determined that a migraine medication called galcanezumab is appropriate to use after birth
- People who are planning to receive galcanezumab after giving birth
Who may not be able to join:
- People who have a medical reason they cannot breastfeed, including due to prior surgery or a condition affecting their baby
- People for whom galcanezumab is medically unsuitable, or for whom insurance does not cover it
- People who are currently using a group of migraine medications called gepants
- People who screen positive for moderately severe or severe depression (a score of 15 or above on a standard depression questionnaire called the PHQ-9)
- People who are currently pregnant or planning to become pregnant within the next 6 months
- People who have a severe breast infection (mastitis) at the time of joining
- People whose baby has significant health concerns noted in medical records, such as developmental issues, complications from birth, or the need for ongoing medications
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.
Contact this trial
Principal Investigator: Riley Bove, MD, MSc, University of California, San Francisco
Phone: 415-514-8330
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
Where this trial is recruiting
Primary endpoints
Determine emgality concentration in mature breastmilk; Determine average emgality concentration in mature breastmilk; Determine maximum emgality concentration in mature breastmilk; Determine average emgality dose to infants through mature breastmilk in a 24-hour period; Determine maximum emgality dose to infants through mature breastmilk in a 24-hour period; Determine average relative infant dose of emgality in mature breastmilk; Determine maximum relative infant dose of emgality in mature breastmilk
Can't join this trial?
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.