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A Global Prospective Observational Study of Women With Fabry Disease and Their Infants During Pregnancy and Breastfeeding
RecruitingObservational study
Who can join
All ages · Women
Full eligibility criteria
Inclusion Criteria: Female patients meeting the following criteria will be eligible for study enrollment: 1. Patients with Fabry disease who are pregnant and/or breastfeeding, whether or not they are exposed to migalastat 2. Able and willing to provide informed consent or assent, if applicable. 3. Able and willing to provide HCP contact information. Exclusion Criteria: None
About the study
This is a global prospective observational study of women with Fabry disease and their infants during pregnancy and/or breastfeeding. The study will evaluate outcomes of pregnancy and/or breastfeeding in women and infants exposed to migalastat.
What is being tested
- migalastat (drug)
Sponsor: Amicus Therapeutics · Participants: 20 · Started: Mar 18, 2025
Contact the study team
- Pregnancy Registry Call Center · Phone: 888-239-0758
Official record on ClinicalTrials.gov — NCT04252066
Locations in the U.S.
| Pennsylvania | Amicus Therapeutics, Inc. Pregnancy Registry, Philadelphia |
Conditions
From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.