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NCT04252066Recruiting

A Global Prospective Observational Study of Women With Fabry Disease and Their Infants During Pregnancy and Breastfeeding

Source: ClinicalTrials.gov · Last updated 28 Oct 2026

Brief summary (registry, in English)

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.

Status (registry)
Recruiting
Study type
Observational
Enrollment
20 (estimated)
First submitted
18 Dec 2019
Start date
18 Mar 2025
Primary completion date
Aug 2029
Lead sponsor
Amicus Therapeutics
NCT number
NCT04252066

What you commit to

  • Study type: Observational
  • Planned participants: 20
  • From 18 Mar 2025 to the primary completion date, Aug 2029
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other

  • None

Who the study is looking for

  • Female patients meeting the following criteria will be eligible for study enrollment:
  • Patients with Fabry disease who are pregnant and/or breastfeeding, whether or not they are exposed to migalastat
  • Able and willing to provide informed consent or assent, if applicable.
  • Able and willing to provide HCP contact information.

Sex: Female · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Amicus Therapeutics, Inc. Pregnancy Registry
Coordinator of this site? Confirm its status
PhiladelphiaUnited StatesRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.