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Found 4 clinical trials
A Long Term Follow-Up Study of Fabry Disease Subjects Treated With FLT190

Fabry disease is a rare, X-linked inborn error of glycosphingolipid metabolism caused by an abnormal gene encoding the -galactosidase A (GLA) enzyme.

fabry's disease
deficiency
gene therapy
glycosphingolipids
breakdown
  • 0 views
  • 16 Feb, 2024
  • 1 location
Fabry Disease Registry & Pregnancy Sub-registry

The Fabry Registry is an ongoing, international multi-center, strictly observational program that tracks the routine clinical outcomes for patients with Fabry disease, irrespective of treatment status.

fabry's disease
replacement therapy
agalsidase beta
deficiency
alpha-galactosidase
  • 0 views
  • 22 Dec, 2020
  • 126 locations
A Global Prospective Observational Study of Women With Fabry Disease and Their Infants During Pregnancy and Breastfeeding

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.

fabry's disease
migalastat
  • 0 views
  • 16 Feb, 2024
  • 1 location
Agalsidase Beta Long-Term Treatment Outcome for Fabry Disease Patients With IVS4 Mutation in Taiwan

This is a national, multicenter, observational, cohort study designed to assess clinical outcomes upon agalsidase beta treatment, to characterize the clinical manifestations, and to collect the natural history on male and female Fabry disease adult patients who carry the GLA IVS4. This study aims to retrospectively and prospectively investigate the …

  • 0 views
  • 15 Nov, 2023
  • 1 location