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French Prospective, Observational Cohort Study of Patients With Fabry Disease Treated With Migalastat

Fabry Disease Clinical Trial

Official title:
A French Prospective, Observational Cohort Study of Patients With Fabry Disease Treated With Migalastat - the MIGA-FAB Study

Clinical Trial Summary

This is a noninterventional cohort study to evaluate the effects of migalastat, on long-term safety, effectiveness, and quality of life (QOL) in patients with Fabry disease.

Clinical Trial Description

Occurrence of key indicators of safety and effectiveness will be evaluated, such as cardiac, cerebrovascular and renal events, and overall survival. The study is designed to provide effectiveness and safety data by Q2 2023 which will cover a period up to 5 years after the migalastat launch date. This will involve a retrospective data collection up to migalastat initiation (for patients already receiving migalastat) and a prospective follow-up from 1 to 3.5 years (depending on the time of enrollment) in migalastat-treated patients with Fabry disease who have a GLA mutation amenable to migalastat. All visits will be scheduled and conducted according to the clinical site's standard of care. Standard of care is defined as a diagnostic and customary clinical treatment/practice process that a clinician chooses according to their clinical judgement for a Fabry disease patient. There are no study- required visits, tests or clinical assessments. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04602364
Study type Observational
Source Amicus Therapeutics France SAS
Contact
Status Completed
Phase
Start date October 15, 2020
Completion date June 30, 2023
View Details
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