clinical trial · NCT06019728
A Prospective Study to Investigate Safety and Tolerability of Shorter Infusion of Fabrazyme
Fabry's DiseaseAGALSIDASE BETA (GZ419828)AcetaminophenDiphenhydramineDexamethasoneMontelukastLoratadineCetirizineFexofenadine
brief summary
This Phase 4 study will evaluate the safety and tolerability of Fabrazyme at current approved dose with increases in the infusion rate and reduced infusion volume. This study aims to generate data to provide the guidance on how infusion rate can be safely increased and minimize the burden of the life-long treatment with Fabrazyme.
started
Nov 10, 2023
primary completion
Oct 25, 2024
completion
Oct 25, 2024
last updated
Oct 21, 2025
detailed description
The total duration will be up to 7 months
official title
A Study to Investigate Safety and Tolerability of Higher Infusion Rate to shORten the duraTion of FabrazymE Infusion
sourced from ClinicalTrials.gov · pharmadog mirrors structured fields, not the full protocol