A Phase 1/2, Open Label, Dose Ranging Study to Evaluate the Safety, Tolerability, Pharmacokinetics and Exploratory Efficacy Parameters of PRX-102 Administered by Intravenous Infusion Every 2 Weeks for 12 Weeks to Adult Fabry Patients
Phase of Trial: Phase I/II
Latest Information Update: 10 May 2017
At a glance
- Drugs Pegunigalsidase alfa (Primary)
- Indications Fabry's disease
- Focus Adverse reactions; First in man; Pharmacokinetics
- Sponsors Protalix Biotherapeutics
- 10 May 2017 According to a Protalix Biotherapeutics media release, results from this trial were presented at the World Congress of Nephrology 2017, titled, The Fifth Update on Fabry Nephropathy.
- 09 May 2017 Results of pharmacokinetic analysis and modeling, which provides a strong rationale for once-monthly dosing of PRX-102, published in a Protalix BioTherapeutics Media Release.
- 16 Mar 2017 According to a Protalix Biotherapeutics media release, results from this trial were presented at the 13th Annual WORLDSymposium 2017.
Most Recent Events
Table of Contents
- At a glance
- Trial Overview
- Trial Details
- Trial Centres
- Trial History