Safety, Efficacy, & PK of PRX-102 in Patients With Fabry Disease Administered Intravenously Every 4 Weeks

Last updated:
2026-07-25
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View trial details

Overview

Official protocol title:

A PHASE 3, OPEN LABEL, SWITCH OVER STUDY TO ASSESS THE SAFETY, EFFICACY AND PHARMACOKINETICS OF PEGUNIGALSIDASE ALFA (PRX-102) 2MG/KG ADMINISTERED BY INTRAVENOUS INFUSION EVERY 4 WEEKS FOR 52 WEEKS IN PATIENTS WITH FABRY DISEASE CURRENTLY TREATED WITH ENZYME REPLACEMENT THERAPY: FABRAZYME (AGALSIDASE BETA) OR REPLAGAL (AGALSIDASE ALFA)

Intervention/treatment:
PRX-102 (PEGUNIGALSIDASE ALFA)
Medical condition:
FABRY DISEASE
Protocol code:
PB-102-F50
Control number:
207219
Status:
Closed
Approved:
August 02, 2017
Date Completed:
Trial phase:
Phase 3
For more information:
ClinicalTrials.gov - NCT03180840
This is an external link. The information is not authorized by the Government of Canada.

Eligibility

Sex: ALL
Age
18 Years to 60 Years
Accepts healthy volunteers: No

Contacts and locations

Contact
Name
Sari Alon
Organization
Protalix Ltd.
Phone:
+972-4-9028100
Extension 215
Sponsor
PROTALIX LTD

Results

See the results from the trial NCT03180840. This is an external link. The information is not authorized by the Government of Canada.

Date posted:
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