drugset / Trial / NCT01124643

Extension Study of TKT028 Evaluating Safety and Clinical Outcomes of Replagal® in Adult Patients With Fabry Disease

NCT01124643

Phase 3 Completed 35 enrolled Shire
NaSingle-groupOpen-labelTreatment

Summary

This study will evaluate safety and clinical outcomes of treatment with Replagal in adult participants with Fabry disease who have completed Study TKT028 (NCT00864851).

Timeline

Start
2010-04-13
Primary completion
2013-07-08
Completion
2013-07-08

Drugs

EvaluationDrugModalityDoseRoute
Subject Replagal Protein / enzyme biologic 0.2 mg/kg Intravenous

Indications