drugset / Trial / NCT00048711

Open-Label Study of Efficacy and Safety of Recombinant Human N-acetylgalactosamine 4-sulfatase in Patients With MPS VI

NCT00048711 ↗

Phase 2 Completed BioMarin Pharmaceutical
Non-randomizedSingle-groupOpen-labelTreatment

Summary

The purpose of the study is evaluate the efficacy, safety, and pharmacokinetics of weekly intravenous infusions of 1 mg/kg recombinant human N-acetylgalactosamine 4-sulfatase (rhASB) in patients diagnosed with Mucopolysaccharidosis VI (MPS VI)

Timeline

Start
2002-03
Primary completion
—
Completion
2006-06

Drugs

EvaluationDrugModalityDoseRoute
Subject Galsulfase Protein / enzyme biologic 1 mg/kg Intravenous