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Mucopolysaccharidosis Type VI - 35 Studies Found

Status Study
Recruiting Study Name: Naglazyme After Allo Transplant for Maroteaux-Lamy Syndrome
Condition: Maroteaux-Lamy Syndrome
Date: 2014-06-03
Interventions: Drug: Naglazyme® 1 mg per kg of body weight administered once weekly as an intravenous infusion
Completed Study Name: Study of rhASB in Patients With Mucopolysaccharidosis VI
Condition: Mucopolysaccharidosis VI
Date: 2005-02-24
Interventions:
  • Drug: N-acetylgalactosamine 4-sulfatase

Completed Study Name: Study of Recombinant Human N-Acetylgalactosamine 4-Sulfatase in Patients With MPS VI
Condition: Mucopolysaccharidosis VI
Date: 2002-11-04
Interventions: Drug: N-acetylgalactosamine 4-sulfatase
Completed Study Name: Open-Label Study of Efficacy and Safety of Recombinant Human N-acetylgalactosamine 4-sulfatase in Patients With MPS VI
Condition: Mucopolysaccharidosis VI
Date: 2002-11-06
Interventions: Drug: N-acetylgalactosamine 4-sulfatase
Completed Study Name: A Phase 4 Two Dose Level Study of Naglazyme(TM) (Galsulfase) in Infants With MPS VI
Condition:
  • Mucopolysaccharidosis VI
  • Maroteaux-Lamy S
    Date: 2006-03-02
    Interventions: Drug: Naglazyme Weekly infusion for minimum of 52 weeks. Naglazyme is diluted in sterile 0.9% sodium chl
Recruiting Study Name: Biomarker for Maroteaux-Lamy Disease
Condition:
  • Maroteaux-lamy Disease
  • Lysosomal Storage Diseases

Date: 2011-10-24
Completed Study Name: Study of Recombinant Human N-acetylgalactosamine 4-sulfatase (rhASB) in Patients With MPS VI
Condition: Mucopolysaccharidosis VI
Date: 2003-08-20
Interventions:
  • Drug: Placebo
  • Drug: N-acetylgalactosamine

Recruiting Study Name: Mucopolysaccharidosis (MPS) VI Clinical Surveillance Program (CSP)
Condition: Mucopolysaccharidosis VI (MPS VI, Maroteaux-Lamy Syndrome)
Date: 2005-09-13
Completed Study Name: Screening an Orthopedic Population for Mildly-affected Individuals With Morquio Syndrome A and Maroteaux-Lamy Syndrome
Condition:
  • Morquio Syndrome A
  • Maroteaux Lamy Syndrome
  • MPS VI
    Date: 2011-06-29
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