Hurler Syndrome - 22 Studies Found

Completed : Study of Aldurazyme® Replacement Therapy in Patients With Mucopolysaccharidosis I (MPS I) Disease
:
  • Mucopolysaccharidosis I
  • Hurler Syndrome
  • Mucopolysaccharidosis I
  • Hurler Syndrome
  • Biological: Aldurazyme (Recombinant Human Alpha-L-Iduronidase)

Recruiting : A Study of the Effect of Aldurazyme® (Laronidase) Treatment on Lactation in Female Patients With Mucopolysaccharidosis I (MPS I) and Their Breastfed Infants
:
  • Mucopolysaccharidosis I
  • Hurler's Syndrome
  • Mucopolysaccharidosis I
  • Hurler's Syndrome
  • Biological: Aldurazyme Placebo
Completed : A Dose-optimization Study of Aldurazyme® (Laronidase) in Patients With Mucopolysaccharidosis I (MPS I) Disease
:
  • Mucopolysaccharidosis I
  • Hurler's Syndrome
  • Biological: Aldurazyme (Recombinant Human Alpha-L-Iduronidase)

Completed : A Study Investigating the Relationship Between the Development of Laronidase Antibody and Urinary GAG (Glycosaminoglycan) Levels in Aldurazyme® Treated Patients
:
  • Mucopolysaccharidosis I
  • Hurler's Syndrome
  • - Hurler Syndrome (MPS-1) With Short Stature and Muscle Wasting
  • : 2006-02-01
    :
    • Drug: Growth Hormone
    • Procedure: Whole body
Not yet recruiting : Safety and Exploratory Efficacy of HSC835 in Patients With Inherited Metabolic Disorders (IMD)
: Inherited Metabolic Disorders IMD
: 2016-03-16
: Drug: Umbilical cord blood transplantation with HSC835 Hematopoietic Stem cell transplantation will be d
Completed : Immune Tolerance Study With Aldurazyme® (Laronidase)
: Mucopolysaccharidosis I
: 2008-08-13
:
  • Biological: Laronidase 0.058 m
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