Clinical Trials on Leukodystrophy, Metachromatic

Total 37 results





    • NCT00639132
      Active, not recruiting
      Conditions: Metachromatic Leukodystrophy
    • NCT01510028
      Completed
      Conditions: Metachromatic Leukodystrophy (MLD)
    • NCT03771898
      Recruiting
      Conditions: Metachromatic Leukodystrophy (MLD)
    • NCT01801709
      Unknown status
      Conditions: Metachromatic Leukodystrophy
    • NCT00683189
      Completed
      Conditions: Metachromatic Leukodystrophy
    • NCT01325025
      Completed
      Conditions: Late Infantile Metachromatic Leukodystrophy
    • NCT01887938
      Active, not recruiting
      Conditions: Metachromatic Leukodystrophy (MLD)
    • NCT00633139
      Completed
      Conditions: Late Infantile Metachromatic Leukodystrophy
    • NCT00418561
      Completed
      Conditions: Metachromatic Leukodystrophy (MLD)
    • NCT03725670
      Recruiting
      Conditions: Metachromatic Leukodystrophy (MLD)
    • NCT01303146
      Completed
      Conditions: Metachromatic Leukodystrophy
    • NCT03392987
      Active, not recruiting
      Conditions: Lysosomal Storage Disease; Metachromatic Leukodystrophy
    • NCT01560182
      Active, not recruiting
      Conditions: Lysosomal Storage Disease; Metachromatic Leukodystrophy
    • NCT04283227
      Recruiting
      Conditions: Lysosomal Storage Diseases; Metachromatic Leukodystrophy
    • NCT02559830
      Recruiting
      Conditions: Metachromatic Leukodystrophy; Adrenoleukodystrophy
    • NCT00681811
      Terminated
      Conditions: Late Infantile Metachromatic Leukodystrophy
    • NCT02084121
      No longer available
      Conditions: Metachromatic Leukodystrophy
    • NCT02021266
      No longer available
      Conditions: Metachromatic Leukodystrophy
    • NCT01536327
      Active, not recruiting
      Conditions: Peripheral Neuropathy; Muscle Weakness
    • NCT01963650
      Terminated
      Conditions: Lipid Metabolism Disorders; Metachromatic Leukodystrophy (MLD); Nervous System Diseases; Brain Diseases; Central Nervous System Diseases; Demyelinating Diseases; Metabolism, Inborn Errors; Genetic Diseases, Inborn; Sphingolipidoses; Hereditary Central Nervous System Demyelinating Diseases; Metabolic Inborn Brain Diseases; Lysosomal Storage Diseases; Metabolic Diseases; Sulfatidosis
    • NCT03639844
      No longer available
      Conditions: Hurler Syndrome; Inherited Metabolic Disorder; Lysosomal Storage Disorder; Metachromatic Leukodystrophy; Inborn Errors of Metabolism
    • NCT02254863
      Recruiting
      Conditions: Adrenoleukodystrophy; Batten Disease; Mucopolysaccharidosis II; Leukodystrophy, Globoid Cell; Leukodystrophy, Metachromatic; Neimann Pick Disease; Pelizaeus-Merzbacher Disease; Sandhoff Disease; Tay-Sachs Disease; Brain Diseases, Metabolic, Inborn; Alpha-Mannosidosis; Sanfilippo Mucopolysaccharidoses
    • NCT00004378
      Completed
      Conditions: Thrombocytopenia; Metachromatic Leukodystrophy; Fanconi's Anemia; Thalassemia Major; Pure Red-Cell Aplasia; Inborn Errors of Metabolism
    • NCT00383448
      Completed
      Conditions: Adrenoleukodystrophy; Metachromatic Leukodystrophy; Globoid Cell Leukodystrophy; Tay Sachs Disease; Sandhoffs Disease; Wolman Disease; I-Cell Disease; Sanfilippo Syndrome; GM1 Gangliosidosis
    • NCT00005900
      Unknown status
      Conditions: I Cell Disease; Fucosidosis; Globoid Cell Leukodystrophy; Adrenoleukodystrophy; Mannosidosis; Niemann-Pick Disease; Pulmonary Complications; Mucopolysaccharidosis I; Mucopolysaccharidosis VI; Metachromatic Leukodystrophy; Gaucher's Disease; Wolman Disease