Clinical Trials on Leukodystrophy, Metachromatic

Total 30 results

  • 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
  • NCT00639132
    Active, not recruiting
    Conditions: Metachromatic Leukodystrophy
  • NCT04283227
    Recruiting
    Conditions: Lysosomal Storage Diseases, Metachromatic Leukodystrophy
  • NCT03771898
    Active, not recruiting
    Conditions: Metachromatic Leukodystrophy (MLD)
  • 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
  • NCT04628364
    Recruiting
    Conditions: Metachromatic Leukodystrophy
  • NCT01372228
    Active, not recruiting
    Conditions: Hurler Syndrome (MPS I), Hurler-Scheie Syndrome, Hunter Syndrome (MPS II), Sanfilippo Syndrome (MPS III), Krabbe Disease (Globoid Leukodystrophy), Metachromatic Leukodystrophy (MLD), Adrenoleukodystrophy (ALD and AMN), Sandhoff Disease, Tay Sachs Disease, Pelizaeus Merzbacher (PMD), Niemann-Pick Disease, Alpha-mannosidosis
  • NCT02084121
    No longer available
    Conditions: Metachromatic Leukodystrophy
  • NCT02021266
    No longer available
    Conditions: Metachromatic Leukodystrophy
  • NCT03639844
    No longer available
    Conditions: Hurler Syndrome, Inherited Metabolic Disorder, Lysosomal Storage Disorder, Metachromatic Leukodystrophy, Inborn Errors of Metabolism
  • NCT02171104
    Recruiting
    Conditions: Mucopolysaccharidosis Disorders, Hurler Syndrome, Hunter Syndrome, Maroteaux Lamy Syndrome, Sly Syndrome, Alpha-Mannosidosis, Fucosidosis, Aspartylglucosaminuria, Glycoprotein Metabolic Disorders, Sphingolipidoses, Recessive Leukodystrophies, Globoid Cell Leukodystrophy, Metachromatic Leukodystrophy, Niemann-Pick B, Niemann-Pick C Subtype 2, Sphingomyelin Deficiency, Peroxisomal Disorders, Adrenoleukodystrophy With Cerebral Involvement, Zellweger Syndrome, Neonatal Adrenoleukodystrophy, Infantile Refsum Disease, Acyl-CoA Oxidase Deficiency, D-Bifunctional Enzyme Deficiency, Multifunctional Enzyme Deficiency, Alpha-methylacyl-CoA Racmase Deficiency, Mitochondrial Neurogastrointestingal Encephalopathy, Severe Osteopetrosis, Hereditary Leukoencephalopathy With Axonal Spheroids (HDLS; CSF1R Mutation), Inherited Metabolic Disorders
  • NCT01887938
    Active, not recruiting
    Conditions: Metachromatic Leukodystrophy (MLD)
  • NCT03392987
    Active, not recruiting
    Conditions: Lysosomal Storage Disease, Metachromatic Leukodystrophy
  • NCT01560182
    Active, not recruiting
    Conditions: Lysosomal Storage Disease, Metachromatic Leukodystrophy
  • NCT01586455
    Active, not recruiting
    Conditions: Mucopolysaccharidosis I, Mucopolysaccharidosis VI, Adrenoleukodystrophy, Niemann-Pick Disease, Metachromatic Leukodystrophy, Wolman Disease, Krabbe's Disease, Gaucher's Disease, Fucosidosis, Batten Disease, Severe Aplastic Anemia, Diamond-Blackfan Anemia, Amegakaryocytic Thrombocytopenia, Myelodysplastic Syndrome, Acute Myelogenous Leukemia, Acute Lymphocytic Leukemia
  • NCT03725670
    Recruiting
    Conditions: Metachromatic Leukodystrophy (MLD)
  • NCT00383448
    Completed
    Conditions: Adrenoleukodystrophy, Metachromatic Leukodystrophy, Globoid Cell Leukodystrophy, Tay Sachs Disease, Sandhoffs Disease, Wolman Disease, I-Cell Disease, Sanfilippo Syndrome, GM1 Gangliosidosis
  • NCT01510028
    Completed
    Conditions: Metachromatic Leukodystrophy (MLD)
  • NCT00418561
    Completed
    Conditions: Metachromatic Leukodystrophy (MLD)
  • NCT01043640
    Completed
    Conditions: Mucopolysaccharidosis, Hurler Syndrome, Hunter Syndrome, Maroteaux-Lamy Syndrome, Sly Syndrome, Alpha Mannosidosis, Fucosidosis, Aspartylglucosaminuria, Adrenoleukodystrophy (ALD), Krabbe Disease, Metachromatic Leukodystrophy (MLD), Sphingolipidoses, Peroxisomal Disorders
  • NCT00176904
    Completed
    Conditions: Adrenoleukodystrophy, Metachromatic Leukodystrophy, Globoid Cell Leukodystrophy, Gaucher's Disease, Fucosidosis, Wolman Disease, Niemann-Pick Disease, Batten Disease, GM1 Gangliosidosis, Tay Sachs Disease, Sandhoff Disease
  • NCT01801709
    Unknown status
    Conditions: Metachromatic Leukodystrophy
  • NCT01325025
    Completed
    Conditions: Late Infantile Metachromatic Leukodystrophy
  • NCT02559830
    Recruiting
    Conditions: Metachromatic Leukodystrophy, Adrenoleukodystrophy
  • NCT00633139
    Completed
    Conditions: Late Infantile Metachromatic Leukodystrophy