Clinical Trials on Sulfatidosis

Total 32 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
    • NCT04628364
      Recruiting
      Conditions: Metachromatic Leukodystrophy
    • NCT04283227
      Recruiting
      Conditions: Lysosomal Storage Diseases; Metachromatic Leukodystrophy
    • NCT03771898
      Active, not recruiting
      Conditions: Metachromatic Leukodystrophy (MLD)
    • NCT03725670
      Recruiting
      Conditions: Metachromatic Leukodystrophy (MLD)
    • NCT03639844
      No longer available
      Conditions: Hurler Syndrome; Inherited Metabolic Disorder; Lysosomal Storage Disorder; Metachromatic Leukodystrophy; Inborn Errors of Metabolism
    • NCT03392987
      Active, not recruiting
      Conditions: Lysosomal Storage Disease; Metachromatic Leukodystrophy
    • NCT03333200
      Recruiting
      Conditions: MLD; Krabbe Disease; ALD; MPS I; MPS II; MPS III; Vanishing White Matter Disease; GM3 Gangliosidosis; PKAN; Tay-Sachs Disease; NP Deficiency; Osteopetrosis; Alpha-Mannosidosis; Sandhoff Disease; Niemann-Pick Diseases; MPS IV; Gaucher Disease; GAN; GM1 Gangliosidoses; Morquio Disease; S-Adenosylhomocysteine Hydrolase Deficiency; Batten Disease; Pelizaeus-Merzbacher Disease; Leukodystrophy; Lysosomal Storage Diseases; Purine Nucleoside Phosphorylase Deficiency; Multiple Sulfatase Deficiency Disease
    • NCT02559830
      Recruiting
      Conditions: Metachromatic Leukodystrophy; Adrenoleukodystrophy
    • 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
    • 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
    • NCT02084121
      No longer available
      Conditions: Metachromatic Leukodystrophy
    • NCT02021266
      No longer available
      Conditions: Metachromatic Leukodystrophy
    • NCT01887938
      Active, not recruiting
      Conditions: Metachromatic Leukodystrophy (MLD)
    • NCT01801709
      Unknown status
      Conditions: 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
    • NCT01560182
      Active, not recruiting
      Conditions: Lysosomal Storage Disease; Metachromatic Leukodystrophy
    • NCT01536327
      Active, not recruiting
      Conditions: Peripheral Neuropathy; Muscle Weakness
    • NCT01510028
      Completed
      Conditions: Metachromatic Leukodystrophy (MLD)
    • 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
    • NCT01325025
      Completed
      Conditions: Late Infantile Metachromatic Leukodystrophy
    • NCT01303146
      Completed
      Conditions: Metachromatic Leukodystrophy
    • 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
    • NCT00683189
      Completed
      Conditions: Metachromatic Leukodystrophy
    • NCT00681811
      Terminated
      Conditions: Late Infantile Metachromatic Leukodystrophy