Clinical Trials on Hereditary Central Nervous System Demyelinating Diseases

Total 81 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
    • 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
    • NCT02714764
      Recruiting
      Conditions: Alexander Disease
    • 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
    • NCT04126005
      Recruiting
      Conditions: Canavan Disease
    • NCT03627416
      Completed
      Conditions: Hereditary Spastic Paraplegia; Adrenomyeloneuropathy
    • NCT02851563
      Completed
      Conditions: Canavan Disease
    • NCT01005004
      Completed
      Conditions: Pelizaeus-Merzbacher Disease
    • NCT02993796
      Recruiting
      Conditions: Krabbe Disease
    • 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
    • NCT01391637
      Completed
      Conditions: Pelizaeus-Merzbacher Disease; PMD
    • NCT01425489
      Active, not recruiting
      Conditions: Krabbe Disease
    • NCT00787865
      Active, not recruiting
      Conditions: Krabbe Disease
    • 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
    • NCT00278707
      Unknown status
      Conditions: Infantile Canavan Disease; Deficiency Disease, Aspartoacylase
    • NCT03639844
      No longer available
      Conditions: Hurler Syndrome; Inherited Metabolic Disorder; Lysosomal Storage Disorder; Metachromatic Leukodystrophy; Inborn Errors of Metabolism
    • NCT03367546
      Recruiting
      Conditions: Sickle Cell Disease; Thalassemia; High Risk Hematologic Disorders; Cerebral Adrenoleukodystrophy; Inherited Metabolic Disorders
    • NCT00383448
      Completed
      Conditions: Adrenoleukodystrophy; Metachromatic Leukodystrophy; Globoid Cell Leukodystrophy; Tay Sachs Disease; Sandhoffs Disease; Wolman Disease; I-Cell Disease; Sanfilippo Syndrome; GM1 Gangliosidosis
    • NCT00724802
      Unknown status
      Conditions: Canavan Disease
    • NCT00657748
      Withdrawn
      Conditions: Canavan Disease; Infantile; Deficiency Disease; Aspartoacylase; Leukodystrophy, Spongiform
    • NCT02021266
      No longer available
      Conditions: Metachromatic Leukodystrophy
    • NCT04528706
      Recruiting
      Conditions: Cerebral Adrenoleukodystrophy
    • NCT01536327
      Active, not recruiting
      Conditions: Peripheral Neuropathy; Muscle Weakness
    • NCT03278899
      Recruiting
      Conditions: X-Linked Adrenoleukodystrophy
    • NCT01938014
      Completed
      Conditions: Mucopolysaccharidosis Type I (MPS I); Mucopolysaccharidosis Type II (MPS II); Mucopolysaccharidosis Type III (MPS III); Mucopolysaccharidosis Type VI (MPS VI); Krabbe Disease