Clinical Trials on Tay-Sachs Disease

Total 23 results

    • NCT01869270
      Completed
      Conditions: Tay Sachs Disease; Sandhoff Disease; Late Onset Tay Sachs Disease
    • NCT02851862
      Recruiting
      Conditions: GM2 Gangliosidosis
    • NCT04221451
      Recruiting
      Conditions: Tay-Sachs Disease Sandhoff Disease
    • NCT01102686
      Completed
      Conditions: Gangliosidoses, GM2; Sandhoff Disease; Tay-Sachs Disease
    • NCT00679744
      Withdrawn
      Conditions: G(M2) Ganglioside; Tay-Sachs Disease Ganglioside; Sandhoff Disease Ganglioside
    • NCT04470713
      Recruiting
      Conditions: GM1 Gangliosidosis; GM2 Gangliosidosis; Gaucher Disease, Type 2; Tay-Sachs Disease; AB Variant Gangliosidosis GM2; Sandhoff Disease
    • NCT03822013
      Recruiting
      Conditions: GM2 Gangliosidosis; Supportive Care
    • NCT03759665
      Recruiting
      Conditions: GM2 Gangliosidosis; Tay-Sachs Disease; Sandhoff Disease
    • NCT00418847
      Completed
      Conditions: Gangliosidoses GM2
    • NCT00672022
      Completed
      Conditions: GM2 Gangliosidoses; Tay-Sachs; Sandhoff Disease
    • NCT01999257
      Completed
      Conditions: Tay Sachs Disease; Canavan Disease; Familial Dysautonomia
    • NCT02030015
      Recruiting
      Conditions: GM1 Gangliosidoses; GM2 Gangliosidoses; Tay-Sachs Disease; Sandhoff Disease
    • NCT00668187
      Completed
      Conditions: Tay-Sachs Disease; Sandhoff Disease; Late Onset Tay-Sachs Disease; GM1 Gangliosidosis; GM2 Gangliosidosis
    • NCT00006057
      Completed
      Conditions: Tay-Sachs Disease; Porphyria, Erythropoietic; Leukodystrophy, Globoid Cell; Metabolism, Inborn Errors
    • 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
    • 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
    • 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
    • NCT00383448
      Completed
      Conditions: Adrenoleukodystrophy; Metachromatic Leukodystrophy; Globoid Cell Leukodystrophy; Tay Sachs Disease; Sandhoffs Disease; Wolman Disease; I-Cell Disease; Sanfilippo Syndrome; GM1 Gangliosidosis
    • 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
    • NCT01626092
      Completed
      Conditions: Lysosomal Storage Disease; Peroxisomal Disorder
    • NCT00654433
      Terminated
      Conditions: Inherited Metabolic Diseases; Lysosomal Storage Disorders; Peroxisomal Storage Diseases; Inborn Errors of Metabolism; Mucopolysaccharidosis
    • NCT01003912
      Withdrawn
      Conditions: Lysosomal Storage Diseases; Inborn Errors of Metabolism
    • NCT00029965
      Recruiting
      Conditions: Neurological Regression; Myoclonus; Cherry Red Spot; Brain Atrophy