Clinical Trials on Lysosomal Storage Diseases

Total 734 results

    • NCT03812042
      Unknown status
      Conditions: Lysosomal Storage Diseases
    • NCT03812055
      Unknown status
      Conditions: Lysosomal Storage Diseases
    • NCT04393701
      Not yet recruiting
      Conditions: Neonatal Screening; Lysosomal Storage Diseases
    • NCT02000310
      Recruiting
      Conditions: Lysosomal Storage Disorders
    • NCT01003912
      Withdrawn
      Conditions: Lysosomal Storage Diseases; Inborn Errors of Metabolism
    • NCT00001671
      Completed
      Conditions: Lysosomal Storage Disease
    • NCT00001215
      Enrolling by invitation
      Conditions: Lysosomal Storage Disease; Gaucher Disease; Parkinson Disease
    • NCT04455230
      Recruiting
      Conditions: Fabry Disease; Lysosomal Storage Diseases
    • NCT04040049
      Recruiting
      Conditions: Fabry Disease; Lysosomal Storage Diseases
    • NCT04283227
      Recruiting
      Conditions: Lysosomal Storage Diseases; Metachromatic Leukodystrophy
    • NCT00046202
      Recruiting
      Conditions: Lysosomal Storage Disease; Cholesterol Metablism
    • NCT03392987
      Active, not recruiting
      Conditions: Lysosomal Storage Disease; Metachromatic Leukodystrophy
    • NCT01626092
      Completed
      Conditions: Lysosomal Storage Disease; Peroxisomal Disorder
    • NCT01560182
      Active, not recruiting
      Conditions: Lysosomal Storage Disease; Metachromatic Leukodystrophy
    • NCT03897361
      Recruiting
      Conditions: Lysosomal Storage Diseases; Cystinosis
    • NCT04189601
      Not yet recruiting
      Conditions: Fabry Disease; Gaucher Disease; Niemann-Pick Disease, Type C; Lysosomal Storage Diseases
    • 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
    • NCT03853876
      Suspended
      Conditions: Aspartylglucosaminuria; Aspartylglucosamidase (AGA) Deficiency; Lysosomal Storage Diseases
    • NCT04532047
      Not yet recruiting
      Conditions: MPS I; MPS II; MPS IVA; MPS VI; Mps VII; Gaucher Disease, Type 2; Gaucher Disease, Type 3; Pompe Disease Infantile-Onset; Wolman Disease
    • NCT02416661
      Completed
      Conditions: Lysosomal Storage Diseases; Gaucher Disease; Sphingolipidoses
    • NCT02120235
      Unknown status
      Conditions: Lysosomal Storage Disorders; Gaucher Disease; Fabry Disease; Pompe Disease; Niemann-Pick Disease
    • NCT02363153
      Recruiting
      Conditions: Pompe Disease; Glycogen Storage Disease Type II; Lysosomal Storage Diseases
    • NCT00215527
      Terminated
      Conditions: Mucopolysaccharidosis I; Lysosomal Storage Diseases; Spinal Cord Compression
    • NCT01416467
      Completed
      Conditions: Galactosialidosis
    • NCT03893240
      Recruiting
      Conditions: Pompe Disease; Pompe Disease (Late-onset); Glycogen Storage Disease Type 2; LOPD; Lysosomal Storage Diseases; Acid Maltase Deficiency