Clinical Trials on Mucopolysaccharidosis Type VI

Total 29 results





    • NCT03173521
      Recruiting
      Conditions: Mucopolysaccharidosis Type VI
    • NCT02156674
      Active, not recruiting
      Conditions: Maroteaux-Lamy Syndrome
    • NCT00104234
      Completed
      Conditions: Mucopolysaccharidosis VI
    • NCT00048620
      Completed
      Conditions: Mucopolysaccharidosis VI
    • NCT00048711
      Completed
      Conditions: Mucopolysaccharidosis VI
    • NCT03370653
      Completed
      Conditions: Mucopolysaccharidosis VI
    • NCT00299000
      Completed
      Conditions: Mucopolysaccharidosis VI; Maroteaux-Lamy Syndrome
    • NCT01387854
      Completed
      Conditions: MPS VI
    • NCT00067470
      Completed
      Conditions: Mucopolysaccharidosis VI
    • NCT00214773
      Recruiting
      Conditions: Mucopolysaccharidosis VI (MPS VI, Maroteaux-Lamy Syndrome)
    • NCT01961518
      Completed
      Conditions: Morquio Syndrome A; Maroteaux Lamy Syndrome; MPS IVA; MPS VI
    • NCT02437253
      Completed
      Conditions: Mucopolysaccharidosis Type I; Mucopolysaccharidosis Type II; Mucopolysaccharidosis Type VI
    • NCT01458613
      Active, not recruiting
      Conditions: Lysosomal Storage Disease; Lung Diseases; Obstructive Sleep Apnoea; Macroglossia; Eye Abnormalities
    • NCT01707433
      Completed
      Conditions: Mucopolysaccharidosis IV A; Mucopolysaccharidosis VI
    • NCT00176917
      Completed
      Conditions: Mucopolysaccharidosis I; Mucopolysaccharidosis VI; Mannosidosis; Mucolipidosis Type II (I-cell Disease)
    • NCT00748969
      Terminated
      Conditions: Mucopolysaccharidosis I; Mucopolysaccharidosis II; Mucopolysaccharidosis VI
    • NCT01870375
      Completed
      Conditions: Mucopolysaccharidosis Type I; Mucopolysaccharidosis Type II; Mucopolysaccharidosis Type VI; Mucopolysaccharidosis Type IV; Mucopolysaccharidosis Type VII
    • 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
    • NCT01586871
      Completed
      Conditions: MPS I; MPS II; MPS VI; Mucopolysaccharidoses
    • NCT01675674
      Terminated
      Conditions: Mucopolysaccharidoses; Mucopolysaccharidosis I; Mucopolysaccharidosis II; Mucopolysaccharidosis IV; Mucopolysaccharidosis VI
    • NCT03632213
      Recruiting
      Conditions: Mucopolysaccharidosis IV A; Mucopolysaccharidosis VI; Mucopolysaccharidoses; MPS IV A; MPS VI; MPS - Mucopolysaccharidosis; Morquio A Syndrome; Morquio Syndrome A; Morquio Syndrome
    • NCT00005900
      Unknown status
      Conditions: I Cell Disease; Fucosidosis; Globoid Cell Leukodystrophy; Adrenoleukodystrophy; Mannosidosis; Niemann-Pick Disease; Pulmonary Complications; Mucopolysaccharidosis I; Mucopolysaccharidosis VI; Metachromatic Leukodystrophy; Gaucher's Disease; Wolman Disease
    • 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
    • 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
    • NCT00668564
      Terminated
      Conditions: Hurler's Syndrome; Maroteaux-Lamy Syndrome; Sly Syndrome; Alpha Mannosidosis; Fucosidosis; Aspartylglucosaminuria; Sphingolipidoses; Krabbe Disease; Wolman's Disease; Niemann-Pick Disease Type B; Niemann-Pick Disease, Type C