Clinical Trials on Peroxisomal Biogenesis Disorders

Total 58 results





    • NCT01626092
      Completed
      Conditions: Lysosomal Storage Disease; Peroxisomal Disorder
    • NCT03163771
      Recruiting
      Conditions: Peroxisomal Disorders; Diagnoses Disease
    • NCT00004348
      Unknown status
      Conditions: Beta-Oxidation Disorder; Peroxisomal Disorders
    • NCT00004442
      Terminated
      Conditions: Infantile Refsum's Disease; Zellweger Syndrome; Bifunctional Enzyme Deficiency; Adrenoleukodystrophy
    • NCT00383448
      Completed
      Conditions: Adrenoleukodystrophy; Metachromatic Leukodystrophy; Globoid Cell Leukodystrophy; Tay Sachs Disease; Sandhoffs Disease; Wolman Disease; I-Cell Disease; Sanfilippo Syndrome; GM1 Gangliosidosis
    • NCT01838941
      Completed
      Conditions: Peroxisome Biogenesis Disorders
    • NCT00007020
      Completed
      Conditions: Infantile Refsum's Disease; Zellweger Syndrome; Adrenoleukodystrophy; Peroxisomal Disorders; Cholestasis
    • 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
    • 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
    • NCT01668186
      Recruiting
      Conditions: Peroxisome Biogenesis Disorders; D-Bifunctional Protein Deficiency; X-linked Adrenoleukodystrophy; Alpha-Methylacyl-CoA Racemase Deficiency; Peroxisomal Acyl-CoA Oxidase Deficiency; Adult Refsum's Disease
    • NCT03856866
      Recruiting
      Conditions: Zellweger Syndrome; Peroxisome Biogenesis Disorders
    • NCT04569162
      Recruiting
      Conditions: RCDP - Rhizomelic Chondrodysplasia Punctata; RCDP1; RCDP2; RCDP3; RCDP4; RCDP5
    • NCT04031287
      Recruiting
      Conditions: Rhizomelic Chondrodysplasia Punctata
    • NCT04528706
      Recruiting
      Conditions: Cerebral Adrenoleukodystrophy
    • NCT04303416
      Not yet recruiting
      Conditions: Adrenomyeloneuropathy; Adrenoleukodystrophy
    • NCT04090268
      Recruiting
      Conditions: Leukemia, Myeloid, Acute; Leukemia, B-cell; Leukemia, T Cell; Lymphoma, Hodgkin; Lymphoma, Non-Hodgkin; Drepanocytosis; Thalassemia Major; Adrenoleukodystrophy
    • NCT03864523
      Completed
      Conditions: Adrenomyeloneuropathy; X-linked Adrenoleukodystrophy
    • NCT03852498
      Recruiting
      Conditions: Cerebral Adrenoleukodystrophy (CALD)
    • NCT03810508
      Recruiting
      Conditions: Charcot-Marie-Tooth Disease; Hereditary Motor and Sensory Neuropathy IV
    • NCT03789721
      Recruiting
      Conditions: ALD (Adrenoleukodystrophy); Adrenoleukodystrophy; Cerebral Adrenoleukodystrophy
    • NCT03727555
      Recruiting
      Conditions: X-linked Adrenoleukodystrophy
    • NCT03627416
      Completed
      Conditions: Hereditary Spastic Paraplegia; Adrenomyeloneuropathy
    • NCT03513328
      Recruiting
      Conditions: Bone Marrow Failure Syndrome; Thalassemia; Sickle Cell Disease; Diamond Blackfan Anemia; Acquired Neutropenia in Newborn; Acquired Anemia Hemolytic; Acquired Thrombocytopenia; Hemophagocytic Lymphohistiocytoses; Wiskott-Aldrich Syndrome; Chronic Granulomatous Disease; Common Variable Immunodeficiency; X-linked Lymphoproliferative Disease; Severe Combined Immunodeficiency; Hurler Syndrome; Mannosidosis; Adrenoleukodystrophy
    • NCT03440905
      Completed
      Conditions: Zellweger Spectrum
    • NCT03367546
      Recruiting
      Conditions: Sickle Cell Disease; Thalassemia; High Risk Hematologic Disorders; Cerebral Adrenoleukodystrophy; Inherited Metabolic Disorders