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Clinical Trials on Adrenomyeloneuropathy
Total 52 results
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NCT04528355RecruitingConditions: Primary Immunodeficiency (PID); Congenital Bone Marrow Failure Syndromes; Inherited Metabolic Disorders (IMD); Hereditary Anemias; Inflammatory Conditions
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NCT04528706RecruitingConditions: Cerebral Adrenoleukodystrophy
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NCT04303416Not yet recruitingConditions: Adrenomyeloneuropathy; Adrenoleukodystrophy
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NCT04090268RecruitingConditions: Leukemia, Myeloid, Acute; Leukemia, B-cell; Leukemia, T Cell; Lymphoma, Hodgkin; Lymphoma, Non-Hodgkin; Drepanocytosis; Thalassemia Major; Adrenoleukodystrophy
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NCT04008849Active, not recruitingConditions: Inherited Metabolic Disorders (IMD)
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NCT03864523CompletedConditions: Adrenomyeloneuropathy; X-linked Adrenoleukodystrophy
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NCT03852498RecruitingConditions: Cerebral Adrenoleukodystrophy (CALD)
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NCT03789721RecruitingConditions: ALD (Adrenoleukodystrophy); Adrenoleukodystrophy; Cerebral Adrenoleukodystrophy
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NCT03727555RecruitingConditions: X-linked Adrenoleukodystrophy
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NCT03649919Not yet recruitingConditions: Xlsma; DMD; X-ALD; TSC
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NCT03627416CompletedConditions: Hereditary Spastic Paraplegia; Adrenomyeloneuropathy
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NCT03513328RecruitingConditions: 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
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NCT03500627CompletedConditions: Healthy
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NCT03406962Active, not recruitingConditions: Inherited Metabolic Disorders (IMD)
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NCT03367546RecruitingConditions: Sickle Cell Disease; Thalassemia; High Risk Hematologic Disorders; Cerebral Adrenoleukodystrophy; Inherited Metabolic Disorders
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NCT03278899RecruitingConditions: X-Linked Adrenoleukodystrophy
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NCT03231878Active, not recruitingConditions: Adrenoleukodystrophy
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NCT03196765WithdrawnConditions: X-Linked Adrenoleukodystrophy
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NCT02961803CompletedConditions: Adrenomyeloneuropathy; Adrenoleukodystrophy; AMN
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NCT02952482CompletedConditions: Adrenoleukodystrophy
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NCT02948062WithdrawnConditions: Adrenoleukodystrophy
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NCT02698579Enrolling by invitationConditions: Cerebral Adrenoleukodystrophy (CALD); Adrenoleukodystrophy (ALD); X-Linked Adrenoleukodystrophy (X-ALD)
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NCT02595489Active, not recruitingConditions: X-linked Adrenoleukodystrophy
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NCT02559830RecruitingConditions: Metachromatic Leukodystrophy; Adrenoleukodystrophy
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NCT02410239WithdrawnConditions: Cerebral Adrenoleukodystrophy
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NCT02254863RecruitingConditions: 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
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NCT02233257No longer availableConditions: X-linked Adrenoleukodystrophy
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NCT02204904TerminatedConditions: X-Linked Adrenoleukodystrophy (X-ALD); Cerebral Adrenoleukodystrophy (CALD); Adrenoleukodystrophy (ALD)
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NCT02171104RecruitingConditions: 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
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NCT01962415RecruitingConditions: Primary Immunodeficiency (PID); Congenital Bone Marrow Failure Syndromes; Inherited Metabolic Disorders (IMD); Hereditary Anemias; Inflammatory Conditions
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NCT01896102Active, not recruitingConditions: Cerebral Adrenoleukodystrophy (CALD)
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NCT01881334AvailableConditions: Hematologic Malignancies; Inborn Errors of Metabolism Disorders; Immune Deficiencies
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NCT01838941CompletedConditions: Peroxisome Biogenesis Disorders
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NCT01787578WithdrawnConditions: X-Linked Adrenoleukodystrophy; Adrenomyeloneuropathy
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NCT01668186RecruitingConditions: Peroxisome Biogenesis Disorders; D-Bifunctional Protein Deficiency; X-linked Adrenoleukodystrophy; Alpha-Methylacyl-CoA Racemase Deficiency; Peroxisomal Acyl-CoA Oxidase Deficiency; Adult Refsum's Disease
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NCT01626092CompletedConditions: Lysosomal Storage Disease; Peroxisomal Disorder
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NCT01594853CompletedConditions: X-linked Adrenoleukodystrophy
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NCT01586455Active, not recruitingConditions: 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
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NCT01495260CompletedConditions: Adrenomyeloneuropathy
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NCT01372228Active, not recruitingConditions: 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
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NCT01165060CompletedConditions: X-linked Adrenoleukodystrophy; Adrenomyeloneuropathy
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NCT01043640CompletedConditions: Mucopolysaccharidosis; Hurler Syndrome; Hunter Syndrome; Maroteaux-Lamy Syndrome; Sly Syndrome; Alpha Mannosidosis; Fucosidosis; Aspartylglucosaminuria; Adrenoleukodystrophy (ALD); Krabbe Disease; Metachromatic Leukodystrophy (MLD); Sphingolipidoses; Peroxisomal Disorders
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NCT00654433TerminatedConditions: Inherited Metabolic Diseases; Lysosomal Storage Disorders; Peroxisomal Storage Diseases; Inborn Errors of Metabolism; Mucopolysaccharidosis
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NCT00545597TerminatedConditions: Adrenomyeloneuropathy; Adrenoleukodystrophy
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NCT00383448CompletedConditions: Adrenoleukodystrophy; Metachromatic Leukodystrophy; Globoid Cell Leukodystrophy; Tay Sachs Disease; Sandhoffs Disease; Wolman Disease; I-Cell Disease; Sanfilippo Syndrome; GM1 Gangliosidosis
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NCT00278044Unknown statusConditions: Adrenoleukodystrophy
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NCT00176904CompletedConditions: Adrenoleukodystrophy; Metachromatic Leukodystrophy; Globoid Cell Leukodystrophy; Gaucher's Disease; Fucosidosis; Wolman Disease; Niemann-Pick Disease; Batten Disease; GM1 Gangliosidosis; Tay Sachs Disease; Sandhoff Disease
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NCT00007020CompletedConditions: Infantile Refsum's Disease; Zellweger Syndrome; Adrenoleukodystrophy; Peroxisomal Disorders; Cholestasis
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NCT00005900Unknown statusConditions: 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
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NCT00004418SuspendedConditions: Adrenoleukodystrophy