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Browse : By Condition : By Disease Heading : Nutritional and Metabolic Diseases : Brain Diseases, Metabolic


Include trials that are no longer recruiting patients.

19 studies were found.
1.RecruitingReplagal Enzyme Replacement Therapy for Children with Fabry Disease
Condition: Fabry Disease
2.RecruitingAlternative Dosing and Regimen of Replagal to Treat Fabry Disease
Condition: Fabry Disease
3.RecruitingExpanded access use of Myozyme (alglucosidase alfa) in patients with infantile-onset Pompe disease
Conditions: Glycogen Storage Disease Type II; Glycogenosis 2
4.RecruitingAn Open-Label Clinical Trial of Replagal Enzyme Therapy in Children Ages 7-17 Years with Fabry Disease
Condition: Fabry Disease
5.RecruitingRegistry of Fabry Disease - A Multicenter Observational Study
Condition: Fabry Disease
6.RecruitingOGT 918-006: A Phase I/II Randomized, Controlled Study of OGT 918 in Patients with Neuronopathic Gaucher Disease
Condition: Gaucher Disease
7.RecruitingNervous System Degeneration in Glycosphingolipid Storage Disorders
Conditions: Gangliosidoses; Gaucher Disease
8.RecruitingThe Natural History and Pathogenesis of Mucolipidosis Type IV
Condition: Mucolipidosis Type IV
9.RecruitingPhase II Study of Allogeneic Bone Marrow or Umbilical Cord Blood Transplantation in Patients With Lysosomal or Peroxisomal Inborn Errors of Metabolism
Conditions: Graft Versus Host Disease; Lysosomal Storage Diseases; Peroxisomal Disorders
10.RecruitingPhase II Randomized Study of Alendronate Sodium for Osteopenia in Patients with Gaucher's Disease
Conditions: Gaucher's Disease; Osteopenia
11.Not yet recruitingStudy of Bile Acids in Patients With Peroxisomal Disorders
Conditions: Infantile Refsum's Disease; Zellweger Syndrome; Bifunctional Enzyme Deficiency; Adrenoleukodystrophy
12.RecruitingStudy of Glyceryl Trierucate and Glyceryl Trioleate (Lorenzo's Oil) Therapy in Male Children with Adrenoleukodystrophy
Condition: Adrenoleukodystrophy
13.RecruitingStudy of the Metabolism of Pyruvate and Related Problems in Patients with Lactic Acidemia
Conditions: Mitochondrial Myopathy; MELAS Syndrome; Lactic Acidosis
14.RecruitingPhase II Study of Glucocerebrosidase in Patients With Gaucher Disease
Condition: Gaucher's Disease
15.RecruitingAnalysis of the Nervous System in Patients with Fabry's Disease
Condition: Fabry's Disease
16.RecruitingEffects of Enzyme Replacement in Gaucher's Disease
Condition: Gaucher's Disease
17.RecruitingCopper Histidine Therapy for Menkes Diseases
Condition: Kinky Hair Syndrome
18.RecruitingGenetic Studies of Lysosomal Storage Disorders
Conditions: Gaucher's Disease; Lysosomal Storage Disease
19.RecruitingLipoprotein Metabolism in Normal Volunteers and Patients with High Levels of Lipoproteins
Conditions: Abetalipoproteinemia; Atherosclerosis; Healthy; Inborn Errors Lipid Metabolism

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