Example: Heart Attack
Clinical Trials on Brain Diseases, Metabolic, Inborn
Total 799 results
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NCT04552691AvailableConditions: Fabry Disease
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NCT04537377Not yet recruitingConditions: Wilson's Disease
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NCT04534842RecruitingConditions: Phenylketonuria
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NCT04532047Not yet recruitingConditions: MPS I; MPS II; MPS IVA; MPS VI; Mps VII; Gaucher Disease, Type 2; Gaucher Disease, Type 3; Pompe Disease Infantile-Onset; Wolman Disease
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NCT04531189Not yet recruitingConditions: Wilson Disease
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NCT04528706RecruitingConditions: Cerebral Adrenoleukodystrophy
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NCT04526197Enrolling by invitationConditions: Wilson Disease
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NCT04526210Enrolling by invitationConditions: Wilson Disease
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NCT04519749Not yet recruitingConditions: Fabry Disease
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NCT04480567RecruitingConditions: Phenylketonuria (PKU)
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NCT04476550RecruitingConditions: Pompe Disease
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NCT04475549Not yet recruitingConditions: MELAS
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NCT04469894RecruitingConditions: Niemann-Pick Diseases
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NCT04470713RecruitingConditions: GM1 Gangliosidosis; GM2 Gangliosidosis; Gaucher Disease, Type 2; Tay-Sachs Disease; AB Variant Gangliosidosis GM2; Sandhoff Disease
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NCT04455230RecruitingConditions: Fabry Disease; Lysosomal Storage Diseases
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NCT04452513RecruitingConditions: Phenylketonurias
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NCT04442347Not yet recruitingConditions: Ornithine Transcarbamylase Deficiency
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NCT04440254Not yet recruitingConditions: Fabry Disease
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NCT04433728Not yet recruitingConditions: Phenylketonurias
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NCT04429984Not yet recruitingConditions: Gaucher Disease
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NCT04430881Active, not recruitingConditions: Gaucher Disease; Splenomegaly
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NCT04422431Not yet recruitingConditions: Wilson Disease
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NCT04416126RecruitingConditions: Ornithine Transcarbamylase Deficiency
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NCT04411654Not yet recruitingConditions: Gaucher Disease, Type 2
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NCT04408300RecruitingConditions: Wilson Disease
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NCT04404530RecruitingConditions: Phenylketonurias
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NCT04395339RecruitingConditions: Brain Metastases; Radiotherapy Side Effect; Cognitive Impairment; Gangliosidosis, GM1; Breast Cancer
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NCT04388969Not yet recruitingConditions: Gaucher Disease; Parkinson Disease; GBA Gene Mutation
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NCT04375592Not yet recruitingConditions: Phenylketonurias; Hyperphenylalaninaemia; Tetrahydrobiopterin Deficiency
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NCT04368624Active, not recruitingConditions: Phenylketonurias
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NCT04353466Active, not recruitingConditions: Gaucher Disease, Type 1
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NCT04348708Enrolling by invitationConditions: Phenylketonuria; PAH Deficiency
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NCT04337684Enrolling by invitationConditions: Menkes Disease
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NCT04327973AvailableConditions: Pompe Disease Infantile-Onset
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NCT04320329Not yet recruitingConditions: Morquio B Disease; GM1 Gangliosidosis Type III
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NCT04318509CompletedConditions: PKU; Phenylketonurias; Inborn Errors of Metabolism; Metabolic Disease
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NCT04316637AvailableConditions: Niemann-Pick Disease, Type C
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NCT04310163RecruitingConditions: GM1 Gangliosidosis
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NCT04309331CompletedConditions: PKU; Phenylketonurias; Inborn Errors of Metabolism; Metabolic Disease
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NCT04303416Not yet recruitingConditions: Adrenomyeloneuropathy; Adrenoleukodystrophy
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NCT04302194Not yet recruitingConditions: Phenylketonurias
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NCT04283227RecruitingConditions: Lysosomal Storage Diseases; Metachromatic Leukodystrophy
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NCT04281537Active, not recruitingConditions: Fabry Disease
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NCT04273269Not yet recruitingConditions: GM1 Gangliosidosis
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NCT04272736Not yet recruitingConditions: Phenylketonurias; Hyperphenylalaninaemia
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NCT04269122CompletedConditions: Ornithine Transcarbamylase Deficiency
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NCT04251494RecruitingConditions: Phenylketonurias; Cardiovascular Diseases
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NCT04252066RecruitingConditions: Fabry Disease
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NCT04256655WithdrawnConditions: Phenylketonurias
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NCT04248062RecruitingConditions: Inborn Errors of Metabolism; Urea Cycle Disorder; Maple Syrup Urine Disease; Phenylketonurias; Methylmalonicacidemia; OTC Deficiency; Aminoacidopathy; Patient Reported Outcome Measurements