Example: Heart Attack
Clinical Trials on Glycogen Storage Disease Type II
Total 112 results
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NCT04349566Enrolling by invitationConditions: Becker Muscular Dystrophy; McArdle Disease; Limb-Girdle Muscular Dystrophy Type 2
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NCT04327973AvailableConditions: Pompe Disease Infantile-Onset
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NCT04174105Not yet recruitingConditions: Pompe Disease (Late-onset)
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NCT04138277RecruitingConditions: Pompe Disease (Late-onset)
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NCT04120168RecruitingConditions: Duchenne Muscular Dystrophy; Pompe Disease (Late-onset)
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NCT04094948Not yet recruitingConditions: Pompe Disease (Late-onset)
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NCT04093349SuspendedConditions: Pompe Disease; Pompe Disease (Late-onset); Glycogen Storage Disease Type 2; Glycogen Storage Disease Type II; LOPD; Lysosomal Storage Diseases; Acid Maltase Deficiency
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NCT03911505RecruitingConditions: Pompe Disease (Late-onset)
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NCT03893240Active, not recruitingConditions: Pompe Disease; Pompe Disease (Late-onset); Glycogen Storage Disease Type 2; LOPD; Lysosomal Storage Diseases; Acid Maltase Deficiency
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NCT03865836AvailableConditions: Pompe Disease
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NCT03812042Active, not recruitingConditions: Lysosomal Storage Diseases
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NCT03729362Active, not recruitingConditions: Pompe Disease (Late-onset)
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NCT03694561RecruitingConditions: Pompe Disease; Pompe Disease (Late-onset); GAA Deficiency
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NCT03687333Active, not recruitingConditions: Glycogen Storage Disease Type II
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NCT03564561RecruitingConditions: Glycogen Storage Disease Type II, Adult
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NCT03533673RecruitingConditions: Pompe Disease
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NCT03347253TerminatedConditions: Late-onset Pompe Disease
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NCT03285126CompletedConditions: Pompe Disease (Late-onset)
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NCT03255213SuspendedConditions: Glycogen Storage Disease
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NCT03211923Enrolling by invitationConditions: Nemaline Myopathy Type 6; Myotonic Dystrophy Type 2; McArdle Disease
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NCT03147664CompletedConditions: Enzyme Replacement Therapy in Pompe Disease
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NCT03112889CompletedConditions: Glycogen Storage Disease Type V; McArdle Disease
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NCT03045042Unknown statusConditions: Late Onset Pompe Disease; Pompe Disease
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NCT03019406Active, not recruitingConditions: Glycogen Storage Disease Type II-Pompe's Disease
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NCT02950298Active, not recruitingConditions: Pompe Disease; Glycogen Storage Disease II
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NCT02904395CompletedConditions: Pompe's Disease
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NCT02903654CompletedConditions: Pompe's Disease
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NCT02898753TerminatedConditions: Pompe Disease
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NCT02838368CompletedConditions: Pompe Disease
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NCT02824068Enrolling by invitationConditions: Pompe Disease
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NCT02801539CompletedConditions: Glycogen Storage Disease Type II
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NCT02782741Active, not recruitingConditions: Glycogen Storage Disease Type II;Pompe's Disease
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NCT02765828CompletedConditions: Myopathy; Neuropathy; Glycogen Storage Disease Type II (Late-onset Pompe Disease)
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NCT02761421Unknown statusConditions: Glycogen Storage Disease Type II
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NCT02746718Unknown statusConditions: Pompe Disease
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NCT02742298Active, not recruitingConditions: Pompe Disease
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NCT02708784Unknown statusConditions: Glycogen Storage Disease Type 2; Dystrophia Myotonica
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NCT02675465Active, not recruitingConditions: Pompe Disease
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NCT02654886CompletedConditions: Pompe Disease; Muscle Weakness
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NCT02635269Active, not recruitingConditions: Metabolism, Inborn Errors; Lipid Metabolism, Inborn Errors; Carbohydrate Metabolism, Inborn Errors; Long-Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency; Glycogenin-1 Deficiency (Glycogen Storage Disease Type XV); Carnitine Palmitoyl Transferase 2 Deficiency; VLCAD Deficiency; Medium-chain Acyl-CoA Dehydrogenase Deficiency; Multiple Acyl-CoA Dehydrogenase Deficiency; Carnitine Transporter Deficiency; Neutral Lipid Storage Disease; Glycogen Storage Disease Type II; Glycogen Storage Disease Type III; Glycogen Storage Disease Type IV; Glycogen Storage Disease Type V; Muscle Phosphofructokinase Deficiency; Phosphoglucomutase 1 Deficiency; Phosphoglycerate Mutase Deficiency; Phosphoglycerate Kinase Deficiency; Phosphorylase Kinase Deficiency; Beta Enolase Deficiency; Lactate Dehydrogenase Deficiency; Glycogen Synthase Deficiency
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NCT02527239Unknown statusConditions: Pompe's Disease
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NCT02525172Unknown statusConditions: Pompe Disease
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NCT02405598CompletedConditions: Pompe Disease
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NCT02405624Unknown statusConditions: Pompe Disease
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NCT02399748RecruitingConditions: Pompe Disease
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NCT02385162Active, not recruitingConditions: Fructose Metabolism, Inborn Errors; Glycogen Storage Disease; Glycogen Storage Disease Type I; Glycogen Storage Disease Type II; Glycogen Storage Disease Type III; Glycogen Storage Disease Type IV; Glycogen Storage Disease Type V; Glycogen Storage Disease Type VI; Glycogen Storage Disease Type VII; Glycogen Storage Disease Type VIII
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NCT02363153RecruitingConditions: Pompe Disease; Glycogen Storage Disease Type II; Lysosomal Storage Diseases
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NCT02357225TerminatedConditions: Pompe Disease
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NCT02354651RecruitingConditions: Pompe Disease
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NCT02354664CompletedConditions: Pompe Disease