Search for Clinical Trial Results
Glycogen Storage Disease - 49 Studies Found
Status | Study |
Recruiting |
Study Name: Effect of Motor Development, Motor Function and Electrophysiologic Findings of IOPD Under ERT Condition: Glycogen Storage Disease Type II Date: 2016-04-26 Interventions: Other: observation study observation study |
Withdrawn |
Study Name: High Protein and Exercise Therapy Plus Nocturnal Enteral Feeding in Juvenile-onset Pompe Disease Condition: Glycogen Storage Disease Type II Date: 2012-08-01 Interventions: Other: High Protein and Exercise Therapy along-with Nocturnal Enteral Feeding |
Completed |
Study Name: Extension Study of Long-term Safety and Efficacy of Myozyme in Patients With Pompe Disease Who Were Previously Enrolled in Genzyme Sponsored Enzyme Replacement Therapy (ERT) Studies Condition:
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Completed |
Study Name: Expanded Access Use of Myozyme (Alglucosidase Alfa) in Patients With Late-onset Pompe Disease Condition:
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Approved for marketing |
Study Name: Expanded Access Use of Myozyme (Alglucosidase Alfa) in Patients With Infantile-onset Pompe Disease Condition:
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Active, not recruiting |
Study Name: Comparison of the Effect of a Novel Starch (Glycosade) Versus Gastrostomy Tube-Dextrose Infusion on Overnight Euglycaemia Control in Children With Glycogen Storage Disease Type I: Open Label Demonstration Trial Condition:
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Completed |
Study Name: Newborn Screening Assay of Pompe's Disease Condition: Pompe Disease Date: 2008-07-09 Interventions: Other: Pompe disease newborn screening DBS will be tested for acid alpha-glucosidase (GAA)activity. Newb |
Terminated |
Study Name: Study to Evaluate the Safety of AT2220 in Pompe Disease Condition: Pompe Disease Date: 2008-05-30 Interventions:
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Completed |
Study Name: Safety and Efficacy of Clenbuterol on Motor Function in Individuals With Late-onset Pompe Disease and Receiving Enzyme Replacement Therapy Condition: Pompe Disease Date: 2013-09-11 Interventions:
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