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A Study of the Safety and Pharmacokinetics of rhGAA in Siblings With Glycogen Storage Disease Type II
This study has been completed.
Study NCT00051935   Information provided by Genzyme
First Received: January 17, 2003   Last Updated: July 6, 2009   History of Changes
Related Studies can be found by searching for the Conditions, Interventions, and Sponsors found in this study:
Conditions listed in this trial
Glycogen Storage Disease Type II
Pompe Disease
Acid Maltase Deficiency Disease
Glycogenosis 2
Additional conditions recognized in this trial
Deficiency Diseases
Glycogen Storage Disease
Metabolic Diseases
More general conditions related to this trial
Brain Diseases
Brain Diseases, Metabolic
Brain Diseases, Metabolic, Inborn
Carbohydrate Metabolism, Inborn Errors
Central Nervous System Diseases
Genetic Diseases, Inborn
Lysosomal Storage Diseases
Lysosomal Storage Diseases, Nervous System
Malnutrition
Metabolism, Inborn Errors
Nervous System Diseases
Nutrition Disorders
Interventions listed in this trial
Alglucosidase alfa
Sponsors listed in this trial
Genzyme


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