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rhGAA in Patients With Infantile-onset Glycogen Storage Disease-II (Pompe Disease)
This study has been completed.
Study NCT00053573   Information provided by Genzyme

First Received on January 31, 2003.   Last Updated on March 14, 2011   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
Myozyme
Sponsors listed in this trial
Genzyme


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