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Expanded Access Use of Myozyme (Alglucosidase Alfa) in Patients With Late-Onset Pompe Disease
This study has been completed.
Study NCT00074932   Information provided by Genzyme
First Received: December 23, 2003   Last Updated: October 14, 2008   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
Glycogenosis 2
Additional conditions recognized in this trial
Glycogen Storage Disease
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
Metabolic Diseases
Metabolism, Inborn Errors
Nervous System Diseases
Interventions listed in this trial
Myozyme
Sponsors listed in this trial
Genzyme


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