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An Observational Study Evaluating Anti-Idursulfase Serum Antibody Response in Hunter Syndrome Patients
This study has been completed.
Study NCT00882921   Information provided by Shire Human Genetic Therapies, Inc.

First Received on April 16, 2009.   Last Updated on May 22, 2013   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
Hunter Syndrome
Additional conditions recognized in this trial
Mucopolysaccharidosis II
More general conditions related to this trial
Carbohydrate Metabolism, Inborn Errors
Connective Tissue Diseases
Genetic Diseases, Inborn
Genetic Diseases, X-Linked
Heredodegenerative Disorders, Nervous System
Lysosomal Storage Diseases
Mental Retardation
Mental Retardation, X-Linked
Metabolic Diseases
Metabolism, Inborn Errors
Mucinoses
Mucopolysaccharidoses
Nervous System Diseases
Neurobehavioral Manifestations
Neurologic Manifestations
Interventions listed in this trial
Idursulfase
Sponsors listed in this trial
Shire Human Genetic Therapies, Inc.


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