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Pompe disease (also known as glycogen storage disease type II) is caused by a deficiency of a critical enzyme in the body called acid alpha-glucosidase (GAA). Normally, GAA is used by the body's cells...
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Lead Sponsor
Genzyme, a Sanofi Company
NCT06666413 · Glycogen Storage Disease Type II, Pompe's Disease
NCT07136844 · Neuromuscular Diseases, Obesity (Disorder), and more
NCT06616545 · Glycogen Storage Disease Type III
NCT04093349 · Pompe Disease, Pompe Disease (Late-onset), and more
NCT04990388 · Glycogen Storage Disease Type III
University of Alabama
Birmingham, Alabama
Shands Hospital at the University of Florida
Gainesville, Florida
Miami Children's Hospital
Miami, Florida
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This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
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