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Pompe disease 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 to break down glycogen (a stored form of sugar) ...
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Lead Sponsor
Genzyme, a Sanofi Company
NCT07282847 · Pompe Disease (Late-onset), Pompe Disease Late-Onset, and more
NCT06666413 · Glycogen Storage Disease Type II, Pompe's Disease
NCT06121011 · Pompe Disease
NCT04808505 · Glycogen Storage Disease Type II Infantile Onset
NCT07136844 · Neuromuscular Diseases, Obesity (Disorder), and more
Duke University Medical Center
Durham, North Carolina
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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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