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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
NCT04174105 · Pompe Disease (Late-onset)
NCT03911505 · Pompe Disease (Late-onset)
NCT03694561 · Pompe Disease, Pompe Disease (Late-onset), and more
NCT04929002 · Glycogen Storage Disease, McArdle Disease, and more
NCT04093349 · Pompe Disease, Pompe Disease (Late-onset), and more
Hopital Raymond Poincare
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Data Source & Attribution
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.
Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.
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