Birmingham

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Trial	Conditions	Status	Phase	Updated	More info	NCT ID
A Gene Transfer Study for Late-Onset Pompe Disease (RESOLUTE)	Brain Diseases, Metabolic, Brain Diseases, Metabolic, Inborn, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Lysosomal Storage Diseases, Nervous System, Nutritional and Metabolic Diseases, brain disorder, central nervous system disorder, disorder of glycogen metabolism, glycogen storage disease II, hereditary disease, inborn carbohydrate metabolic disorder, inborn errors of metabolism, lysosomal storage disease, metabolic disease, nervous system disorder	Active, not recruiting	Phase 1 / Phase 2	2024-11-27		NCT04093349

Clinical trials