Vall d'Hebron Barcelona Hospital Campus

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Trial	Conditions	Status	Phase	Updated	More info	NCT ID
Phase I/II/III Gene Transfer Clinical Trial of scAAV9.U1a.hSGSH	Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Mucopolysaccharidosis III, Nutritional and Metabolic Diseases, Skin and Connective Tissue Diseases, connective tissue disorder, cutaneous mucinosis, hereditary disease, inborn carbohydrate metabolic disorder, inborn errors of metabolism, lysosomal storage disease, metabolic disease, mucopolysaccharidosis, mucopolysaccharidosis type 3A	Recruiting	Phase 2 / Phase 3	2026-09-22		NCT02716246

Clinical trials