Washington University/Barnes Jewish Hospital

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Trial	Conditions	Status	Phase	Updated	More info	NCT ID
Study of YOLT-203 in Children and Adults With Primary Hyperoxaluria Type 1 (PH1)	Calculi, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Female Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Hyperoxaluria, Kidney Calculi, Male Urogenital Diseases, Nutritional and Metabolic Diseases, Pathological Conditions, Anatomical, Pathological Conditions, Signs and Symptoms, Urinary Calculi, Urogenital Diseases, hereditary disease, inborn carbohydrate metabolic disorder, inborn errors of metabolism, kidney disorder, metabolic disease, nephrolithiasis, primary hyperoxaluria, primary hyperoxaluria type 1, urinary system disorder, urolithiasis	Recruiting	Phase 2	2026-10-09		NCT07587021

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