University of Coloardo Anschutz Medical Campus

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Trial	Conditions	Status	Phase	Updated	More info	NCT ID
Feasibility of Study of Empagliflozin in Patients With Autosomal Dominant Polycystic Kidney Disease	Abnormalities, Multiple, Ciliopathies, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Female Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Male Urogenital Diseases, Urogenital Diseases, autosomal dominant polycystic kidney disease, cystic kidney disease, hereditary disease, kidney disorder, polycystic kidney disease, urinary system disorder	Active, not recruiting	Phase 2	2026-05-01		NCT05510115

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