congenital hereditary endothelial dystrophy of cornea

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Trial	Conditions	Status	Phase	Updated	More info	NCT ID
Study of EO2002 in Subjects With Corneal Edema Secondary to Corneal Endothelial Dysfunction	Chandler syndrome, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Corneal Endothelial Cell Loss, Corneal Endothelial Dystrophy 1, Eye Diseases, Hereditary, Eye Manifestations, Fuchs' endothelial dystrophy, Pathologic Processes, Pathological Conditions, Signs and Symptoms, Postoperative Complications, Signs and Symptoms, congenital hereditary endothelial dystrophy of cornea, corneal disorder, corneal dystrophy, corneal edema, eye disorder, hereditary disease	Recruiting	Phase 2	2026-10-09		NCT07729137

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