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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
Study of EO2002 in Subjects With Corneal Edema Secondary to Corneal Endothelial DysfunctionChandler 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 diseaseRecruitingPhase 22026-10-09NCT07729137

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OrganizationsLinked trials
Emmecell3

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Research sitesCityCountryLinked trials
Atlanta, GeorgiaAtlantaUnited States1
Carmel, IndianaCarmelUnited States1
Chicago, IllinoisChicagoUnited States1
Garden City, NYGarden CityUnited States1
Kansas City, MissouriKansas CityUnited States1
Largo, FloridaLargoUnited States1
Minnetonka, MinnesotaMinnetonkaUnited States1
Overland Park, KansasOverland ParkUnited States1
Salt Lake City, UtahSalt Lake CityUnited States2
Torrance, CaliforniaTorranceUnited States1