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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
Phase 1 Study of C.001 in Retinal DegenerationCongenital, Hereditary, and Neonatal Diseases and Abnormalities, Eye Diseases, Hereditary, Geographic Atrophy, Stargardt disease, age-related macular degeneration, eye disorder, hereditary disease, macular degeneration, retinal degeneration, retinal disorderRecruitingPhase 12026-08-17NCT07594236