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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
A Study of AAVB-039 in Participants With Stargardt Disease (STGD1)Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Eye Diseases, Hereditary, Stargardt disease, eye disorder, hereditary disease, macular degeneration, retinal degeneration, retinal disorderRecruitingPhase 1 / Phase 22026-09-30NCT07161544