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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
Study to Evaluate ACDN-01 in ABCA4-related Stargardt Retinopathy (STELLAR)Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Eye Diseases, Hereditary, Juvenile Macular Degeneration, Stargardt Disease 1, Stargardt disease, cone-rod dystrophy, eye disorder, hereditary disease, inherited retinal dystrophy, macular degeneration, retinal degeneration, retinal disorderRecruitingPhase 1 / Phase 22026-10-07NCT06467344