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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
Study of ALK-001 on the Progression of Stargardt DiseaseCongenital, Hereditary, and Neonatal Diseases and Abnormalities, Eye Diseases, Hereditary, Stargardt disease, eye disorder, hereditary disease, macular degeneration, retinal degeneration, retinal disorderRecruitingPhase 32026-09-18NCT07419334