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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
Study of Serine Supplementation to Protect Vision in MacTelMacular Telangiectasia Type 2 (MacTel)Not yet recruitingPhase 32026-01-15NCT07342439
An Observational Study in Subjects to Follow the Progression of Stargardt Disease Type 1 (STGD1) Caused by Bi-Allelic Autosomal Recessive Mutations in the ABCA4 GeneCongenital, Hereditary, and Neonatal Diseases and Abnormalities, Eye Diseases, Hereditary, Stargardt disease, eye disorder, hereditary disease, macular degeneration, retinal degeneration, retinal disorderRecruitingNot stated2025-09-19NCT06435000