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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
Interventional Study of Implantation of hESC-derived RPE in Patients With RP Due to Monogenic MutationCongenital, Hereditary, and Neonatal Diseases and Abnormalities, Eye Diseases, Hereditary, eye disorder, hereditary disease, inherited retinal dystrophy, retinal degeneration, retinal disorder, retinitis pigmentosaActive, not recruitingPhase 1 / Phase 22023-11-28NCT03963154