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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
Rate of Progression of PCDH15-Related Retinal Degeneration in Usher Syndrome 1FCongenital, Hereditary, and Neonatal Diseases and Abnormalities, Eye Diseases, Hereditary, autosomal recessive nonsyndromic hearing loss 23, eye disorder, hereditary disease, inherited retinal dystrophy, retinal degeneration, retinal disorder, retinitis pigmentosaActive, not recruitingNot stated2026-02-04NCT04765345