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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
BS01 in Patients With Retinitis PigmentosaCongenital, Hereditary, and Neonatal Diseases and Abnormalities, Eye Diseases, Hereditary, eye disorder, hereditary disease, inherited retinal dystrophy, retinal degeneration, retinal disorder, retinitis pigmentosaRecruitingPhase 1 / Phase 22026-01-23NCT04278131

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OrganizationsLinked trials
Bionic Sight LLC2

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Research sitesCityCountryLinked trials
New Jersey RetinaTeaneckUnited States3