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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
Personalized Antisense Oligonucleotide Therapy for a Single Participant With PRPH2 Mutation Associated With Retinal Dystrophyeye disorder, inherited retinal dystrophy, retinal degeneration, retinal disorderActive, not recruitingPhase 1 / Phase 22025-09-16NCT07177196

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1 results · Page 1 of 1

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Research sitesCityCountryLinked trials
University of California San DiegoSan DiegoUnited States22