drugset / Trial / NCT05805007

Safety and Tolerability Study of Gene Editing Drug ZVS203e in Participants With Retinitis Pigmentosa

NCT05805007 ↗

Phase 0 Unknown 9 enrolled Peking University Third Hospital
NaSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to evaluate the safety, tolerability and efficacy of a single escalating doses of ZVS203e administered via subretinal injection in participants with RP caused by RHO site-specific gene mutation (RHO-RP).

Timeline

Start
2023-09-12
Primary completion
2026-04
Completion
2026-04

Drugs

EvaluationDrugModalityDoseRoute
Subject ZVS203e CRISPR / gene editing — Other

Indications