drugset / Trial / NCT04560790

Safety and Efficacy of CRISPR/Cas9 mRNA Instantaneous Gene Editing Therapy to Treat Refractory Viral Keratitis

NCT04560790

NaSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to evaluate the safety, tolerability and efficacy of a single escalating doses of BD111 CRISPR/Cas9 mRNA Instantaneous Gene Editing Therapy administered via corneal injection in participants with refractory herpetic viral keratitis.

Timeline

Start
2020-11-04
Primary completion
2022-07-05
Completion
2022-07-05

Drugs

EvaluationDrugModalityDoseRoute
Subject BD111 CRISPR / gene editing 0.2 ml Other