NCT06196827

A Multi-center Clinical Study to Evaluate the Safety, Tolerability, and Efficacy of rAAV2-RPE65 Gene Therapy (LX101) in Subjects With Biallelic RPE65 Mutation-associated Inherited Retinal Dystrophy

Study Summary

The purpose of the study is to evaluate the safety, tolerability and efficacy of LX101 in subjects with biallelic RPE65 mutation-associated inherited retinal dystrophy.

Want to learn more about this trial?

Request More Info

Interventions

LX101GENETIC
Subretinal Administration

Study Locations

FacilityCityStateCountry
Beijing Tongren Hospital, Capital Medical UniversityBeijingChina
Shanghai General HospitalShanghaiChina

Official Trial Information

View on ClinicalTrials.gov

Data sourced from ClinicalTrials.gov. Last updated: April 14, 2026