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ACTIVE NOT RECRUITING
NCT07054632
PHASE3

Efficacy and Safety of LX101 for Inherited Retinal Dystrophy Associated With RPE65 Mutations

Sponsor: Innostellar Biotherapeutics Co.,Ltd

View on ClinicalTrials.gov

Summary

The purpose of the study is to evaluate the efficacy and safety of LX101 in subjects with biallelic RPE65 mutation-associated inherited retinal dystrophy. This is an open-label, multicenter, randomized controlled Phase III clinical trial. Subjects were randomly assigned in a 1:1 ratio to either the intervention group or the control group. Subjects in the intervention group received subretinal injection of LX101, while those in the control group received no treatment.

Official title: Efficacy and Safety of Gene Therapy rAAV-RPE65 (LX101) in Biallelic RPE65 Mutation-associated Inherited Retinal Dystrophy: a Phase III, Multicenter, Randomized Controlled Trial (STAR)

Key Details

Gender

All

Age Range

6 Years - Any

Study Type

INTERVENTIONAL

Enrollment

30

Start Date

2023-09-13

Completion Date

2029-08

Last Updated

2026-03-05

Healthy Volunteers

No

Interventions

GENETIC

LX101

Subretinal administration of LX101 to the study eye

Locations (4)

Zhongshan Ophthalmic Center, Sun Yat sen University

Guangzhou, Guangdong, China

Southwest Hospital of AMU

Chongqing, China

Shanghai General Hospital

Shanghai, China

Tianjin Medical University Ophthalmology Hospital

Tianjin, China