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Efficacy and Safety of LX101 for Inherited Retinal Dystrophy Associated With RPE65 Mutations
Sponsor: Innostellar Biotherapeutics Co.,Ltd
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
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