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Safety and Efficacy Evaluation of LX111 Gene Therapy in nAMD Patients
Sponsor: Shanghai General Hospital, Shanghai Jiao Tong University School of Medicine
Summary
The goal of this study is to evaluate the safety and efficacy of LX111 treatment of nAMD. This study will enroll subjects aged ≥ 50 vears old to receive a single unilateral intravitreal (lVT) injection of LX111 to evaluate its safety and efficacy.
Official title: An Exploratory Clinical Study Evaluating LX111 Gene Therapy in Patients With Neovascular Age-related Macular Degeneration (nAMD)
Key Details
Gender
All
Age Range
50 Years - Any
Study Type
INTERVENTIONAL
Enrollment
10
Start Date
2025-07-02
Completion Date
2029-12-30
Last Updated
2026-03-10
Healthy Volunteers
No
Interventions
LX111 Injection
Qualified subjects will receive a single unilateral intravitreal injection of LX111 at Day 0.
Locations (1)
Shanghai General Hospital, Shanghai Jiao Tong University School of Medicine
Shanghai, China