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RECRUITING
NCT07053358
EARLY_PHASE1

Safety and Efficacy Evaluation of LX111 Gene Therapy in nAMD Patients

Sponsor: Shanghai General Hospital, Shanghai Jiao Tong University School of Medicine

View on ClinicalTrials.gov

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

GENETIC

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