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UnknownNCT05831007

Safety and Efficacy Study of LX102-C01 Treatment of Neovascular Age-Related Macular Degeneration (nAMD)

An Open Label Dose Escalation Clinical Trial to Evaluate the Safety and the Efficacy of LX102-C01 in Patients With Neovascular Age-Related Macular Degeneration (nAMD)

Status
Unknown
Phase
N/A
Study type
Interventional
Enrollment
6 (actual)
Sponsor
Shanghai General Hospital, Shanghai Jiao Tong University School of Medicine · Academic / Other
Sex
All
Age
50 Years
Healthy volunteers
Not accepted

Summary

The goal of this study is to evaluate the safety and efficacy of LX102-C01 treatment of nAMD. This study will enroll subjects aged ≥ 50 years old to receive a single unilateral intravitreal (IVT) injection of LX102-C01 to evaluate its safety and efficacy.

Conditions

Interventions

TypeNameDescription
GENETICLX102-C01 InjectionQualified subjects will receive a single unilateral intravitreal injection of LX102-C01 at Day 0 in the trial.

Timeline

Start date
2021-12-06
Primary completion
2023-06-01
Completion
2024-06-01
First posted
2023-04-26
Last updated
2023-04-26

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT05831007. Inclusion in this directory is not an endorsement.

Safety and Efficacy Study of LX102-C01 Treatment of Neovascular Age-Related Macular Degeneration (nAMD) (NCT05831007) · Clinical Trials Directory