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ACTIVE NOT RECRUITING
NCT06817343
PHASE1

A Long-term Follow up Study of EXG102-031 in Patients With wAMD (Everest LTFU)

Sponsor: Exegenesis Bio

View on ClinicalTrials.gov

Summary

In neovascular (wet) age-related macular degeneration (nAMD), the macula, or the part of the eye that provides the clear, detailed central vision, is being affected by abnormal blood vessel growth and leakage. This leakage affects the vision over time and can lead to severe blurriness or blinding. EXG102-031 was made to block the extra vessel formation which would lead to less leakage affecting the vision. Before EXG102-031 can be tested for its efficacy (if it makes vision better), it must be tested to see if it is safely tolerated to confirm it can continue to be studied in more patients with nAMD. This study is designed to fulfill the long-term safety monitoring of EXG102-031. Participants that enroll in this long-term follow-up study have been treated with EXG102-031 under the main study (EXG102-031-211).

Official title: An Open-label, Long-term Follow-Up Study to Evaluate the Safety and Tolerability of Gene Therapy With EXG102-031 in Participants With Neovascular Age-related Macular Degeneration

Key Details

Gender

All

Age Range

Any - Any

Study Type

INTERVENTIONAL

Enrollment

12

Start Date

2024-09-10

Completion Date

2029-02

Last Updated

2026-04-08

Healthy Volunteers

No

Interventions

BIOLOGICAL

Aflibercept (2.0 mg)

PRN IVT Aflibercept

Locations (2)

Sierra Eye Associates

Reno, Nevada, United States

Erie Retina Research

Erie, Pennsylvania, United States