drugset / Trial / NCT06659445

Study to Evaluate Efficacy and Safety of ONL1204 in Patients With GA Associated With AMD

NCT06659445

Phase 2 Recruiting 324 enrolled ONL Therapeutics
RandomizedParallel-groupDouble-blindTreatment

Summary

The purpose of this study is to collect efficacy and safety information of intravitreal injection for 3 experimental arms, including 2 dose levels of ONL1204 and 2 treatment frequencies in patients with GA associated with AMD. GA associated with AMD is one of the world's leading causes of visual disability and legal blindness globally. Associated with aging, cigarette smoking, obesity, diets low in certain nutrients, a lifestyle related to cardiac risk, and a growing list of genetic factors, AMD is becoming an increasingly prevalent public health concern, especially as the global population ages. ONL1204 is a first-in-class inhibitor of fragment apoptosis stimulator receptor-mediated cell death that has demonstrated protection of multiple retinal cell types in numerous preclinical models of retinal disease, including models of dry AMD.

Timeline

Start
2025-10-28
Primary completion
2028-11
Completion
2028-11

Drugs

EvaluationDrugModalityDoseRoute
Comparator Avacincaptad Pegol Aptamer 2 mg Intravitreal
Subject XELAFASLATIDE Protein / enzyme biologic 100 ug Intravitreal
Subject XELAFASLATIDE Protein / enzyme biologic 200 ug Intravitreal