drugset / Trial / NCT07668804

A Study to Evaluate the Safety and Effect of TO-O-1007 Intravitreal Implant in Subjects With Geographic Atrophy

NCT07668804 ↗

Phase 1/2 Recruiting 31 enrolled Theratocular Biotek Co.
RandomizedParallel-groupSingle-blindTreatment

Summary

This study will evaluate the safety, tolerability, pharmacokinetics, and preliminary efficacy of TO-O-1007, a biodegradable sustained-release intravitreal implant, for the treatment of Geographic Atrophy (GA) secondary to Age-related Macular Degeneration (AMD). A long-acting intravitreal implant providing sustained delivery of API over 6 months may slow the progression of GA lesions while reducing treatment burden associated with frequent intravitreal injections. TO-O-1007 may offer a convenient treatment option with the potential to preserve retinal structure and visual function while maintaining an acceptable safety profile.

Timeline

Start
2026-06-02
Primary completion
2027-08-31
Completion
2027-12-31

Drugs

EvaluationDrugModalityDoseRoute
Subject TO-O-1007 Unknown — Intravitreal