drugset / Trial / NCT06176352

A Study to Evaluate the Efficacy and Safety of Faricimab in Patients With Choroidal Neovascularization Secondary to Pathologic Myopia

NCT06176352

Phase 3 Completed 280 enrolled Hoffmann-La Roche
RandomizedParallel-groupTriple-blindTreatment

Summary

This is a Phase III, multicenter, randomized, double-masked, active comparator-controlled study evaluating the efficacy and safety of faricimab in patients with myopic choroidal neovascularization (CNV). This non-inferiority study will compare 6.0 mg faricimab versus 0.5 mg ranibizumab administered at a pro-re-nata (PRN) dosing regimen after an initial active IVT treatment administration at randomization (Day 1).

Timeline

Start
2024-03-06
Primary completion
2025-09-11
Completion
2026-05-22

Drugs

EvaluationDrugModalityDoseRoute
Subject Faricimab Monoclonal antibody 6 mg Intravitreal
Comparator Ranibizumab Monoclonal antibody 0.5 mg Intravitreal