drugset / Trial / NCT00967213

Combination of Ranibizumab and Verteporfin Therapy in Neovascular Age-related Macular Degeneration

NCT00967213

Phase 3 Completed 10 enrolled Novartis
NaSingle-groupOpen-label

Summary

The purpose of this study is to evaluate changes in preferential hyperacuity perimeter (PHP) and fundus autofluorescence (FAF) in patients with neovascular age-related macular degeneration receiving combination of ranibizumab (LucentisTM) and verteporfin (Visudyne®) therapy

Timeline

Start
2006-08
Primary completion
2008-02
Completion

Drugs

EvaluationDrugModalityDoseRoute
Subject Ranibizumab Monoclonal antibody 0.3 mg Intravitreal