drugset / Trial / NCT00320788

Safety and Efficacy of Repeated Intravitreal Administration of Vascular Endothelial Growth Factor (VEGF) Trap in Patients With Wet Age-Related Macular Degeneration (AMD)

NCT00320788

Phase 2 Completed 159 enrolled Regeneron Pharmaceuticals Bayer · collab
RandomizedParallel-groupTriple-blindTreatment

Summary

This study examines the effect of intravitreally administered VEGF Trap in patients with wet AMD. The purpose of this trial is to assess the ocular and systemic safety and tolerability of repeated intravitreal doses of VEGF Trap in patients with subfoveal choroidal neovascularization (CNV) due to AMD.

Timeline

Start
2006-04
Primary completion
2008-06
Completion
2008-08

Drugs

EvaluationDrugModalityDoseRoute
Subject Aflibercept Protein / enzyme biologic 0.5 mg Intravitreal
Subject Aflibercept Protein / enzyme biologic 2 mg Intravitreal
Subject Aflibercept Protein / enzyme biologic 4 mg Intravitreal