drugset / Trial / NCT02698566

A Study in Patients With Neovascular Age Related Macular Degeneration or Macular Edema Secondary To Retinal Vein Occlusion to Evaluate Usability of the Ranibizumab (Lucentis®) Prefilled Syringe (PFS)

NCT02698566

Phase 3 Completed 35 enrolled Genentech, Inc.
NaSingle-groupOpen-labelOther

Summary

This is a multicenter study designed to evaluate usability of ranibizumab PFS in patients with neovascular age related macular degeneration or macular edema secondary to retinal vein occlusion.

Timeline

Start
2016-03-21
Primary completion
2016-04-05
Completion
2016-04-05

Drugs

EvaluationDrugModalityDoseRoute
Background Ranibizumab Monoclonal antibody 0.5 mg Intravitreal

Indications