drugset / Trial / NCT02032173

Efficacy and Safety of Lucentis® Use in Patients With Diabetic Macular Edema Evaluating a Spaced Out Follow-up After Intensive Treatment Phase

NCT02032173

Phase 3 Terminated 31 enrolled Novartis Pharmaceuticals
NaSingle-groupOpen-labelTreatment

Summary

The study was designed to assess the efficacy and safety of Lucentis® (ranibizumab 0.5 mg) in diabetic patients presenting with reduced visual acuity due to diabetic macular edema and evaluating spacing out of follow-up after initial intensive treatment phase.

Timeline

Start
2014-05-19
Primary completion
2015-04-29
Completion
2015-04-29

Drugs

EvaluationDrugModalityDoseRoute
Subject Ranibizumab Monoclonal antibody 0.5 mg Intravitreal