drugset / Trial / NCT02540954

Efficacy and Safety of Two Different Aflibercept Regimens in Subjects With Neovascular Age-related Macular Degeneration (nAMD)

NCT02540954

Phase 3 Completed 336 enrolled Bayer
RandomizedParallel-groupOpen-labelTreatment

Summary

To compare the efficacy of 2 mg aflibercept administered by two different intravitreal (IVT) treatment regimens to subjects with neovascular age-related macular degeneration (nAMD)

Timeline

Start
2015-09-29
Primary completion
2019-12-24
Completion
2020-06-04

Drugs

EvaluationDrugModalityDoseRoute
Subject Aflibercept Protein / enzyme biologic 2 mg Intravitreal

Indications