drugset / Trial / NCT04522167

Efficacy and Safety of the Aflibercept FYB203 Biosimilar in Comparison to Eylea® in Patients With Neovascular Age-Related Macular Degeneration

NCT04522167

Phase 3 Completed 434 enrolled Bioeq GmbH
RandomizedParallel-groupQuadruple-blindTreatment

Summary

This is a randomized, double-masked, multicenter study to evaluate the efficacy and safety of FYB203 compared to Eylea® in patients with neovascular age related macular degeneration.

Timeline

Start
2020-07-21
Primary completion
2022-06-23
Completion
2023-05-18

Drugs

EvaluationDrugModalityDoseRoute
Comparator Aflibercept Protein / enzyme biologic 2 mg Intravitreal
Comparator Aflibercept Protein / enzyme biologic 2 mg