drugset / Trial / NCT04270747

A Study to Understand Effectiveness and Safety of ABP 938 Compared to Aflibercept (Eylea®) in Patients Suffering With Neovascular Age-related Macular Degeneration [Neovascular (Wet) AMD]

NCT04270747

Phase 3 Completed 576 enrolled Amgen Parexel · collab
RandomizedParallel-groupTriple-blindTreatment

Summary

The purpose of this study is to compare the efficacy and safety of ABP 938 versus Aflibercept (Eylea®) in the treatment of neovascular age-related macular degeneration. Subjects will be randomized in a masked 1:1 ratio to receive 2 mg (0.05 mL) of either ABP 938 (Treatment Group A) or aflibercept (Treatment Group B) administered by intravitreal (IVT) injection.

Timeline

Start
2020-06-22
Primary completion
2022-07-18
Completion
2023-01-30

Drugs

EvaluationDrugModalityDoseRoute
Subject ABP 938 Unknown 2 mg Intravitreal
Comparator Aflibercept Protein / enzyme biologic 2 mg Intravitreal