drugset / Trial / NCT04964089

A Study to Evaluate the Efficacy and Safety of Intravitreal KSI-301 Compared With Intravitreal Aflibercept in Participants With Neovascular (Wet) Age-related Macular Degeneration (wAMD)

NCT04964089

Phase 3 Completed 557 enrolled Kodiak Sciences Inc
RandomizedParallel-groupTriple-blindTreatment

Summary

This Phase 3 study will evaluate the efficacy and safety of KSI-301 compared to aflibercept, in participants with neovascular (wet) age-related macular degeneration (wAMD)

Timeline

Start
2021-06-23
Primary completion
2023-03-28
Completion
2023-04-06

Drugs

EvaluationDrugModalityDoseRoute
Comparator Aflibercept Protein / enzyme biologic 2 mg Intravitreal
Subject Tarcocimab tedromer Protein / enzyme biologic 5 mg Intravitreal