drugset / Trial / NCT04592419

A Study to Evaluate the Efficacy, Durability, and Safety of KSI-301 Compared to Aflibercept in Patients With Macular Edema Due to Retinal Vein Occlusion (RVO)

NCT04592419

Phase 3 Completed 568 enrolled Kodiak Sciences Inc
RandomizedParallel-groupTriple-blindTreatment

Summary

This Phase 3 study will evaluate the efficacy, durability, and safety of KSI-301 compared to aflibercept, in participants with macular edema due to treatment-naïve branch (BRVO) or central retinal vein occlusion (CRVO).

Timeline

Start
2020-09-25
Primary completion
2022-06-10
Completion
2023-01-19

Drugs

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