drugset / Trial / NCT05066230

A Study to Evaluate the Efficacy and Safety of Intravitreal KSI-301 in Non-proliferative Diabetic Retinopathy (NPDR)

NCT05066230

Phase 3 Terminated 253 enrolled Kodiak Sciences Inc
RandomizedParallel-groupTriple-blindTreatment

Summary

This Phase 3 Study will evaluate the efficacy and safety of KSI-301 in participants with moderately severe to severe non-proliferative diabetic retinopathy (NPDR).

Timeline

Start
2021-09-07
Primary completion
2023-08-03
Completion
2023-08-31

Drugs

EvaluationDrugModalityDoseRoute
Subject Tarcocimab tedromer Protein / enzyme biologic 5 mg Intravitreal

Indications