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Clinical Trial 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).


Clinical Trial Description

This is a Phase 3, prospective, randomized, double-masked, sham-controlled, two-arm, multicenter study evaluating the efficacy and safety of repeated intravitreal dosing of KSI-301 5 mg in participants with moderately severe to severe non-proliferative diabetic retinopathy (NPDR). The primary endpoint will be assessed at Week 48; additional secondary endpoints for efficacy will be assessed at Week 48, Week 96 and if applicable, over time. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05066230
Study type Interventional
Source Kodiak Sciences Inc
Contact Kodiak Sciences Inc.
Phone (650) 281-0850
Email [email protected]
Status Recruiting
Phase Phase 3
Start date August 30, 2021
Completion date November 1, 2024

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