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Clinical Trial Summary

This Phase 3 study will evaluate the efficacy, durability, and safety of KSI-301 compared to aflibercept in participants with treatment-naïve DME.


Clinical Trial Description

This is a Phase 3, prospective, randomized, double-masked, two-arm, multi-center non-inferiority study evaluating the efficacy and safety of repeated intravitreal dosing of KSI-301 5 mg in participants with treatment-naïve DME. The primary endpoint will be assessed at Year 1; additional secondary endpoints for efficacy will be assessed at Years 1 and 2. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04611152
Study type Interventional
Source Kodiak Sciences Inc
Contact
Status Terminated
Phase Phase 3
Start date September 30, 2020
Completion date August 31, 2023

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