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Clinical Trial 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)


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 visual impairment due to treatment-naïve neovascular (wet) age-related macular degeneration (wAMD) The primary endpoint will be assessed as an average of Weeks 40, 44, and 48; additional secondary endpoints for efficacy will be assessed by visit over time ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04964089
Study type Interventional
Source Kodiak Sciences Inc
Contact
Status Completed
Phase Phase 3
Start date June 23, 2021
Completion date April 6, 2023

See also
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