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Clinical Trial Summary

This is a randomized, double-masked study to evaluate the tolerability and safety of IRX-101 versus 5% povidone-iodine (PI) in subjects receiving intravitreal anti-VEGF injections. The study will be conducted in up to 15 centers in the United States (US).


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05747430
Study type Interventional
Source iRenix Medical, Inc.
Contact Stephen Smith, MD
Phone 650-785-1316
Email stephen@irenix.com
Status Recruiting
Phase Phase 2
Start date February 22, 2023
Completion date August 30, 2024

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