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Safety and Tolerability of IRX-101 in Patients Receiving Intravitreal Injections — COMFORT  

Retinal Disease Clinical Trial

Official title:
Randomized, Controlled, Double-Masked Study to Evaluate the Efficacy of IRX-101 in Reducing Post-Intravitreal Pain and Corneal Epitheliopathy

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.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05750589
Study type Interventional
Source iRenix Medical, Inc.
Contact Stephen Smith, MD
Phone 650-785-1316
Email stephen@irenix.com
Status Recruiting
Phase Phase 3
Start date February 22, 2023
Completion date August 30, 2024
View Details
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