drugset / Trial / NCT05750589

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

NCT05750589

Phase 3 Not yet recruiting 240 enrolled iRenix Medical, Inc.
RandomizedParallel-groupDouble-blindTreatment

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.

Timeline

Start
2026-09-01
Primary completion
2027-01-31
Completion
2027-12-31

Drugs

EvaluationDrugModalityDoseRoute
Subject IRX-101 Unknown
Comparator Providone-Iodine Unknown

Indications