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Clinical Trial Summary

Intravitreal topotecan has anti-inflammatory, anti-proliferative and anti-fibrotic activity that we hypothesize may exhibit high efficacy for the treatment of proliferative vitreoretinopathy (PVR) in patients with rhegmatogenous retinal detachment (RRD). A high efficacy for intravitreal topotecan has been exhibited in cell cultures of PVR. At the same time, intravitreal topotecan has been routinely used in the treatment of vitreous seeds from retinoblastoma. At doses of 5-30 micrograms per injection, no adverse events have been reported with the use of intravitreal topotecan. Therefore, the current prospective matched phase II trial aims to investigate the efficacy and safety of intravitreal topotecan for severe PVR in patients with RRD.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05523869
Study type Interventional
Source Unity Health Toronto
Contact Rajeev Muni, MD
Phone 416-867-7411
Email rajeev.muni@utoronto.ca
Status Recruiting
Phase Phase 2
Start date February 23, 2023
Completion date February 2025