drugset / Trial / NCT05309135

A Safety and Efficacy Study of Corneal Injection for Endothelial Dysfunction Using Human Corneal Endothelial Cell Therapy in Subjects With Corneal Edema Secondary to Endothelial Dysfunction

NCT05309135 ↗

Phase 1 Completed 22 enrolled Aurion Biotech
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The purpose of this study is to assess the safety of a fixed dose of human corneal endothelial cells when administered with varying concentrations of Rho kinase inhibitor (Y-27632) in patients with corneal edema secondary to endothelial dysfunction.

Timeline

Start
2022-03-24
Primary completion
2023-03-09
Completion
2023-03-09

Drugs

EvaluationDrugModalityDoseRoute
Comparator HCEC-1 Cell therapy — —
Subject Y27632 Small molecule — —

Indications