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Clinical Trial Summary

This study is a longitudinal assessment using a classic dose-escalation study design to assess the safety and maximal tolerated dose (MTD) of locally delivered allogeneic mesenchymal stromal cells (MSC) for promoting corneal repair. The study will be conducted at Illinois Eye and Ear Infirmary located at University of Illinois at Chicago. The study will use digital conjunctival and corneal photography and corneal Scheimpflug Imaging, densitometry, and pachymetry for assessment of safety and corneal wound healing.


Clinical Trial Description

The "Safety of Locally Delivered Allogeneic Mesenchymal Stem Cells for Promoting Corneal Repair Study" otherwise known as the "MSC Study," is designed to assess the safety of allogeneic bone marrow-derived MSC secreted factor on the ocular surface via subconjunctival injection of MSC, and also obtain a preliminary observation on the following: 1. Epithelial barrier integrity and/or wound closure. 2. Development of Scarring. 3. Final Visual Acuity. The objective is to improve clinical outcomes in significant non-healing corneal wounds. To achieve these goals, the MSC Study will include a Phase I dose-escalation safety study. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04626583
Study type Interventional
Source University of Illinois at Chicago
Contact Ali R Djalilian, MD
Phone 312-996-8937
Email adjalili@uic.edu
Status Recruiting
Phase Phase 1
Start date March 5, 2021
Completion date December 30, 2024

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