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Clinical Trial Summary

This is a single center, randomized, double-blind, placebo-controlled, dose-Escalation clinical study to investigate the safety and efficacy of EPCs transplantation in Acute ischemic stroke.


Clinical Trial Description

Acute ischemic stroke (AIS) occurs when blood flow to the brain is blocked by a clot or mechanical event and is the most common type of stroke. However, due to the limitation of time and contraindications, only a few patients with AIS are eligible candidates. Endothelial progenitor cells (EPCs) have the potential to reduce brain damage from AIS. They can effectively repair endothelial cells with vascular injuries by directly differentiating into endothelial cells or releasing corresponding regulatory factors, which is a potentially important means for the prevention and treatment of a series of vascular system disorders. The introduction of induced pluripotent stem cells (iPSCs) technology provides a highly feasible option for clinical application of EPCs. Allogeneic iPSC-EPCs can be produced on a large scale to provide enough cells, fundamentally solving the problem of insufficient dosage, and making them a feasible clinical option for treatment of AIS. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05993884
Study type Interventional
Source Allife Medical Science and Technology Co., Ltd.
Contact Xingquan Zhao, Dr
Phone 01059978555
Email ttyyirb@163.com
Status Not yet recruiting
Phase Phase 1
Start date August 15, 2023
Completion date August 15, 2025

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