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Clinical Trial Summary

This clinical trial is a Phase 1, multiple administration, dose-escalasion clinical trial of human umbilical cord-derived mesenchymal stem cells for the treatment of decompensated cirrhosis. The primary objective of this study is to assess the safety of intravenous infusion of human umbilical cord-derived mesenchymal stem cells in patients with decompensated cirrhosis.


Clinical Trial Description

Decompensated cirrhosis has a high overall mortality rate. There is unmet need for safe and alternative therapeutic potions. This clinical trial is a Phase 1, multiple administration, dose-escalasion clinical trial of human umbilical cord-derived mesenchymal stem cells for the treatment of decompensated cirrhosis. The primary objective of this study is to assess the safety of intravenous infusion of human umbilical cord-derived mesenchymal stem cells in patients with decompensated cirrhosis.In order to illustrate the safety and effectiveness of human umbilical cord-derived mesenchymal stem cells and the patient's dose tolerance to human umbilical cord-derived mesenchymal stem cells. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05984303
Study type Interventional
Source Beijing 302 Hospital
Contact Lei Shi, MD,PhD
Phone 86-10-66949623
Email shilei302@126.com
Status Not yet recruiting
Phase Phase 1
Start date August 30, 2023
Completion date August 30, 2025

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