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Clinical Trial Summary

This is a multicenter, randomized, controlled, open-label phase 1/2 clinical study conducted in China to evaluate the efficacy, safety and tolerability of hiHep cell-based bio-artificial liver support system (HepaCure) plus DPMAS versus DPMAS alone in Chinese subjects with acute-on-chronic liver failure(ACLF). Phase 1 is a multicenter, open label study to evaluate the safety and tolerability of single dose and multiple doses of HepaCure with different treatment duration plus DPMAS in ACLF subjects respectively.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05989958
Study type Interventional
Source Hexaell Biotech Co., Ltd.
Contact YU Chen, MD
Phone 86-13391663900
Email chybeyond@163.com
Status Recruiting
Phase Phase 1
Start date September 22, 2023
Completion date September 2024

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