Clinical trial

Mesenchymal Stem Cells-Derived Extracellular Vesicles (MSC-EV) in Acute-on-Chronic Liver Failure After Liver Transplantationa:a Prospective, Randomized, Controlled Clinical Study

Name
MSC-EV of ThirdSunYatSen
Description
Acute-on-chronic liver failure refers to a liver failure syndrome in which some patients with chronic liver disease with relatively stable liver function suffer from acute liver decompensation and liver failure due to the effects of various acute injury factors. Liver transplantation is the only curative treatment for this type of end-stage liver disease. The potential of MSCs to repair or regenerate damaged tissue and suppress immune responses makes them promising in the treatment of liver diseases, especially in the field of liver transplantation. Many studies have shown that MSC-based therapies can reduce the symptoms of liver disease due to their paracrine effects. Therefore, compared to the cells they derive from, mesenchymal stem cells-derived extracellular vesicles (MSC-EV) are gradually gaining attention for their enhanced safety, as they do not replicate or cause microvascular embolism, and can be easily stored without losing their properties. It represents a novel and effective cell-free therapeutic agent as alternative to cell-based therapies for liver diseases, and liver failure was also concerned. This study was designed to evaluate the safety and tolerability of MSC-EV in acute-on-chronic liver failure after liver transplantation.
Trial arms
Trial start
2023-09-30
Estimated PCD
2024-09-30
Trial end
2025-04-30
Status
Withdrawn
Phase
Early phase I
Treatment
MSC-EV
10 E10 MSC-EV particles per 100ml for a single dose. No prior HLA matching between MSC donors and recipients or liver donors
Arms:
MSC-EV group
Primary endpoint
Number of participants with MSC-EV infusion-related toxicity as assessed by CTCAE v4.0.
24 hours after injection
Aspartate aminotransferase (AST)
6 months after transplantation
Alanine aminotransferase (ALT)
6 months after transplantation
Bilirubin level
6 months after transplantation
International normalized ratio (INR)
6 months after transplantation
carbohydrate Compound antigen (GGT) level
6 months after transplantation
Adverse events
6 months
Eligibility criteria
Inclusion Criteria: * aged 18-60 years; * Acute on chronic liver failure-which is characterized by acute hepatic insult manifesting as jaundice (serum total bilirubin \[TBil\] ≥ 10×ULN umol/L) and coagulopathy (international normalized ratio \[INR\] ≥ 1.5 or prothrombin activity \< 40%), complicated within 4 weeks by ascites and/or encephalopathy as determined by physical examination, in patients with previously diagnosed or undiagnosed chronic liver disease; Requiring liver transplantation due to acute on chronic liver failure; * Obtain the patients' consent after informing patients of the purpose and method of the clinical trial; Exclusion Criteria: * Past history of malignant disease * Active uncontrolled infection; * Combined transplantation * EBV-negative; * HIV or HCV positive; * Retransplantation;
Protocol
{'studyType': 'INTERVENTIONAL', 'phases': ['PHASE1'], 'designInfo': {'allocation': 'RANDOMIZED', 'interventionModel': 'PARALLEL', 'primaryPurpose': 'TREATMENT', 'maskingInfo': {'masking': 'NONE'}}, 'enrollmentInfo': {'count': 0, 'type': 'ACTUAL'}}
Updated at
2023-10-12

1 organization

1 product

2 indications

Product
MSC-EV
Indication
Liver Failure