drugset / Trial / NCT04822922

Safety of UC-MSC Transfusion for ACLF Patients

NCT04822922

Phase 2 Unknown 16 enrolled Hai Li
Non-randomizedParallel-groupOpen-labelTreatment

Summary

Acute on chronic liver failure (ACLF) is a type of critically ill liver disease with high short-term mortality in liver disease. Liver transplantation is currently the only method to improve survival. Current clinical research evidence shows that mesenchymal stem cells can reduce the mortality of ACLF patients and are safe. This study aims to explore the safety of umbilical cord mesenchymal stem cells (UC-MSCs) in the treatment of ACLF. The study population is ACLF patients with 1-2 organ failures. To explore the safety of 3 doses of UC-MSCs, 16 patients need to be enrolled. The main observation indicators are the short-term and long-term safety of the treatment. All patients need to receive the standard medical treatment (SMT) at the same time. Stem cell treatment is given by intravenous infusion on the first, fourth, seventh, and tenth day. The occurrence of adverse events (AE) and serious adverse events(SAE) before and after the infusion will be observed. After the patient is discharged from the hospital, patients will be followed , the follow-up time is 5 years.

Timeline

Start
2021-09-30
Primary completion
2022-07-31
Completion
2024-07-21

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Human Umbilical Cord-derived Mesenchymal Stem Cells Cell therapy 400000 cells/kg Intravenous
Subject Human Umbilical Cord-derived Mesenchymal Stem Cells Cell therapy 800000 cells/kg Intravenous
Subject Human Umbilical Cord-derived Mesenchymal Stem Cells Cell therapy 1.2e+06 cells/kg Intravenous

Indications