Decompensated Cirrhosis
Conditions
Brief 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.
Detailed 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.
Interventions
Human Umbilical Cord-derived Mesenchymal Stem Cells will be administered intravenously.
Sponsors
Wuhan Optics Valley Zhongyuan Pharmaceutical Co., Ltd., Hubei, China
Beijing 302 Hospital
Study design
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
No
Inclusion criteria
1. Willing to provide written informed consent; 2. Aged 18 to 75 years (including 18 and 75 years), male or female; 3. Patients diagnosed with decompensated liver cirrhosis based on clinical findings, laboratory tests, imaging findings and/or representative pathological findings (decompensated liver cirrhosis is defined as the occurrence of at least one serious complication, including esophageal and gastric varices bleeding, hepatic encephalopathy, ascites, spontaneous bacterial peritonitis and other serious complications); 4. Child-Turcotte-Pugh (CTP) score 7 to 12 points.
Exclusion criteria
1. Hepatitis B virus (HBV) DNA ≥ detection limit at the time of screening, or patients with hepatitis B virus-related decompensated liver cirrhosis may discontinue antiviral therapy during the study, or those who with antiviral therapy for HBV for less than 12 months. 2. Hepatitis C virus (HCV) RNA ≥ detection limit at the time of screening, or patients with hepatitis C virus-related decompensated liver cirrhosis not more than 12 months on antiviral therapy. 3. Patients under treatment with corticosteroids for autoimmune hepatitis for less than 6 months. 4. Trans-jugular intrahepatic portosystemic shunts (TIPS) insertion within 6 months prior to study inclusion. 5. Active drinkers with alcohol-related decompensated cirrhosis are unwilling to stop alcohol abuse after inclusion. 6. Patients with biliary obstruction, or portal patients with vein spongiosis. 7. Patients are known with other malignancies within 5 years prior to the signing of ICF, except have had curative therapy of Basal Cell Cancer, Squamous Cell Carcinoma and/or radical resection of Carcinoma in Situ. Known to have had other malignancies within 5 years prior to signing the informed consent, except for basal cell carcinoma of the skin, squamous cell carcinoma of the skin, and/or carcinoma in situ with curable resection. 8. Patients with history of organ transplantation. 9. Patients with severe heart, lung, kidney and blood system diseases. 10. Patients with drug abuse, drug dependence and patients who receive methadone treatment or with psychosis. 11. Patients with history of immunodeficiency disease, including a positive test result for human immunodeficiency virus (HIV) antibodies, or other acquired or congenital immunodeficiency diseases; 12. Pregnant or lactating female. Fertile patients who were unable or unwilling to use effective non-pharmaceutical contraception during the trial and within 6 months after the end of the trial. 13. Patients who had cardiovascular and cerebrovascular events (such as Unstable Angina, Brain Hemorrhage, severe Ischemic Infarction) within 3 months before the first dose；Patients who had Myocardial Infarct or a clinically significant Arrhythmia/Conduction Abnormalities within 12 months before the first dose. 14. Patients with hypersensitivity (allergic to more than two foods or drugs) or with a history of severe allergy, or patients with Severe allergy to a known experimental drug or to any excipient. 15. Patients previously received stem cell therapy or are intolerance to cell therapy; 16. Participants in other clinical trials within the last 3 months. 17. Any other clinical condition which the investigator considers would make the patient unsuitable for the trial.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Incidence of Adverse Events | from baseline to 28th day | — |
| incidence of dose-limiting toxicity-related adverse events | from baseline to 28th day | — |
| maximum tolerated dose | from baseline to 28th day | — |
| Change in Model for End-Stage Liver Disease (MELD) score from baseline to 28th day | at 28th day | The Model for End-stage Liver Disease (MELD) is a scoring system that evaluates the liver function reserve and prognosis of patients with chronic liver disease by creatinine, international normalized ratio (INR), and bilirubin-conjugated cirrhosis etiology. The MELD score is calculated by the formula: R = 9.6 × ln (creatinine mg/dl) + 3.8 × ln (bilirubin mg/dl) + 11.2 × ln (INR) + 6.4 × etiology, and the results are taken as integers. ( 0 for cholestatic and alcoholic cirrhosis and 1 for other causes of cirrhosis such as viruses). |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| plasma albumin (ALB) | up to 24 months | — |
| plasma prealbumin (PALB) | up to 24 months | — |
| total bilirubin (TBIL) | up to 24 months | — |
| serum cholinesterase (CHE) | up to 24 months | — |
| Change in Model for End-Stage Liver Disease (MELD) score from baseline to 3 days, 7days, 14 days, 21 days, 1 month, 2 months, 3 months, 6 months, 12 months, 18 months, and 24 months | 3 days, 7days, 14 days, 21 days, 1 month, 2 months, 3 months, 6 months, 12 months, 18 months, and 24 months | — |
| Child-Turcotte-Pugh (CTP) score | up to 24 months | Child-Turcotte-Pugh (CTP) score is a scoring system that evaluates the liver function. Maximum is 15, minimum is 5. Higher scores mean a worse outcome. |
| EuroQol Group 5-Dimension Self-Report Questionnaire (EQ-5D) | up to 24 months | Quality of life assessment. Maximum is 5, minimum is 1. Lower scores mean a better outcome. |
| Incidence of liver cancer | up to 24 months | — |
| ChronicLiver Disease Questionnaire (CLDQ) | up to 24 months | Quality of life assessment. The Chronic Liver Disease Questionnaire (CLDQ) was developed as an evaluative instrument to measure longitudinal change in health status within individuals with chronic liver disease. In addition to measuring both physical and mental health, the instrument was designed to be a disease-specific tool for assessing areas of function important to patients with chronic liver disease. Maximum is 7, minimum is 1. Higher scores mean a better outcome. |
| prothrombin time (PT) | up to 24 months | Prothrombin time (PT) is a blood test that measures the time it takes for plasma to clot, to check for bleeding problems, or to check whether medicine to prevent blood clots is working. |
| Incidence of each complication associated with decompensated cirrhosis | up to 24 months | — |
| liver transplant-free survival | up to 24 months | — |
| Incidence of liver failure | up to 24 months | — |
Countries
China
Contacts
Primary ContactLei Shi, MD,PhD
Backup ContactFu-Sheng Wang, MD,PhD
Outcome results
None listed