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Completed

NCT Number: NCT05080465

Long Term Follow up Mesenchymal Stem Cell Therapy for Patients Virus-related Liver Cirrhosis

This is a study to assess safety and preliminary clinical activity of treatments of liver cirrhosis in patients with caused by Hepatitis C and Hepatitis B or Nonalcoholic Steatohepatitis of Mesenchymal stem cell.

Patients who will be enrolled in the study will be under supervision and monitoring to ensure clinical significance

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Key information

Age range

18 year–69 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 3

Primary location

Institute of Bio-Stem Cell Rehabilitation

Kharkiv, Ukraine

About this study

Liver cirrhosis refers to extreme scarring of the liver, resulting in suboptimal function of the liver. It can result from a variety of causes, ranging from hepatitis B and C infection, excessive alcohol consumption, autoimmune causes, fatty liver and others. Irrespective of the cause, once the liver becomes cirrhotic, it is a downhill course.

Liver cirrhosis is irreversible and most patients will progressively worsen over time. Once liver cirrhosis has reached the stage of decompensation, that is, development of jaundice, ascites, variceal bleeding, hepatic encephalopathy and coagulopathy the two-year survival drops to about 50%.

The definitive treatment of decompensated cirrhosis is liver transplantation. While a liver transplantation is potentially curative, the high costs, lack of a donor, treatment-related mortality and the immunosuppression complications make this option possible only for a limited number of patients. The vast majority do not have an effective option at all, thus the need to develop alternative therapies. Various types of Stem Cells had been investigated as a regenerative therapy for liver cirrhosis. These stem cells include bone marrow mesenchymal stem cells (MSC). Some early studies have shown encouraging results in patients who had autologous bone marrow stem cell transplantation. There was improved liver function in these patients with cirrhotic livers.

The sponsor is proposing a study to look into the role of MSC therapy for patients with liver cirrhosis in Ukraine. This will be a Phase I study with the main emphasis on the safety and efficiency profile first. The trial will be conducted in compliance with the protocol, GCP and local regulatory requirement(s).

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

Provision of written informed consent for this study by subject or as applicable legal guardians Able to comply with study requirements Еру rates with RVR defined as serum HCV RNA undetectable after 12 month after antiviral therapy.

Subject must have documented compensated cirrhosis and no current or past clinical evidence of decompensated liver disease Subject must have documented history Screening laboratory result indicating hepatitis C virus (HCV) Genotype 1, 2, 4, 5 or 6 (GT1,2,4,5,6) infection

Exclusion criteria

Positive test result at screening for Hepatitis B surface antigen or anti-human immunodeficiency virus (anti-HIV) antibody HCV genotype performed during screening indicating co-infection with more than 1 HCV genotype.

Treatment and study plan

Autologous BM MSC

Biological

A total of 100-200ml will be harvested from the subject, in either a single or multiple punctures. This will be processed for autologous MSC infusion.

Primary outcomes

  1. MR Elastography

    Time frame: Change from Baseline (Day 0) until 40 weeks

    The detect liver stiffness of significant or severe fibrosis (≥stage F2)(≥stage F3)

  2. The level of serum alanine aminotransferase (ALT)

    Time frame: Change from Baseline (Day 0) until 40 weeks

    level of serum alanine aminotransferase less 40 (IU/L)

  3. Clinical Examination

    Time frame: Change from Baseline (Day 0) until 40 weeks

    To observe for the following:

    absence of grade IV anaphylactic reactions (in reference to CTCAE 4.03)

  4. The level of glomerular filtration rate (GFR)

    Time frame: Change from Baseline (Day 0) until 40 weeks

    The level of glomerular filtration range from 90 to 120 mL/min/1.73 m2

Secondary outcomes

  1. The level of serum albumin (ALB)

    Time frame: Up to 6 months, post-infusion

    The level of serum albumin to 5.4 g/dL

  2. The level of serum total bilirubin (TB)

    Time frame: Up to 6 months, post-infusion

    The level of serum total bilirubin 1.8 mg/dL

Sponsors and collaborators

Lead sponsor

Ukraine Association of Biobank

Other

Registry information

Official study title

Long Term Follow up Autologous Mesenchymal Stem Cell Therapy for Patients Virus-related Liver Cirrhosis

Important dates

Study start
2018
Primary completion
2024
Study completion
2025
First posted
Oct 15, 2021
Registry last updated
Dec 22, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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