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Mesenchymal Stem Cell Therapy for Liver Cirrhosis

Primary Purpose

Liver Cirrhosis

Status
Unknown status
Phase
Phase 1
Locations
Singapore
Study Type
Interventional
Intervention
Autologous BM MSC
Sponsored by
Stem Med Pte. Ltd.
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Liver Cirrhosis focused on measuring Liver, Cirrhosis, Child B, Child C, Advance, Advanced, Singapore, MSC, Mesenchymal, Stem Cell, Cell Therapy, MSC Therapy, Treatment

Eligibility Criteria

21 Years - 69 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

Subjects must meet all the inclusive criteria to participate in the study:

  1. with definite liver cirrhosis, irrespective of aetiology
  2. must have Child's B or C stage
  3. must have signed an informed consent form

Exclusion Criteria:

Subjects with any of the following criteria are regarded as an exclusion from the study and will not be permitted to participate:

  1. age ≤21 years and >70 years old
  2. with life expectancy of < 6 months
  3. cancers and bone marrow malignancies
  4. patients with an active infection or multiple infections
  5. patients with uncontrolled hypertension and diabetes
  6. immunosuppressed patients (IST must have stopped at least 4 weeks prior to trial enrolment)
  7. patients who are HIV positive
  8. patients who are pregnant or lactating

Sites / Locations

  • Asian American Liver Centre - Gleneagles Hospital (Annexe Block)Recruiting
  • Parkway Cancer Centre - Gleneagles HospitalRecruiting
  • Desmond Wai Liver & Gastrointestinal Disease Centre - Mount Elizabeth Novena Specialist CentreRecruiting

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Treatment Arm

Arm Description

A single dose of 0.5 to 1 x 10^6/kg autologous BM MSCs (Total volume: 30 - 50 ml) will be infused via peripheral venous access.

Outcomes

Primary Outcome Measures

Clinical Examination
To observe for the following: absence of grade IV anaphylactic reactions (in reference to CTCAE 4.03) absence of grade IV febrile reactions or septic/ infective complications (in reference to CTCAE 4.03).
MR Elastography
To detect liver stiffness
The level of serum alanine aminotransferase (ALT)
To ensure the absence of deterioration of liver function.
The level of glomerular filtration rate (GFR)
To ensure the absence of deterioration of renal function.

Secondary Outcome Measures

The level of serum prothrombin time (PT)
To assess the efficacy of treatment
The level of serum total bilirubin (TB)
To assess the efficacy of treatment
The level of serum albumin (ALB)
To assess the efficacy of treatment
MELD Score
To assess the efficacy of treatment

Full Information

First Posted
July 26, 2018
Last Updated
March 15, 2021
Sponsor
Stem Med Pte. Ltd.
Collaborators
Parkway Cancer Centre, Asian American Liver Centre, Desmond Wai Liver & Gastrointestinal Diseases Centre
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1. Study Identification

Unique Protocol Identification Number
NCT03626090
Brief Title
Mesenchymal Stem Cell Therapy for Liver Cirrhosis
Official Title
Mesenchymal Stem Cell Therapy for Liver Cirrhosis: A Phase I/II Study
Study Type
Interventional

2. Study Status

Record Verification Date
March 2021
Overall Recruitment Status
Unknown status
Study Start Date
August 18, 2018 (Actual)
Primary Completion Date
October 22, 2021 (Anticipated)
Study Completion Date
October 22, 2021 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Stem Med Pte. Ltd.
Collaborators
Parkway Cancer Centre, Asian American Liver Centre, Desmond Wai Liver & Gastrointestinal Diseases Centre

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
MSCs have been studied for the treatment of liver diseases as well as non-liver diseases. MSCs have been successful in treating conditions like acute steroid-resistant GVHD in hematopoietic stem cell transplanted patients and also have shown to improve the MELD score in end-stage liver disease. There were no severe side effects observed in using autologous MSCs as a treatment option. The outcome of the studies done so far have been positive and it is encouraged to study the use of MSCs as cell therapy for treating liver diseases. The estimated rate of cirrhosis in HBV patients in Singapore is about 1.6% per year, rate of hepatocellular carcinoma is about 0.8% per year overall and 3.0% per year in cirrhotic patients. Knowing that there are not many options currently available for Liver Cirrhosis patients and that they have a poor prognosis with an average life expectancy of < 12 months, this study uses autologous MSCs to treat Liver Cirrhosis patients in Singapore. The objective of the study is to demonstrate that autologous bone marrow is safe to be used in patients with liver cirrhosis as well as demonstrate that bone marrow MSC may improve liver function and prolong patient survival.
Detailed Description
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), bone marrow mononuclear cells (MNC) and peripheral CD34 positive cells. 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 Singapore. This will be a Phase I/II study with the main emphasis on the safety profile first. The trial will be conducted in compliance with the protocol, GCP and local regulatory requirement(s).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Liver Cirrhosis
Keywords
Liver, Cirrhosis, Child B, Child C, Advance, Advanced, Singapore, MSC, Mesenchymal, Stem Cell, Cell Therapy, MSC Therapy, Treatment

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 1, Phase 2
Interventional Study Model
Single Group Assignment
Model Description
As the primary objective of the study is to assess safety of MSC infusion, a single arm non-blinded study design has been adopted.
Masking
None (Open Label)
Allocation
N/A
Enrollment
20 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Treatment Arm
Arm Type
Experimental
Arm Description
A single dose of 0.5 to 1 x 10^6/kg autologous BM MSCs (Total volume: 30 - 50 ml) will be infused via peripheral venous access.
Intervention Type
Biological
Intervention Name(s)
Autologous BM MSC
Intervention Description
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 Outcome Measure Information:
Title
Clinical Examination
Description
To observe for the following: absence of grade IV anaphylactic reactions (in reference to CTCAE 4.03) absence of grade IV febrile reactions or septic/ infective complications (in reference to CTCAE 4.03).
Time Frame
Up to 34 weeks
Title
MR Elastography
Description
To detect liver stiffness
Time Frame
Up to 34 weeks
Title
The level of serum alanine aminotransferase (ALT)
Description
To ensure the absence of deterioration of liver function.
Time Frame
Up to 34 weeks
Title
The level of glomerular filtration rate (GFR)
Description
To ensure the absence of deterioration of renal function.
Time Frame
Up to 34 weeks
Secondary Outcome Measure Information:
Title
The level of serum prothrombin time (PT)
Description
To assess the efficacy of treatment
Time Frame
Up to 6 months, post-infusion
Title
The level of serum total bilirubin (TB)
Description
To assess the efficacy of treatment
Time Frame
Up to 6 months, post-infusion
Title
The level of serum albumin (ALB)
Description
To assess the efficacy of treatment
Time Frame
Up to 6 months, post-infusion
Title
MELD Score
Description
To assess the efficacy of treatment
Time Frame
Up to 6 months, post-infusion

10. Eligibility

Sex
All
Minimum Age & Unit of Time
21 Years
Maximum Age & Unit of Time
69 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Subjects must meet all the inclusive criteria to participate in the study: with definite liver cirrhosis, irrespective of aetiology must have Child's B or C stage must have signed an informed consent form Exclusion Criteria: Subjects with any of the following criteria are regarded as an exclusion from the study and will not be permitted to participate: age ≤21 years and >70 years old with life expectancy of < 6 months cancers and bone marrow malignancies patients with an active infection or multiple infections patients with uncontrolled hypertension and diabetes immunosuppressed patients (IST must have stopped at least 4 weeks prior to trial enrolment) patients who are HIV positive patients who are pregnant or lactating
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Clinical Trial Department
Phone
63699191
Email
clinicaltrials@stem-med.sg
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Teo Cheng Peng
Organizational Affiliation
Parkway Cancer Centre
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Wai Chun Tao, Desmond
Organizational Affiliation
Desmond Wai Liver & Gastrointestinal Diseases Centre
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Lee Kang Hoe
Organizational Affiliation
Asian American Liver Centre
Official's Role
Principal Investigator
Facility Information:
Facility Name
Asian American Liver Centre - Gleneagles Hospital (Annexe Block)
City
Singapore
ZIP/Postal Code
258500
Country
Singapore
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Clinical Trial Department
Phone
63699191
Email
clinicaltrials@stem-med.sg
First Name & Middle Initial & Last Name & Degree
Lee Kang Hoe
Facility Name
Parkway Cancer Centre - Gleneagles Hospital
City
Singapore
ZIP/Postal Code
258500
Country
Singapore
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Clinical Trial Department
Phone
63699191
Email
clinicaltrials@stem-med.sg
First Name & Middle Initial & Last Name & Degree
Teo Cheng Peng
Facility Name
Desmond Wai Liver & Gastrointestinal Disease Centre - Mount Elizabeth Novena Specialist Centre
City
Singapore
ZIP/Postal Code
329563
Country
Singapore
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Clinical Trial Department
Phone
63699191
Email
clinicaltrials@stem-med.sg
First Name & Middle Initial & Last Name & Degree
Wai Chun Tao, Desmond

12. IPD Sharing Statement

Plan to Share IPD
No
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Mesenchymal Stem Cell Therapy for Liver Cirrhosis

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