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临床试验/NCT01661842
NCT01661842Unknown1 期

Phase 1/2 Study of UC-MSC Treatment for Evaluation the Efficacy and Safety in Patients With Autoimmune Liver Disease

Beijing 302 Hospital1 个研究点 分布在 1 个国家目标入组 100 人开始时间: 2011年10月1日最近更新:
适应症

试验速览

阶段
1 期
发起方
入组人数
100
试验地点
1
主要终点
Liver Histology change

研究概览

简要总结

Autoimmune hepatitis (AIH) is characterized by chronic inflammation of the liver, interface hepatitis, hypergammaglobulinemia, and the presence of autoantibodies. Disease presentation is varied but typically is based on characteristic aminotransferase elevations, histological abnormalities, elevated levels of serum globulins, and the presence of one or more autoantibodies. Two types of juvenile AIH have been identified according to seropositivity for smooth muscle and /or antinuclear antibody (AIH type 1) or liver kidney microsomal antibody (AIH type 2). Standard therapy in clinic consists of a combination of corticosteroids and azathioprine, which displays the efficacy in 80% of patients. However, 7% of patients deteriorate despite compliance with the standard corticosteroid regiments (treatment failure),13% of patients improve but not to a degree that satisfies remission criteria (incomplete response), 13% of patients develop serious drug-induced complications, and 50%-86% of patients will relapse after drug withdrawal. These serious drawbacks counterbalance the benefits of conventional therapy, and they are compelling reasons to refine current treatment strategies and pursue alternative therapies. UC-MSC has been the application for the treatment of several severe autoimmune diseases, such as immune thrombocytopenia, systemic lupus erythematosus, and therapy-resistant rheumatoid arthritis. In this study, the safety and efficacy of UC-MSC transplantation for AIH patients will be evaluated.

详细描述

Autoimmune hepatitis (AIH) is an immune-mediated necroinflammatory disease of the liver characterized by elevation of IgG, presence of characteristic autoantibodies, and histological feature of interface hepatitis. Standard therapy consists of a combination of corticosteroids and azathioprine, which is efficacious in 80% of patients. However, current treatment strategies are complicated by frequent relapse after drug withdrawal, medication intolerance, and refractory disease. Alternative medical therapy may be need for AIH.

The potential for stem cells to differentiate into hepatocytes cells was recently confirmed. In particular, bone marrow-derived mesenchymal stem cell (BM-MSC) transplantation has been applicated in the clinic for treat several human disease such as GVHD, cardiac injury and brain injury, and displayed good tolerance and efficiency. Recently, umbilical cord-derived MSCs (UC-MSC) has also been used to treat severe autoimmune diseases, such as immune thrombocytopenia, systemic lupus erythematosus, and therapy-resistant rheumatoid arthritis.

The purpose of this study is to learn whether and how UC-MSC can improve the disease condition in patients with autoimmune hepatitis (AIH). This study will also look at how well UC-MSC is tolerated and its safety in AIH patients

Participants in the study will be randomly assigned to one of two treatment arms:

Arm A: Participants will receive 12 weeks of UC-MSC treatment plus conventional treatment (combination of corticosteroids and azathioprine) Arm B: Participants will receive 12 weeks of placebo plus conventional treatment. (combination of corticosteroids and azathioprine) UC-MSC will be prepared according to standard procedures and is collected in plastic bags containing anticoagulant. UC-MSCs are given via i.v. under sonography monitoring. After cell therapy, patients are followed up at week 12, 24, 36, 48, 72, 96. The evaluation of some clinical parameters such as the level of serum alanine aminotransferase (ALT), aspartate aminotransferase (AST), γ-globulin, total bilirubin (TB), prothrombin time (PT), albumin (ALB), prealbumin (PA) and IgG, are detected at these time points. MELD score, Liver histology, treatment side effects, relapse rate and clinical symptoms were also observed simultaneously.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Written informed consent
  • Autoimmune hepatitis (according to the criteria defined by the international autoimmune hepatitis Group ,Hepatology, 2008;48:169-176)
  • Negative pregnancy test (female patients in fertile age)

排除标准

  • Hepatocellular carcinoma or other Malignancies
  • Pregnant or lactating women
  • Viral Hepatitis ( HAV,HBV,HCV, et al )
  • Vital organs failure (Cardiac, Renal or Respiratory, et al)
  • Active thrombosis in the portal or hepatic veins

结局指标

主要结局

Liver Histology change

时间窗: baseline and 96 weeks

Serum alanine aminotransferase (ALT)

时间窗: 0,12, 24, 36, 48, 72, 96 weeks after treatment

次要结局

  • Serum AST(At baseline and at week 12, 24, 36, 48, 72, 96)
  • Serum Tbil(At baseline and at week 12, 24, 36, 48, 72, 96)
  • Serum immunoglobulin G (IgG)(At baseline and at week 12, 24, 36, 48, 72, 96)
  • Serum γ-globulin(At baseline and at week 12, 24, 36, 48, 72, 96)
  • MELD score(At base line and at week 12, 24, 36, 48, 72, 96)
  • Number of participants with treatment side effects(At base line and at week 12, 24, 36, 48, 72, 96)
  • Number of participants with improvement of clinical symptoms(At base line and at week 12, 24, 36, 48, 72, 96)

研究者

发起方
Beijing 302 Hospital
申办方类型
Other
责任方
Principal Investigator
主要研究者

Fu-Sheng Wang

Director of both the Research Center for Biological Therapy and the Beijing Institute of Translational Hepatology

Beijing 302 Hospital

研究点 (1)

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