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临床试验/NCT00291616
NCT00291616已完成4 期

A Multicenter, Randomized, Controlled Trial of Combination Therapy for HBeAg Positive Chronic Hepatitis B: Comparing Thymosin Alpha 1 and Pegylated Interferon-alpha2a With Pegylated Interferon-alpha2a Alone.

Seoul National University Hospital1 个研究点 分布在 1 个国家目标入组 52 人开始时间: 2005年12月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
状态
已完成
入组人数
52
试验地点
1
主要终点
HBeAg seroconversion, HBV DNA titer<20,000 IU/mL

研究概览

简要总结

The purpose of this study is to determine the optimal treatment duration of antiviral therapy for chronic hepatitis B.

详细描述

Thymosin alpha1/interferon combination therapy has been known as an effective antiviral therapy for chronic hepatitis B. It is superior to interferon single therapy since the sustained viral response rate of combination therapy used to be about 70% compared with that of single interferon therapy(20%). Until now, the combination therapy including 6-month treatment of thymosin alpha1 has been as effective as 12-month treatment of thymosin alpha1. We hypothesized that thymosin alpha1 is an immune potentiator so, the shorter duration of thymosin alpha1 treatment might be as effective as the prolonged treatment duration.

In detail, we designed to perform this clinical study comparing the combination of pegylated interferon and thymosin alpha1 with pegylated interferon alone. Total treatment duration of both parallel groups will be 12 months, and the combination therapy will be lasted for the first 3 months followed by the next, ongoing pegylated interferon single therapy for 9 months.

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 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • HBsAg positive and anti-HBs negative for more than 6 months
  • HBeAg positive
  • HBV DNA titer more than 100,000 IU/mL
  • serum ALT more than upper normal limit value, but no more than 10 times upper normal limit value

排除标准

  • the history of antiviral therapy for chronic hepatitis B within the recent 6 months
  • HAV IgM Ab + and/or HCV Ab + and/or HDV Ab and/or HIV Ab +
  • the sign of decompensated liver disease
  • the history of hemoglobinopathy, autoimmune hepatitis, alcoholic liver disease
  • pregnant or lactating woman
  • neutrophil count less than 1,500/mm3 or platelet count less than 90,000/mm3
  • serum creatinine more than 1.5 times upper normal limit value
  • the sign of alcoholic or drug addiction within the recent 1 year
  • the history of psychotic disorder especially like depression
  • immunologically mediated disease
  • the history of esophageal varix
  • the history of severe heart disease or respiratory disease
  • the history of severe epilepsy or current use of antiepileptic drug
  • the sign of malignancy or suggestive of malignancy or the history of malignancy, the recurrence rate within 2 years of which is more than 20%
  • the history of systemic anticancer treatment including radiation therapy or immunotherapy including systemic corticosteroid
  • the history of major organ transplantation
  • the history of medically uncontrolled thyroid disease
  • the history or sign of severe retinopathy

研究组 & 干预措施

1

Active Comparator

Pegylated Interferon-alpha2a

干预措施: Pegylated Interferon-alpha2a (Drug)

2

Active Comparator

Thymosin alpha1 & Pegylated Interferon-alpha2a

干预措施: Thymosin alpha1 & Pegylated Interferon-alpha2a (Drug)

结局指标

主要结局

HBeAg seroconversion, HBV DNA titer<20,000 IU/mL

时间窗: 48 week and 96 week

次要结局

  • Normalization of serum ALT, loss of HBeAg and HBsAg, production of anti-HBs(48 week and 96 week)

研究者

申办方类型
Other

研究点 (1)

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