跳至主要内容
临床试验/EUCTR2017-002574-39-DE
EUCTR2017-002574-39-DE进行中(未招募)1 期

Ancillary study evaluating ChAd155-hIi-HBV shedding in a subset of chronic hepatitis B patients enrolled in the first-time-in-human, Phase I/II, randomised, multi-centric, single-blind study TH HBV VV-001 - TH HBV VV-031 HBS:001

GlaxoSmithKline Biologicals0 个研究点目标入组 76 人开始时间: 2018年4月20日最近更新:

试验速览

阶段
1 期
状态
进行中(未招募)
入组人数
76

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional clinical trial of medicinal product

入排标准

性别
All

入选标准

  • Patients who, in the opinion of the investigator, can and will comply with the requirements of the protocol.
  • Written informed consent obtained from the patient prior to performance of any study specific procedure.
  • Patients who met all inclusion criteria and were randomised to the Step B of the TH HBV VV-001 study.
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range 38
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 38

排除标准

  • Patients met any exclusion criterion of the TH HBV VV-001 study.

研究者

相似试验