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临床试验/NCT01867957
NCT01867957已完成1 期

A Single Blind, Randomized, Placebo Control, Phase I Study to Evaluate the Safety and Immunogenicity of the GC1109 Administered by the Intramuscular Route in Healthy Men

Seoul National University Hospital1 个研究点 分布在 1 个国家目标入组 20 人开始时间: 2009年2月最近更新:
适应症
干预措施

试验速览

阶段
1 期
状态
已完成
入组人数
20
试验地点
1
主要终点
Adverse Event

研究概览

简要总结

  1. BACKGROUND The newly developed anthrax vaccine GC1109 has been proven safe and effective in preclinical studies.
  2. OBJECTIVE
  • To evaluate the immunogenicity and safety of the anthrax vaccine GC1109 in healthy male volunteers.
  1. STUDY DESIGN
  • single-blinded
  • randomized
  • placebo controlled
  • phase 1 study

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
Single (Participant)

入排标准

年龄范围
18 Years 至 45 Years(Adult)
性别
Male
接受健康志愿者

入选标准

  • Healthy male subjects between 18 and 45 years of age at the time of screening visit
  • 18.5kg/m2 ≤BMI < 30kg/m2 at the time of screening visit
  • Subjects without congenital or chronic disorder

排除标准

  • 未提供

研究组 & 干预措施

High-dose GC1109

Experimental

干预措施: High-dose GC1109 (Biological)

Low-dose Placebo

Placebo Comparator

干预措施: Low-dose Placebo (Biological)

High-dose Placebo

Placebo Comparator

干预措施: High-dose Placebo (Biological)

Low-dose GC1109

Experimental

干预措施: Low-dose GC1109 (Biological)

结局指标

主要结局

Adverse Event

时间窗: 0 - 28 Days

次要结局

  • Anti-protective antigen(PA) antibody level (by TNA)(Day 14, Day 28)
  • Anti-PA Immunoglobulin G (IgG) (by ELISA)(Day 14, Day 28)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Myoung-don Oh

Professor, Division of Infectious Diseases, Department of Internal Medicine

Seoul National University Hospital

研究点 (1)

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