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临床试验/NCT03357263
NCT03357263已完成1 期

Randomized, Single-Blind, Active Comparator-controlled Study to Evaluate the Safety and Immunological Efficacy of GC3114 in Healthy Adults.

Green Cross Corporation1 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2017年11月20日最近更新:
适应症
干预措施

试验速览

阶段
1 期
状态
已完成
入组人数
40
试验地点
1
主要终点
Adverse Event

研究概览

简要总结

Healthy adults will be once administered GC3114A(High-dose Quadrivalent influenza vaccine) or GCFLU Quadrivalent Pre-filled syringe inj..

详细描述

Healthy adults will be once administered GC3114A(High-dose Quadrivalent influenza vaccine) or GCFLU Quadrivalent Pre-filled syringe inj.. Safety and immunological efficacy will be evaluated.

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
19 Years 至 64 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Healthy adults aged 19-64 years old
  • Informed consent form has been signed and dated
  • Able to comply with the requirements of the study

排除标准

  • Known systemic hypersensitive to eggs, chicken proteins, or any of the vaccine components
  • Personal history of Guillain-Barre syndrome(GBS)
  • Subjects with severe chronic disease who are considered by investigator to be ineligible for the study
  • Subjects who received a vaccination within 28 days before enrollment or who are scheduled for another vaccination during the study
  • Immunocompromised subjects with immunodeficiency disease or subjects receiving immunosuppressive or immunomodulating therapy
  • Pregnant or lactating women

研究组 & 干预措施

GC3114

Experimental

Pre-filled syringe inj., 0.5ml, Once, IM

干预措施: GC3114 (Biological)

GCFLU Quadrivalent

Active Comparator

Pre-filled syringe inj., 0.5ml, Once, IM

干预措施: GCFLU Quadrivalent (Biological)

结局指标

主要结局

Adverse Event

时间窗: for 7 days from Day0/during study period

Solicited/Unsolicited Adverse Event

次要结局

  • Percentage of participants achieving pre-defined Seroconversion Before and following vaccination(Day 0 and Day 21)
  • Percentage of participants achieving pre-defined Seroprotection Before and following vaccination(Day 0 and Day 21)
  • Geometric Mean Titer and Geometric Mean Titer Ratios of Antibodies to the Investigational Product Before and Following vaccination(Day 0 and Day 21)

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (1)

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