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临床试验/NCT07838298
NCT07838298招募中4 期

Immunogenicity of Different Influenza Vaccine Strategies in Older Adults in a Repeated Vaccination Setting

Korea University Guro Hospital1 个研究点 分布在 1 个国家目标入组 180 人开始时间: 2026年9月21日最近更新:
适应症
干预措施

试验速览

阶段
4 期
状态
招募中
入组人数
180
试验地点
1
主要终点
Geometric mean titers of hemagglutination inhibition antibodies at 1 month after vaccination

研究概览

简要总结

The goal of this clinical trial is to compare immune responses to different influenza vaccine formulations in older adults and to understand how immune aging and repeated annual influenza vaccination affect these responses.

The main questions it aims to answer are:

  • Do standard dose, MF59 adjuvanted, and high dose influenza vaccines produce different immune responses in adults aged 65 years or older?
  • How does immune aging affect responses to different influenza vaccine formulations?
  • How do immune responses change with repeated annual influenza vaccination, and do these changes differ among vaccine formulations?

Researchers will compare older adults who receive a standard dose, MF59 adjuvanted, or high dose influenza vaccine. Younger adults aged 19-49 years who receive a standard dose influenza vaccine will also be included as a reference group to help evaluate age related differences in immune responses.

Participants will:

  • Receive an influenza vaccine.
  • Provide blood samples before and after vaccination to measure antibody and other immune responses.
  • Some participants will provide additional blood or nasal samples for more detailed evaluation of immune responses.

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
None

入排标准

年龄范围
19 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者
是

入选标准

  • •Older adult group: aged 65 years or older
  • •Younger reference group: aged 19 to 49 years
  • •Able to receive influenza vaccination and complete the scheduled follow up

排除标准

  • •Receipt of an influenza vaccine or any other vaccine within 4 weeks prior to enrollment
  • •Immunocompromised status, including ongoing chemotherapy or immunosuppressive therapy, high dose corticosteroid therapy, history of solid organ or hematopoietic stem cell transplantation, active malignancy, HIV infection, or other clinically significant immunocompromising conditions
  • •Moderate or severe acute infection
  • •History of allergic reaction to an influenza vaccine or any of its components, or any other condition that precludes influenza vaccination
  • •Inability, as determined by the investigator, to understand the purpose and procedures of the study and provide voluntary informed consent

研究组 & 干预措施

older adults- standard dose influenza vaccine

Active Comparator

干预措施: Standard dose influenza vaccine (Biological)

older adults- adjuvanted influenza vaccine

Experimental

干预措施: MF59 adjuvanted influenza vaccine (Biological)

older adults- high dose influenza vaccine

Experimental

干预措施: High dose influenza vaccine (Biological)

younger adults- standard dose influenza vaccine

Other

Younger adults aged 19-49 years who receive a standard dose influenza vaccine and serve as a reference group for evaluating age related differences in immune responses

干预措施: Standard dose influenza vaccine (Biological)

结局指标

主要结局

Geometric mean titers of hemagglutination inhibition antibodies at 1 month after vaccination

时间窗: 1 month after vaccination, annually for up to 3 years

Geometric mean titers (GMTs) of hemagglutination inhibition antibodies against each influenza vaccine strain will be assessed at 1 month after vaccination.

Geometric mean fold rise in hemagglutination inhibition antibody titers at 1 month after vaccination

时间窗: Baseline to 1 month after vaccination, annually for up to 3 years

Geometric mean fold rises (GMFRs) in hemagglutination inhibition antibody titers from baseline to 1 month after vaccination will be assessed for each influenza vaccine strain.

次要结局

  • Seroconversion rate following influenza vaccination(Baseline and 1 month after vaccination, annually for up to 3 years)
  • Frequency of influenza specific B cells following vaccination(Baseline, 1 week, and 1 month after vaccination, annually for up to 3 years)
  • normalized level of influenza specific secretory IgA in nasal samples(1 month after vaccination in the first season; baseline and 1 month after vaccination annually in year 2 and 3)
  • Frequency of influenza specific T cells following vaccination(Baseline, 1 week, and 1 month after vaccination, annually for up to 3 years)

研究者

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

Choi, Min Joo

Associated Professor

Korea University Guro Hospital

研究点 (1)

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