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Reactogenicity, Safety and Immunogenicity of a LAIV H7N9 Influenza Vaccine

2015年6月19日 更新者:Oleg Kiselev、Research Institute of Influenza, Russia

Reactogenicity, Safety and Immunogenicity of a Live Monovalent A/17/Anhui/2013/61 (H7N9) Influenza Vaccine

This is a single centre phase I, double-blind placebo-controlled study to assess reactogenicity, safety and immunogenicity of a live monovalent A/17/Anhui/2013/61 (H7N9) influenza vaccine in healthy male and female adults, 18 through 49 years of age .

研究概览

研究类型

介入性

注册 (实际的)

40

阶段

  • 阶段1

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

18年 至 49年 (成人)

接受健康志愿者

是的

有资格学习的性别

全部

描述

Inclusion Criteria:

  • Legal male or female adult 18 through 49 years of age at the enrollment visit.
  • Literate and willing to provide written informed consent.
  • A signed informed consent.
  • Free of obvious health problems, as established by the medical history and screening evaluations, including physical examination.
  • Capable and willing to complete diary cards and willing to return for all follow-up visits
  • Willing to comply with the rules of the isolation unit (including willing and able to take oseltamivir influenza antiviral medication, should that be recommended by a study physician).
  • For females, willing to take reliable birth control measures through day 56.

Exclusion Criteria:

  • Participation in another clinical trial involving any therapy within the previous three months or planned enrollment in such a trial during the period of this study.
  • Receipt of any non-study vaccine within four weeks prior to enrollment or refusal to postpone receipt of such vaccines until four weeks after study completion.
  • Practice of nasal irrigation on a regular basis within the past six months or has engaged in nasal irrigation within two weeks prior to enrollment.
  • Recent history of frequent nose bleeds (more than 5 within the past year).
  • Clinically relevant abnormal paranasal anatomy.
  • Recent history (within the past month) of rhino or sinus surgery, or surgery for any traumatic injury of the nose.
  • Current or recent (within two weeks of enrollment) acute respiratory illness with or without fever.
  • Other acute illness at the time of study enrollment.
  • Receipt of immune globulin or other blood products within three months prior to study enrollment or planned receipt of such products during the period of subject participation in the study.
  • Chronic administration (defined as more than 14 consecutively-prescribed days) of immunosuppressants or other immune-modulating therapy within six months prior to study enrollment (for corticosteroids, this means prednisone or equivalent, 0.5 mg per kg per day; topical steroids are allowed, exclusive of nasal.)
  • Participation in any previous trial of any H7 or H5 containing influenza vaccine.
  • History of bronchial asthma.
  • Hypersensitivity and allergy reactions after previous administration of any vaccine.
  • History of wheezing after past receipt of any live influenza vaccine.
  • Other AE following immunization (body temperature more than 40°C, collapse, non-febrile seizures, anaphylaxis), at least possibly related to previous receipt of any vaccine (not only influenza).
  • Suspected or known hypersensitivity to any of the study vaccine components, including chicken or egg protein.
  • Seasonal (autumnal) hypersensitivity to the natural environment.
  • Acute or chronic clinically significant pulmonary, cardiovascular, hepatic, metabolic, neurologic, psychiatric or renal functional abnormality, as determined by medical history, physical examination or clinical laboratory screening tests, which in the opinion of the investigator, might interfere with the study objectives. Subjects with physical examination findings or clinical laboratory screening results which would be graded 2 or higher on the AE severity grading scale will be excluded from entry into the study and will be excluded from receipt of dose two of study vaccine or placebo.
  • History of leukemia or any other blood or solid organ cancer.
  • History of thrombocytopenic purpura or known bleeding disorder.
  • History of seizures.
  • Known or suspected immunosuppressive or immunodeficient condition of any kind, including HIV infection.
  • Known chronic HBV or HCV infection.
  • Known tuberculosis infection or evidence of previous tuberculosis exposure.
  • History of chronic alcohol abuse and/or illegal drug use.
  • Claustrophobia or sociophobia.
  • Pregnancy or lactation (a negative pregnancy test will be required before administration of study vaccine or placebo for all women of childbearing potential).
  • Any condition that, in the opinion of the investigator, would increase the health risk to the subject if he/she participates in the study or would interfere with the evaluation of the study objectives.
  • Allergic, including anaphylactic, reactions to the introduction of any vaccines in the subject's medical history (not only flu vaccine).

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 主要用途:预防
  • 分配:随机化
  • 介入模型:并行分配
  • 屏蔽:四人间

武器和干预

参与者组/臂
干预/治疗
有源比较器:H7N9 LAIV
H7N9 live influenza vaccine
H7N9 live influenza vaccine
其他名称:
  • LAIV H7N9
安慰剂比较:Placebo
Lyophilized purified allantoic fluid of chicken embryos with stabilizers
Lyophilized purified allantoic fluid of chicken embryos with stabilizers

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
Immediate reactions
大体时间:2 hours
Immediate reactions occurring within two hours of administration of any dose, measured as observed by study staff or reported by the subject to study staff
2 hours
Solicited adverse events
大体时间:Greater than two hours after administration of any dose of study vaccine or placebo through 6 days following any dose
Adverse events commonly associated with intranasal vaccination (solicited local and systemic reactions), measured as observed by study staff or reported by the subject to study staff
Greater than two hours after administration of any dose of study vaccine or placebo through 6 days following any dose
Changes from baseline in laboratory findings
大体时间:Days 3, 6 and 34
Abnormal laboratory findings from blood and urine specimens
Days 3, 6 and 34
Serious adverse events (SAEs)
大体时间:4 weeks of receipt of any dose
All SAEs during 56 days, as observed by study staff, reported by the subject to study staff, or noted by the subject on a diary card, including abnormal laboratory findings from blood specimens collected on Days 28 (pre-vaccination) and 56
4 weeks of receipt of any dose

次要结果测量

结果测量
措施说明
大体时间
Immune responses
大体时间:Days 0, 28 and 56

Immune responses was parameterized as the proportion of subjects with at least a four-fold rise after each dose from baseline or as the mean titer after each dose in any of the following:

  • Serum hemagglutination inhibition (HAI) antibodies
  • Serum neutralizing antibodies
  • Serum immunoglobulin class A (IgA) or immunoglobulin class G (IgG) antibodies measured by enzyme-linked immunosorbent assay (ELISA)
  • Secretory IgA antibodies from the nasal mucosa detected in nasal wick specimens using ELISA
  • Secretory IgA antibodies in saliva specimens using ELISA
Days 0, 28 and 56
Virus shedding
大体时间:Days 0-6 after each dose
Virus shedding with virus detected by real-time reverse transcriptase polymerase chain reaction rRTPCR in nasal swabs at any time point (at day of vaccination and daily during hospitalization).
Days 0-6 after each dose
Virus stability
大体时间:Days 0-6 after each dose
Virus stability (virus detected and sequenced after inoculation into chicken eggs)
Days 0-6 after each dose

其他结果措施

结果测量
措施说明
大体时间
Cellular immune responses (cytokine and T-cell)
大体时间:Days 0, 28 and 56
Cellular immune responses (cytokine and T-cell) was measured using isolated peripheral blood mononuclear cells (PBMCs) tested by flow cytometry and/or enzyme-linked immunosorbent spot (ELISPOT) assay.
Days 0, 28 and 56

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

调查人员

  • 学习椅:Larisa G Rudenko, MD PhD DSc、Institute of Experimental Medicine

出版物和有用的链接

负责输入研究信息的人员自愿提供这些出版物。这些可能与研究有关。

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始

2014年10月1日

初级完成 (实际的)

2014年12月1日

研究完成 (实际的)

2015年4月1日

研究注册日期

首次提交

2015年6月16日

首先提交符合 QC 标准的

2015年6月19日

首次发布 (估计)

2015年6月24日

研究记录更新

最后更新发布 (估计)

2015年6月24日

上次提交的符合 QC 标准的更新

2015年6月19日

最后验证

2015年6月1日

更多信息

与本研究相关的术语

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