跳至主要内容
临床试验/NCT02335164
NCT02335164已完成1 期

A Randomised, Controlled, Blinded Phase 1 Study to Evaluate the Immunogenicity and Safety of a Pandemic Avian H5 Influenza Vaccine in Adults

Vaxine Pty Ltd2 个研究点 分布在 1 个国家目标入组 270 人开始时间: 2015年7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
270
试验地点
2
主要终点
The incidence of adverse events

研究概览

简要总结

Recombinant hemagglutinin has been shown to induce protective neutralising antibodies against avian influenza virus but is relatively non-immunogenic. An ideal pandemic avian influenza influenza vaccine would combine hemagglutinin antigen with an appropriate adjuvant to increase its immunogenicity. This Phase 1 study will collect preliminary human safety and efficacy data on combined formulations of recombinant hemagglutinin with Advax adjuvant formulations administered by intramuscular injection

详细描述

This is a study to test new vaccine formulations against pandemic avian influenza ("bird flu"). Bird flu is a potentially deadly disease that is caused by influenza virus from birds. It is not the same as the common seasonal flu for which there is a seasonal vaccine released around March each year. To date, bird flu due to the H5N1 strain of influenza virus has infected over 500 people mainly in Asia resulting in death in more than half the cases. More recently there has been an outbreak of another bird flu virus in China known as H9N7 that is also highly lethal when it infects humans. Vaccination is the single most effective measure to prevent infection from bird flu viruses such as H5N1 or H9N7 should such a pandemic occur. In the event of a major bird flu pandemic outbreak, vaccine supplies are likely to be very limited, as there is not currently sufficient manufacturing capacity to provide enough vaccine quickly for the whole population. Research is needed on how to make the pandemic flu vaccine more effective but also how to stretch vaccine supplies using a strategy called 'antigen-sparing'. This can potentially be achieved by using an important ingredient called an 'adjuvant'. Adjuvants act by stimulating the immune system to make vaccines more effective. This study will test Advax adjuvants which are based on delta inulin in combination with recombinant hemagglutinin from the H5N1 influenza virus serotype.

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
Triple (Participant, Investigator, Outcomes Assessor)

入排标准

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

入选标准

  • Ambulatory males or females aged 18 years and over
  • Able to provide written informed consent
  • Willing and able to comply with the protocol for the duration of the study.
  • Not planning to have seasonal influenza vaccine within 2 months from the time of the first trial immunization

排除标准

  • Pregnant or lactating women.
  • Women of childbearing potential unless using a reliable and appropriate contraceptive method.
  • Receipt of another investigational agent within 28 days preceding initiation of treatment.
  • Any other serious medical, social or mental condition which, in the opinion of the investigator, would be detrimental to the subjects or the study.

研究组 & 干预措施

HA 45ug

Experimental

recombinant influenza hemagglutinin (H5) 45ug, i.m. injection, 2 doses

干预措施: recombinant influenza hemagglutinin (Biological)

HA 45ug+Advax1

Experimental

recombinant influenza hemagglutinin(H5) 45ug, Advax1 adjuvant 20mg, i.m. injection, 2 doses

干预措施: recombinant influenza hemagglutinin (Biological)

HA 45ug+Advax1

Experimental

recombinant influenza hemagglutinin(H5) 45ug, Advax1 adjuvant 20mg, i.m. injection, 2 doses

干预措施: Advax1 (Biological)

HA 45ug+Advax2

Experimental

recombinant influenza hemagglutinin (H5) 45ug, Advax2 adjuvant 20mg, i.m. injection, 2 doses

干预措施: recombinant influenza hemagglutinin (Biological)

HA 45ug+Advax2

Experimental

recombinant influenza hemagglutinin (H5) 45ug, Advax2 adjuvant 20mg, i.m. injection, 2 doses

干预措施: Advax2 (Biological)

HA 15ug+Advax1

Experimental

recombinant influenza hemagglutinin (H5) 15ug, Advax1 adjuvant 20mg, i.m. injection, 2 doses

干预措施: recombinant influenza hemagglutinin (Biological)

HA 15ug+Advax1

Experimental

recombinant influenza hemagglutinin (H5) 15ug, Advax1 adjuvant 20mg, i.m. injection, 2 doses

干预措施: Advax1 (Biological)

HA 15ug+Advax2

Experimental

recombinant influenza hemagglutinin (H5) 15ug, Advax2 adjuvant 20mg, i.m. injection, 2 doses

干预措施: recombinant influenza hemagglutinin (Biological)

HA 15ug+Advax2

Experimental

recombinant influenza hemagglutinin (H5) 15ug, Advax2 adjuvant 20mg, i.m. injection, 2 doses

干预措施: Advax2 (Biological)

HA 5ug+Advax1

Experimental

recombinant influenza hemagglutinin (H5) 5ug, Advax1 adjuvant 20mg, i.m. injection, 2 doses

干预措施: recombinant influenza hemagglutinin (Biological)

HA 5ug+Advax1

Experimental

recombinant influenza hemagglutinin (H5) 5ug, Advax1 adjuvant 20mg, i.m. injection, 2 doses

干预措施: Advax1 (Biological)

HA 5ug+Advax2

Experimental

recombinant influenza hemagglutinin (H5) 5ug, Advax2 adjuvant 20mg, i.m. injection, 2 doses

干预措施: recombinant influenza hemagglutinin (Biological)

HA 5ug+Advax2

Experimental

recombinant influenza hemagglutinin (H5) 5ug, Advax2 adjuvant 20mg, i.m. injection, 2 doses

干预措施: Advax2 (Biological)

HA 2.5ug+Advax2

Experimental

recombinant influenza hemagglutinin (H5) 2.5ug, Advax2 adjuvant 20mg, i.m. injection, 2 doses

干预措施: recombinant influenza hemagglutinin (Biological)

HA 2.5ug+Advax2

Experimental

recombinant influenza hemagglutinin (H5) 2.5ug, Advax2 adjuvant 20mg, i.m. injection, 2 doses

干预措施: Advax2 (Biological)

HA 15ug

Experimental

recombinant influenza hemagglutinin (H5) 15ug, i.m. injection, 2 doses

干预措施: recombinant influenza hemagglutinin (Biological)

结局指标

主要结局

The incidence of adverse events

时间窗: 12 months

The frequency of adverse events will be compared between groups

次要结局

  • Hemagglutination inhibition assay(1 month post each immunization and 11 months post final immunization)

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (2)

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