Safety and Reactogenicity of a H1N1 Influenza Challenge Virus in Healthy Volunteers
2013年12月12日 更新者:Immune Targeting Systems Ltd
A Phase I, Open-label, Ascending Dose Study to Determine the Safety and Reactogenicity of a Wild Type Seasonal A/California/ H1N1 2009 Influenza Challenge Virus in Healthy Volunteers, Following a Single Intranasal Administration
The primary objective is to determine the dose level of live, wild-type A/California/ H1N1 2009 virus that has an appropriate safety and illness/infectivity profile to be used as an influenza virus, challenge strain in future intervention studies.
Illness parameters were collected by subject symptom scores as well as by physical examination. Virus parameters were measured by PCR and cell culture assay (performed by VisMederi srl).
研究概览
地位
完全的
条件
研究类型
介入性
注册 (实际的)
29
阶段
- 阶段1
联系人和位置
本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。
学习地点
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-
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Antwerpen、比利时
- SGS Life Sciences
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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 45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:
- Male or female aged 18-45 years inclusive.
- Able to give written informed consent to participate.
- Healthy, as determined by medical history, physical examination, vital signs, 12 lead ECG, and clinical safety laboratory examinations at baseline, as determined by the Investigator.
- Absent or low levels of detectable pre-existing antibodies to influenza virus subtypes, including as a minimum the challenge strain, as determined by an HAI titre of ≤ 10 prior to challenge.
- Non-habitual smoker (habitual smokers are persons who smoke more than 4 cigarettes or other tobacco products on a weekly basis) and agree to not use tobacco products during participation in the study.
Females should fulfil one of the following criteria:
- At least one year post-menopausal;
- Surgically sterile;
- Will use oral, implantable, transdermal or injectable contraceptives for 30 days prior to administration of the A/California/H1N1 2009 virus until the follow-up visit is performed.
- Use another reliable form of contraception approved by the Investigator (e.g., intrauterine device, female condom, diaphragm with spermicide, cervical cap, use of condom by the sexual partner or a sterile sexual partner) from the time of screening until the follow up visit is performed.
- Women of childbearing potential must have a negative serum pregnancy test at screening and a negative urine pregnancy test on Day -1.
- Comprehension of the study requirements, expressed availability for the required study period, and ability to be quarantined for up to 10 days and to attend the scheduled follow-up visit.
- Negative alcohol and urine drug screening tests prior to entering quarantine.
- Being willing to adhere to the prohibitions and restrictions specified in this protocol
Exclusion Criteria:
- Prior receipt of any influenza vaccine for the previous 2 years.
- Significant adulthood history of seasonal hay fever or a seasonal allergic rhinitis or perennial allergic rhinitis or chronic or nasal or sinus condition such as chronic sinusitis.
- Abnormal nasal structure including septal deviation and nasal polyps.
- Suffering from asthma, bronchiectasis, emphysema, chronic obstructive pulmonary disease or any other chronic lung disease.
- Pregnant or who is breast feeding.
- Diastolic BP < 50 or > 90 mmHg, a systolic BP < 100 or > 150 mmHg, a pulse < 50 or > 100 bpm after resting for 5 min.
- Current use or use within the last 7 days of intranasal corticosteroids.
- Presence of significant uncontrolled medical, neurological or psychiatric illness (acute or chronic) as assessed by the Investigator. This includes, but is not limited to, institution of new surgical or medical treatment (for a chronic condition), or a significant dose alteration for uncontrolled symptoms or drug toxicity within 3 months of screening and reconfirmed on Day -1 prior to challenge.
- Positive serology for HIV-1 or HIV-2, or HBsAg or HCV antibodies.
- Cancer or treatment for cancer, within 3 years, excluding basal cell carcinoma of the skin, which is allowed.
- Presence of immunosuppression or any medical condition that may be associated with impaired immune responsiveness, including, but not limited to, diabetes mellitus inflammatory bowel disease.
- Presently receiving (or history of receiving) or during the preceding 3-month period prior to screening, any medications or other treatments that may adversely affect the immune system such as allergy injections, immune globulin, interferon, immunomodulators, cytotoxic drugs or other drugs known to be frequently associated with significant major organ toxicity, or systemic corticosteroids (oral or injectable) azathioprine or mercaptopurine. Topical corticosteroids except intranasal will be allowed.
- Anticipated presence of a household contact with documented severe immunosuppression (as defined by CD4 < 200/mm³ or an absolute neutrophil count < 1500/mm³), either as a result of disease and/or therapy.
- Anticipated presence of a household contact age 5 years or younger, within 2 weeks following challenge.
- Anticipated presence of a household contact age 65 years or older, within 2 weeks following challenge.
- Current professional activity as a carer or healthcare workers who will return to work within 2 weeks following challenge.
- Anticipated presence of a pregnant household contact, within 2 weeks following challenge.
- History of anaphylactic type reaction to egg or egg protein.
- History of Guillain-Barré syndrome.
- History of drug or chemical abuse in the year before the study.
- Receipt of any investigational virus product or nonregistered drug within the 30 days prior to challenge or currently enrolled in any investigational drug study or intends to enrol in such a study within the ensuing study period.
- Receipt of blood or blood products 6 months prior to challenge or planned administration during the study period.
- Blood donation in the last 12 weeks.
- Acute disease within 72 h prior to challenge, defined as the presence of a moderate or severe illness with or without fever (as determined by the Investigator through medical history and physical examination), or presence of a fever ≥ 38ºC oral.
- Elevated white cell count above 10.5 x 109/L or an absolute neutrophil count above 7.5 x 109/L.
- Any condition that, in the opinion of the Investigator, might interfere with the primary study objective.
- Habitual smoker (habitual smokers are persons who smoke more than 4 cigarettes or other tobacco products on a weekly basis).
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
- 分配:非随机化
- 介入模型:单组作业
- 屏蔽:无(打开标签)
武器和干预
参与者组/臂 |
干预/治疗 |
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实验性的:Cohort 1
1:1000 dilution of neat virus
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1:1000 dilution of neat virus
其他名称:
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实验性的:Cohort 2
1:100 dilution of neat virus
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1:100 dilution of neat virus
其他名称:
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实验性的:Cohort 3
1:10 dilution of neat virus
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1:10 dilution of neat virus
其他名称:
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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 |
|---|---|---|
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Safety
大体时间:Day 1 - 29
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Frequency and severity of treatment-emergent adverse events as a measure of which dose of H1N1 challenge virus is safe for future intervention studies
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Day 1 - 29
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Infectivity
大体时间:Day 1- 8
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Frequency and severity of influenza signs and symptoms experienced and incidence of laboratory confirmed infections, as a measure of which dose of H1N1 virus induces an appropriate level of illness/ infectivity for future intervention studies
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Day 1- 8
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次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
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Kinetics
大体时间:Day 1 -8
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Record influenza signs, symptoms, and viral load/shedding over time to assess kinetics of infection
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Day 1 -8
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Immunology
大体时间:Day 1 - 29
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Assess immunological responses over the study period, including
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Day 1 - 29
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Biomarkers
大体时间:Day 1 -29
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investigate gene expression to explore potential markers of influenza A infection that may be used in future intervention studies and, as such, determine mechanisms of vaccine efficacy
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Day 1 -29
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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。
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。
一般刊物
- Muller J, Parizotto E, Antrobus R, Francis J, Bunce C, Stranks A, Nichols M, McClain M, Hill AVS, Ramasamy A, Gilbert SC. Development of an objective gene expression panel as an alternative to self-reported symptom scores in human influenza challenge trials. J Transl Med. 2017 Jun 8;15(1):134. doi: 10.1186/s12967-017-1235-3.
- Watson JM, Francis JN, Mesens S, Faiman GA, Makin J, Patriarca P, Treanor JJ, Georges B, Bunce CJ. Characterisation of a wild-type influenza (A/H1N1) virus strain as an experimental challenge agent in humans. Virol J. 2015 Feb 3;12:13. doi: 10.1186/s12985-015-0240-5.
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
2013年6月1日
初级完成 (实际的)
2013年10月1日
研究完成 (实际的)
2013年10月1日
研究注册日期
首次提交
2013年12月5日
首先提交符合 QC 标准的
2013年12月12日
首次发布 (估计)
2013年12月18日
研究记录更新
最后更新发布 (估计)
2013年12月18日
上次提交的符合 QC 标准的更新
2013年12月12日
最后验证
2013年12月1日
更多信息
此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.