Safety of Tuberculosis Vaccine, MVA85A, Administered by the Intramuscular Route and the Intradermal Route
Safety and Immunogenicity of Candidate Tuberculosis (TB) Vaccine MVA85A Administered by the Intramuscular Route and the Intradermal Route: a Phase I Randomised Active Controlled Trial
研究概览
详细说明
We postulate that the intramuscular route is not inferior to the intradermal route of administration of MVA85A in BCG vaccinated adults when evaluated for safety and immunogenicity.
If MVA85A can be given safely by intramuscular route and it is at least equally immunogenic and efficacious in a prime-boost strategy, then it would probably be the preferred route in subsequent phase II and III trials. There are several reasons for this:
- Reduced pain associated with injection.
- Reduced local reaction at the injection site.
- More straightforward procedure; less technically demanding; less time consuming.
- Easier production and storage of vaccine.
- Larger volume of vaccine can be given.
Trials of MVA85A to date have established 1 x 10^8 pfu as the optimal dose for intradermal injection in adults. We therefore intend to administer this same dose intramuscularly in order to directly compare the two routes for both safety and immunogenicity. These results will guide future trials in which the intramuscular route, if safe, could be further evaluated at either higher or lower dose depending on immunogenicity at 1 x 10^8 pfu dosage.
研究类型
注册 (预期的)
阶段
- 阶段1
联系人和位置
学习地点
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Oxford、英国、OX3 7LJ
- Centre of Clinical Vaccinology and Tropical Medicine (CCVTM) Churchill Hospital
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参与标准
资格标准
适合学习的年龄
接受健康志愿者
有资格学习的性别
描述
Inclusion Criteria:
- Healthy adult aged 18 - 55 years (both male and female)
- Resident in or near Oxford for the duration of the study period
- Confirmation of prior vaccination with BCG not less than 3 months prior to projected study vaccination date (by visible BCG scar on examination or written documentation)
- Normal medical history and physical examination
- Willingness to allow the Investigators to discuss the individual's medical history with their GP
- Willingness to use continuous effective barrier contraception for three months after receiving the vaccination (males and females)
- Willingness to use effective contraception for the duration of the study period (females only)
- Agreement to refrain from blood donation during the course of the study
- Give written informed consent
- Agreement to allow the Investigator to register volunteer details with a confidential database to prevent concurrent entry into clinical trials
- Able and willing (in the Investigator's opinion) to comply with all the study requirements
Exclusion Criteria:
- Clinical, radiological, or laboratory evidence of current active TB infection
- Laboratory evidence at screening of latent TB infection as indicated by a positive ELISPOT test (greater than 17 sfc/million PBMC) in any ESAT6 peptide or CFP10 peptide poola
- Previous vaccination with candidate vaccine MVA85A or another recombinant MVA vaccine
- Clinically significant history of skin disorder, allergy, immunodeficiency (including human immunodeficiency virus [HIV]), cancer (except basal cell carcinoma [BCC] or carcinoma in situ [CIS]), cardiovascular disease, respiratory disease, gastrointestinal disease, liver disease, renal disease, endocrine disorder, neurological illness, psychiatric disorder, drug or alcohol abuse
- History of serious psychiatric condition
- Concurrent oral or systemic steroid medication or the use of other immunosuppressive agents
- History of anaphylaxis to vaccination or any allergy likely to be exacerbated by any component of the study vaccine
- Any clinically significant abnormality of screening blood or urine tests
- Positive hepatitis B surface antigen (HBsAg), hepatitis C virus (HCV) or HIV antibodies
- Female currently lactating, confirmed pregnancy or intention to become pregnant during study period
- Use of an investigational medicinal product or non-registered drug, live vaccine, or medical device other than the study vaccine for 30 days prior to dosing with the study vaccine, or planned use during the study period
- Administration of immunoglobulins and/or any blood products within the three months preceding the planned trial vaccination date
- Any other significant disease, disorder, or finding, which, in the opinion of the Investigator, may either put the volunteer at risk or may influence the result of the study or may affect the volunteer's ability to participate in the study
学习计划
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: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:Group A
Intramuscular immunisation
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Single injection of 1 x 108 pfu MVA85A
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实验性的:Group B
Intradermal immunisation
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Single injection of 1 x 108 pfu MVA85A
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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:6 months following vaccination
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Safety data in both groups, as assessed by the frequency, incidence, and nature of adverse events (AEs) and serious adverse events (SAEs) during the study.
Safety is measured throughout the 6 months follow up period, but specifically on the following days: 2, 7, 14, 28, 56, 84 and 168 and.
Blood for safety testing is taken at Days 7 and 28.
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6 months following vaccination
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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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Immunogenicity
大体时间:6 months following vaccination
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Immunogenicity data in both groups.
This will be obtained from exploratory immunological laboratory investigations on blood samples taken at screening, and throughout follow up.
Immunogenicity is measured throughout the 6 months follow up period, but specifically on the following days: 2, 7, 14, 28, 56, 84 and 168.
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6 months following vaccination
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合作者和调查者
出版物和有用的链接
研究记录日期
研究主要日期
学习开始
初级完成 (实际的)
研究完成 (实际的)
研究注册日期
首次提交
首先提交符合 QC 标准的
首次发布 (估计)
研究记录更新
最后更新发布 (估计)
上次提交的符合 QC 标准的更新
最后验证
更多信息
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