此页面是自动翻译的,不保证翻译的准确性。请参阅 英文版 对于源文本。

A Study to Evaluate Safety and Immunogenicity of AERAS-402 Administered in HIV-negative, BCG-vaccinated, QFT (+) and (-) Adults Without Evidence of TB (C-012-402)

2016年4月25日 更新者:Aeras

A Phase I Randomized Placebo-controlled Double-blind Study to Evaluate Safety and Immunogenicity of AERAS-402 Administered in HIV-negative, BCG-vaccinated, QuantiFERON®-TB Gold (+) and QuantiFERON®-TB Gold (-) Adults Without Evidence of Tuberculosis.

The available live tuberculosis vaccine Bacillus Calmette-Guérin (BCG) provides incomplete protection against pulmonary tuberculosis. For unknown reasons, a BCG revaccination or "booster", while not toxic, does not provide much additional protection. AERAS-402 presents tuberculosis antigens in the setting of a new, live, replication deficient adenovirus vaccine that may increase T cell immunity and thus protection from tuberculosis. Since BCG-vaccinated individuals are the population for which AERAS-402 might be indicated, AERAS-402 will be administered to individuals in Kenya who have already been vaccinated with BCG.

研究概览

地位

完全的

条件

详细说明

This Phase I study will be conducted as a double-blind, randomized, placebo-controlled study in 20 healthy adult subjects. The study will enroll 10 subjects who are QFT-G positive at screening and 10 subjects who are QFT-G negative at screening. Within QFT-G group, subjects will be randomized to receive AERAS-402 or placebo in a ratio of 4:1. One dose level of AERAS-402 (3 x 10^10 vp) will be investigated in this study. All subjects will receive a single dose of study vaccine (AERAS-402 or placebo) on Study Day 0 and a second dose of study vaccine (AERAS-402 or placebo) on Study Day 56. All vaccinations will be administered by IM injection into the deltoid muscle.

The sample size was selected as adequate for preliminary safety evaluations and initial immunogenicity reviews for this phase study, rather than for statistical reasons. If no serious adverse events are observed in 16 subjects who receive AERAS-402, the upper bound of the 95% confidence interval on the rate of serious adverse event occurrence is 17.1 percent.

The selection of AERAS-402 dose level for evaluation in this study was derived from animal studies and based on the safety profile for the completed and ongoing clinical studies in the U.S. and South Africa.The total duration of follow-up is 182 days for each subject with a total of eleven follow-up clinic visits. The study is planned at a single site in Kisumu, Kenya.

研究类型

介入性

注册 (实际的)

20

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

      • Kisumu、肯尼亚
        • Kenya Medical Research Institute

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

有资格学习的性别

全部

描述

Inclusion Criteria:

  1. Is male or female
  2. Is age 18 through 45 years on Study Day 0
  3. Has completed the written informed consent process
  4. Had BCG vaccination at least 5 years ago, documented through medical history or presence of scar
  5. Females: Ability to avoid pregnancy from 28 days prior to administration of the study vaccine through the end of the study.
  6. Has general good health, confirmed by medical history and physical examination.
  7. Has Body Mass Index (BMI) between 18 and 30 (wt./ht.2) by nomogram
  8. Has ability to complete follow-up period of 182 days as required by the protocol
  9. Is able and willing to commit to avoiding elective surgery for the duration of the study.
  10. Is able and willing to stay in contact with the study site for the duration of the study.
  11. Has completed simultaneous enrollment in Aeras Vaccine Development Registry Protocol.

Exclusion Criteria:

  1. Acute illness on the day of randomization.
  2. Fever ≥37.5°C on the day of randomization.
  3. Evidence of any significant active infection on the day of randomization.
  4. Used immunosuppressive medication within 45 days before entry into the study (inhaled and topical corticosteroids are permitted).
  5. Received immunoglobulin or blood products within 45 days before entry into the study.
  6. Received any investigational drug therapy or vaccine within 182 days before the first dose of study vaccine in this protocol.
  7. Received any standard vaccine within 45 days before the first dose of study vaccine in this protocol, through the last study visit (the use of licensed drugs or vaccines medically indicated during the study is permitted).
  8. Received any adenovector based vaccine previously.
  9. Current chronic drug therapy including hormones such as thyroxin, insulin, etc. (Estrogen and progesterone replacement and contraceptives are permitted)
  10. History or laboratory evidence of any past, present or future possible immunodeficiency state which will include, but is not limited to, any laboratory indication of HIV-1 infection.
  11. History of allergic disease or reactions likely to be exacerbated by any component of the study vaccine.
  12. Previous medical history that may compromise the safety of the subject in the study.
  13. Evidence of a new acute illness that may compromise the safety of the subject in the study.
  14. Pregnant or lactating/nursing females.
  15. Evidence of chronic hepatitis including a positive test for hepatitis B core antibody, or hepatitis C antibody.
  16. Inability to discontinue daily medications except contraceptives during the study.
  17. History of alcohol or drug abuse within the past 2 years.
  18. Tobacco or cannabis smoking three or more days per week
  19. Positive urine test for illicit drugs (opiates, cocaine, amphetamines).
  20. History or evidence of any systemic disease on physical examination or any acute or chronic illness that may interfere with the evaluation of the safety or immunogenicity of the vaccine, including axillary lymphadenopathy
  21. History or evidence (including chest X-ray) of active or past tuberculosis
  22. Abnormal hemoglobin, hematocrit, white blood cell count, absolute neutrophil count, absolute lymphocyte count, PT, PTT, GGT, ALT, AST, total bilirubin, ALP, and creatinine drawn within 36 hours of randomization. CPK must be drawn but the CPK value is not an exclusion criteria.
  23. History of high risk sexual behaviors.

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
安慰剂比较:Placebo
1.0 mL sterile buffer administered by intramuscular (IM) injection to deltoid area on days 0 and 56.
This is the identical buffer solution in which AERAS-402 is formulated.
实验性的:AERAS-402
1.0 mL containing 3 x 10^10 vp/mL suspended in 20 mM Tris buffer, 2 mM MgCl2, 25 mM NaCl, 10% w/v sucrose, 0.02% w/v PS-80 (polysorbate-80, non-animal source) and water. Administered intramuscular (IM) injection to deltoid area on days 0 and 56.
Given to 8 participants that were QFT-G(-) at screening and 8 participants that were GFT-G(+) at screening.

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
Safety of AERAS-402 in healthy, HIV-negative, BCG-vaccinated, QuantiFERON®-TB Gold In-Tube test (QFT-G)(+) and QFT-G(-) adults without evidence of tuberculosis disease in Kenya.
大体时间:Day 0 thru Day 182
Collection of solicited and unsolicited adverse events.
Day 0 thru Day 182

次要结果测量

结果测量
措施说明
大体时间
Immunogenicity profile of AERAS-402 in healthy, HIV-negative, BCG-vaccinated, QFT-G(+) and QFT-G(-) adults without evidence of tuberculosis disease in Kenya.
大体时间:Day 0 thru day 182
Percentage of CD4 and CD8 T cells that produce any of three cytokines (IFN-γ, TNF-α, and/or IL-2) or a combination of the three cytokines simultaneously.
Day 0 thru day 182

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。

赞助

调查人员

  • 首席研究员:Doug Walsh, MD、U. S. Army Medical Research Unit- Kenya

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

2008年9月1日

初级完成 (实际的)

2009年6月1日

研究完成 (实际的)

2010年7月1日

研究注册日期

首次提交

2015年4月27日

首先提交符合 QC 标准的

2015年4月29日

首次发布 (估计)

2015年4月30日

研究记录更新

最后更新发布 (估计)

2016年4月27日

上次提交的符合 QC 标准的更新

2016年4月25日

最后验证

2016年4月1日

更多信息

与本研究相关的术语

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.

订阅