A Randomized, Placebo-controlled, Partially Blinded Phase 1b Clinical Trial to Evaluate the Safety and Immunogenicity of BCG Revaccination, H4:IC31, and H56:IC31 in Healthy, HIV-1-Uninfected Adolescent Participants
试验速览
- 阶段
- 1 期
- 状态
- 已完成
- 发起方
- 入组人数
- 84
- 试验地点
- 1
- 主要终点
- Number of Participants With Adverse Events
研究概览
简要总结
The aims of the phase 1b trial described here are to facilitate identification of assays and immune responses that could then be evaluated as correlates of risk and correlates of protection in efficacy studies and ultimately to provide leads for biomarkers of protection against tuberculosis. This study will complement one ongoing study (NCT02075203) evaluating the prevention of M. Tuberculosis infection using H4:IC31 (also known as AERAS-404).
详细描述
This study proposes to further evaluate the safety and immunogenicity of H4:IC31, H56:IC31, and BCG revaccination. The study will be conducted in previously BCG vaccinated healthy adolescents, and will entail a thorough immunogenicity evaluation of these regimens incorporating unbiased systems vaccinology approaches and novel assessments of baseline and elicited responses that may impact vaccine responses. A major goal for this study is to generate immunological data on a wide range of immune responses using a variety of approaches including validated assessments, unbiased strategies, and novel exploratory assays to increase the likelihood of detecting responses correlating with risk or protection in the prevention of infection study. Investigators contributing to the proposed study have participated in a correlates analysis for an HIV vaccine exhibiting modest efficacy in which 2 correlates of risk were identified.
An additional aim of this study is to explore factors affecting vaccine induced responses that may also impact efficacy. For example, it is hypothesized that exposure to environmental mycobacteria may alter protection provided by BCG vaccination. Reagents for evaluating levels of exposure to environmental mycobacteria are in development as part of a concurrent collaborative study. An exploratory objective for this trial is to apply these reagents to examine whether such exposures influence immune responses elicited by the study vaccine and regimens.
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
- Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
入排标准
- 年龄范围
- 12 Years 至 17 Years（Child）
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •Age of 12 to ≤ 17 years at enrollment
- •Minimum weight ≥ 40 kg
- •Previous BCG vaccination at least 5 years ago documented by scarification or medical card
- •No evidence of active TB disease, as determined by history, physical examination and, if deemed appropriate, sputum investigation and / or chest x-ray.
- •Negative QFT-GIT test at screening, using the manufacturer's recommended threshold of 0.35 IU/mL
- •Assessed by the clinic staff as being at low risk for HIV infection
- •Hemoglobin ≥ 11.7 g/dL for females, ≥ 12.5 g/dL for males
- •Negative HIV-1 and -2 blood test
- •Agree to consistently use effective contraception for sexual activity that could lead to pregnancy from at least 20 days prior to enrollment through the last required protocol clinic visit.
- •(additional minor criteria not added due to space constraints)
排除标准
- •Blood products received within 120 days before first vaccination
- •Investigational research agents received within 182 days before first vaccination
- •Intent to participate in another study of an investigational research agent during the planned duration of the HVTN 602 / AERAS A-042 study
- •Pregnant or breastfeeding
- •History of alcohol or drug abuse
- •A significant contact with active TB disease: for example, shared residency with an individual receiving anti-TB treatment, or with an individual known to have incompletely treated culture or smear positive TB
- •TB prophylaxis within 90 days prior to enrollment
- •History of treatment for active TB disease or latent Mtb infection
- •Positive and indeterminate QFT-GIT result
- •Received a tuberculin skin test (TST) within 90 days prior to enrollment
- •Vaccines and other Injections
- •Immunosuppressive medications received within 168 days before first vaccination.
- •Serious adverse reactions to vaccines including history of anaphylaxis and related symptoms such as hives, respiratory difficulty, angioedema, and/or abdominal pain.
- •Immunoglobulin received within 60 days before first vaccination
- •Autoimmune disease Not excluded: mild, well-controlled psoriasis
- •Clinically significant medical condition, physical examination findings, clinically significant abnormal laboratory results, or past medical history with clinically significant implications for current health. Including but not limited to: Diabetes mellitus type 1 or type 2, Thyroidectomy, or Thyroid disease, Asthma, Asplenia, Bleeding disorders, malignancy, Seizure disorder, and Angioedema
- •(additional minor criteria not added due to space constraints)
结局指标
主要结局
Number of Participants With Adverse Events
时间窗: Up to 8 months
The number of solicited and unsolicited adverse events (AEs), including serious adverse events (SAEs), recorded post-vaccination for all participants.
Percentage of Participants With Response Rates to TB Antigens as Compared to Baseline
时间窗: Days 70 and 168
Flow cytometry was used to examine TB Mb-specific CD4+ and CD8+ T-cell responses using the ICS assay. The antigens used to stimulate cells in this assay included peptide pools for the vaccine-matched proteins (Ag85B, ESAT-6, Rv2660c, and TB 10.4) as well as complex TB antigens (TB whole cell lysate \[TB WCL\], and BCG Pasteur strain.
次要结局
- Evaluate Humoral Responses Elicited by the Different Vaccine Regimens.(Up to day 168.)
- Evaluate Changes in Innate Cells in Response to the Vaccine Regimens(Up to day 168)
- Measure Non-classical Major Histocompatibility Complex (MHC)-Restricted T-cell Vaccine-induced Responses, Such as to Mycobacterial Lipids (CD1-restricted) and Metabolites (MR1-restricted).(Up to day 168)
- * Evaluate Immune Response From Vaccine Regimens by Measuring Early (Innate) Vaccine-induced Peripheral Blood Transcription Profiles; Determine Which Responses Are Associated With Antigen-specific Adaptive Responses * Evaluate Adaptive Immune Response.(Up to day 168)
- Evaluate QFT-GIT and ESAT-6 Free IGRA Discordance and Conversion/Reversion Rate During the Course of the Trial.(Up to day 168)