Phase 1/II, Safety and Immunogenicity Study of a Recombinant Protein Tuberculosis Vaccine (AERAS-404) in BCG-Primed Infants
试验速览
- 阶段
- 1 期
- 状态
- 已完成
- 发起方
- 入组人数
- 243
- 试验地点
- 7
- 主要终点
- Investigate the safety of AERAS-404 in HIV-uninfected, HIV-unexposed, BCG-primed infants.
研究概览
简要总结
Phase I/II, randomized, double-blind, placebo-controlled, safety, immunogenicity and dose-range finding study of AERAS-404 Tuberculosis (TB) vaccine administered intramuscularly in Bacille Calmette-Guerin (BCG) primed infants.
详细描述
This is a Phase I/II, randomized, double-blind, placebo-controlled, safety, immunogenicity and dose-range finding study in HIV-uninfected, HIV-unexposed, BCG-primed infants. The study vaccine AERAS-404 or placebo will be administered without concomitant EPI vaccines (Cohorts 1 to 5, N = 159 subjects) and with concomitant EPI vaccines (Cohort 6, N = 70 subjects). Study vaccine or placebo will be administered as a single dose (injection) at Study Day 0 ( ≥168 to ≤ 196 days of age, Cohorts 1 and 2), a 2-dose schedule at Study Day 0 (≥ 168 to ≤ 189 days of age) and Study Day 28 (Cohorts 3A and 3B) or a 3-dose schedule at Study Day 0 (≥ 84 to ≤ 98 days of age), Study Day 42 and Study Day 98 (Cohorts 4 and 5). Subjects in Cohort 6 will receive the study vaccine or placebo at Study Day 0 (≥ 64 to ≤ 83 days of age), Study Day 28 (≥ 91 to ≤ 105 days of age), and Study Day 210 (≥ 273 to ≤ 287 days of age). A cohort will enroll once safety in the previous cohort has been established. AERAS-404 is an investigational vaccine manufactured by Sanofi Pasteur (SP) and Statens Serum Institute (SSI).
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
- 64 Days 至 196 Days（Child）
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •Age at time of entry:
- •Cohorts 1 to 6
- •Cohorts 1 and 2: ≥ 168 to ≤ 196 days
- •Cohorts 3A and 3B: ≥ 168 to ≤ 189 days
- •Cohorts 4 and 5: ≥ 84 to ≤ 98 days (≥ 2 weeks after receipt of EPI vaccine doses at 10 weeks of age)
- •Cohort 6 - coincident with EPI vaccine doses at 10 weeks of age (≥ 64 to ≤ 83 days of age)
- •Source documentation of birth weight ≥ 2.5 kg.
- •Documented BCG vaccination within 72 hours of birth.
- •Documented receipt of all age-appropriate EPI vaccines, except Rotavirus, for Cohorts 4 to 6 (see Appendix II).
- •Source documentation of a negative HIV status in the mother, from any time during pregnancy with this child through randomization.
- •Documentation of infant HIV negative exposure or infection status with negative HIV ELISA and HIV DNA PCR tests.
- •Parent or legal guardian able and willing to provide signed informed consent.
- •Participant/parent/legal guardian able to attend all scheduled visits and to comply with all trial procedures.
排除标准
- •History of TB exposure in household or non-household contact.
- •History/Evidence of TB disease or infection.
- •Quantiferon positive.
- •Prior TST test.
- •Any one of Anemia, Neutropenia, Thrombocytopenia, SGPT (ALT), SGOT (AST) or Creatinine ≥ Grade 2
- •Receipt of a live vaccine within 28 days prior to randomization.
- •Receipt or planned receipt of any investigational vaccine.
- •Known or suspected congenital immunodeficiency.
- •Receipt of immunosuppressive therapy or long-term systemic corticosteroid therapy (prednisone or equivalent for more than 2 consecutive weeks within the past 3 months).
- •Known or suspected autoimmune disease
- •Hypersensitivity to any of the vaccine components, or history of a life-threatening reaction to a vaccine containing any of the same substances as the vaccine used in the trial.
- •Participation in another clinical trial for an investigational product (IP).
- •Bleeding disorder or receipt of anticoagulants in the 3 weeks preceding randomization, contraindicating IM vaccination.
- •Chronic illness that, in the opinion of the investigator, is at a stage where it might interfere with trial conduct or completion.
- •Febrile illness (temperature ≥ 100.4°F [≥ 38.0°C]) within 24 hours prior to randomization.
- •Note: A subject may enroll after recovery from febrile illness if the subject is still within the age window.
- •Systemic antibiotic use within 48 hours prior to randomization.
研究组 & 干预措施
Cohort 1 Aeras404 (5ug H4/100nmol IC31) or Placebo
1 Dose; Subject ≥ 168 to ≤ 196 days of age
干预措施: AERAS-404 (Biological)
Cohort 3B AERAS-404 (15ug H4/500nmol IC31) or Placebo
2 Doses; Subject ≥ 168 to ≤ 189 days of age
干预措施: AERAS-404 (Biological)
Cohort 3A AERAS-404 (5ug H4/500nmol IC31) or Placebo
2 Doses; Subject ≥ 168 to ≤ 189 days of age
干预措施: AERAS-404 (Biological)
Cohort 2 AERAS-404 (5ug H4/500nmol IC31) or Placebo
1 Dose; Subject ≥ 168 to ≤ 196 days of age
干预措施: AERAS-404 (Biological)
Cohort 1 Aeras404 (5ug H4/100nmol IC31) or Placebo
1 Dose; Subject ≥ 168 to ≤ 196 days of age
干预措施: Placebo (Biological)
Cohort 2 AERAS-404 (5ug H4/500nmol IC31) or Placebo
1 Dose; Subject ≥ 168 to ≤ 196 days of age
干预措施: Placebo (Biological)
Cohort 3A AERAS-404 (5ug H4/500nmol IC31) or Placebo
2 Doses; Subject ≥ 168 to ≤ 189 days of age
干预措施: Placebo (Biological)
Cohort 3B AERAS-404 (15ug H4/500nmol IC31) or Placebo
2 Doses; Subject ≥ 168 to ≤ 189 days of age
干预措施: Placebo (Biological)
Cohort 5 AERAS-404 (50ug H4/500nmol IC31) or Placebo
3 Doses; Subject ≥ 84 to ≤ 98 days of age
干预措施: AERAS-404 (Biological)
Cohort 4 AERAS-404 (15ug H4/500nmol IC31) or Placebo
3 Doses; Subject ≥ 84 to ≤ 98 days of age
干预措施: Placebo (Biological)
Cohort 5 AERAS-404 (50ug H4/500nmol IC31) or Placebo
3 Doses; Subject ≥ 84 to ≤ 98 days of age
干预措施: Placebo (Biological)
Cohort 6 AERAS-404 (dose level pending) or Placebo
3 Doses; Subject ≥ 64 to ≤ 83 days of age
干预措施: Placebo (Biological)
Cohort 6 AERAS-404 (dose level pending) or Placebo
3 Doses; Subject ≥ 64 to ≤ 83 days of age
干预措施: AERAS-404 (Biological)
Cohort 4 AERAS-404 (15ug H4/500nmol IC31) or Placebo
3 Doses; Subject ≥ 84 to ≤ 98 days of age
干预措施: AERAS-404 (Biological)
结局指标
主要结局
Investigate the safety of AERAS-404 in HIV-uninfected, HIV-unexposed, BCG-primed infants.
时间窗: Subjects will be followed for up to 1 year and 4 months.
Adverse Events and Serious Adverse Events (SAE) will be collected on subjects throughout their participation in the study. Solicited adverse events are captured 28 days post each vaccination. Evaluation of the safety profile of AERAS-404 will be performed using data from all subjects who received at least one dose and has 7 days of safety data, and will be summarized by cohort and treatment group. The number (percentage) of subjects with any adverse event (including solicited, unsolicited, and serious adverse events) will be summarized by Medical Dictionary for Regulatory Activities (MedDRA) system organ class and Preferred Term. Additional summaries will present the number (percentage) of subjects with any adverse events by severity and by relationship to study vaccine; parameters evaluable by the Aeras 404 Pediatric Toxicity Table provided in the protocol, will be summarized by severity corresponding to Toxicity Grade, as appropriate.
次要结局
- Investigate the safety of a 3-dose AERAS-404 regimen in HIV-uninfected, HIV-unexposed, BCG-primed infants(Subjects will be followed for up to 1 year and 4 months.)