Study to Demonstrate Non-inferiority of GSK Biologicals' Hib-MenC With Priorix™, Versus MenC-CRM197 Vaccine With Hiberix™ & Priorix™ in Toddlers Primed With Hib But Not MenC & to Evaluate Persistence up to 5 Years After Vaccination.
试验速览
- 阶段
- 3 期
- 状态
- 已完成
- 入组人数
- 433
- 试验地点
- 7
- 主要终点
- Number of Subjects With Anti-polyribosylribitol Phosphate (Anti-PRP) Antibody Concentration Greater Than or Equal to 0.15 Micrograms Per Milliliter (µg/mL)
研究概览
简要总结
The purpose of the primary phase of the study is to demonstrate the non-inferiority of a single dose of GSK Biologicals' Haemophilus influenzae type b and meningococcal C (Hib-MenC) conjugate vaccine when given in the second year of life to subjects primed in infancy with a Hib vaccine, but not with a meningococcal serogroup C vaccine, versus commercially available Hib and MenC vaccines.
In the extension phase, at Years 1, 2, 3, 4 & 5, one blood sample is taken at each year to follow the antibody persistence up to 5 years after vaccination. No additional vaccine is administered during the extension phase. The Protocol Posting has been updated in order to comply with the FDA Amendment Act, Sep 2007.
详细描述
This multicenter study is open and has 2 treatment groups with Hiberix™ + a commercially available MenC vaccine as active controls. Priorix™ is given concomitantly in both groups. In the primary phase, two blood samples are taken from all subjects for immunogenicity analyses: before and one month after vaccination. In the extension phase, at Year 1, 2, 3, 4 & 5, one blood sample is taken at each year to follow the antibody persistence up to 5 years after vaccination. No additional vaccine is administered during the extension phase.
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
- None
入排标准
- 年龄范围
- 12 Months 至 18 Months（Child）
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •Primary phase:
- •Subjects whom the investigator believes that their parents/guardians can and will comply with the requirements of the protocol.
- •A male or female between, and including, 12 and 18 months of age at the time of vaccination.
- •Written informed consent obtained from the parent or guardian of the subject.
- •Free of obvious health problems as established by medical history and clinical examination before entering into the study.
- •Previously completed routine childhood vaccinations to the best of his/her parents'/guardians knowledge.
- •Having completed primary vaccination with two doses of Haemophilus influenzae type b outer membrane protein (Hib-OMP) containing vaccine OR three doses of diphtheria, tetanus, acellular pertussis and Haemophilus influenzae type b (DTPa/Hib) containing vaccine at least 6 months before the study start.
- •Long-term persistence phase:
- •Having participated in the vaccination study 106445
排除标准
- •For the primary vaccination phase:
- •Use of any investigational or non-registered product (drug or vaccine) other than the study vaccine(s) within 30 days preceding the first dose of study vaccine, or planned use during the study period.
- •Chronic administration (defined as more than 14 days) or planned administration of immuno-suppressants or other immune-modifying drugs within six months prior to vaccination.
- •Planned administration/administration of a vaccine not foreseen by the protocol during the period starting from 30 days before vaccination and ending 30 days after vaccination.
- •Administration of a meningococcal vaccine not foreseen by the study protocol during the period starting at birth and ending at first dose.
- •Previous administration of a booster dose of Hib vaccine.
- •Previous vaccination against measles, mumps, rubella.
- •History of H. influenzae type b, meningococcal serogroup C and/or confirmed measles, mumps or rubella diseases.
- •Known exposure to measles, mumps or rubella within 30 days prior to the start of the study.
- •Any confirmed or suspected immunosuppressive or immunodeficient condition, including human immunodeficiency virus infection.
- •A family history of congenital or hereditary immunodeficiency.
- •History of allergic disease or reactions likely to be exacerbated by any component of the vaccine.
- •Major congenital defects or serious chronic illness.
- •History of neurological disorders or more than one episode of febrile convulsion.
- •Acute disease at the time of enrolment.
- •Administration of immunoglobulins and/or any blood products since birth or planned administration during the study period.
- •Additional exclusion criteria for the long-term persistence phase: to be checked each year.
- •Previous administration of a booster dose of Hib, meningococcal serogroup C vaccines.
- •History of H. influenzae type b, meningococcal serogroup C diseases.
结局指标
主要结局
Number of Subjects With Anti-polyribosylribitol Phosphate (Anti-PRP) Antibody Concentration Greater Than or Equal to 0.15 Micrograms Per Milliliter (µg/mL)
时间窗: 1 month after vaccination
Anti-PRP antibody concentration greater than or equal to 0.15 µg/mL is indicative of short-term protection.
Number of Subjects With Meningococcal Serogroup C Serum Bactericidal Assay Using Rabbit Complement (rSBA-MenC) Titers Greater Than or Equal to 1:8 Titer
时间窗: 1 month after vaccination
rSBA-MenC titers greater than or equal to 1:8 titer are indicative of seroprotection.
次要结局
- Number of Subjects With Meningococcal Serogroup C Serum Bactericidal Assay Using Rabbit Complement (rSBA-MenC) Titers Above the Cut-off Values(5 years after vaccination)
- Number of Subjects With Anti-polysaccharide C (Anti-PSC) Antibody Concentration Above the Cut-off Values(Prior to, 1 month, 1 year, 2 years and 3 years after vaccination)
- Meningococcal Serogroup C Serum Bactericidal Assay Using Rabbit Complement (rSBA-MenC) Titers(5 years after vaccination)
- Anti-polysaccharide C (Anti-PSC) Antibody Concentrations(Prior to, 1 month, 1 year, 2 years and 3 years after vaccination)
- Number of Subjects With Anti-polyribosylribitol Phosphate (Anti-PRP) Antibody Concentration Above Cut-off Values(5 years after vaccination)
- Number of Subjects Reporting Unsolicited Symptoms(Within 31 days (Day 0 - Day 30) after vaccination)
- Number of Subjects Reporting Serious Adverse Events (SAEs)(Throughout the entire study period (up to year 5))
- Anti-polyribosylribitol Phosphate (Anti-PRP) Antibody Concentrations(5 years after vaccination)
- Number of Subjects Reporting Solicited Local and General Symptoms(Within 4 days (Day 0 -Day 3) after vaccination)