Safety and Immunogenicity of Fluzone Influenza Virus Vaccine (2005-2006 Formulation) Among Healthy Children 6 to 12 Weeks of Age
试验速览
- 阶段
- 2 期
- 状态
- 已完成
- 入组人数
- 1,375
- 试验地点
- 2
- 主要终点
- To demonstrate the safety of Fluzone vaccine administered to 2-month old children
研究概览
简要总结
Study of the safety and immunogenicity (antibody producing capability) comparing inactivated influenza vaccine to placebo given to infants at 2 and 3 months of age. Infants will receive inactivated influenza vaccine at the same time as other vaccines on the routine immunization schedule. Infants will be randomized at enrollment to receive inactivated influenza vaccine or placebo at a 2:1 ratio. This study is double-blind, randomized, and placebo-controlled.
详细描述
Methods: A double-blind, randomized, placebo-controlled trial was conducted in 1375 healthy US infants 6-12 weeks of age. Subjects received either 2 doses of trivalent inactivated influenza vaccine (TIV, Fluzone®, sanofi pasteur 2005-6 pediatric formulation) (N=915) or placebo (N=460) 1 month apart, along with indicated concomitant vaccines. Solicited adverse events were collected for 7 days following each vaccination, unsolicited adverse events for 28 days, and serious adverse events for 6 months. Hemagglutination inhibition antibodies to all 3 vaccine strains were measured following the second TIV/placebo dose.
Results: No significant differences were seen between TIV and placebo groups for any safety outcomes. Fever ≥38oC rectal within 3 days of vaccination was seen in 11.2% vs 11.7% of TIV vs placebo recipients. Serious adverse events within 28 days of vaccine/placebo were reported in 1.9% of TIV and 1.5% of placebo recipients; only one (hypersensitivity reaction in a TIV recipient) was considered vaccine-related. Significantly increased antibody responses (p<0.001) were seen against all 3 strains in TIV recipients by titer ≥ 1:40 or geometric mean titer (GMT) (p<0.001). Altogether, 50% of infants had antibody titers ≥ 1:40 for H1N1, 86% for H3N2, and 11% for B compared with 7%, 10%, and 0.3% in the placebo group. The reciprocal GMT for influenza recipients was 33, 95, and 11 for H1N1, H3N2, and B vs. 7, 9, and 5 for placebo recipients. Over 90% of infants who received TIV had antibody ≥ 1:40 for at least one vaccine strain and 49.6% for 2 strains, vs. 16.4% and 0.9% in the placebo group.
Conclusions: TIV administered to young infants beginning at 6-12 weeks of age is safe and immunogenic.
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
- 42 Days 至 84 Days（Child）
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •Age 42 to 84 days on the day of inclusion
- •Full term (born at >=36 weeks with birth weight >=2.5 kg
- •Considered to be in good health
- •Parental consent obtained and available
- •Available for the study duration (6 months)
排除标准
- •Reported allergy to egg proteins, chicken proteins
- •Previous history of influenza vaccination or disease
- •Receipt of any vaccine other than Hepatitis B prior to enrollment
- •Acute illness with rectal temperature >= 38.0 (defer enrollment)
- •Known bleeding disorder
- •Participation in other interventional clinical trial within 30 days prior to enrollment
结局指标
主要结局
To demonstrate the safety of Fluzone vaccine administered to 2-month old children
时间窗: within 6 months
次要结局
未报告次要终点