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临床试验/NCT01406509
NCT01406509已完成1 期

A Phase I Clinical Trial for Safety of A Group A, C Polysaccharide Meningococcal and Type b Haemophilus Influenzal Conjugate Vaccine in Children

Jiangsu Province Centers for Disease Control and Prevention1 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2011年8月最近更新:
适应症

试验速览

阶段
1 期
状态
已完成
入组人数
40
试验地点
1
主要终点
The adverse reactions in healthy children (6-23 months) after the second vaccination

研究概览

简要总结

Haemophilus influenzae is an important pathogen which can cause primary infection and respiratory viral infection in infants and leaded to secondary infections. The infection of haemophilus is a major cause of morbidity and mortality in infants and children. At present, the developed conjugant Hib vaccine is proved to be safe and effective, 90-99% of children will produce antibody of protection after 3 doses. Because Hib vaccine can prevent meningitis, pneumonia, epiglottis inflammation and other serious infection caused by Hib bacteria, the WHO suggested that Hib vaccine should be included in the infant's normal immune programming.

Since the use of meningitis aureus polysaccharide vaccine, incidence of a disease in recent years is declined and maintain to the level of 0.5 per 1/100 thousand. But meningitis aureus polysaccharide vaccine with a relatively poor immune response in the infants under the age of two, and the remaining 60% with a low antibody level and a short duration.

According to the present immunization schedule, to reach the median level of antibody levels there are at least 4 doses in need. So it is meaningful to improving vaccine immunogenicity, to provide high levels of long-term protection and to reduce the number of injections.

The objective of this study is to evaluate the safety of the group A, C polysaccharide meningococcal and type b haemophilus Influenzal Conjugate vaccine.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Single Group
主要目的
Prevention
盲法
None

入排标准

年龄范围
6 Months 至 5 Years(Child)
性别
All
接受健康志愿者

入选标准

  • Healthy subjects aged from 6 months to 5years old of normal intelligence
  • The subjects'guardians are able to understand and sign the informed consent
  • Subjects established as healthy after medical history questioning,physical examination and clinical decision and in accordance with vaccination requirements of the experimental vaccine
  • Subjects who can comply with the requirements of the clinical trial program according to the researcher's views
  • Subjects who have never received group A, C polysaccharide meningococcal vaccine and type b haemophilus Influenzal vaccine
  • Subjects with temperature <37°C on axillary setting

排除标准

  • Exclusion Criteria for the first dose:
  • Subject who has a medical history of Meningitis
  • Subject that has a medical history of any of the following: allergies, seizures, epilepsy, encephalopathy history and so on
  • Subject who is allergic with tetanus toxoid components
  • Subject suffering from thrombocytopenia or other coagulation disorder may lead to contraindication to intramuscular injection
  • Subject who has a history of allergic reactions
  • Any known immunological dysfunction
  • Had received gamma globulin or immune globulin, in the past two weeks
  • Subject suffering from congenital malformations, dysgenopathy or serious chronic disease
  • Any acute infections
  • Any condition that in the opinion of the investigator, may interfere with the evaluation of study objectives
  • Exclusion Criteria for the second dose:
  • Had any Grade 3 or Grade 4 adverse reactions or events
  • Any situation meets the exclusion criteria stated in the exclusion criteria for first dose
  • Any condition the investigator believed may affect the evaluation of the vaccine

结局指标

主要结局

The adverse reactions in healthy children (6-23 months) after the second vaccination

时间窗: 7 days after the second vaccination

to evaluate the adverse reactions of the group A, C polysaccharide meningococcal and type b haemophilus Influenzal Conjugate vaccine in healthy children (6-23 months) after the second vaccination

The adverse reactions in healthy children (2-5 years) after the first vaccination

时间窗: 7 days after the first vaccination

to evaluate the adverse reactions of the group A, C polysaccharide meningococcal and type b haemophilus Influenzal Conjugate vaccine in healthy children (2-5 years) after the first vaccination

The adverse reactions in healthy children (6-23 months) after the first vaccination

时间窗: 7 days after the first vaccination

to evaluate the adverse reactions of the group A, C polysaccharide meningococcal and type b haemophilus Influenzal Conjugate vaccine in healthy children (6-23 months) after the first vaccination

次要结局

未报告次要终点

研究者

申办方类型
Network
责任方
Principal Investigator
主要研究者

Fengcai Zhu

Professor, Director of Center for Vaccine Clinical Trials

Jiangsu Province Centers for Disease Control and Prevention

研究点 (1)

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