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临床试验/NCT00385320
NCT00385320已完成2 期

To Assess the Efficacy, Immuno & Safety of 2 Doses of GSK HRV Vaccine at Different Virus Concentrations in Healthy Infants Aged 2 Months & Previously Uninfected With HRV, Concurrently Given With DTPw-HBV, Hib.

GlaxoSmithKline0 个研究点目标入组 2,640 人开始时间: 2001年5月31日最近更新:
适应症

试验速览

阶段
2 期
状态
已完成
入组人数
2,640
主要终点
Occurrence of RV GE

研究概览

简要总结

The purpose of this study is to test how infants respond to different strengths of the human rotavirus vaccine.

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
Double

入排标准

年龄范围
6 Weeks 至 12 Weeks(Child)
性别
All
接受健康志愿者

入选标准

  • Healthy male or female infant between, and including, 6 and 12 weeks of age born after a gestation period of 36 to 42 weeks or a birth weight of >2000g.
  • Written informed consent obtained from the parent or guardian of the subject.

排除标准

  • Planned administration of oral polio vaccine during the period starting from 2 weeks before each dose of study vaccine(s) and ending 2 weeks after.
  • Any confirmed or suspected immunosuppressive or immunodeficient condition, including human immunodeficiency virus (HIV) infection
  • History of diphtheria, tetanus, pertussis, Hib disease and/ or hepatitis B.
  • Previous vaccination against diphtheria, tetanus, pertussis, and/or Haemophilus influenzae type b.
  • History of allergic disease
  • Any clinically significant history of chronic gastrointestinal disease including any uncorrected congenital malformation of the GI tract or other serious medical condition as determined by the investigator.
  • Gastroenteritis within 7 days preceding the study vaccine administration (warrants deferral of the vaccination)
  • Previous confirmed occurrence of RV GE.
  • Household contact with an immunosuppressed individual or pregnant women.
  • Administration of immunoglobulins and/or blood products since birth or planned administration during the study period

结局指标

主要结局

Occurrence of RV GE

次要结局

  • Serum RV IgA antibody titre, Viral shedding, Seroprotection/seropositivity status for DTPwHBVHib antigens, Solicited, unsolicited & SAE

研究者

申办方类型
Industry
责任方
Sponsor

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