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临床试验/NCT01470287
NCT01470287已完成3 期

A Phase-III, Single Arm, Multi-Center, Open-Label Study to Assess the Immunogenicity, Safety and Tolerability of a Fully Liquid Pentavalent Vaccine (DTwP-Hib-HepB Vaccine) When Administered to Indian Infants at 6, 10, and 14 Weeks of Age

Novartis Vaccines3 个研究点 分布在 1 个国家目标入组 175 人开始时间: 2011年12月最近更新:
适应症

试验速览

阶段
3 期
状态
已完成
发起方
入组人数
175
试验地点
3
主要终点
Seroprotection rate one month after the last dose of vaccine administration

研究概览

简要总结

This study will evaluate immunogenicity, safety and tolerability of fully liquid pentavalent vaccine (DTwP-Hib-HepB Vaccine) in infants 6-8 weeks of age.

研究设计

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

入排标准

年龄范围
42 Days 至 64 Days(Child)
性别
All
接受健康志愿者

入选标准

  • Male and female subjects ≥ 42 days to ≤ 64 days of age.
  • Written informed consent obtained from either parents/ legal guardian after the nature of the study has been explained according to local regulatory requirements

排除标准

  • Subjects whose parents or legal guardians are unwilling or unable to give written informed consent to participate in the study.
  • History of previous immunization with a vaccine containing any of the 5 antigen components of investigational vaccine.
  • History of anaphylactic shock(immediate hypersensitivity reactions), urticaria or other allergic reactions after previous vaccination or known hypersensitivity to any vaccine component.
  • Administration of parenteral immunoglobulin preparation and/or blood products since birth.

结局指标

主要结局

Seroprotection rate one month after the last dose of vaccine administration

时间窗: One month after last vaccination

次要结局

  • Seroprotection rate and GMCs one month after the last vaccine administration(One month after last vaccination)

研究者

发起方
Novartis Vaccines
申办方类型
Industry
责任方
Sponsor

研究点 (3)

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