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临床试验/NCT01456715
NCT01456715已完成3 期

Immunogenicity and Safety of Gardasil and Twinrix Vaccines Co-administered or Administered a Month Apart, According to the 0, 6 Months Schedule and the Effect of a Third Dose of Gardasil or Cervarix Administered 42 Months Later.

Laval University2 个研究点 分布在 1 个国家目标入组 418 人开始时间: 2008年9月最近更新:
适应症

试验速览

阶段
3 期
状态
已完成
入组人数
418
试验地点
2
主要终点
Antibody to HPV

研究概览

简要总结

Two human papillomavirus vaccines are now commercially available.

No clinical data exist regarding:

  • The immunogenicity and safety of Gardasil and Twinrix when co-administered.
  • The immunogenicity and safety of Cervarix when administered to subjects previously vaccinated with Gardasil.

The main objective of the first phase of this clinical trial was:

• To assess and compare the immunogenicity of Gardasil and Twinrix Junior when co-administered or administered at one month interval according to a 0, 6 month schedule to 9-10 year-old girls.

The main objective of the seconde phase of this clinical trial is:

• To determine the effect of a booster dose of Gardasil or Cervarix on HPV antibodies when given 42 months post-vaccination of 9-10 year-old girls with two doses of Gardasil.

Study Design & Duration:

Experimental Design: Blind for the third HPV vaccine dose, randomized, single centre study with two treatment groups.

Duration of the study:

Participants will be followed for the duration of 10 years post-primary vaccination.

Number of Centres:

One Center.

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
Single (Participant)

入排标准

年龄范围
12 Years 至 14 Years(Child)
性别
Female
接受健康志愿者

入选标准

  • In 2008-2009 received two doses of Gardasil at the age of 9-10 years according to 0, 6 months schedule.

排除标准

  • Received less than two doses of Gardasil or received an HPV vaccine outside the study protocol.

结局指标

主要结局

Antibody to HPV

时间窗: 1 month post booster dose

The effect of a booster dose of Gardasil or Cervarix administered randomly (1:1) to subjects vaccinated 42 months before with two doses of Gardasil.

次要结局

  • Safety of a booster dose of Gardasil and Cervarix administered 42 months after the second dose of Gardasil.(Solicited adverse events 5 days post vaccine administration. Serious adverse events during the study period.)

研究者

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

Vladimir Gilca

Principal investigator

Laval University

研究点 (2)

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