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临床试验/NCT00835380
NCT00835380已完成3 期

A Phase III Open-Label Study of Immunogenicity, Safety, and Tolerability of 2 Doses of VAQTA™ (Formalin, Inactivated, Alum-Adjuvanted Hepatitis A Vaccine) in Healthy Children 12 to 23 Months of Age

Merck Sharp & Dohme LLC0 个研究点目标入组 80 人开始时间: 2008年3月1日最近更新:
适应症
干预措施

试验速览

阶段
3 期
状态
已完成
入组人数
80
主要终点
Hepatitis A Virus (HAV) Seroconversion Rate, i.e. the Percentage of Subjects Who Were Seronegative at Baseline and Developed Seropositive at Month 7 After Administration of a 2-dose Regime of Vaccines.

研究概览

简要总结

This study will demonstrate the immunogenicity and evaluate the safety/tolerability of the vaccine in Chinese children between 12 and 23 months of age.

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
12 Months 至 23 Months(Child)
性别
All
接受健康志愿者
是

入选标准

  • •Healthy Chinese children 12 to 17 months old at receipt of the first study vaccination

排除标准

  • •Subject is Hepatitis A virus antibody positive at screening or has a history of Hepatitis A infection
  • •Subject has a fever 72 hours prior to first injection
  • •Subject has already been vaccinated for Hepatitis A
  • •Subject is allergic to aluminum, formaldehyde, sodium borate, latex, or any component of the vaccine
  • •Subject has received inactivated vaccines within 14 days of screening or live vaccines within 30 days of screening

研究组 & 干预措施

1

Experimental

VAQTA™

干预措施: Hepatitis A Vaccine, Purified Inactivated (VAQTA™) (Biological)

结局指标

主要结局

Hepatitis A Virus (HAV) Seroconversion Rate, i.e. the Percentage of Subjects Who Were Seronegative at Baseline and Developed Seropositive at Month 7 After Administration of a 2-dose Regime of Vaccines.

时间窗: Collect blood sample for HAV antibody testing at Day 0 prior to vaccination, and Month 7 (4 weeks after administration of a 2-dose regimen of vaccines at Month 6)

Seroconversion rate = (number of subjects with seronegative at baseline and developed seropositive at Month 7)/(number of subjects with seronegative at baseline regardless HAV serum status at Month 7). Measure serum HAV (hepatitis A virus) antibody at Day 0 prior to vaccination and at Month 7 after administration of a 2-dose regimen of vaccines. HAV antibody titers were determined by Wantai ELISA kit for serum antibody response to HAV. Seropositive was defined as HAV antibody titer ≥ 50 mIU/mL. Seronegative was defined as HAV antibody titer \< 50 mIU/mL.

次要结局

  • Serious Adverse Experiences and Systemic Adverse Experiences Occurring Within 14 Days After Each Vaccination, and Injection-site Complaints Occurring Day 1 Through Day 5 After Each Vaccination(For serious adverse experiences and systemic adverse experiences: 14 days follow-up after each dose of vaccination; For injection-site adverse experiences: 5 days follow-up after each dose of vaccination)

研究者

申办方类型
Industry
责任方
Sponsor

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