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临床试验/NCT00735839
NCT00735839已完成1 期

A Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Safety, Tolerability, and Immunogenicity of a Single Dose of Merck S. Aureus Vaccine (V710) in Healthy Male Japanese Subjects

Merck Sharp & Dohme LLC0 个研究点目标入组 40 人开始时间: 2008年3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
主要终点
Geometric Mean Fold Rise (GMFR) From Baseline in Antibody Level

研究概览

简要总结

This study is to evaluate the safety and immunogenicity of V710 in Japanese male subjects.

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 (Participant, Investigator)

入排标准

年龄范围
20 Years 至 80 Years(Adult, Older Adult)
性别
Male
接受健康志愿者

入选标准

  • Generally Good Physical Health

排除标准

  • Received V710 Vaccine, Any Other Investigational S. Aureus Vaccine, Or Investigational S. Aureus Antibodies Before
  • Temperature Of Equal/Greater Than 100.4 Degrees F(38 Degrees C) Within The Past 48 Hours

结局指标

主要结局

Geometric Mean Fold Rise (GMFR) From Baseline in Antibody Level

时间窗: Baseline (Day 1) to Day 14 postvaccination

Geometric mean fold rise is calculated as the natural logarithm of the ratio of Day 14 and baseline antibody titers.

Number of Participants With Vaccine-related Serious Adverse Experiences

时间窗: Baseline (Day 1) to Day 84 postvaccination

Vaccine-related adverse experiences are those determined by the investigator to be possibly, probably, or definitely vaccine-related.

次要结局

未报告次要终点

研究者

申办方类型
Industry
责任方
Sponsor

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