跳至主要内容
临床试验/NL-OMON31421
NL-OMON31421已完成3 期

An open-label, randomised, comparative, multi-centre study of the immunogenicity and safety of a 1-dose regimen and different 2-dose regimens of a Zoster vaccine (Live), ZOSTAVAX, in subjects >= 70 years of age - Zostavax-study

Sanofi Pasteur MSD S.N.C.0 个研究点目标入组 150 人开始时间: 待定最近更新:
适应症

试验速览

阶段
3 期
状态
已完成
发起方
入组人数
150

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
18 至 99(—)

入选标准

  • 70 years or older, varicella history-positive or residence for > 30 years in a country with endemic VZV infection

排除标准

  • Febrile within the last 72 hours before vaccination, history of hypersensitivity/anaphylactoid reaction to ZOSTAVAX components including gelatine or neomycin, prior herpes-zoster episode clinically diagnosed by a physician

研究者

发起方
Sanofi Pasteur MSD S.N.C.

相似试验

进行中(未招募)
不适用
An open-label, randomised, comparative, multi-centre study of the immunogenicity and safety of a 2-dose regimen of ProQuad® manufactured with rHA administered to healthy children from 9 months of ageMeasles, mumps, rubella and varicella vaccine administered to healthy children from 9 months of age
EUCTR2007-002468-88-FISanofi Pasteur MSD SNC1,620
进行中(未招募)
1 期
An open-label, randomised, comparative, multi-centre study of the immunogenicity and safety of a 1-dose regimen and different 2-dose regimens of a Zoster vaccine (Live), ZOSTAVAX ®, in subjects = 70 years of age
EUCTR2007-000744-28-NLSanofi Pasteur MSD S.N.C.
进行中(未招募)
不适用
An open-label, randomised, comparative, multi-centre study of the immunogenicity and safety of a 2-dose regimen of ProQuad® manufactured with rHA administered to healthy children from 9 months of ageMeasles, mumps, rubella and varicella vaccine administered to healthy children from 9 months of age
EUCTR2007-002468-88-DESanofi Pasteur MSD SNC1,620
进行中(未招募)
不适用
An open-label, randomised, comparative, multi-centre study of the immunogenicity and safety of a 1-dose regimen and different 2-dose regimens of a Zoster vaccine (Live), ZOSTAVAX , in subjects equal or over 70 years of age - ND
EUCTR2007-000744-28-ITSanofi Pasteur MSD S.N.C.750
进行中(未招募)
不适用
An open-label, randomised, comparative, multi-centre study of the immunogenicity and safety of the concomitant use of a live pentavalent rotavirus vaccine (RotaTeq®) and a meningococcal group C conjugate (MCC) vaccine in healthy infantsRotaTeq® is indicated for the active immunisation of infants from age of 6 weeks for prevention of gastroenteritis due to rotavirus infection.NeisVac-C® is indicated for active immunisation of children from 2 months of age for the prevention of invasive disease caused by Neisseria meningitidis serogroup C
EUCTR2006-005445-11-FISanofi Pasteur MSD S.N.C.