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临床试验/EUCTR2016-001104-36-NL
EUCTR2016-001104-36-NL进行中(未招募)1 期

Immunogenicity and safety study of a third measles mumps rubella (MMR-3) vaccine dose in healthy young adults in The Netherlands - Third MMR vaccine dose in young adults (acronym: MMR-3)

RIVM0 个研究点目标入组 147 人开始时间: 2016年5月23日最近更新:
适应症
相关药物

试验速览

阶段
1 期
状态
进行中(未招募)
发起方
入组人数
147

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional clinical trial of medicinal product

入排标准

性别
All

入选标准

  • Healthy young adult 18-25 years of age.
  • Previously been immunized with two doses of the MMR vaccine according to the Dutch NIP (MMR-1 at ~14 months and MMR-2 at ~9 years).
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range 150
  • F.1.3 Elderly (>=65 years) no
  • F.1.3.1 Number of subjects for this age range

排除标准

  • Medical conditions that will severely affect immunological responses to vaccinations, such as, but not limited to, cancer or an immune disorder.
  • Vaccination should be postponed during any illness with fever >38.5°C until the fever has disappeared.
  • Vaccination with any vaccine during the first two weeks before and four weeks after MMR-3.
  • An additional MMR vaccination during the study.
  • Coagulation disorder and/or anticoagulant medication.
  • Be or have been under immunosuppressive medical treatment, like cytostatics, high-dose corticosteroids, immune globulins, blood or plasma transfusions that might interfere with the results of the study (within the previous 3 months).
  • Have or previously had clinical symptoms of mumps virus infection.
  • Have or previously had cases of mumps disease within your Household.
  • Had experienced a previous severe adverse reaction to any vaccine.
  • Being pregnant; Furthermore, pregnancy should be avoided for 1 month following vaccination.
  • Breast-feeding women.

研究者

发起方
RIVM

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