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临床试验/CTRI/2012/08/002922
CTRI/2012/08/002922已完成3 期

A Phase III Clinical Trial to Study the Safety, Tolerability, and Immunogenicity of ZOSTAVAXâ?¢ in Healthy Adults in India

Merck Sharp and Dohme0 个研究点目标入组 250 人开始时间: 待定最近更新:

试验速览

阶段
3 期
状态
已完成
发起方
入组人数
250

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

入选标准

  • A subject will be eligible to participate in this study if all of the following criteria apply:
  • a.Greater than or equal to 50 years of age.
  • b.Females have a negative pregnancy test and use an acceptable method of birth control, or are postmenopausal
  • c.Any underlying chronic illness must be in stable condition.
  • Note: We have entered maximum age of 99 yrs, as there is no upper limit defined in the study protocol, the same is approved by the directorate(DCGI).

排除标准

  • A subject will not be eligible to participate in this study if any of the following criteria apply:
  • a.History of hypersensitivity reaction to any vaccine component
  • b.Prior history of HZ
  • c.Previously received a varicella or zoster vaccine
  • d.Pregnant or breastfeeding
  • e.Have recently received blood products other than autologous blood transfusion
  • f.Use of immunosuppressive therapy
  • g.Known or suspected immune dysfunction
  • h.Use of nontopical antiviral therapy with activity against herpes virus

研究者

发起方
Merck Sharp and Dohme

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