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临床试验/TCTR20210628005
TCTR20210628005已完成3 期

Safety and immunogenicity of heterologous prime/boost inactivated COVID-19 vaccine and viral vector vaccine: an experimental clinical study

ational Research Council of Thailand (NRCT)0 个研究点目标入组 100 人开始时间: 2021年6月28日最近更新:
适应症

试验速览

阶段
3 期
状态
已完成
发起方
入组人数
100

研究概览

简要总结

Given the shorter completion time of two doses, heterologous CoronaVac followed by ChAdOx1-S can be considered as an alternative regimen to homologous efficacy-proven ChAdOx1-S in countries with circulating variants. Additional studies on the efficacy and durability of immune responses induced by heterologous vaccine regimens are warranted.

研究设计

研究类型
Interventional

入排标准

年龄范围
18 Years 至 N/A (No limit)(—)
性别
All

入选标准

  • 1. Healthy individuals above 18 years of age
  • 2. Have never been infected with SARS-CoV-2
  • 3. Have never been vaccinated with COVID-19 vaccine
  • 4. Not in the immunocompromised status

排除标准

  • 1. Are being infected with COVID-19
  • 2. Bleeding disorders

研究者

发起方
ational Research Council of Thailand (NRCT)

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