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临床试验/TCTR20211120001
TCTR20211120001已完成4 期

Immunogenicity of the booster dose COVID-19 vaccine after complete primary series of inactivated vaccine (Sinovac) and viral vector vaccine (AstraZeneca) with full and half dose of mRNA vaccine

ational Research Council of Thailand (NRCT)0 个研究点目标入组 222 人开始时间: 2021年11月20日最近更新:
适应症

试验速览

阶段
4 期
状态
已完成
发起方
入组人数
222

研究概览

简要总结

Results showed that headache, joint pain, and diarrhea were more frequent in the 15 ug- than the 30 ug-BNT162b2 groups, whereas joint pain and chilling were more frequent in the 100 ug- than the 50 ug-mRNA-1273 groups. No significant differences in immunogenicity were detected. These findings demonstrated that the reduced dose of mRNA vaccines elicited antibody response against the SARS-CoV-2 delta and omicron variants that were comparable to the standard dose.

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 adults aged more than 18 years
  • •2. Provide informed consent
  • •3. Not previously infected with COVID-19

排除标准

  • •1. Infected with COVID-19
  • •2. Immunocompromised individuals

研究者

发起方
ational Research Council of Thailand (NRCT)

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