跳至主要内容
临床试验/TCTR20210910002
TCTR20210910002已完成4 期

Safety and immunogenicity of full or half dose of COVID-19 booster vaccine after completion of two-dose inactivated and viral vector vaccines

The Health Systems Research Institute0 个研究点目标入组 224 人开始时间: 2021年9月10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
224

研究概览

简要总结

The solicited adverse events were mild to moderate and well tolerated. Total RBD Ig, anti-RBD IgG, neutralizing antibodies against delta and omicron variants, and T-cell response were highest in the mRNA-1273 group followed by the BNT162b2, AZD1222, and BBIBP groups, respectively. All booster vaccines significantly increased binding and neutralizing antibodies in individuals immunized with 2 doses of CoronaVac. The result benefit vaccine strategies to thwart variants of concern, including omicron variant.

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

  • •Healthy Thai individuals above 18 years
  • •Have never been infected with COVID-19

排除标准

  • •Immunosuppressed conditions

研究者

发起方
The Health Systems Research Institute

相似试验