...
首页> 外文期刊>The Lancet >Single-dose administration and the influence of the timing of the booster dose on immunogenicity and efficacy of ChAdOx1 nCoV-19 (AZD1222) vaccine: a pooled analysis of four randomised trials
【24h】

Single-dose administration and the influence of the timing of the booster dose on immunogenicity and efficacy of ChAdOx1 nCoV-19 (AZD1222) vaccine: a pooled analysis of four randomised trials

机译:单剂量给药和增强剂量的影响对Chadox1 NcoV-19(AZD1222)疫苗的免疫原性和功效:四种随机试验的合并分析

获取原文
获取原文并翻译 | 示例
   

获取外文期刊封面封底 >>

       

摘要

Background The ChAdOx1 nCoV-19 (AZD1222) vaccine has been approved for emergency use by the UK regulatory authority, Medicines and Healthcare products Regulatory Agency, with a regimen of two standard doses given with an interval of 4-12 weeks. The planned roll-out in the UK will involve vaccinating people in high-risk categories with their first dose immediately, and delivering the second dose 12 weeks later. Here, we provide both a further prespecified pooled analysis of trials of ChAdOx1 nCoV-19 and exploratory analyses of the impact on immunogenicity and efficacy of extending the interval between priming and booster doses. In addition, we show the immunogenicity and protection afforded by the first dose, before a booster dose has been offered.
机译:背景英国药品和保健品管理局(Medicines and Healthcare products regulatory Agency)已批准ChAdOx1 nCoV-19(AZD1222)疫苗紧急使用,其方案为两次标准剂量,间隔4-12周。计划在英国推广的疫苗将包括立即为高危人群接种第一剂疫苗,并在12周后提供第二剂疫苗。在此,我们对ChAdOx1 nCoV-19的试验进行了进一步的预先指定汇总分析,并对延长启动剂量和增强剂量之间的间隔对免疫原性和疗效的影响进行了探索性分析。此外,我们还展示了在提供增强剂之前,第一剂疫苗所提供的免疫原性和保护作用。

著录项

相似文献

  • 外文文献
  • 中文文献
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号