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临床试验/NCT05667116
NCT05667116已完成不适用

An Observational Study to Assess the Real-world Effectiveness of EVUSHELD™ (Tixagevimab/Cilgavimab) as Pre-exposure Prophylaxis Against COVID-19 Among EVUSHELD-eligible Populations Receiving Care at UPMC in the United States

AstraZeneca1 个研究点 分布在 1 个国家目标入组 4,232 人开始时间: 2023年1月9日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
已完成
发起方
AstraZeneca
入组人数
4,232
试验地点
1
主要终点
All-cause mortality

研究概览

简要总结

An AstraZeneca-sponsored observational, electronic healthcare record (EHR)-embedded retrospective cohort study to assess the real-world effectiveness of EVUSHELD against SARS-CoV-2 infection, COVID-19-related hospitalization, and other COVID-19 related outcomes in the total EUA-eligible patient population in the University of Pittsburgh Medical Center (UPMC) Health System.

详细描述

This a Phase IV observational, secondary data study to assess the effectiveness of Evusheld in preventing COVID-19 infection and severe outcomes using the electronic medical records from the nationwide integrated health system.

The study is designed as an AstraZeneca-sponsored observational, electronic healthcare record (EHR)-embedded retrospective cohort study to assess the real-world effectiveness of EVUSHELD against SARS-CoV-2 infection, COVID-19-related hospitalization, and other COVID-19 related outcomes in the total EUA-eligible patient population in UPMC health system

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Retrospective

入排标准

年龄范围
12 Years 至 —(Child, Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Receipt of EVUSHELD under the FDA EUA for EVUSHELD
  • Eligibility for assess Evusheld use under the EUA. -

排除标准

  • 未提供

研究组 & 干预措施

EVUSHELD arm

3,000 Individuals given EVUSHELD for pre-exposure prophylaxis

干预措施: EVUSHELD (Drug)

结局指标

主要结局

All-cause mortality

时间窗: 6 months

To assess the effectiveness of EVUSHELD as PrEP against all-cause mortality

COVID-19 hospitalisation

时间窗: 6 months

To assess the effectiveness of EVUSHELD as PrEP against COVID-19 hospitalisation

次要结局

  • SARS-CoV-2 infection(6 & 12 months)
  • Medically attended COVID-19(6 & 12 months)
  • Medically attended acute COVID-19(6 & 12 months)
  • COVID-19 hospitalisation(12 months)
  • COVID-19 intensive care unit (ICU) admission(6 & 12 months)

研究者

发起方
AstraZeneca
申办方类型
Industry
责任方
Sponsor

研究点 (1)

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