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eVusheld Assessment reaL wORld Effectiveness in DoD Health System
eVusheld Assessment reaL wORld Effectiveness in DoD Health System

NCT05569408

CompletedN/A

Sponsor: AstraZeneca

Conditions: COVID-19; SARS-CoV-2; 2019 Novel Coronavirus Disease

Interventions: EVUSHELD

Countries: United States

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 treated in DoD Health system.

Eligibility overview

Sex: ALL

Age: 12 Years to

Healthy volunteers: No

Study type: OBSERVATIONAL

Eligibility criteria
Inclusion Criteria:

1. Receipt of Evusheld under the FDA EUA for Evusheld
2. Eligibility for Evusheld use under the EUA. -

Exclusion Criteria:

* None
Locations (1)
  • Bethesda, Maryland, United States