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