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NCT05235347 Clinical Trial

Sotrovimab Expanded Access Treatment Protocol (COVID-19)

Covid19 Clinical Trial

Official title:
Sotrovimab Expanded Access Treatment Protocol

Clinical Trial Details — Status: No longer available

Administrative data
NCT number NCT05235347
Other study ID # VIR-7831-6406
Secondary ID
Status No longer available
Phase
First received
Last updated

Study information
Verified date November 2022
Source Vir Biotechnology, Inc.
Contact n/a
Is FDA regulated No
Health authority
Study type Expanded Access

Clinical Trial Summary

An expanded access program for sotrovimab administered intravenously to participants with COVID-19 illness who meet current authorized/approved criteria for use of sotrovimab.

Recruitment information / eligibility
Status No longer available
Enrollment 0
Est. completion date
Est. primary completion date
Accepts healthy volunteers
Gender All
Age group 12 Years and older
Eligibility Inclusion Criteria: - In the opinion of the investigator, meets the current Emergency Use Authorization (EUA) eligibility criteria for sotrovimab OR - patients currently hospitalized for a non-COVID-19 illness who acquire COVID-19 (nosocomial infection) and otherwise meets all the current EUA eligibility criteria Exclusion Criteria: - Hospitalized due to COVID-19 (excludes nosocomial infection) - Require oxygen therapy due to COVID-19, OR who require an increase in baseline oxygen flow rate due to COVID-19

Study Design

Related Conditions & MeSH terms

Intervention

Biological:
• Sotrovimab
500mg IV

Locations
Country Name City State
United States Site Boston Massachusetts
United States Site Palo Alto California
United States Site Saint Louis Missouri
United States Site Seattle Washington

Sponsors (1)
Lead Sponsor Collaborator
Vir Biotechnology, Inc.

Country where clinical trial is conducted

United States, 

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