Sotrovimab
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Sotrovimab - Wikipedia
sotrovimab, sold under the brand name Xevudy, is a human neutralizing monoclonal antibody with activity against severe acute respiratory syndrome coronavirus 2, known as SARS-CoV-2. [10][12][13] It was developed by GlaxoSmithKline and Vir Biotechnology, Inc. [12][14] sotrovimab is designed to attach to the spike protein of SARS-CoV-2. [12][13][15]
En.wikipedia.orgSotrovimab (sotrovimab) - COVID-19 vaccines and treatments portal
Information about sotrovimab (sotrovimab) authorized by Health Canada as a Treatment for COVID-19.
Covid-vaccine.canada.caEarly Treatment for Covid-19 with SARS-CoV-2 Neutralizing …
Oct 27, 2021 · sotrovimab is a pan-sarbecovirus monoclonal antibody that was designed to prevent progression of Covid-19 in high-risk patients early in the course of disease.
Nejm.orgGSK Sotrovimab Fact Sheet for Patients, Parents, and …
sotrovimab is an investigational medicine used for the treatment of adults and children (12 years of age and older weighing at least 88 pounds [40 kg]) with positive results of direct SARS-Co-V-2
Fda.govSotrovimab: First Approval - PMC - National Center for …
Mar 14, 2022 · sotrovimab (Xevudy ®) is a recombinant human monoclonal antibody targeted against the severe acute respiratory syndrome coronavirus 2. It is being developed by Vir Biotechnology in collaboration with GlaxoSmithKline for …
Ncbi.nlm.nih.govXevudy - European Medicines Agency (EMA)
Dec 17, 2021 · The active substance of Xevudy, sotrovimab, is a monoclonal antibody, a type of protein that has been designed to recognise and attach to a specific structure (called an antigen). sotrovimab has been designed to attach to the spike protein of SARS-CoV-2 (the virus that causes COVID-19).
Ema.europa.euSotrovimab for Early Covid-19 | New England Journal of Medicine
Oct 27, 2021 · sotrovimab is a human monoclonal antibody that neutralizes SARS-CoV-2 and numerous other sarbecoviruses, but its effects on clinical outcomes in high-risk outpatients with Covid-19 are
Nejm.orgGSK Sotrovimab Fact Sheet for HCP 03172023 - U.S. Food and …
sotrovimab is not authorized for treatment of mild-to-moderate COVID-19 when infection is likely to have been caused by a non-susceptible SARS-CoV-2 variant based on available information
Fda.govReal-World Effectiveness of Sotrovimab for the Early Treatment …
Feb 20, 2024 · sotrovimab is an engineered, dual-action human immunoglobulin G1κ mAb derived from the parental mAb S309, a potent neutralising mAb directed against the spike protein of SARS-CoV-2 [19–22].
Ncbi.nlm.nih.govCoronavirus (COVID-19) Update: FDA Authorizes Additional …
May 26, 2021 · The FDA issued an emergency use authorization for the investigational monoclonal antibody therapy sotrovimab for the treatment of mild-to-moderate COVID-19 in adult and pediatric patients.
Fda.gov