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Contact the study team using the details below to take part. If there are no contact details below please ask your doctor in the first instance.

Contact Information:

EU GSK Clinical Trials Call Center +44 (0) 20 89904466
GSKClinicalSupportHD@gsk.com


US GSK Clinical Trials Call Center 877-379-3718
GSKClinicalSupportHD@gsk.com


Study Location:

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Be Part of Research - Trial Details - Study to Monitor the Occurrence of Viral Variants in Patients With Compromised Immune Systems Being Treated for COVID-19

Study to Monitor the Occurrence of Viral Variants in Patients With Compromised Immune Systems Being Treated for COVID-19

Recruiting

Open to: ALL

Age: 18.0 - N/A

Medical Conditions

COVID-19


This information is provided directly by researchers, and we recognise that it isn't always easy to understand. We are working with researchers to improve the accessibility of this information. In some summaries, you may come across links to external websites. These websites will have more information to help you better understand the study.


Sotrovimab binds to a conserved epitope on the severe acute respiratory syndrome coronavirus (SARS-CoV) and SARS-CoV-2 spike protein outside the receptor-binding motif and has been shown to reduce the risk of hospitalization and/or death when administered as early treatment in non-hospitalized patients that are at risk for progression to severe disease. Immunocompromised (IC) patients are prioritized to receive early treatment for COVID-19 as they are at high risk of disease progression, and because of their potential for prolonged viral shedding and the resulting increased risk of emergent viral mutations and potential onward community transmission.

This genomic surveillance study will aim to describe changes in the SARS-CoV-2 spike protein observed in IC participants receiving sotrovimab as standard of clinical care in sentinel sites at a national level to assess potential emergence of viral variants.

Start dates may differ between countries and research sites. The research team are responsible for keeping the information up-to-date.  

The recruitment start and end dates are as follows:

Jul 2022 Jul 2023

Publications

"Case JB, Mackin S, Errico JM, Chong Z, Madden EA, Whitener B, Guarino B, Schmid MA, Rosenthal K, Ren K, Dang HV, Snell G, Jung A, Droit L, Handley SA, Halfmann PJ, Kawaoka Y, Crowe JE Jr, Fremont DH, Virgin HW, Loo YM, Esser MT, Purcell LA, Corti D, Diamond MS. Resilience of S309 and AZD7442 monoclonal antibody treatments against infection by SARS-CoV-2 Omicron lineage strains. Nat Commun. 2022 Jul 2;13(1):3824. doi: 10.1038/s41467-022-31615-7."; "35780162"

INTERVENTIONAL

Intervention Type : DRUG
Intervention Description : Sotrovimab dose and administration per standard of clinical care

Intervention Arm Group : Cohort receiving Sotrovimab;



You can take part if:



You may not be able to take part if:


This is in the inclusion criteria above


Below are the locations for where you can take part in the trial. Please note that not all sites may be open.

  • GSK Investigational Site
    London
    SE1 7EH
  • GSK Investigational Site
    Cambridge
    CB2 0QQ
  • GSK Investigational Site
    Newcastle Upon Tyne
    NE1 4LP
  • GSK Investigational Site
    London
    NW1 2BU
  • GSK Investigational Site
    Cardiff
    CF14 4XW
  • GSK Investigational Site
    Middlesbrough
    TS4 3BW
  • GSK Investigational Site
    Plymouth
    PL6 5FP

US GSK Clinical Trials Call Center 877-379-3718
GSKClinicalSupportHD@gsk.com


EU GSK Clinical Trials Call Center +44 (0) 20 89904466
GSKClinicalSupportHD@gsk.com



The study is sponsored by GlaxoSmithKline




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Read full details for Trial ID: NCT05305651
Last updated 23 January 2023

This page is to help you find out about a research study and if you may be able to take part

You can print or share the study information with your GP/healthcare provider or contact the research team directly.