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PROphylaxis for paTiEnts at risk of COVID-19 infecTion (PROTECT-V).
Humphrey, Toby J L; Dosanjh, Davinder; Hiemstra, Thomas F; Richter, Alex; Chen-Xu, Michael; Qian, Wendi; Jha, Vivekanand; Gatley, Katrina; Adhikari, Rakshya; Dowling, Francis; Smith, Rona M.
Afiliación
  • Humphrey TJL; Cambridge University Hospitals NHS Foundation Trust, Cambridge, UK.
  • Dosanjh D; University of Cambridge, Cambridge, UK.
  • Hiemstra TF; Birmingham and West Midlands Lung Research Unit, University Hospitals Birmingham NHS Foundation Trust, Birmingham, UK.
  • Richter A; Cambridge University Hospitals NHS Foundation Trust, Cambridge, UK.
  • Chen-Xu M; Birmingham and West Midlands Lung Research Unit, University Hospitals Birmingham NHS Foundation Trust, Birmingham, UK.
  • Qian W; Institute of Immunology and Immunotherapy, University of Birmingham, Birmingham, UK.
  • Jha V; Cambridge University Hospitals NHS Foundation Trust, Cambridge, UK.
  • Gatley K; University of Cambridge, Cambridge, UK.
  • Adhikari R; Cambridge University Hospitals NHS Foundation Trust, Cambridge, UK.
  • Dowling F; George Institute for Global Health, New Delhi, India.
  • Smith RM; School of Public Health, Imperial College, London, UK.
Trials ; 24(1): 185, 2023 Mar 13.
Article en En | MEDLINE | ID: mdl-36915199
BACKGROUND: Despite the introduction of vaccination, there remains a need for pre-exposure prophylactic agents against SARS-CoV-2. Several patient groups are more vulnerable to SARS-CoV-2 infection by virtue of underlying health conditions, treatments received or suboptimal responses to vaccination. METHODS: PROTECT-V is a platform trial testing pre-exposure prophylactic interventions against SARS-CoV-2 infection in vulnerable patient populations (organ transplant recipients; individuals with oncological/haematological diagnoses, immune deficiency or autoimmune diseases requiring immunosuppression or on dialysis). Multiple agents can be evaluated across multiple vulnerable populations sharing placebo groups, with the option of adding additional treatments at later time points as these become available. The primary endpoint is symptomatic SARS-CoV-2 infection, and each agent will be independently evaluated in real time when the required number of events occurs. Presently, three agents are approved in the platform: intranasal niclosamide, nasal and inhaled ciclesonide and intravenous sotrovimab. DISCUSSION: Despite the introduction of vaccination, there remains a need for pre-exposure prophylactic agents against SARS-CoV-2. Several patient groups are more vulnerable to COVID-19 disease by virtue of underlying health conditions, treatments received or suboptimal responses to vaccination. TRIAL REGISTRATION: ClinicalTrials.gov NCT04870333. EudraCT 2020-004144-28.
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: COVID-19 Tipo de estudio: Clinical_trials / Etiology_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: Trials Asunto de la revista: MEDICINA / TERAPEUTICA Año: 2023 Tipo del documento: Article

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: COVID-19 Tipo de estudio: Clinical_trials / Etiology_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: Trials Asunto de la revista: MEDICINA / TERAPEUTICA Año: 2023 Tipo del documento: Article