Study identity card

Huygens

The Netherlands
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  • Disease: Acute SARS-CoV-2
  • Study type: Observational Cohort Study
  • Study type descriptors: Prospective, Multicentre
  • Study aim: To evaluate the clinical outcome, viral clearance, and incidence of resistance-associated mutations that emerged during therapy in a cohort of 245 ICPs with COVID-19 treated with casirivimab/imdevimab, sotrovimab, and tixagevimab/cilgavimab
  • Number of participants enrolled: 245
  • Study enrolling from to
  • Study includes follow-up for 3 months

Study Data

  • Adults
  • Elderly
  • Fragile population
  • Immunocompromised host
  • Hospital wide
  • Outpatient clinic
  • SARS-CoV-2
  • Acute SARS-CoV-2
  • Pharmacological intervention
  • Monoclonal antibodies
  • Sotrovimab
  • Tixagevimab/Cilgavimab
  • Casirivimab/Imdevimab

Other information

Funders:

  • Roche
  • Horizon Europe
  • ZorgOnderzoek Nederland

If you would like to contact the Principal Investigator of the study please email: ccb@ateneo.univr.it

The data is updated up to