Study identity card

Orth

Germany
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  • Disease: Acute SARS-CoV-2
  • Study type: Observational Cohort Study
  • Study type descriptors: Retrospective, Multicentre
  • Study aim: To analyse first-line COVID-19 combination regimens for virological and clinical outcomes and safety in a large cohort of immunocompromised patients
  • Number of participants enrolled: 144
  • Study enrolling from to
  • Study includes follow-up for 3 months

Study Data

  • Adults
  • Elderly
  • Fragile population
  • Hospital wide
  • SARS-CoV-2
  • Acute SARS-CoV-2
  • Pharmacological intervention
  • Antivirals
  • Remdesivir
  • Monoclonal antibodies
  • Nirmatrelvir/Ritonavir
  • Sotrovimab
  • Molnupiravir
  • Tixagevimab/Cilgavimab
  • Casirivimab/Imdevimab

Other information

Funders:

  • Projekt DEAL

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

The data is updated up to