Study identity card

Rotundo

Italy
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  • Disease: Acute SARS-CoV-2
  • Study type: Observational Cohort Study
  • Study type descriptors: Retrospective, Single centre
  • Study aim: To evaluate the safety and efficacy of early combination therapy involving both antivirals and monoclonal antibody therapy in severely immunocompromised patients with COVID-19 while assessing the outcomes and duration of viral shedding this patient population
  • Number of participants enrolled: 48
  • Study enrolling from to
  • Study includes follow-up for 1.5 years

Study Data

  • Adults
  • Fragile population
  • Immunocompromised host
  • Outpatient clinic
  • SARS-CoV-2
  • Acute SARS-CoV-2
  • Pharmacological intervention
  • Antivirals
  • Remdesivir
  • Monoclonal antibodies
  • Nirmatrelvir/Ritonavir
  • Sotrovimab
  • Molnupiravir
  • Tixagevimab/Cilgavimab
  • Casirivimab/Imdevimab

Other information

Funders:

  • Regione Calabria, Italy

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

The data is updated up to