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Early combination of sotrovimab with nirmatrelvir/ritonavir or remdesivir is associated with low rate of persisting SARS CoV-2 infection in immunocompromised outpatients with mild-to-moderate COVID-19: a prospective single center study.

Gentile, I.; Viceconte, G.; Cuccurullo, F.; Pietroluongo, D.; D'Agostino, A.; Silvitelli, M.; Mercinelli, S.; Scotto, R.; Grimaldi, F.; Palmieri, S.; Gravetti, A.; Trastulli, F.; Moccia, M.; Buonomo, A. R.

2024-07-15 infectious diseases
10.1101/2024.07.15.24310384 medRxiv
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BackgroundImmunocompromised patients are at high risk of developing persisting/prolonged COVID-19 Data concerning early combined use of antivirals and monoclonal antibodies in this population are scarce. Research design and methodsWe performed an observational, prospective study, enrolling immunocompromised outpatient adults with mild-to-moderate COVID-19 treated with a combination of sotrovimab plus one antiviral (remdesivir or nirmatrelvir/ritonavir) within 7 days from symptoms onset. ResultsWe enrolled 52 patients. No patient was hospitalized within 30 days from the disease onset, needed oxygen administration or died within 60 days, or experienced a reinfection or a clinical relapse within 90 days. Clearance rates were 67% and 97% at 14th day after the end of therapy and at the end of follow-up, respectively. Factors associated with longer infection were initiation of therapy after 3 days from symptoms onset, and enrollment more than 180 days from the beginning of the study. However, only the latter factor was independently associated with longer SARS-CoV-2 infection, suggesting a loss of efficacy of this strategy with the evolution of SARS-CoV-2 variants ConclusionsEarly administration of combination therapy with a direct antiviral and sotrovimab seems to be effective in preventing hospitalization, progression to severe COVID-19 and the development of prolonged/persisting SARS-CoV-2 infection in immunocompromised patients.

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