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.

Publication date: Jul 14, 2024

Background Immunocompromised 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 methods We 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. Results We 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 Conclusions Early 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.

PDF

Concepts Keywords
Biotechnology Clinical
Chicago Combination
Immunosuppressive Cov
July Covid
Days
Early
Immunocompromised
Infection
Onset
Patient
Preprint
Prolonged
Sars
Symptoms
Therapy

Semantics

Type Source Name
drug DRUGBANK Ritonavir
disease MESH infection
disease MESH COVID-19
disease MESH Immunocompromised patients
disease VO population
drug DRUGBANK Oxygen
disease MESH reinfection
pathway REACTOME SARS-CoV-2 Infection
disease VO effective
disease MESH Infectious Diseases
drug DRUGBANK Coenzyme M
disease MESH complications
disease IDO cell
disease MESH hematologic malignancies
disease VO viable
disease MESH morbidity
disease MESH malignancy
disease MESH persistent infection
pathway KEGG Primary immunodeficiency
disease IDO primary immunodeficiency
disease MESH lymphoblastic leukemia
disease MESH Chronic lymphoblastic leukemia
disease MESH Non Hodgkin lymphoma
disease MESH hypogammaglobulinemia
drug DRUGBANK Medical air
disease MESH chronic conditions
disease VO time
disease MESH contraindications
disease MESH viral shedding
disease MESH Death
disease VO dose
disease IDO history
disease MESH drug interactions
disease IDO blood
disease MESH diabetes mellitus
disease MESH hypertension
disease VO USA

Download Document

(Visited 4 times, 1 visits today)