Effect of the Neutralizing SARS-CoV-2 Antibody Sotrovimab in Preventing Progression of COVID-19: A Randomized Clinical Trial

التفاصيل البيبلوغرافية
العنوان: Effect of the Neutralizing SARS-CoV-2 Antibody Sotrovimab in Preventing Progression of COVID-19: A Randomized Clinical Trial
المؤلفون: Anil Gupta, Manuel Crespo, Daren Austin, Adrienne E. Shapiro, Erick Juarez, Jennifer Sager, Joel Solis, Elizabeth Alexander, Amanda Peppercorn, Yaneicy Gonzalez-Rojas, Cynthia Brinson, Hanzhe Zheng, Nicola Scott, Elias Sarkis, Melissa Aldinger, Andrea L. Cathcart, Jaynier Moya, Diego R. Falci, Sergio Parra, Wendy W. Yeh
بيانات النشر: Cold Spring Harbor Laboratory, 2021.
سنة النشر: 2021
مصطلحات موضوعية: Mechanical ventilation, medicine.medical_specialty, biology, business.industry, medicine.medical_treatment, Phases of clinical research, Placebo, law.invention, Randomized controlled trial, law, Internal medicine, biology.protein, Medicine, Respiratory system, Antibody, Risk factor, business, Adverse effect
الوصف: ImportanceOlder patients and those with underlying comorbidities infected with SARS-CoV-2 may be at increased risk of hospitalization and death from COVID-19. Sotrovimab is a neutralizing antibody designed for treatment of high-risk patients to prevent COVID-19 progression.ObjectiveTo evaluate the efficacy and safety of sotrovimab in preventing progression of mild to moderate COVID-19 to severe disease.DesignRandomized, double-blind, multicenter, placebo-controlled, phase 3 study.Setting57 centers in 5 countries.ParticipantsNonhospitalized patients with symptomatic, mild to moderate COVID-19 and at least 1 risk factor for disease progression.InterventionPatients were randomized (1:1) to an intravenous infusion of sotrovimab 500 mg or placebo.Main Outcomes and MeasuresThe primary efficacy outcome was the proportion of patients with COVID-19 progression, defined as all-cause hospitalization longer than 24 hours for acute illness management or death through day 29. Key secondary outcomes included the proportion of patients with COVID-19 progression, defined as emergency room visit, hospitalization of any duration, or death, and proportion of patients developing severe/critical respiratory COVID-19 requiring supplemental oxygen.ResultsAmong 1057 patients randomized (sotrovimab, 528; placebo, 529), all-cause hospitalization longer than 24 hours or death was significantly reduced with sotrovimab (6/528 [1%]) vs placebo (30/529 [6%]) by 79% (95% CI, 50% to 91%; PPP=.002). No patients receiving sotrovimab required high-flow oxygen, oxygen via nonrebreather mask, or mechanical ventilation compared with 14 patients receiving placebo. The proportion of patients reporting adverse events was similar between treatment groups; sotrovimab was well tolerated, and no safety concerns were identified.Conclusions and RelevanceAmong nonhospitalized patients with mild to moderate COVID-19, a single 500-mg intravenous dose of sotrovimab prevented progression of COVID-19, with a reduction in hospitalization and need for supplemental oxygen. Sotrovimab is a well-tolerated, effective treatment option for patients at high risk for severe morbidity and mortality from COVID-19.Trial RegistrationClinicalTrials.gov Identifier: NCT04545060
تدمد: 0454-5060
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::a11230f5e0001f5702dcccf0ad2543a0
https://doi.org/10.1101/2021.11.03.21265533
حقوق: OPEN
رقم الأكسشن: edsair.doi...........a11230f5e0001f5702dcccf0ad2543a0
قاعدة البيانات: OpenAIRE