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Elsevier - PMC COVID-19 Collection logoLink to Elsevier - PMC COVID-19 Collection
. 2021 Oct 30;242:172–173. doi: 10.1016/j.ahj.2021.10.067

COVID-19 prevention with subcutaneous administration of the monoclonal antibodies casirivimab and imdevimab: Subgroup analysis in participants with cardiovascular disease and diabetes

Meagan P O'Brien 1, Eduardo Forleo-Neto 1, Bret J Musser 1, Flonza Isa 1, Kuo-Chen Chan 1, Neena Sarkar 1, Katharine J Bar 2, Ruanne V Barnabas 3, Dan H Barouch 4, Myron S Cohen 5, Mary A Marovich 6, Peijie Hou 1, Ingeborg Heirman 1, John D Davis 1, Kenneth C Turner 1, Divya Ramesh 1, Adnan Mahmood 1, Lisa Purcell 1, Andrea T Hooper 1, Jennifer D Hamilton 1, Yunji Kim 1, Alina Baum 1, Christos A Kyratsous 1, James Krainson 7, Richard Perez-Perez 8, Rizwana Mohseni 9, Bari Kowal 1, A Thomas DiCioccio 1, Neil Stahl 1, Leah Lipsich 1, Ned Braunstein 1, Gary Herman 1, George D Yancopoulos 1, David M Weinreich 1, for the COVID-19 Phase 3 Prevention Trial Team
PMCID: PMC8556497

Abstract

Background

In a Phase 3 prevention trial, the monoclonal antibody combination casirivimab and imdevimab (REGEN-COVTM) administered subcutaneously (SC) prevented symptomatic SARS-CoV-2 infection in asymptomatic adults/adolescents living in the same household as a SARS-CoV-2-infected individual (index case). Individuals with cardiovascular disease (CVD) and/or diabetes are at increased risk of moderate/severe COVID-19.

Methods

Uninfected individuals ≥12 years, identified ≤96 hours of index case being diagnosed SARS-CoV-2 positive, were randomized 1:1 to REGEN-COV 1200mg SC or placebo. The primary endpoint was the proportion of participants who developed symptomatic infection (COVID-19) during the 28-day efficacy assessment period among those who were SARS-CoV-2 RT-qPCR negative and without evidence of immunity (seronegative) at baseline. A post-hoc analysis assessed efficacy in participants with CVD (including hypertension) and/or diabetes. Overall safety is reported.

Results

The study included SARS-CoV-2 RT-qPCR negative participants at baseline (n=2067). There was an 81.4% relative risk reduction (RRR) of symptomatic infection with REGEN-COV in the overall seronegative population (n=1505; Figure 1; Table 1). In participants with CVD (n=332) or diabetes (n=103), the RRRs of developing symptomatic infection with REGEN-COV versus placebo were 54.9% and 69.0%, respectively. Similar results were observed when analyses were performed regardless of baseline serology status. Treatment-emergent adverse events occurring at ≥2% included COVID-19, asymptomatic COVID-19, headache, and injection-site reaction (Table 2).

Conclusions

In study participants with CVD and/or diabetes, who are known to be at increased risk of severe disease if infected, treatment with REGEN-COV SC reduced the risk of developing symptomatic SARS-CoV-2 infection, consistent with the overall study results..


Articles from American Heart Journal are provided here courtesy of Elsevier

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