Abstract
The safety of casirivimab + imdevimab (CAS + IMD) (anti-severe acute respiratory syndrome coronavirus 2 [SARS-CoV-2] monoclonal antibodies [mAbs]) in pediatric outpatients with coronavirus disease 2019 (COVID-19) was evaluated in a randomized phase 1/2/3 trial. Consistent with adults, CAS + IMD was generally well tolerated with low drug-induced immunogenicity rates. The findings support the development of next-generation anti-SARS-CoV-2 mAbs for at-risk pediatric patients.
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Norton, T. D., Thakur, M., Ganguly, S., Ali, S., Chao, J., Waldron, A., … Herman, G. A. (2024). Safety and Pharmacokinetics of Casirivimab and Imdevimab (CAS + IMD) in Pediatric Outpatients With COVID-19. Journal of the Pediatric Infectious Diseases Society, 13(11), 589–593. https://doi.org/10.1093/jpids/piae105
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