Article
Pemivibart is less active against recent SARS-CoV-2 JN.1 sublineages
2024-08-13
Abstract excerpt
Protection from COVID-19 vaccination is suboptimal in many immunocompromised individuals. In March 2024, the Food and Drug Administration issued an Emergency Use Authorization for pemivibart (Permagard/VYD222), an engineered human monoclonal antibody, for pre-exposure prophylaxis in this vulnerable population. However, SARS-CoV-2 has since evolved extensively, resulting in multiple Omicron JN.1 sublineages. We the...
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Identifiers and source
- Literature Corpus work
- 39730744-cab0-5c29-b2b2-9dba490bd60f
- DOI
- 10.1101/2024.08.12.607496
