FDA Restricts Sotrovimab Use in More States Over BA.2 Subvariant Efficacy Concerns

HHS and the FDA have expanded the list of states where GlaxoSmithKline’s and Vir Biotechnology’s COVID-19 monoclonal antibody, sotrovimab, may not be used due to concerns about the treatment’s efficacy against the Omicron subvariant BA.2.
Source: Drug Industry Daily