GlaxoSmithKline and Vir submit Covid-19 mAb for emergency authorization
As the US continues to monitor the impact of variants on authorized monoclonal antibodies (mAbs) and shake up which mAbs are distributed where, GlaxoSmithKline and Vir Biotechnology said Friday that they’re seeking an emergency use authorization for their own mAb.
The companies are submitting an application for their mAb, known as VIR-7831, as a treatment for adults and adolescents (12 years and older) with mild-to-moderate Covid-19 who are at risk for progression to hospitalization or death.
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