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EMA review for GSK, Vir's COVID-19 antibody launched

A review has been initiated by the European Medicines Agency for VIR-7831, the investigational monoclonal antibody co-developed by GlaxoSmithKline and Vir Biotechnology as an early treatment for COVID-19. Included in the review will be an interim analysis of safety and efficacy data for 583 randomized patients, which showed the treatment reduced hospitalization or mortality by 85% in participants who received the monoclonal antibody in comparison to those given a placebo. PharmaTimes online (UK) (4/16)

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