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GSK and Vir Biotechnology Late Wednesday Announced Sotrovimab Receives Emergency Use Authorization from the US FDA for Treatment of Mild-to-Moderate COVID-19 in High-Risk Adults and Pediatric Patients


Benzinga | May 27, 2021 09:52AM EDT

GSK and Vir Biotechnology Late Wednesday Announced Sotrovimab Receives Emergency Use Authorization from the US FDA for Treatment of Mild-to-Moderate COVID-19 in High-Risk Adults and Pediatric Patients






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