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  1. The Medicines and Healthcare products Regulatory Agency approves the sotrovimab made by GSK and Vir Biotechnology named Xerudy, after a clinical trial found it reduced vulnerable adults’ risk of hospital admission and death by 79% and should be given within five days of symptoms developing.
  2. The Medicines and Healthcare products Regulatory Agency approves GSK and Vir Biotechnology's sotrovimab antibody treatment, after a clinical trial found that the treatment reduced the risk of hospital admission and death by 79% in vulnerable adults if administered within five days of symptoms developing.

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