AstraZeneca PLC’s long-acting antibody combination Evusheld (150mg each of tixagevimab and cilgavimab, formerly AZD7442) has received a global first approval in Japan for the treatment of COVID-19, the country’s Ministry of Health, Labour and Welfare (MHLW) and the UK-based company announced on 30 August.
Japan also approved the drug the same day for prevention (pre-exposure prophylaxis) of the disease, the same indication for which the product has already been approved in Europe and in the US, where the Food and Drug Administration issued an Emergency Use Authorization
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