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GSK’s regulatory application for Arexvy accepted for review by China’s CDE

GSK (GSK) announced that its regulatory application for Arexvy, has been accepted for review by China’s Center for Drug Evaluation, CDE, for the prevention of lower respiratory tract disease, LRTD, caused by respiratory syncytial virus, RSV, in adults aged 60 years and older. If approved, Arexvy will be the first vaccine available to this population in China to help protect against the potentially serious consequences of RSV disease.

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