GlaxoSmithKline: FDA Approves Broader Use Application for Arexvy, a Respiratory Syncytial Virus Vaccine
2025-07-14 / Read about 0 minute
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GlaxoSmithKline (GSK) has announced that the U.S. Food and Drug Administration (FDA) has accepted its application to expand the use of Arexvy, a respiratory syncytial virus (RSV) vaccine. The approval now extends the indication for Arexvy to include high-risk adults aged 18-49. Previously, Arexvy was approved in the United States for use in individuals aged 60 and older, as well as high-risk individuals aged 50-59, to prevent lower respiratory tract diseases caused by RSV.