New data for Arexvy, GSK's RSV vaccine
UK pharma major GSK (LSE: GSK) today announced positive preliminary results from its Phase III trial the immune response and safety of Arexvy (respiratory syncytial virus vaccine, adjuvanted) in adults aged 50 to 59, including those at increased risk of respiratory syncytial virus (RSV) lower respiratory tract disease (LRTD) due to certain underlying medical conditions.
Arexvy is currently approved by the US Food and Drug Administration for active immunization for the prevention of RSV-LRTD in adults 60 years of age and older. It is also approved in Europe, Japan and several other countries.
It is in direct competition with Pfizer (NYSE: PFE), which has also gained FDA clearance for its RSV vaccine Abrysvo.
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