GSK gets US FDA approval for expanded use of RSV vaccine

GSK gets US FDA approval for expanded use of RSV vaccine

March 13 (Reuters) - British drugmaker GSK said on Friday the U.S. Food and ‌Drug Administration has expanded the approved age ‌range for its respiratory syncytial virus vaccine, Arexvy, to ​include adults aged 18 to 49 who are at increased risk of lower respiratory tract disease caused by the virus.

Reuters

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* The vaccine ‌is already approved ⁠in the U.S. for preventingRSV-related disease in adults aged 60 and above, ⁠and in at-riskadults aged 50 to 59. * RSV is a common respiratory virus that causes ​seasonalinfections such ​as the flu ​and is a ‌leading cause of pneumoniaand death in infants and older adults. * In the U.S., an estimated 21 million adults under 50 haveat least one risk factor for severe RSV infection, the ‌companysaid. * GSK's vaccine, Arexvy, ​would be competing for market ​sharein the ​18-49 age group with Moderna's mRESVIA ‌and Pfizer'sAbrysvo. * In December, ​a panel ​of the European Medicines Agency hadalso backed the use of Arexvy for all adults ​above the ‌age of18, paving the way for broader ​use.

(Reporting by Siddhi Mahatole in Bengaluru; ​Editing by Devika Syamnath)

 

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