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GSK Gets RSV Vaccine Expansion To Younger Adults

 
• By Jessica Merrill

Arexvy was approved by the US FDA for adults 50-59 with medical conditions that put them at increased risk of severe RSV. Separately, the company ended a cancer deal with SpringWorks.

GSK received an FDA approval for Arexvy • Source: Shutterstock

GSK plc has scored a notch on the respiratory syncytial virus (RSV) vaccine development leaderboard, beating rival Pfizer Inc. to a younger adult population. The US Food and Drug Administration on 7 June approved GSK’s RSV vaccine Arexvy in adults aged 50-59 who have medical conditions that put them at increased risk of severe RSV.

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