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The FDA has accepted for review the sBLA to expand the indication of Arexvy (RSV vaccine, adjuvanted) to adults aged 18 to 49 years who are at increased risk.
Guillain-Barre syndrome is a rare but serious condition which needs urgent treatment in hospital to prevent it progressing.
London: GSK plc has announced that the US Food and Drug Administration (FDA) has accepted for review an application to extend ...
GSK announces US FDA accepts application to review expanded use of RSV vaccine, Arexvy for adults 18-49 at increased risk: London, UK Wednesday, July 16, 2025, 14:00 Hrs [IST] GSK ...
GSK's vaccine is currently approved in the U.S. for preventing RSV-related disease in adults aged 60 and above, and in ...
5d
Zacks Investment Research on MSNFDA Accepts GSK Filing for Expanded Use of RSV Shot in Younger AdultsGSK plc GSK announced that the FDA has accepted its regulatory filing seeking to expand the use of its RSV vaccine, Arexvy, in adults under 50 who are at a higher risk of the disease. A final decision ...
The UK's medicines regulator has warned NHS healthcare staff about an increased risk of a condition affecting the nerves in ...
Residents in public residential aged care services aged 60 and over can now claim a free vaccine for Respiratory Syncytial ...
Frailty strongly predicts worse RSV outcomes in older adults, highlighting the need for targeted care as aging populations face rising infection risks.
Recent studies have shown convincingly that vaccines against shingles (Herpes zoster) reduce the risk of dementia.
A new study from the University of Oxford has revealed a surprising benefit of the respiratory syncytial virus (RSV) vaccine: it may reduce the risk of developing dementia.
Medical staff in Western Australia have been warned after reports of the wrong immunisations being given to patients.
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