mResvia’s prescribing information indicates that the vaccine was 78.7% effective at preventing RSV that presents with two or more symptoms at 3.7 ... Arexvy is out in front in the ...

GSK plc (LSE/NYSE:LON: GSK), a leading pharmaceutical company, announced today that the European Medicines Agency (EMA) has commenced the review process for the use of its adjuvanted recombinant ...

Two AS01-adjuvanted vaccines for different pathogens -- the respiratory syncytial virus (RSV) vaccine (Arexvy) and the ...

A new study by the University of Oxford, published in the journal npj Vaccines, shows that a vaccine against respiratory ...

GSK is currently seeking approval for the expanded use of Arexvy in adults aged 18 years and above in the United States and Japan. Year to date, shares of GSK have risen 20.8% against the industry ...

(Alliance News) - GSK PLC on Friday said its respiratory syncytial virus vaccine, Arexvy, has been accepted for regulatory review by the European Medicines Agency to expand its use in adults 18 ...

Arexvy was the first RSV vaccine approved in the European Economic Area for the prevention of lower respiratory tract disease (LRTD) caused by RSV in adults aged 60 and older, and for those aged 50-59 ...

GSK's RSV vaccine, Arexvy, accepted for regulatory review by the European Medicines Agency to expand use in adults 18 years and older · Regulatory decision anticipated H1 2026 ...

The U.S. Army’s 1st Information Operations Command is no more. The active-duty unit shut down in May, after 23 years of operations, citing changing needs in the wider force.

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