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Prefilled syringe presentation offers a convenient administration option to healthcare professionals· An estimated one million people develop shingles in the US each year[1]GSK plc ...
London: GSK plc has received approval from the US Food and Drug Administration (FDA) for a prefilled syringe presentation of ...
(Alliance News) - GSK PLC on Thursday said the prefilled syringe version of its vaccine Shingrix has been approved for use in the US for the prevention of shingles.
GSK PLC closed 15.32% short of its 52-week high of £16.79, which the company reached on September 9th.
GSK PLC closed 16.45% short of its 52-week high of £16.79, which the company reached on September 9th.
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Zacks.com on MSNFDA Accepts GSK Filing for Expanded Use of RSV Shot in Younger AdultsFDA accepts GSK's filing to extend Arexvy's RSV vaccine use to high-risk adults under 50, with a decision due in 2026.
Haleon plc had a decent quarter, mostly driven by price. Click here to read more about HLNCF stock and why it is a Hold.
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 ...
PDUFA date nears for GSK plc’s Blenrep (belantamab mafodotin), the U.S. FDA’s Oncologic Drugs Advisory Committee will decide July 17 on whether available data justify the return to market of the ...
GSK supports seasonal flu immunization in the US by shipping FLULAVAL (Influenza Vaccine) and FLUARIX (Influenza Vaccine) in ...
"A regulatory decision by the FDA on this submission is expected in H1 2026. GSK is continuing to seek expanded indications for its RSV vaccine in other geographies including in the European Economic ...
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