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(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.
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 Shingrix (GSK's Recombinant Zoster Vaccine or RZV) for the prevention ...
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.
FDA accepts GSK's application to expand Arexvy vaccine use to at-risk adults aged 18–49, with a decision expected in the ...
London: GSK plc has announced that the US Food and Drug Administration (FDA) has accepted for review an application to extend ...
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Asianet Newsable on MSNUS FDA Reviewers Highlight Safety Concerns With GSK’s Investigational Cancer Drug: Retail’s On The FenceFDA reviewers said in briefing documents that the benefit-risk profile of the drug for the treatment of multiple myeloma “remains unclear.” ...
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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 ...
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 ...
British drugmaker GSK said on Monday it had submitted an application to the U.S. Food and Drug Administration to extend the ...
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