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London: GSK plc has announced that the US Food and Drug Administration (FDA) has accepted for review an application to extend ...
(Reuters) -British drugmaker GSK said on Monday it had submitted an application to the U.S. Food and Drug Administration to ...
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Pharmaceutical Technology on MSNGSK eyes FDA label expansion for RSV vaccine Arexvy to include younger patientsThe label expansion sought by GSK is a bid to compete with Pfizer and Moderna in the younger age groups of the RSV vaccine market. Pfizer’s Abrysvo and Moderna’s mRESVIA are both approved to prevent ...
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Zacks.com on MSNFDA Accepts GSK Filing for Expanded Use of RSV Shot in Younger AdultsArexvy is currently approved for use in all individuals aged 60 and older, as well as for high-risk individuals aged 50-59.
Welcome to Fierce Pharma's regulatory tracker for the second half of 2025. | In this tracker, Fierce Pharma is recording the ...
OPEN The FTSE 100 was expected to open 9.7 points lower ahead of the bell on Monday after wrapping up the previous session 0.38% softer at 8,941.12.
Recent health news highlights various developments, including Trump's spending bill impacting insurance costs, a major acquisition in the bioscience sector, and GSK's efforts to expand RSV vaccine ...
The disease was found following tests on a severely emaciated doe that was euthanized and tested in early June, Andrea Korman ...
OVER 20 people developed a potentially paralysing illness after getting the respiratory syncytial virus (RSV) vaccine. The UK ...
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News-Medical.Net on MSNShingles and RSV vaccines with AS01 adjuvant reduce dementia riskResearchers found that older adults who received AS01-adjuvanted shingles or RSV vaccines had a significantly lower risk of ...
Compared with flu vaccine recipients, those given the RSV or shingles vaccine had 18% to 37% lower odds of receiving a ...
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