GSK

GSK plc RSV vaccine Arexvy approved in Japan

GSK's Arexvy vaccine receives approval in Japan to protect adults aged 50-59 at increased risk from severe RSV infection, expanding its coverage...

GSK Plc confirms 2024 guidance; Q3 dividend of 15p declared

GSK Plc reports Q3 2024 results with strong growth in Specialty Medicines offsetting lower Vaccine sales. Core earnings rose by 5%, despite Zantac charges...

FDA accepted New Drug Application for GSK’s Gepotidacin

GSK's new antibiotic gepotidacin earns FDA's Priority Review, marking potential first new uUTI oral treatment in 20 years, with decision due March 2025...

GSK plc to seek dismissal of upcoming Wilson case in Florida

GSK welcomes the Florida State Court's Daubert ruling excluding unreliable expert testimony, seeking dismissal of the Wilson case alleging ranitidine-prostate cancer link...

GSK wins jury verdict in Illinois ranitidine cancer case

GSK plc welcome favorable jury verdict in Illinois, ruling out any liability for plaintiff's colorectal cancer linked to ranitidine use...

GSK and CureVac to restructure collaboration into new licensing agreement

GSK plc and CureVac N.V. restructure their collaboration into a licensing agreement, enhancing mRNA vaccine development for influenza and COVID-19...

GSK’s Omjjara approved in Japan for treatment of myelofibrosis

GSK's Omjjara (momelotinib) gains approval from Japan's MHLW for treating myelofibrosis, addressing anaemia, symptoms, and splenomegaly in patients...

GSK starts appeal process of recent Delaware Daubert decision

GSK seeks appeal of recent Daubert ruling in Zantac litigation in Delaware Superior Court. Scientific consensus disputes claim of increased cancer risk...

GSK’s Arexvy RSV vaccine approved for adults 50-59 at risk of LRTD

GSK secures FDA approval for Arexvy in adults aged 50-59 at increased risk for RSV-LRTD. Clinical development ongoing, expanding vaccine benefits globally...

GSK Plc Second trial to show robust efficacy for a Blenrep combination

GSK plc announces positive results from DREAMM-8 trial at ASCO 2024, showing significant improvements in PFS for Blenrep combination therapy...

GSK Plc wins jury verdict in Zantac case and dismissal of next trial

GSK plc celebrates favorable jury verdict in first Zantac trial, highlighting scientific consensus on ranitidine safety and ongoing defense against claims...
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GSK plc RSV vaccine Arexvy approved in Japan

GSK's Arexvy vaccine receives approval in Japan to protect adults aged 50-59 at increased risk from severe RSV infection, expanding its coverage...

GSK Plc confirms 2024 guidance; Q3 dividend of 15p declared

GSK Plc reports Q3 2024 results with strong growth in Specialty Medicines offsetting lower Vaccine sales. Core earnings rose by 5%, despite Zantac charges...

FDA accepted New Drug Application for GSK’s Gepotidacin

GSK's new antibiotic gepotidacin earns FDA's Priority Review, marking potential first new uUTI oral treatment in 20 years, with decision due March 2025...

GSK plc to seek dismissal of upcoming Wilson case in Florida

GSK welcomes the Florida State Court's Daubert ruling excluding unreliable expert testimony, seeking dismissal of the Wilson case alleging ranitidine-prostate cancer link...

GSK wins jury verdict in Illinois ranitidine cancer case

GSK plc welcome favorable jury verdict in Illinois, ruling out any liability for plaintiff's colorectal cancer linked to ranitidine use...

GSK and CureVac to restructure collaboration into new licensing agreement

GSK plc and CureVac N.V. restructure their collaboration into a licensing agreement, enhancing mRNA vaccine development for influenza and COVID-19...

GSK’s Omjjara approved in Japan for treatment of myelofibrosis

GSK's Omjjara (momelotinib) gains approval from Japan's MHLW for treating myelofibrosis, addressing anaemia, symptoms, and splenomegaly in patients...

GSK starts appeal process of recent Delaware Daubert decision

GSK seeks appeal of recent Daubert ruling in Zantac litigation in Delaware Superior Court. Scientific consensus disputes claim of increased cancer risk...

GSK’s Arexvy RSV vaccine approved for adults 50-59 at risk of LRTD

GSK secures FDA approval for Arexvy in adults aged 50-59 at increased risk for RSV-LRTD. Clinical development ongoing, expanding vaccine benefits globally...

GSK Plc Second trial to show robust efficacy for a Blenrep combination

GSK plc announces positive results from DREAMM-8 trial at ASCO 2024, showing significant improvements in PFS for Blenrep combination therapy...

GSK Plc wins jury verdict in Zantac case and dismissal of next trial

GSK plc celebrates favorable jury verdict in first Zantac trial, highlighting scientific consensus on ranitidine safety and ongoing defense against claims...
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GSK

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