Press release archive
Browse GSK's global press release archive for media and investors. Search by keyword or browse by year/business category.
Press releases issued by our local operating companies can be viewed on our market websites.
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GSK aims to redefine the future of respiratory medicine at the European Respiratory Society International Congress
Presenting 56 abstracts to advance scientific understanding and support ambition to improve the lives of people with respiratory conditions
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European Commission approves expanded age indication for GSK’s Arexvy, the first respiratory syncytial virus (RSV) vaccine for adults aged 50-59 at increased risk
Authorisation helps protect this population for the first time ahead of this RSV season
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GSK’s Nucala (mepolizumab) approved in Japan for treatment of adults with chronic rhinosinusitis with nasal polyps
Nucala is the first and only biologic in Japan with a four-weekly dosing schedule for this condition
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Bepirovirsen granted SENKU designation in Japan for chronic hepatitis B
Designation expedites review of bepirovirsen as a potential treatment for people living with chronic hepatitis B (CHB)
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Statement: Zantac (ranitidine) litigation – Delaware Supreme Court to review Superior Court’s Daubert decision
Zantac (ranitidine) litigation – Delaware Supreme Court to review Superior Court’s Daubert decision
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GSK receives US FDA Breakthrough Therapy Designation for its B7-H3-targeted antibody-drug conjugate in relapsed or refractory extensive-stage small-cell lung cancer
Regulatory designation based on promising early clinical evidence observed with GSK5764227 in this tumour type
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Statement: Zantac (ranitidine) litigation – Florida State Court Daubert Ruling in Wilson case
Zantac (ranitidine) litigation – Florida State Court Daubert Ruling in Wilson case
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Statement: Zantac (ranitidine) litigation – Joiner case
Jury in Joiner case in Illinois state court finds GSK not liable for plaintiff’s colorectal cancer
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US FDA expands Jemperli (dostarlimab) plus chemotherapy approval to all adult patients with primary advanced or recurrent endometrial cancer as the first and only immuno-oncology-based treatment to show an overall survival benefit
Jemperli approval now includes MMRp/MSS tumours, which represent majority of endometrial cancer cases.
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GSK delivers continued strong performance and upgrades 2024 guidance
Q2 2024 performance highlights
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GSK presents new data at the Alzheimer's Association International Conference 2024
ZOSTER-122 retrospective study presented during Featured Research Session on shingles and dementia risk
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Arexvy, GSK’s Respiratory Syncytial Virus (RSV) vaccine, receives positive European Medicines Agency CHMP opinion for adults aged 50-59 at increased risk for RSV disease
If approved, this will be the first vaccine in the EU for adults aged 50-59 who are at increased risk of RSV disease.
Download (PDF, 432.6KB) -
Statement: Zantac (ranitidine) litigation – Kimbrow case
GSK has reached a confidential settlement with Ronald Kimbrow resolving the case he filed in Illinois state court.
Download (PDF, 110.4KB) -
GSK and Flagship Pioneering partner to discover novel medicines and vaccines
Collaboration brings together GSK disease area expertise and development capability with Flagship portfolio of 40+ bioplatform companies
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ViiV Healthcare premieres early data showing antiviral activity against integrase resistance from its investigational, third-generation integrase inhibitor
Data, along with results from a phase I study, are the first public presentation of VH4524184.
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ViiV Healthcare announces positive data demonstrating 2-drug regimen Dovato is as effective as 3-drug regimen Biktarvy for maintenance therapy of HIV-1
Largest head-to-head randomised clinical trial between DTG/3TC and BIC/FTC/TAF showed DTG/3TC demonstrated non-inferior efficacy
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ViiV Healthcare announces positive new data for Apretude use during pregnancy at AIDS 2024
Open label extension show maternal and pregnancy outcomes with Apretude exposure were comparable to those with no cabotegravir exposure.
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Blenrep (belantamab mafodotin) combinations in multiple myeloma application accepted for review by the European Medicines Agency
Regulatory submission supported by phase III head-to-head DREAMM-7 and DREAMM-8 trials
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ViiV Healthcare to announce data from largest head-to-head randomised clinical trial for 2-drug regimen Dovato against 3-drug regimen Biktarvy at AIDS 2024
The presentation is one of 25 abstracts evaluating the company’s portfolio of marketed HIV treatment and prevention options.
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Brazil and Thailand become first malaria-endemic countries to launch new single-dose radical cure medicine to prevent the relapse of Plasmodium vivax malaria
Launch of single-dose tafenoquine, co-administered with chloroquine, is another step closer to global elimination of malaria.
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