Press releases
Browse GSK global press releases issued since 2009. Search them 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 shares positive data for Arexvy, its respiratory syncytial virus (RSV) older adult vaccine, indicating protection over two RSV seasons
Results from the ongoing AReSVi-006 phase III trial show vaccine efficacy over two full seasons
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GSK announces extension of FDA review period for momelotinib
GSK is confident in the momelotinib NDA and looks forward to working with the FDA as they finalise their review.
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European Commission authorises GSK’s Arexvy, the first respiratory syncytial virus (RSV) vaccine for older adults
Authorisation will help protect adults 60 years of age and older in 30 European countries from RSV disease for the first time
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GSK receives US FDA file acceptance for Jemperli (dostarlimab) plus chemotherapy for the treatment of dMMR/MSI-H primary advanced or recurrent endometrial cancer
Submission accepted for Priority Review
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GSK presents pivotal data at ESPID confirming effectiveness of its 5-in-1 meningococcal ABCWY vaccine candidate, with demonstrated coverage against a panel of 110 MenB strains
GSK today presented preliminary positive results from the phase III trial
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Statement: Zantac (ranitidine) litigation
GSK welcomes the decision of the British Columbia Supreme Court in Dussiaume v. Sandoz Canada Inc. 2023 BCSC 795
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US FDA approves GSK’s Arexvy, the world’s first respiratory syncytial virus (RSV) vaccine for older adults
Ground-breaking approval enables adults aged 60 years and older to be protected from RSV disease for the first time
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GSK’s respiratory syncytial virus older adult vaccine candidate gains positive European Medicines Agency CHMP opinion
Positive opinion advances GSK’s goal to provide the first vaccine to help protect older adults from respiratory syncytial virus disease
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GSK momentum continues with strong start to 2023
Q1 2023 performance highlights
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European Medicines Agency validates marketing authorisation application for Jemperli (dostarlimab) plus chemotherapy for the treatment of dMMR/MSI-H primary advanced or recurrent endometrial cancer
Regulatory submission based on pivotal data from Part 1 of the RUBY phase III trial
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GSK reaches agreement to acquire late-stage biopharmaceutical company BELLUS Health
Acquisition further strengthens specialty medicines and respiratory pipeline.
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Gepotidacin’s positive phase III data shows potential to be the first in a new class of oral antibiotics for uncomplicated urinary tract infections in over 20 years
Gepotidacin is a late-stage antibiotic in development in GSK’s growing infectious diseases portfolio
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GSK and SCYNEXIS announce an exclusive agreement to commercialise and further develop Brexafemme (ibrexafungerp), a novel, first-in-class medicine to treat fungal infection
Brexafemme complements GSK’s industry-leading infectious disease portfolio with an FDA approved treatment for vulvovaginal candidiasis.
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Medicines Patent Pool signs sublicences with Aurobindo, Cipla and Viatris to produce generic versions of ViiV Healthcare’s innovative long-acting HIV prevention medicine
Licences should enable potentially millions of people living in areas most impacted by HIV to access innovative prevention medicine.
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Phase III RUBY clinical trial demonstrates potential of Jemperli (dostarlimab) plus chemotherapy to redefine the treatment of primary advanced or recurrent endometrial cancer versus chemotherapy alone
Interim results from Part 1 of the RUBY clinical trial in primary advanced or recurrent endometrial cancer.
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Statement: Zantac (ranitidine) litigation
In response to the Sargon ruling by the California state court in respect of the Goetz case, GSK plc issued the following statement.
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China National Medical Products Administration accepts regulatory submission for Nucala (mepolizumab) in severe eosinophilic asthma
The China National Medical Products Administration (NMPA) has accepted for review a new drug application for Nucala (mepolizumab)
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GSK announces positive pivotal phase III data for 5-in-1 Meningococcal ABCWY vaccine candidate
MenABCWY combination vaccine candidate met all its primary endpoints of the pivotal phase III clinical trial
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US FDA Advisory Committee votes to support effectiveness and safety of GSK’s respiratory syncytial virus older adult vaccine candidate
Committee votes unanimously that the data support the effectiveness of the vaccine and 10-2 that the data support the safety of the vaccine
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ViiV Healthcare announces positive data demonstrating long-acting injectable Cabenuva (cabotegravir, rilpivirine) is as effective as daily oral Biktarvy (BIC/FTC/TAF) for the treatment of HIV-1
ViiV Healthcare announced positive 12-month findings from the SOLAR study.