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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EMA issues positive scientific opinion on GSK and Vir Biotechnology’s sotrovimab for the early treatment of COVID-19
Opinion based on the EMA’s CHMP review of available data on sotrovimab (previously VIR-7831) for the early treatment of COVID-19.
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GSK announces sale of stake in Innoviva Inc
Shares to be sold back to Innoviva at $12.25 per share
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Medicago and GSK announce positive interim Phase 2 results for adjuvanted COVID-19 vaccine candidate
Neutralizing antibody responses were ten times higher than in people recovering from COVID-19.
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Sanofi and GSK COVID-19 vaccine candidate demonstrates strong immune responses across all adult age groups in Phase 2 trial
Adjuvanted recombinant COVID-19 vaccine candidate triggered strong neutralizing antibody responses in all adult age groups.
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GSK Consumer Healthcare commits to make over a billion toothpaste tubes recyclable by 2025 as part of its ongoing sustainability journey
GSKCH’s initiatives support GSK’s company wide commitment to achieve a net zero impact on climate and a positive impact on nature by 2030.
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GSK and Vir Biotechnology announce the start of the EMA rolling review of VIR-7831 (sotrovimab) for the early treatment of COVID-19
Review will support a formal Marketing Authorisation Application.
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European Commission approves Benlysta for adult patients with active lupus nephritis
First and only biologic approved for both systemic lupus erythematosus and lupus nephritis
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ViiV Healthcare initiates rolling submission of new drug application with US FDA for long-acting cabotegravir for prevention of HIV
If approved, cabotegravir would be the first, long-acting therapy for HIV PrEP
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GSK delivers Q1 sales of £7.4 billion -18% AER, -15% CER Total EPS 21.5p, -32% AER, -25% CER; Adjusted EPS 22.9p -39% AER, -33% CER
Q1 performance reflects expected year-on-year impact and disruption from COVID-19
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European Commission approves GSK’s JEMPERLI (dostarlimab), the first anti-PD-1 therapy approved for recurrent or advanced endometrial cancer
The approval makes dostarlimab the first anti-PD-1 therapy available for endometrial cancer in Europe.
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FDA grants accelerated approval for GSK’s JEMPERLI (dostarlimab-gxly) for women with recurrent or advanced dMMR endometrial cancer
FDA grants accelerated approval for GSK’s JEMPERLI (dostarlimab-gxly) for women with recurrent or advanced dMMR endometrial cancer
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GSK and Vir Biotechnology announce EMA review of dual-action monoclonal antibody VIR-7831 for the early treatment of COVID-19
GSK and Vir continue discussions with global regulators to make VIR-7831 available to patients with COVID-19.
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GSK provides update on feladilimab, an investigational inducible T cell co-stimulatory (ICOS) agonist
GSK provides update on feladilimab, an investigational inducible T cell co-stimulatory (ICOS) agonist
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GSK announces Dr Anne Beal to join the Board as Non-Executive Director
GlaxoSmithKline plc (LSE/NYSE: GSK) today announces that Dr Anne Beal will join the Board of the Company as a Non-Executive Director.
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GSK to support manufacture of Novavax’ COVID-19 vaccine
GSK to support manufacture of up to 60 million doses of Novavax’ COVID-19 vaccine.
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Lilly, Vir Biotechnology and GSK announce positive topline data from the phase 2 BLAZE-4 trial evaluating bamlanivimab with VIR-7831 in low-risk adults with COVID-19
In combination, the 2 monoclonal antibodies demonstrated 70% relative reduction in persistent high viral load at day 7 compared to placebo.
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GSK and Vir Biotechnology announce submission of Emergency Use Authorization request to FDA for VIR-7831 for the early treatment of COVID-19
The FDA EUA submission is based on an interim analysis of efficacy and safety data from the Phase 3 COMET-ICE trial.
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GSK receives CHMP positive opinion recommending approval of Benlysta for adult patients with active lupus nephritis
This CHMP opinion follows the recent label expansion by the US FDA to include lupus nephritis
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Moncef Slaoui Departs Galvani Bioelectronics Board of Directors
Moncef Slaoui has been terminated as Chair of the Galvani Board of Directors, effective immediately.
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Half of parents surveyed either cancelled or delayed their child’s scheduled meningitis vaccination during the COVID-19 pandemic – GSK survey shows [1]
The Ipsos survey on behalf of GSK offers insight into the pandemic's impact on meningitis vaccinations over the last 12 months.