Press releases
Press releases dating back to 2009 are available below. Search them by keyword or browse by year/business category. Press releases for our local operating companies can be viewed on our market websites.
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GSK appoints Charles Bancroft to the Board as a Non-Executive Director
GlaxoSmithKline plc today announced that Charles Bancroft will join the Board of the Company as a Non-Executive Director on 1 May 2020.
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ViiV Healthcare announces first global regulatory approval of CABENUVA; the first complete, long-acting, regimen for the treatment of HIV
ViiV Healthcare, today announced that Health Canada has approved CABENUVA.
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ViiV Healthcare presents positive long-term data from phase III study demonstrating efficacy and safety of cabotegravir and rilpivirine, its investigational, long-acting, injectable treatment regimen in adults living with HIV-1
ViiV Healthcare presents positive long-term data from phase III study
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ViiV Healthcare presents positive 48-week data from phase III study showing every-two-month regimen of investigational long-acting, injectable cabotegravir and rilpivirine has similar efficacy to once-monthly dosing
ViiV Healthcare presents positive 48-week data from phase III study
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ViiV Healthcare and UNC-Chapel Hill announce five-year renewal of innovative HIV cure partnership
ViiV Healthcare and UNC-Chapel Hill announce five-year renewal of innovative HIV cure partnership
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GSK receives EC approval for the sale of ThermaCare
GSK receives EC approval for the sale of ThermaCare
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FDA approves GSK’s Advil Dual Action with Acetaminophen for over-the-counter use in the United States
First combination of ibuprofen and acetaminophen for pain relief to be available OTC in 2020
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GSK filing accepted by European Medicines Agency for Trelegy Ellipta use in adult patients with asthma
GSK filing accepted by European Medicines Agency for Trelegy Ellipta use in adult patients with asthma
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First-of-its-kind global collaboration launched to develop transformative treatment regimens for tuberculosis
First-of-its-kind global collaboration launched to develop transformative treatment regimens for tuberculosis
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European Medicines Agency accepts submission of GSK’s Marketing Authorisation Application for Zejula (niraparib) in first-line maintenance treatment for women with platinum-responsive advanced ovarian cancer
Submission based on data from the Phase III PRIMA clinical study.
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U.S. FDA accepts GSK’s sNDA application for Zejula (niraparib) for first-line maintenance treatment for women with platinum-responsive advanced ovarian cancer
U.S. FDA accepts GSK’s sNDA application for Zejula (niraparib)
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Clover and GSK announce research collaboration to evaluate coronavirus (COVID-19) vaccine candidate with pandemic adjuvant system
Clover and GSK Announce Research Collaboration to Evaluate Coronavirus (COVID-19) Vaccine Candidate with Pandemic Adjuvant System
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FDA approves GSK’s Voltaren Arthritis Pain for over-the-counter use in the United States
U.S. Food and Drug Administration (FDA) has approved Voltaren Arthritis Pain as an over-the-counter (OTC) product.
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GSK delivers 2019 sales of £33.8 billion +10% AER, +8% CER (Pro-forma +4% CER*)
Total EPS 93.9p; +27% AER; +23% CER; Adjusted EPS 123.9p +4% AER, +1% CER
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CEPI and GSK announce collaboration to strengthen the global effort to develop a vaccine for the 2019-nCoV virus
GSK to make adjuvant technology available to support rapid development of candidate vaccines
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GSK announces European Medicines Agency (EMA) accepted marketing authorisation application for belantamab mafodotin for the treatment of relapsed or refractory multiple myeloma
Belantamab mafodotin accepted for accelerated assessment by the EMA’s Committee for Human Medicinal Products (CHMP)
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GSK licenses tuberculosis vaccine candidate to the Bill & Melinda Gates Medical Research Institute for continued development
GSK announced that it has licensed its M72/AS01E3 tuberculosis disease (TB) vaccine.
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World’s first meningitis B national infant vaccination programme shows 75% drop in cases over three years
New England Journal of Medicine also publishes results of Australian carriage study with Bexsero
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US Food and Drug Administration (FDA) grants priority review of belantamab mafodotin for patients with relapsed or refractory multiple myeloma
Belantamab mafodotin has potential to be the first anti-BCMA treatment available to patients
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Dovato (dolutegravir/lamivudine), the once-daily, single-pill, 2-drug regimen for the treatment of HIV-1 infection, granted marketing approval by Japan Ministry of Health, Labour and Welfare
ViiV Healthcare, the global specialist HIV company announced that it has obtained approval of Dovato.
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