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.
FDA approves US label update on ICS/LABA combinations in asthma, based on review of safety data
Boxed warning removed from ICS/LABA combination products, including BREO ELLIPTA, ADVAIR DISKUS and ADVAIR HFA.
GSK submits regulatory application for single-dose tafenoquine for the treatment of Plasmodium vivax malaria to Australia’s Therapeutic Goods Administration
Innovative science drives progress in developing medicines for infectious diseases.
GSK achieves approval for Nucala (mepolizumab) for the treatment of eosinophilic granulomatosis with polyangiitis (EGPA) for adults in the US
First targeted treatment approved for this rare eosinophil-driven disease
GSK presents promising new data for priority BCMA asset from its emerging Oncology pipeline at 59th ASH meeting
Data from dose expansion phase of DREAMM-1 study
New data supports the safety and efficacy of GSK’s Shingrix in preventing shingles in autologous haematopoietic stem cell transplant patients
GSK announced new data from a Phase III clinical study
GSK welcomes launch of the UK Government’s Life Sciences Sector Deal
New £40 million GSK investment in genomic research
ViiV Healthcare announces start of phase III study of long-acting cabotegravir for HIV prevention in women
The HPTN 084 study will evaluate injections given every two months
GSK submits US regulatory application for single-dose tafenoquine for Plasmodium vivax malaria
Regulatory milestone affirms GSK's strong commitment and scientific capabilities to fighting infectious diseases
ViiV Healthcare starts third phase III HIV treatment study investigating long-acting two-drug regimen of cabotegravir plus rilpivirine
ViiV announced start of phase III study with a two-drug regimen of long-acting, injectable cabotegravir & rilpivirine in adults with HIV-1.
GSK responds to UK Industrial Strategy
Read our response to the UK Industrial Strategy White Paper.
GSK submits landmark IMPACT data to US regulatory authority to support expanded label for Trelegy Ellipta
GSK submits landmark IMPACT data to US regulatory authority to support expanded label for Trelegy Ellipta
Juluca® (dolutegravir and rilpivirine) approved in US as first 2-drug regimen, once-daily, single pill - a complete regimen for the maintenance treatment of virologically suppressed HIV-1 infection
ViiV announced the FDA has approved Juluca®, complete regimen for the maintenance treatment of HIV-1 infection in virologically suppressed..
Trelegy Ellipta once-daily single inhaler triple therapy gains marketing authorisation in Europe for the treatment of COPD
GlaxoSmithKline plc and Innoviva, Inc. today announced that the European Commission has granted marketing authorisation for Trelegy Ellipta
GSK receives European marketing authorisation for self-injectable formulation of Benlysta for the treatment of systemic lupus erythematosus
The approval is for a single-dose prefilled syringe and a single-dose prefilled pen presentation, administered as a once weekly
Patrick Vallance, President, R&D, GSK to become UK Government's Chief Scientific Adviser
Patrick Vallance, President, R&D, GSK to become UK Government’s Chief Scientific Adviser
First long-term efficacy analysis on the effect of GSK’s Benlysta on rate of organ damage progression in SLE versus standard therapy alone
GSK announced results of the first study assessing levels of organ damage in patients with active systemic lupus erythematosus (SLE)
Dr Hal Barron appointed Chief Scientific Officer and President, Research & Development, GSK
Dr Hal Barron appointed Chief Scientific Officer and President, Research & Development, GSK
GSK submits US regulatory application for mepolizumab in eosinophilic chronic obstructive pulmonary disease (COPD)
GlaxoSmithKline plc today announced the submission of a supplemental Biologics License Application (sBLA) to the United States FDA
New multi-country survey reveals need for improved awareness around long-term impact and appropriate use of corticosteroids in SLE management
EnABLE highlight opportunity for increased awareness on appropriate corticosteroid use and a more proactive approach to management of SLE.
GSK’s investigational BCMA antibody-drug conjugate receives Breakthrough Therapy Designation from US FDA for relapsed and refractory multiple myeloma
GlaxoSmithKline plc (LSE/NYSE: GSK) announced it has received Breakthrough Therapy Designation from the U.S. Food and Drug Administration