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.
-
GSK adds detailed clinical trial data to multi-sponsor request system as part of continued commitment to data transparency
GSK added its anonymised patient-level data from the online request system it launched in May 2013 to a new multi-sponsor request system.
-
GSK completes divestment of thrombosis brands and related manufacturing site to Aspen
GlaxoSmithKline (GSK) today completed the previously announced divestment of its thrombosis brands, ArixtraTM and FraxiparineTM.
-
GSK completes divestment of Lucozade and Ribena to Suntory
GSK today completed the previously announced divestment of its nutritional drinks brands Lucozade and Ribena.
-
GSK Cervarix® two-dose schedule receives European marketing authorisation
GSK announced today that the European Commission has granted marketing authorisation for its cervical cancer vaccine Cervarix.
-
GSK and MMV announce FDA Breakthrough Therapy designation for tafenoquine for Plasmodium vivax malaria
GSK and Medicines for Malaria Venture (MMV) announced today that the FDA has granted Breakthrough Therapy designation for tafenoquine.
-
Update on Patent Ruling on ViiV Healthcare's EPZICOM® and TRIZIVIR®
Update on Patent Ruling on ViiV Healthcare's EPZICOM® and TRIZIVIR®
-
GSK announces 1 million innovation prize for bioelectronics research
GSK is announcing today a $1 million dollar prize for innovation in the emerging area of bioelectronics research.
-
ANORO™ ELLIPTA™ approved as first once-daily dual bronchodilator for the treatment of COPD in the US
GlaxoSmithKline plc and Theravance, Inc. today announced that the US Food and Drug Administration (FDA) has approved ANORO ELLIPTA.
-
GSK announces changes to its global sales and marketing practices to further ensure patient interests come first
GSK today set out plans to evolve the way it sells and markets its products to healthcare professionals.
-
GSK and Genmab Receive Priority Review from FDA for Arzerra® (ofatumumab) as 1st Line Treatment for Chronic Lymphocytic Leukaemia (CLL)
GSK and Genmab Receive Priority Review from FDA for Arzerra® (ofatumumab) as 1st Line Treatment for Chronic Lymphocytic Leukaemia (CLL)
-
GSK initiates voluntary open offer to increase stake in its pharmaceuticals subsidiary in India
GSK today announced a Voluntary Open Offer to increase its stake in its publicly-listed pharmaceuticals subsidiary in India.
-
GSK announces £200 million investment in UK advanced manufacturing and science
GSK announced a series of investments totalling approx £200million for new medicines and to create a centre for pharmaceutical manufacturing
-
Update regarding 2010 Nature Medicine study
A GSK research paper published in 2010 that was found earlier this year to contain incorrect data has now been retracted by Nature Medicine.
-
GSK and Theravance announce positive results from pivotal phase III study for fluticasone furoate/vilanterol in asthma
GSK & THRX announced positive results from a phase III efficacy and safety study of fluticasone furoate “FF”/vilanterol “VI”.
-
Synflorix™ receives European marketing authorisation for additional pneumonia indication
GSK today announced that the European Commission (EC) has granted marketing authorisation for an additional indication for Synflorix™
-
GSK launches global consortium with six renowned cancer research centres
GSK announced today the formation of the Oncology Clinical and Translational Consortium (OCTC)
-
Regulatory Update - GSK receives positive CHMP opinion for Cervarix™ two-dose schedule
CHMP is recommending marketing authorisation for a 2-dose schedule in 9-14yo girls for GSK's cervical cancer vaccine, Cervarix™.
-
H5N1 vaccine approved by the U.S. FDA as pandemic influenza preparedness measure
GSK announced FDA has approved its pandemic Influenza A (H5N1) Virus Monovalent Vaccine, Adjuvanted for the immunisation of adults 18+.
-
GSK Responds to FDA Decision on Avandia (rosiglitazone)
GSK announced the FDA has eased restrictions on patient access to Avandia (rosiglitazone), following an committee review in June 2013.
-
Tivicay® (dolutegravir) receives positive CHMP opinion in Europe for the treatment of HIV
ViiV announced that the CHMP of EMA has issued a positive opinion recommending marketing authorisation for Tivicay® (dolutegravir).