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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RELVAR™ ELLIPTA™ gains approval in Japan for the treatment of asthma
GSK & THRX announced that JMHLW has approved RELVAR™ ELLIPTA™ for the treatment of bronchial asthma.
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GSK and Prosensa announce primary endpoint not met in Phase III study of drisapersen in patients with Duchenne Muscular Dystrophy
GSK & Prosensa announced that Phase III clinical study of drisapersen, treatment for DMD did not meet the primary endpoint.
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GSK signs a multi-year agreement with BARDA to supply the US government with anthrax treatment
GlaxoSmithKline (GSK) plc today announced a new four year contract with the Biomedical Advanced Research and Development Authority (BARDA).
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RELVAR™ ELLIPTA™ receives positive opinion from the CHMP in Europe for the treatment of asthma and COPD
GSK and Theravance, Inc. has issued a positive opinion for fluticasone furoate/vilanterol under the proposed brand name RELVAR™ ELLIPTA™.
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GSK receives Priority Review from FDA for dabrafenib/trametinib combination in metastatic melanoma
GSK announced that the FDA has granted Priority Review designation to the use of Tafinlar® & Mekinist® for the treatment of melanoma
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GSK statement in response to patent ruling reversal on Lovaza
the Court of Appeals for the Federal Circuit has ruled against Pronova Biopharma Norge AS in its patent litigation regarding Lovaza®
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FDA grants GSK and Genmab’s Arzerra® (ofatumumab) Breakthrough Therapy designation for previously untreated chronic lymphocytic leukaemia
GSK & Genmab A/S announced today that FDA has granted Breakthrough Therapy designation for Arzerra® (ofatumumab) with chlorambucil for CLL
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ViiV Healthcare Presents Positive Data from Phase IIIb/IV Study of Dolutegravir vs Darunavir in Treatment-Naïve Adults with HIV-1
ViiV Healthcare today announced initial results from the Phase IIIb/IV FLAMINGO (ING114915) study.
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FDA Advisory Committee recommends approval in US of umeclidinium/vilanterol for the treatment of COPD
GSK & THRX announced that the PADAC voted 11/2 Yes/No for the efficacy & safety of umeclidinium/ vilanterol, treatment of COPD
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GSK reaches agreement to divest Lucozade and Ribena for £1.35 billion
GSK today announced it has reached agreement to sell its nutritional drinks brands Lucozade and Ribena to Suntory Beverage & Food Ltd.
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The investigational MAGE-A3 antigen-specific cancer immunotherapeutic does not meet first co-primary endpoint in Phase III melanoma clinical trial
In line with IDMC unanimous recommendation, GSK will continue the DERMA trial until the second co-primary endpoint is assessed.
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GSK receives marketing authorisation from the European Commission for Tafinlar™
GSK announced today that the European Commission has granted marketing authorisation for Tafinlar™ (dabrafenib).
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GSK announces phase III study of vercirnon in patients with moderate-to-severe Crohn’s disease did not meet its primary endpoint
GSK announced Phase III studies, investigating vercirnon in patients with Crohn's disease did not achieve the primary endpoint
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GSK receives marketing authorisation from the European Commission for additional indication: Tyverb™ (lapatinib)
GSK announced today that the EC has granted an additional indication for Tyverb™ (lapatinib) to be used in combination with trastuzumab.
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ViiV Healthcare announces U.S. approval of Tivicay® (dolutegravir) for the treatment of HIV-1
ViiV Healthcare is pleased to announce today that the U.S. Food and Drug Administration (FDA) has approved Tivicay® (dolutegravir)
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GSK launches 50 million venture capital fund to invest in pioneering bioelectronic medicines and technologies
GSK launch of Action Potential Venture, a $50 million strategic venture that will invest in companies that pioneer bioelectronic medicines
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Regulatory Update - GSK announces EU submission seeking additional indication for Votrient® as maintenance therapy for advanced ovarian cancer
GSK today announced submission to the European Medicines Agency of a variation to the Marketing Authorisation for Votrient® (pazopanib)
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Regulatory update – GSK announces EU submission for Cervarix® two dose schedule
GSK announced, submission of a regulatory application in the EU for two dosing schedule in 9-14yo girls for its cervical cancer vaccine.
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Regulatory update: albiglutide US PDUFA date extended by three months
GSK announced that PDUFA goal date for albiglutide, treatment for adult patients with type 2 diabetes, has been extended by three months.
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GSK adds to its commitment to GAVI Alliance to help protect millions more children against infectious diseases
Extension of Synflorix vaccine supply agreement will help protect an additional 80 million children in the world's poorest countries.