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.
GSK announces US FDA approval of Priorix for the prevention of measles, mumps and rubella in individuals 12 months of age and older
Priorix becomes an additional source of measles, mumps and rubella vaccine for US patients
Update: Proposed demerger of the Consumer Healthcare business from GSK to form Haleon
The proposed Demerger is the most significant corporate change for GSK in the last 20 years
GSK publishes Prospectus and Circular for proposed demerger of its Consumer Healthcare business to form Haleon
The Circular is available at www.gsk.com/demerger and the Prospectus is available at www.haleon.com
GSK to acquire clinical-stage biopharmaceutical company Affinivax, Inc.
Supports development of a strong portfolio of innovative vaccines and specialty medicines
ViiV Healthcare announces marketing approval by Japan’s Ministry of Health, Labour and Welfare for Vocabria (cabotegravir) used in combination with Rekambys (rilpivirine)
Long-acting treatment enables people living with HIV to reduce the days they receive treatment.
GSK announces further appointments to Designate Haleon Board
Demerger and listing of Haleon expected in July 2022
China approves Cervarix two-dose vaccine schedule for girls aged 9 to 14 against certain types of cancer-causing human papillomavirus
China’s National Medical Products Administration has approved a two-dose vaccine schedule for Cervarix in girls aged between 9 to 14 years.
ViiV Healthcare commits to grant voluntary licence for patents relating to cabotegravir long-acting for PrEP to Medicines Patent Pool
ViiV Healthcare and MPP are actively negotiating voluntary licensing terms to help widen access to innovative HIV prevention measure
GSK unveils latest research advances demonstrating strength of its portfolio and pipeline at ASCO and EHA
GSK plc will present 25 abstracts at the 2022 American Society of Clinical Oncology (ASCO) Annual Meeting
GSK announces Dr Vishal Sikka to join the Board as Non-Executive Director
GSK has announced that Dr Vishal Sikka, founder and CEO of Vianai Systems, will join the Board of the Company as a Non-Executive Director.
SK bioscience and GSK’s adjuvanted COVID-19 vaccine candidate meets coprimary objectives in a phase III study; Biologics License Application submitted for SKYCovione™(GBP510/GSK adjuvant) in South Korea
SK submits license application to MFDS to support vaccine sovereignty in South Korea
GSK delivers strong Q1 2022 sales of £9.8 billion, +32% AER, +32% CER; Total EPS 35.9p +67% AER, +66% CER and Adjusted EPS 32.8p +43% AER, +43% CER
Sales growth across Pharmaceuticals, Vaccines and Consumer Healthcare driven by strong commercial execution and underlying demand
US Food and Drug Administration accepts New Drug Application for daprodustat
US FDA regulatory submission acceptance is the third major regulatory milestone for daprodustat
GSK reaches agreement to acquire late-stage biopharmaceutical company Sierra Oncology for $1.9bn
Myelofibrosis is a fatal cancer of the bone marrow impacting the normal production of blood cells.
ViiV Healthcare announces US FDA approval of Triumeq PD, the first dispersible single tablet regimen containing dolutegravir, a once-daily treatment for children living with HIV
According to UNAIDS, approximately 1.7 million children globally were living with HIV in 2020.
ViiV Healthcare announces label update for its long-acting HIV treatment, Cabenuva (cabotegravir, rilpivirine), to be initiated with or without an oral lead-in period
US FDA approval of updated label streamlines the initiation process for the first and only complete long-acting HIV treatment.
GSK to demonstrate its commitment to improving outcomes for patients with gynaecologic cancer at the 2022 SGO Annual Meeting
The meeting will take place in Phoenix, Arizona, and virtually from 18-21 March 2022
GSK announces appointments to Designate Haleon Board
GlaxoSmithKline plc (GSK) (LSE/NYSE: GSK) today announced the appointment of six directors to the designate Board of Haleon.
European Medicines Agency (EMA) accepts marketing authorisation application for daprodustat
The EMA has validated the MAA for daprodustat, for the treatment of patients with anaemia of chronic kidney disease.
GSK introduces Haleon to investors
Global leader in consumer health set to be a newly independent company