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GSK announces positive headline results from five Phase 3 studies of daprodustat for patients with anaemia

GSK plc today announced positive headline results from five studies of the Phase 3 ASCEND programme, for patients with anaemia due to chronic kidney disease (...
Jul 17

ViiV Healthcare and Halozyme enter global collaboration and license agreement for ENHANZE drug delivery technology

Halozyme’s drug delivery technology provides the opportunity to administer large volume subcutaneous injections that may enable dosing intervals of every three months and up ...
Jun 22

GSK and iTeos Therapeutics announce development and commercialisation collaboration for EOS-448

With this collaboration GSK is uniquely positioned with access to antibodies that synergistically target all three known CD226 checkpoints - TIGIT, CD96 and PVRIG....
Jun 14

FDA Approves GlaxoSmithKline's immunotherapy for Endometrial Cancer with specific biomarker

GSK gets FDA nod for Jemperli indicated for endometrial cancer...
Apr 26

GSK presents positive efficacy data of dostarlimab in mismatch repair-deficient solid cancers at ASCO Gastrointestinal Cancers Symposium

GSK plc announced updated data from GARNET cohort F evaluating dostarlimab in mismatch repair-deficient non-endometrial advanced solid cancers being presented today at the ...
Jan 18

ViiV Healthcare receives EU Marketing Authorisation for the first-ever dispersible-tablet formulation of dolutegravir, Tivicay

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Jan 13

Vir Biotechnology and GSK announce NHS-supported AGILE study to evaluate VIR-7832 in the early treatment of COVID-19

Vir Biotechnology, Inc. and GlaxoSmithKline plc today announced an agreement with the U.K.-based AGILE initiative to evaluate VIR-7832 in patients with mild ...
Jan 12

GSK, MMV filing for Kozenis in paediatric populations with Plasmodium vivax malaria accepted by Australian Therapeutic Goods Administration

The application includes data for a new, 50 mg tablet that can be dispersed in water and which was developed to facilitate use in children, ...
Jan 08

ViiV Healthcare announces the Marketing Authorisation of the first complete long-acting injectable HIV treatment in Europe

This authorization represents the first time people living with HIV in Europe may be able to receive a long-acting injectable treatment that removes the ...
Dec 21

FDA approves GSK’s BENLYSTA as the first medicine for adult patients with active lupus nephritis in the US

BENLYSTA is the first medicine approved to treat systemic lupus and adults with active lupus nephritis, an important treatment advance for patients with this incurable ...
Dec 18

Vir Biotechnology and GSK announce start of NIH-sponsored ACTIV-3 trial evaluating VIR-7831 in hospitalized adults with COVID-19

ACTIV-3 is an NIH-led public-private partnership designed to accelerate the development of the most promising treatments and vaccine candidates for COVID-19....
Dec 18

GSK starts phase 3 study of RSV maternal candidate vaccine

Currently no vaccine is available for respiratory syncytial virus...
Nov 23

GSK and MMV present positive data on treatment for Plasmodium vivax malaria in children

GSK and MMV today presented positive data from the TEACH study of tafenoquine, an 8-aminoquinoline, for the prevention of relapse of Plasmodium vivax malaria ...
Nov 20

ViiV Healthcare announces CHMP positive opinion for the first-ever dispersible-tablet formulation of dolutegravir, Tivicay, a treatment for children living with HIV in Europe

Dolutegravir is the first integrase inhibitor available as a dispersible tablet for children...
Nov 13

Medicago and GSK announce start of Phase 2/3 clinical trials of adjuvanted COVID-19 vaccine candidate

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Nov 12

ViiV healthcare development program on cabotegravir and rilivirine has no pandemic interruptions

ViiV Healthcare, today announced the positive findings of a pooled analysis of COVID-19-related impacts across the investigational long-acting cabotegravir and rilpivirine clinical ...
Oct 21

GSK presents positive clinical data on maternal and older adults RSV candidate vaccines

Both candidate vaccines contain a recombinant subunit pre-fusion RSV antigen which is believed to trigger the required immune response...
Oct 21

ViiV Healthcare receives positive CHMP opinion for long-acting regimen for the treatment of HIV

ViiV Healthcare announced CHMP issed positive opinion recommending Vocabria in combination with Rekambys and Edurant for the treatment of HIV-1 ...
Oct 16

Vir Biotechnology and GSK announce global expansion to Phase 3 of COMET-ICE study

Vir Biotechnology, Inc. and GlaxoSmithKline today announced the global expansion to Phase 3 of the COMET-ICE study for the early treatment of COVID-19 ...
Oct 06

ViiV Healthcare to present long-term safety and efficacy data for 2-drug regimen

Data presented may shift the treatment paradigm to 2-drug regimens (2DRs) for people living with HIV ...
Oct 01

FDA approves Nucala as the first and only biologic treatment for Hypereosinophilic Syndrome

Third US indication for Nucala demonstrates GSK’s commitment to finding new ways to help patients with eosinophil-driven diseases...
Sep 25

Sanofi and GSK partners for supplying 300 million doses of COVID-19 vaccine to EU countries

Sanofi and GSK finalised and signed today an advanced purchase agreement with the European Commission (EC) for supplying their vaccine...
Sep 20

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