Sanofi and GSK to seek regulatory authorization for COVID-19 vaccine
Final analysis of the global VAT02 booster trial confirms universal ability to boost neutralizing antibodies 18- ...
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Tag: gsk
Sotrovimab receives EUA from US FDA for treatment of COVID-19 in adults and pediatrics
GSK and Vir announce sotrovimab receives Emergency Use Authorization from the US FDA for treatment of ...
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GSK and Vir’s sotrovimab receives positive scientific opinion of EMA for COVID-19
Opinion based on the EMA’s Committee for Human Medicinal Products (CHMP) review of available data on ...
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Medicago and GSK announce positive interim Phase 2 results for adjuvanted COVID-19 vaccine
Similar antibody response in adults and in the elderly after two doses Neutralizing antibody responses were ...
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EU approves Benlysta (belimumab) for adult patients with active lupus nephritis
GlaxoSmithKline plc announced the European Commission has approved the expanded use of intravenous and subcutaneous BENLYSTA ...
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ViiV Healthcare initiates rolling submission of new drug application with US FDA for long-acting cabotegravir for prevention of HIV
ViiV Healthcare, the global specialist HIV company majority owned by GlaxoSmithKline plc (“GSK”), with Pfizer Inc. ...
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GSK reports slower Q1 numbers
Strong growth in new pharmaceutical products offset by stocking and pandemic disruption Pharmaceuticals £3.9 billion -12% ...
Read moreFDA Approves Immunotherapy for Endometrial Cancer with Specific Biomarker
U.S. Food and Drug Administration granted accelerated approval to Jemperli (dostarlimab) for treating patients with recurrent ...
Read moreGSK to Reduce Plastic in Over 80 Million Bottles of Advil by 20% with New Sustainable Plastic Technology
GSK Consumer Healthcare the maker of Advil, today announced its commitment to reducing the plastic in ...
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EMA starts review of monoclonal antibody by GSK & VIR biotech for the early treatment of COVID-19
GlaxoSmithKline plc and Vir Biotechnology, Inc. today announced that the European Medicines Agency (EMA) has started ...
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