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GSK, Vir Seek Emergency Use Authorization for COVID-19 Antibody

GSK, Vir Seek Emergency Use Authorization for COVID-19 Antibody
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Vir Biotechnology and GSK Announce VIR-7831 Reduces Hospitalization and Risk of Death in Early Treatment of Adults with COVID-19

Vir Biotechnology and GSK Announce VIR-7831 Reduces Hospitalization and Risk of Death in Early Treatment of Adults with COVID-19
March 10, 2021 20:22 ET
| Source:
Vir Biotechnology, Inc.
Vir Biotechnology, Inc.
San Francisco, California, UNITED STATES
– Independent Data Monitoring Committee recommends stopping Phase 3 COMET-ICE trial early given an 85% reduction in hospitalization or death –
– Vir and GSK plan to immediately seek Emergency Use Authorization in the U.S. and authorizations in other countries –
– Additional new in vitro studies indicate VIR-7831 maintains activity against major circulating COVID-19 variants –
SAN FRANCISCO and LONDON, March 10, 2021 (GLOBE NEWSWIRE) Vir Biotechnology, Inc. (Nasdaq: VIR) and GlaxoSmithKline plc (LSE/NYSE: GSK) today announced that an Independent Data Monitoring Committee (IDMC) recommended that the Phase 3 COMET-ICE (COVID-19 Monoclonal ....

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Vir Biotechnology and GSK Announce VIR-7831 Reduces Hospitalization and Risk of Death in Early Treatment of Adults with COVID-19

Vir Biotechnology and GSK Announce VIR-7831 Reduces Hospitalization and Risk of Death in Early Treatment of Adults with COVID-19
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United Kingdom , South Africa , City Of , South African , Vir Biotechnology Inc , Drug Administration , Data Monitoring Committee , Independent Data Monitoring , Efficacy Trial , Care Early , Emergency Use Authorization , Biologics License Application , ஒன்றுபட்டது கிஂக்டம் , நகரம் ஆஃப் , வீர் உயிரி தொழில்நுட்பவியல் இன்க் , தகவல்கள் கண்காணிப்பு குழு , சுயாதீனமான தகவல்கள் கண்காணிப்பு , பராமரிப்பு ஆரம்ப , அவசரம் பயன்பாடு அங்கீகாரம் , உயிரியல் உரிமம் விண்ணப்பம் ,

Vir Biotechnology and GSK Announce VIR-7831 Reduces Hospitalization and Risk of Death in Early Treatment of Adults with COVID-19

Vir Biotechnology and GSK Announce VIR-7831 Reduces Hospitalization and Risk of Death in Early Treatment of Adults with COVID-19
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Lilly, Vir Biotechnology and GSK announce first patient dosed in expanded BLAZE-4 trial evaluating bamlanivimab (LY-CoV555) with VIR-7831 (GSK4182136) for COVID-19

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INDIANAPOLIS and SAN FRANCISCO and LONDON, Jan. 27, 2021 /PRNewswire/ Eli Lilly and Company (NYSE: LLY), Vir Biotechnology, Inc. (NASDAQ: VIR) and GlaxoSmithKline plc (LSE/NYSE: GSK) today announced a collaboration to evaluate a combination of two COVID-19 therapies in low-risk patients with mild to moderate COVID-19. Lilly has expanded its ongoing BLAZE-4 trial to evaluate the administration of bamlanivimab (LY-CoV555) 700mg with VIR-7831 (also known as GSK4182136) 500mg, two neutralizing antibodies that bind to different epitopes of the SARS-CoV-2 spike protein. This unique collaboration marks the first time that monoclonal antibodies from separate companies will be brought together to explore potential outcomes. ....

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