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All Studies   Meta Analysis    Recent:   

Lack of Ronapreve (REGN-CoV; casirivimab and imdevimab) virological efficacy against the SARS-CoV 2 Omicron variant (B.1.1.529) in K18-hACE2 mice

Tatham et al., bioRxiv, doi:10.1101/2022.01.23.477397
Jan 2022  
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16th treatment shown to reduce risk in March 2021
 
*, now known with p = 0.000018 from 28 studies, recognized in 42 countries. Efficacy is variant dependent.
No treatment is 100% effective. Protocols combine complementary and synergistic treatments. * >10% efficacy in meta analysis with ≥3 clinical studies.
4,000+ studies for 60+ treatments. c19early.org
K18-hACE2 mouse study showing that casirivimab/imdevimab was not effective for omicron at doses 2x higher than those effective for previous variants.
Tatham et al., 24 Jan 2022, preprint, 15 authors.
This PaperCasirivimab/i..All
Lack of Ronapreve (REGN-CoV; casirivimab and imdevimab) virological efficacy against the SARS-CoV-2 Omicron variant (B.1.1.529) in K18-hACE2 mice
Lee Tatham, Joanne Sharp, Edyta Kijak, Joanne Herriott, Megan Neary, Helen Box, Anthony Valentijn, Helen Cox, Henry Pertinez, Paul Curley, Usman Arshad, Rajith Kr Rajoli, Steve Rannard, James Stewart, Andrew Owen
doi:10.1101/2022.01.23.477397
AO and SR are Directors of Tandem Nano Ltd and co-inventors of patents relating to drug delivery. AO has received research funding from ViiV, Merck, Janssen and consultancy from Gilead, ViiV and Merck not related to the current paper. SR has received research funding from ViiV and AstraZeneca and consultancy from Gilead not related to the current paper. No other conflicts are declared by the authors.
References
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Bentley, SARS-CoV-2 Omicron-B.1.1.529 Variant leads to less severe disease than Pango B and Delta variants strains in a mouse model of severe COVID-19
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Choudhary, Emergence of SARS-CoV-2 Resistance with Monoclonal Antibody Therapy (Cold Spring Harbor Laboratory
Dejnirattisai, Reduced neutralisation of SARS-CoV-2 omicron B.1.1.529 variant by post-immunisation serum, The Lancet, doi:10.1016/s0140-6736(21)02844-0
Dejnirattisai, leads to widespread escape from neutralizing antibody responses
Hiscox, Khoo, Stewart, Owen, Shutting the gate before the horse has bolted: is it time for a conversation about SARS-CoV-2 and antiviral drug resistance?, Journal of Antimicrobial Chemotherapy, doi:10.1093/jac/dkab189
Horby, Casirivimab and imdevimab in patients admitted to hospital with COVID-19 (RECOVERY): a randomised, controlled, open-label, platform trial
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Medigeshi, Sub-optimal Neutralisation of Omicron
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Rothenberger, a novel trispecific DARPin candidate that protects against SARS-CoV-2 variants (Cold Spring Harbor Laboratory
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Salzer, Single-dose immunisation with a multimerised SARS-CoV-2 receptor binding domain (RBD) induces an enhanced and protective response in mice (Cold Spring Harbor Laboratory
Torjesen, Covid-19: Omicron may be more transmissible than other variants and partly resistant to existing vaccines, scientists fear, BMJ, doi:10.1136/bmj.n2943
Vanblargan, An infectious SARS-CoV-2 B.1.1.529 Omicron virus escapes neutralization by several therapeutic monoclonal antibodies (Cold Spring Harbor Laboratory
Weinreich, REGEN-COV Antibody Combination and Outcomes in Outpatients with Covid-19, New England Journal of Medicine, doi:10.1056/nejmoa2108163
Who, None
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