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Rockefeller grants commercial license for development of monoclonal antibodies for treatment of COVID-19

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Bristol Myers Squibb and The Rockefeller University Announce License Agreement for SARS-CoV-2 Neutralizing Monoclonal Antibody Combination for the Treatment of COVID-19

Bristol Myers Squibb and The Rockefeller University Announce License Agreement for SARS-CoV-2 Neutralizing Monoclonal Antibody Combination for the Treatment of COVID-19 Bristol Myers Squibb and The Rockefeller University today announced that they have entered into a definitive agreement under which Bristol Myers Squibb has been granted a global exclusive license to develop, manufacture and commercialize Rockefeller’s novel monoclonal antibody duo treatment that neutralizes the SARS-CoV-2 virus for therapy or prevention of COVID-19. Despite the increasing availability of the … Bristol Myers Squibb (NYSE: BMY) and The Rockefeller University today announced that they have entered into a definitive agreement under which Bristol Myers Squibb has been granted a global exclusive license to develop, manufacture and commercialize Rockefeller’s novel monoclonal antibody (“mAb”) duo treatment that neutralizes the SARS-CoV-2 virus for therapy or prevention of COVID-19.

Enhanced SARS-CoV-2 neutralization by dimeric IgA

n 111) and contacts ( K and L) The normalized AUC of anti-RBD IgA (K) or IgG (L) ELISA for patients with gastrointestinal (GI) symptoms ( n 32) and without GI symptoms ( n 117) was plotted. The r and P values for the correlations in (C) to (G) were determined by two-tailed Spearman’s correlations. For (H) to (L), horizontal bars indicate median values. Statistical significance was determined using a two-tailed Mann-Whitney U test. P 0.005) and severity of symptoms ( P 0.0001) but not timing of sample collection relative to onset ( P 0.69) or age ( P 0.22) (Fig. 1, C to F). Concentrations of anti-RBD IgA antibodies correlated strongly with anti-RBD IgG concentrations (

Rockefeller begins testing of new COVID-19 antibody drug in people

Monoclonal antibodies attaching to coronaviruses. With green light from the FDA, Rockefeller scientists started human trials this week for a new monoclonal antibody drug as a potential treatment for COVID-19. Monoclonal antibodies are mass-produced replicas of natural antibodies made by the immune system to fight viruses. Designed to prevent people with early COVID-19 from developing severe disease, the treatment can be life-saving and is urgently needed as hospitals continue to be inundated by repeated surges of infection, and mass vaccinations are still several months away. “If administered early, monoclonal antibodies could stop the virus in its tracks before the immune system has had enough time to develop its own antibodies,” says Michel C. Nussenzweig, head of the Laboratory of Molecular Immunology, who led the project in collaboration with Paul Bieniasz, Marina Caskey, Theodora Hatziioannou, Charles M. Rice, and others.

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