AbCellera’s Rapid Pandemic Response Platform Contributes to the World’s First COVID-19 Clinical Trial for a Potential Monoclonal Antibody Treatment
Retrieved on:
Monday, June 1, 2020
Medical Supplies, Health, Infectious diseases, Clinical trials, Pharmaceutical, Biotechnology, Medical specialties, Medicine, Viruses, Immunology, Monoclonal antibodies, Zoonoses, Severe acute respiratory syndrome-related coronavirus, Antibody, Coronavirus, Middle East respiratory syndrome-related coronavirus, Severe acute respiratory syndrome, Ocaratuzumab, LY-CoV555, AbCellera Biologics Inc.
LY-CoV555 is developed from a fully human monoclonal antibody identified from the first blood sample obtained from a North American patient who recovered from COVID-19.
Key Points:
- LY-CoV555 is developed from a fully human monoclonal antibody identified from the first blood sample obtained from a North American patient who recovered from COVID-19.
- LY-CoV555 was developed at record speed, taking less than three months to advance from screen to first-in-human clinical trials.
- Lilly is independently leading the clinical development and testing of the resulting potential antibody therapeutics.
- LY-CoV555 is a highly potent, neutralizing IgG1 monoclonal antibody that targets the spike protein of SARS-CoV-2, the novel coronavirus that causes COVID-19.