AbCellera-Discovered Antibody Granted Interim Authorization by Health Canada as a Treatment for COVID-19
Retrieved on:
Friday, November 20, 2020
FDA, Health, Infectious diseases, Clinical trials, Pharmaceutical, Biotechnology, Life sciences, Health sciences, Biotechnology, Pharmaceutical industry, Draft:Bamlanivimab, AbCellera, Emergency Use Authorization, Eua, Food and Drug Administration, Biopharmaceutical, Bamlanivimab, BLAZE-1, AbCellera Biologics Inc.
Details regarding the interim authorization can be found here .
Key Points:
- Details regarding the interim authorization can be found here .
- Bamlanivimab received emergency use authorization (EUA) from the U.S. Food and Drug Administration on November 9, 2020.
- Bamlanivimab emerged from the collaboration between Lilly and AbCellera to create antibody therapies for the prevention and treatment of COVID-19.
- AbCellera's partners include leading biotechnology companies, global health organizations, and many of the top 10 biopharmaceutical companies.