Antibodies: Timeline of key events
Mouseover the event title for a more detailed description of the event (if available). To search for particular terms in the description of the event enter the term in the box below 'Event' on the table and press 'enter'. Alternatively use the dropdown lists to filter by Person, Place or Science. Click here to clear the filter.
Date | Event | People | Places | Sciences |
---|---|---|---|---|
22 Oct 2019 | Monoclonal drug originally dismissed for treating Alzheimers got new green light from FDA for testing for the disease | Biogen | Monoclonal antibodies | |
15 Nov 2019 | FDA approved first monoclonal antibody drug to help treat painful complications associated with sickle-cell disease | Novartis | Monoclonal antibodies | |
18 Dec 2019 | FDA granted accelerated approval for Seattle Genetics drug for advanced urothelial cancer | Seattle Genetics | Monoclonal antibodies, Oncology | |
21 Nov 2020 | FDA issued emergency authorisation for the first monoclonal antibody treatment for patients with mild to moderate COVID-19 | Regeneron Pharmaceuticals | Monoclonal antibodies | |
8 Dec 2021 | FDA issued emergency authorisation for long-acting monoclonal antibodies for pre-exposure prevention of COVID-19 in certain patients | AstraZeneca | Monoclonal antibodies | |
11 Feb 2022 | FDA issued emergency use authorisation for a new monoclonal antibody treatment for COVID-19 that is active against the omicron variant. | AbCellera, Eli Lilly | Monoclonal antibodies | |
22 Oct 2019
Monoclonal drug originally dismissed for treating Alzheimers got new green light from FDA for testing for the disease
15 Nov 2019
FDA approved first monoclonal antibody drug to help treat painful complications associated with sickle-cell disease
18 Dec 2019
FDA granted accelerated approval for Seattle Genetics drug for advanced urothelial cancer
21 Nov 2020
FDA issued emergency authorisation for the first monoclonal antibody treatment for patients with mild to moderate COVID-19
8 Dec 2021
FDA issued emergency authorisation for long-acting monoclonal antibodies for pre-exposure prevention of COVID-19 in certain patients
11 Feb 2022
FDA issued emergency use authorisation for a new monoclonal antibody treatment for COVID-19 that is active against the omicron variant.
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