Full approval for Actemra as option for severe COVID-19
Roche (ROG: SIX) company Genentech has won US approval for its intravenous Actemra (tocilizumab) product, for adults that have been hospitalized with COVID-19.
Full approval for the blockbuster antibody, which was originally developed for autoimmune conditions such as rheumatoid arthritis, comes after an Emergency Use Authorization (EUA) was granted by the Food and Drug Administration (FDA) in June 2021.
While full approval for children has not been granted at this time, the EUA for this age group currently remains in place.
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