Among the list of the top 10 most promising COVID-19 therapeutics just published by the European Commission is a monoclonal antibody that was last month rejected by the US Food and Drug Administration for an emergency use authorization – Humanigen, Inc.’s lenzilumab for preventing and treating the “cytokine storm” often seen in patients newly hospitalized with COVID-19.
Other products added to the commission’s expanded portfolio include AstraZeneca PLC’s Evusheld (tixagevimab + cilgavimab), Atea Pharmaceuticals, Inc./








