Eli Lilly and Company's bebtelovimab receives Emergency Use Authorization for the treatment of mild-to-moderate COVID-19
Posted:
FDA has authorized bebtelovimab for emergency use for certain non-hospitalized patients with mild-to-moderate COVID-19 at high risk of progression to severe disease for whom alternative COVID-19 treatment options approved or authorized by FDA are not accessible or clinically appropriate Bebtelovimab neutralizes Omicron as demonstrated by pseudovirus and authentic virus data.
At GIANT Health Event #GIANT2025, meet with exhibitor Cineon to discuss ELE-Stress - an immersive resource hub developed with Torbay & South Devon NHS Foundation Trust and the University of Bath.
Powered by Cineon’s Empathic Learning Engine (ELE), it offers:
Adaptive,…
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