1. Cromer Berman S Emergency Use Authorization (EUA) for EVUSHELD (Tixagevimab 150 mg and Ci lgavimab 150 mg injection co-packaged for intramuscular use) center for drug evaluation and research (CDER) review identifying information application type (EUA or Pre-EUA) EUA If E. FDA website. https://www.fda.gov/media/155107/download. Published 2021. Accessed 2021. Accessed Jun 27, 2022 Jun 27.
2. Evusheld | European medicines agency. https://www.ema.europa.eu/en/medicines/human/EPAR/evusheld. Published 2022. Accessed 2022. Accessed Oct 10, 2022 Oct 10.
3. Agenzia Italiana del Farmaco (AIFA). AIFA autorizza l’utilizzo terapeutico del monoclonale Evusheld per il trattamento precoce del COVID-19 in soggetti a rischio di progressione. AIFA official website. https://www.aifa.gov.it/-/aifa-autorizza-l-utilizzo-terapeutico-del-monoclonale-evusheld-per-il-trattamento-precoce-del-covid-19-in-soggetti-a-rischio-di-progressione. Accessed 2022 Oct 10.
4. EMA Committee for Medicinal Products for Human Use (CHMP). Committee for medicinal products for human use (CHMP) assessment report. EMA website. www.ema.europa.eu/contact. Published 2021. Accessed June 27, 2022.
5. A Critical Analysis of the Use of Cilgavimab plus Tixagevimab Monoclonal Antibody Cocktail (Evusheld™) for COVID-19 Prophylaxis and Treatment