Tixagevimab + cilgavimab against SARS-CoV-2: the preclinical and clinical development and real-world evidence

Author:

Convertino Irma1ORCID,Ferraro Sara1ORCID,Cappello Emiliano1ORCID,Valdiserra Giulia1ORCID,Bonaso Marco1ORCID,Tuccori Marco12ORCID

Affiliation:

1. Unit of Pharmacology and Pharmacovigilance, Department of Clinical and Experimental Medicine, University of Pisa, Pisa, Italy

2. Unit of Adverse Drug Reactions Monitoring, Pisa University Hospital, Pisa, Italy

Publisher

Informa UK Limited

Subject

Drug Discovery

Reference63 articles.

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

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