Drug intelligence / Profile preview

tixagevimab + cilgavimab

Development stage
Phase 4
Lead developer
AstraZeneca
Modality
Monoclonal Antibodies → Antibody-Based Therapeutics
Administration
Intramuscular, Intravenous
01

Overview

**Tixagevimab + cilgavimab** is a co-packaged, long-acting combination of two Fc-engineered human IgG1 monoclonal antibodies developed for prevention and treatment of COVID-19. The antibodies bind distinct, non-overlapping epitopes in the receptor-binding domain of the SARS-CoV-2 spike glycoprotein, blocking viral attachment to host-cell ACE2 and thereby preventing viral entry. Both antibodies contain YTE substitutions to extend serum half-life and TM substitutions that reduce Fc receptor and complement binding. The product was marketed as **Evusheld** for COVID-19 pre-exposure prophylaxis, particularly in people unlikely to mount an adequate vaccine response; however, loss of activity against later viral variants led to loss of U.S. authorization and withdrawal of the European Union marketing authorization. ([nejm.org](https://www.nejm.org/doi/pdf/10.1056/NEJMoa2116620))

Brand names
Evusheld
Other names
cilgavimab + tixagevimabtixagevimab + cilgavimabtixagevimab co-packaged with cilgavimabtixagevimab-cilgavimabtixagevimab/cilgavimab
02

Targets

RBD (SARS-CoV-2 spike receptor-binding domain)

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