Drug intelligence / Profile preview

crexavibart

Development stage
Phase 3
Lead developer
Bristol Myers Squibb
Modality
Monoclonal Antibodies → Antibody-Based Therapeutics, Recombinant Proteins and Enzymes
Administration
Subcutaneous
01

Overview

Crexavibart (BMS-986413; also known as C144-LS) is a fully human recombinant monoclonal antibody of the IgG1λ2 subtype that targets the receptor-binding domain (RBD) of the SARS-CoV-2 spike glycoprotein. It was developed by Bristol Myers Squibb in partnership with Rockefeller University for the treatment of COVID-19. The antibody binds to a specific epitope on the spike protein RBD and neutralizes SARS-CoV-2 by preventing viral entry into host cells. Crexavibart was engineered with Fc modifications to extend its half-life in humans. It has been evaluated both alone and in combination with another monoclonal antibody (BMS-986414/C135-LS) for outpatient treatment of mild-to-moderate COVID-19[1][3][4]. Clinical trials have shown it is safe but did not demonstrate significant efficacy at treating COVID-19 in low-risk outpatients when administered subcutaneously[1][7].

Other names
crexavibartBMS-986413BMS986413BMS 986413C144-LSC-144-LSC 144-LS
02

Targets

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

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