Drug intelligence / Profile preview

ETI-311

Development stage
Discontinued
Lead developer
Elusys Therapeutics
Modality
Monoclonal Antibodies → Antibody-Based Therapeutics
Administration
Intravenous
01

Overview

ETI-311 is a chimeric monoclonal antibody developed by Elusys Therapeutics for the treatment and prophylaxis of anthrax, a life-threatening infection caused by *Bacillus anthracis*. The antibody is designed to bind with high affinity to the protective antigen (PA) component of the anthrax toxin complex. By binding to PA, ETI-311 prevents the assembly of the lethal toxin and edema toxin complexes and blocks their entry into host cells, thereby neutralizing the primary virulence factors of the bacteria. ETI-311 underwent early-stage clinical evaluation, including a Phase 1 trial to assess safety and pharmacokinetics in healthy volunteers. However, development of this specific chimeric version was superseded by ETI-204 (obiltoxaximab), a de-immunized version of the same antibody designed to reduce potential immunogenicity for long-term use and repeated administration in humans.

Other names
chimeric 14B7chimeric14B7chimeric-14B7
02

Targets

PA (Influenza polymerase acidic protein)

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