Drug intelligence / Profile preview

opebacan

Development stage
Phase 2
Lead developer
XOMA
Modality
Recombinant Proteins and Enzymes, Peptides
Administration
Intravenous
01

Overview

Opebacan is a recombinant fragment of human bactericidal/permeability-increasing protein (BPI), specifically a 21 kDa peptide corresponding to amino acids 1–193 of BPI. It is an injectable biologic drug with potential anti-infective and anti-inflammatory activity. Opebacan acts by neutralizing endotoxins, particularly lipopolysaccharides from Gram-negative bacteria, thereby reducing inflammation and infection risk in clinical settings characterized by neutropenia or compromised immune function. The drug has been investigated for use in conditions such as burns and burn infections, Crohn's disease, cardiovascular disorders, congenital anomalies, pediatric indications, wound infections, graft-versus-host disease following hematopoietic stem cell transplantation (HSCT), surgical wound infection, and radiation injuries. Its development was initially led by XOMA Royalty Corp., with clinical trials reaching up to Phase 3 for some indications[1][2][3][4][5].

Brand names
Neuprex
Other names
1-193-bactericidal/permeability-increasing protein (132-alanine) (human reduced)1-193-bactericidal/permeability-increasing protein (132-alanine) (human)bactericidal permeability-increasing protein opebacan
02

Targets

BPI (Bactericidal permeability-increasing protein)

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