Drug intelligence / Profile preview

dEGF4KDEL

Development stage
Preclinical
Lead developer
University of Minnesota
Modality
Bacterial Toxin Conjugates → Immunotoxins → Antibody Conjugates → Antibody-Based Therapeutics, Fc-Fusion Proteins → Carrier/Scaffold Proteins → Recombinant Proteins and Enzymes
Administration
Intraperitoneal
01

Overview

**dEGF4KDEL** is an investigational, single-chain deimmunized bispecific ligand-directed toxin developed at the University of Minnesota. It fuses human epidermal growth factor and interleukin-4 targeting ligands to a truncated, deimmunized *Pseudomonas aeruginosa* exotoxin A payload with a C-terminal KDEL retention sequence. The molecule binds epidermal growth factor receptor and interleukin-4 receptor-positive tumor cells, is internalized, and delivers the exotoxin catalytic domain to inhibit protein synthesis and induce cell death. It showed preclinical antitumor activity in pancreatic cancer xenograft models, including inhibition of orthotopic MIA PaCa-2 tumors and metastasis, and related publications describe activity in breast cancer and malignant mesothelioma models. ([pubmed.ncbi.nlm.nih.gov](https://pubmed.ncbi.nlm.nih.gov/22258068/))

Other names
dEGF4KDELdEGF-4KDELdEGF 4KDELdeimmunized EGF4KDELEGF4KDEL 7mutEGF-4KDEL 7mutEGF 4KDEL 7mut
02

Targets

EGFR (Epidermal growth factor receptor)IL4R (Interleukin-4 receptor alpha subunit)

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