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OZC-003

Development stage
Preclinical
Lead developer
ONCOZEN
Modality
PROTACs (E3 ligase recruitment) → Targeted Protein Degraders (TPDs) → Small Molecules, Bivalent/Multivalent Binders → Multivalent & Scaffold-Based Small Molecules → Small Molecules
Administration
Oral
01

Overview

OZC-003 is a preclinical-stage therapeutic candidate developed by ONCOZEN for the treatment of resistant non-small cell lung cancer (NSCLC). It utilizes a novel modality known as Chaperone-Mediated Protein Degradation (CMPD) to target and degrade the c-MET protein (hepatocyte growth factor receptor). Unlike traditional tyrosine kinase inhibitors that merely block signaling, OZC-003 is designed to eliminate the c-MET protein entirely by leveraging the cell's internal chaperone-mediated degradation machinery. This approach is intended to overcome resistance mechanisms associated with c-MET alterations, such as amplification or mutations, which frequently occur in advanced lung cancers.

02

Targets

HSP90 (Heat shock protein 90 (HSP90) chaperone complex)MET (Mesenchymal-epithelial transition factor receptor)

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