Drug intelligence / Profile preview

OMO-1 + EGFR-TKI

Development stage
Unknown
Lead developer
Octimet Oncology
Modality
Small Molecules
Administration
Oral
01

Overview

OMO-1 + EGFR-TKI is a combination therapy under investigation for the treatment of advanced solid malignancies, particularly non-small cell lung cancer (NSCLC) that has developed resistance to EGFR tyrosine kinase inhibitors. OMO-1 is a highly selective oral small molecule inhibitor of MET kinase, a recognized driver of resistance in tumors progressing during EGFR-TKI therapy. The combination is designed to inhibit both MET and EGFR signaling pathways, aiming to overcome resistance and potentially improve clinical outcomes in patients with MET-amplified or EGFR-mutant cancers. OCTIMET Oncology licensed OMO-1 from Janssen Pharmaceuticals and is leading its development, with a Phase I/II modular proof-of-concept study (NCT03138083) evaluating safety, tolerability, and preliminary efficacy of OMO-1 in combination with EGFR-TKIs such as afatinib, erlotinib, and gefitinib[1][2].

02

Targets

MET (Mesenchymal-epithelial transition factor receptor)OCT2 (Organic cation transporter 2)

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