Drug intelligence / Profile preview

andamertinib

Development stage
Phase 3
Lead developer
Avistone Biotechnology
Modality
Orthosteric Ligands → Classical Binding Small Molecules → Small Molecules, Allosteric Modulators → Classical Binding Small Molecules → Small Molecules, Irreversible Covalent Inhibitors → Covalent Small Molecules → Small Molecules
Administration
Oral
01

Overview

Andamertinib (PLB1004) is an oral, potent, irreversible, and highly selective epidermal growth factor receptor tyrosine kinase inhibitor (EGFR-TKI). It demonstrates strong blood-brain barrier penetration and broad tyrosine kinase activity. Andamertinib is designed to target both classical EGFR mutations (such as Del19, L858R, T790M) as well as exon 20 insertions with high selectivity. The drug is being developed primarily for the treatment of non-small cell lung cancer (NSCLC), particularly in patients who have developed resistance to prior EGFR-TKI therapy due to MET amplification or overexpression. Clinical studies have shown promising efficacy in this population, including those with brain metastases[5][10].

Other names
andamertinibPLB1004PLB-1004PLB 1004
02

Targets

EGFR T790M (Epidermal growth factor receptor T790M mutant)MET (Mesenchymal-epithelial transition factor receptor)

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