Drug intelligence / Profile preview

BEBT-109

Development stage
Phase 2
Lead developer
BeBetter Med
Modality
Orthosteric Ligands → Classical Binding Small Molecules → Small Molecules, Reversible Covalent Inhibitors → Covalent Small Molecules → Small Molecules, Allosteric Modulators → Classical Binding Small Molecules → Small Molecules, Irreversible Covalent Inhibitors → Covalent Small Molecules → Small Molecules
Administration
Oral
01

Overview

BEBT-109 is an oral, small molecule pan-mutant-selective inhibitor of the epidermal growth factor receptor (EGFR). It is designed to target a broad spectrum of EGFR mutations, including T790M and exon 20 insertion mutations that are commonly associated with resistance to earlier-generation EGFR inhibitors in non-small cell lung cancer (NSCLC). Preclinical and early clinical studies have demonstrated promising antitumor activity and an acceptable safety profile. The drug has shown efficacy in patients with advanced or refractory NSCLC harboring EGFR T790M or exon 20 insertion mutations, with objective response rates around 44% and median progression-free survival of approximately 8 months. Common adverse events include diarrhea, rash, and anemia. BEBT-109 is being developed by BeBetter Med as a new molecular entity for the treatment of NSCLC[1][3][5][9].

Other names
BEBT109BEBT-109BEBT 109
02

Targets

EGFR T790M (Epidermal growth factor receptor T790M mutant)M1 (Muscarinic acetylcholine receptor M1)HTR2A (5-hydroxytryptamine receptor 2A)VEGFR2 (Vascular endothelial growth factor receptor 2)

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