Drug intelligence / Profile preview

LNF1802

Development stage
Phase 1
Lead developer
Shandong New Era Pharmaceutical
Modality
Small Molecules
Administration
Oral
01

Overview

LNF1802 is an investigational, orally bioavailable small molecule inhibitor of the fibroblast growth factor receptor (FGFR) family, specifically targeting FGFR1, FGFR2, and FGFR3. Developed by Shandong New Era Pharmaceutical (a subsidiary of Lunan Pharmaceutical Group), LNF1802 is designed to treat advanced solid tumors characterized by FGFR alterations, such as gene amplifications, mutations, or fusions. By selectively binding to the ATP-binding site of these receptors, the drug inhibits their tyrosine kinase activity, thereby blocking downstream signaling pathways including MAPK/ERK and PI3K/AKT that drive tumor cell proliferation, survival, and angiogenesis. It is currently undergoing Phase 1 clinical evaluation to determine its safety, tolerability, and preliminary efficacy in patients with refractory advanced malignancies.

02

Targets

FGFR1 (Fibroblast growth factor receptor 1)FGFR2 (Keratinocyte growth factor receptor)FGFR3 (Fibroblast growth factor receptor 3)

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