Drug intelligence / Profile preview

JRF103

Development stage
Unknown
Lead developer
Shenzhen Jinruijiye Biotechnology
Modality
Small Molecules
Administration
Oral
01

Overview

JRF103 is a novel, orally administered pan-HER inhibitor that demonstrates potent in vitro activity against HER1 (also known as EGFR), HER2, and HER4. It is designed to target multiple members of the human epidermal growth factor receptor (HER/ErbB) family, including EGFR, which are implicated in the development and progression of various solid tumors. The drug is being developed primarily for the treatment of advanced solid tumors, particularly those with mutations such as EGFR/HER2 exon 20 insertions where no targeted therapies have previously been approved. Clinical studies are ongoing to evaluate its safety, pharmacokinetics, and anti-tumor efficacy in patients with advanced malignancies[1][2][3][4][6].

02

Targets

EGFR T790M (Epidermal growth factor receptor T790M mutant)ERBB2 (Erb-b2 receptor tyrosine kinase 2)ERBB4 (Erb-b2 receptor tyrosine kinase 4)

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