Drug intelligence / Profile preview

seratinib

Development stage
Phase 1
Lead developer
Qilu Pharmaceutical
Modality
Small Molecules
Administration
Oral
01

Overview

Seratinib (QLH11906) is an orally bioavailable, irreversible pan-HER tyrosine kinase inhibitor (TKI) developed by Qilu Pharmaceutical. It targets the human epidermal growth factor receptors EGFR (HER1), HER2, and HER4. By covalently binding to the ATP-binding site of these receptors, seratinib inhibits their autophosphorylation and downstream signaling pathways, such as PI3K/Akt and MAPK, which are critical for the proliferation and survival of HER2-amplified or EGFR-mutated cancer cells. It is primarily being investigated for the treatment of advanced HER2-positive breast cancer and other solid tumors expressing HER family members.

Other names
pan-RAF inhibitor QLH11906
02

Targets

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

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