Drug intelligence / Profile preview

KFRX06

Development stage
Preclinical
Lead developer
KeifeRx
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

KFRX06 is a novel, orally delivered small molecule tyrosine kinase inhibitor (TKI) under development by KeifeRx for the treatment of neurodegenerative, neuroinflammatory, and mast cell-associated diseases. The drug is designed to penetrate the brain, induce autophagy, and promote the clearance of disease-causing toxic proteins—mechanisms believed to be beneficial in conditions such as Alzheimer's disease, Parkinson's disease, amyotrophic lateral sclerosis (ALS), Lewy Body Dementia, frontotemporal dementia, and other immune-related disorders. Preclinical research has demonstrated that KFRX06 inhibits multiple kinases including ABL1 (ABL proto-oncogene 1), FYN (tyrosine-protein kinase FYN), and LRRK2 (leucine-rich repeat serine/threonine-protein kinase 2). These actions are thought to reduce tau hyperphosphorylation and neuronal loss while improving cognitive and behavioral outcomes in relevant models. The intellectual property covering KFRX06 extends through at least 2037[1][4][5].

02

Targets

ABL1 (ABL proto-oncogene 1, non-receptor tyrosine kinase)KIT (c-KIT proto-oncogene receptor tyrosine kinase)FYN (Proto-oncogene tyrosine-protein kinase Fyn)LRRK2 (Leucine-rich repeat serine/threonine-protein kinase 2)TYRO3 (TYRO3 protein tyrosine kinase)

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