Drug intelligence / Profile preview

LNK01002

Development stage
Phase 1
Lead developer
Lynk Pharmaceuticals
Modality
Orthosteric Ligands → Classical Binding Small Molecules → Small Molecules, Reversible Covalent Inhibitors → Covalent Small Molecules → Small Molecules, Irreversible Covalent Inhibitors → Covalent Small Molecules → Small Molecules, Allosteric Modulators → Classical Binding Small Molecules → Small Molecules
Administration
Oral
01

Overview

LNK01002 is an orally bioavailable, innovative triple kinase inhibitor developed by Lynk Pharmaceuticals. It is designed to simultaneously inhibit three kinases—FLT3, JAK1, and JAK2—which are key drivers in certain hematological malignancies such as primary myelofibrosis (PMF), post-polycythemia vera myelofibrosis (PV-MF), post-essential thrombocythemia myelofibrosis (ET-MF), polycythemia vera (PV), and acute myeloid leukemia (AML). The drug acts by inhibiting the activity of these kinases, thereby exerting antineoplastic effects. As a proteolysis-targeting chimera (PROTAC) molecule, it may also promote targeted degradation of these proteins via the ubiquitin–proteasome system. LNK01002 is currently in phase I clinical trials for patients with malignant myeloid hematologic neoplasms who are unresponsive or resistant to conventional therapies[1][2][3][4][5].

02

Targets

JAK1 (Janus kinase 1)FLT3 (Fms related receptor tyrosine kinase 3)JAK2 (Janus kinase 2)

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