Drug intelligence / Profile preview

NF2105

Development stage
Unknown
Lead developer
Shenzhen Taili Biomedical
Modality
Small Molecules
Administration
Oral
01

Overview

NF2105 is an investigational small molecule tyrosine kinase inhibitor (TKI) developed by Shenzhen Taili Biomedical and Shenzhen Xinyang Weikang Technology for the treatment of chronic myeloid leukemia (CML). It is designed as a potent inhibitor of the BCR-ABL1 fusion protein, specifically targeting the T315I gatekeeper mutation which confers resistance to first-, second-, and some third-generation TKIs. By binding to the ATP-binding site of the ABL1 kinase domain, NF2105 suppresses the constitutive signaling activity that drives leukemic cell proliferation. The drug is currently undergoing early-phase clinical evaluation in China to determine its safety, tolerability, and preliminary efficacy in patients with Philadelphia chromosome-positive (Ph+) leukemias who have failed prior therapies.

02

Targets

ABL1 (ABL proto-oncogene 1, non-receptor tyrosine kinase)

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