Drug intelligence / Profile preview

kenitinib

Development stage
Unknown
Lead developer
Teligene
Modality
Small Molecules
Administration
Oral
01

Overview

Kenitinib (also known as TSN222) is an orally bioavailable small molecule inhibitor of Bruton's tyrosine kinase (BTK) developed by Teligene. It is designed to treat various B-cell malignancies by disrupting the B-cell receptor (BCR) signaling pathway, which is essential for the growth and survival of neoplastic B cells. The drug is currently undergoing exploratory clinical evaluation in patients with relapsed or refractory B-cell lymphomas, with specific cohorts focusing on primary central nervous system lymphoma (PCNSL), chronic lymphocytic leukemia (CLL), small lymphocytic lymphoma (SLL), and mantle cell lymphoma (MCL). As a BTK inhibitor, kenitinib aims to provide a targeted therapeutic option for patients who have failed prior lines of therapy.

Other names
克耐替尼kenitinib
02

Targets

STING (Stimulator of interferon genes protein)P4HB (Protein disulfide-isomerase)

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