Drug intelligence / Profile preview

beceltinib

Development stage
Unknown
Lead developer
Hangzhou Bangshun Pharmaceutical
Modality
Small Molecules
Administration
Oral
01

Overview

Beceltinib (BS-1101) is an orally bioavailable, irreversible covalent inhibitor of Bruton's tyrosine kinase (BTK) being developed by Hangzhou Biosun Pharmaceutical. It is primarily under investigation for the treatment of persistent or chronic primary immune thrombocytopenia (ITP) and various B-cell malignancies. By forming a covalent bond with the BTK enzyme, beceltinib inhibits B-cell receptor (BCR) signaling and Fcγ receptor-mediated signaling in macrophages, which are critical pathways in the pathogenesis of ITP and B-cell proliferation. Clinical data from Phase 1/2 trials in ITP patients have shown that beceltinib can effectively increase platelet counts with a manageable safety profile, predominantly consisting of mild adverse events.

02

Targets

BTK (Bruton tyrosine kinase)

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