Drug intelligence / Profile preview

DTRMWXHS-12

Development stage
Phase 1
Lead developer
Zhejiang DTRM Biopharma
Modality
Multivalent & Scaffold-Based Small Molecules → Small Molecules, Classical Binding Small Molecules → Small Molecules, Covalent Small Molecules → Small Molecules, Nucleic Acid-Directed Small Molecules → Small Molecules
Administration
Oral
01

Overview

DTRMWXHS-12 is a selective, irreversible small molecule inhibitor of Bruton tyrosine kinase (BTK), developed by Zhejiang DTRM Biopharma. It is being investigated primarily for the treatment of B-cell malignancies such as chronic lymphocytic leukemia (CLL), diffuse large B cell lymphoma (DLBCL), follicular lymphoma, non-Hodgkin's lymphoma, and mantle cell lymphoma. The drug has also been studied in combination regimens with everolimus and pomalidomide to enhance antitumor activity and address acquired drug resistance. Preclinical studies demonstrated potent BTK inhibition with an IC50 of 0.7 nM and favorable selectivity over other kinases[3][7]. Clinical trials have evaluated its safety, tolerability, pharmacokinetics, and preliminary efficacy as both monotherapy and in combination therapies[1][6].

02

Targets

BTK (Bruton tyrosine kinase)

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