Drug intelligence / Profile preview

zanubrutinib + lenalidomide

Development stage
Unknown
Lead developer
BeiGene
Modality
Orthosteric Ligands → Classical Binding Small Molecules → Small Molecules, Molecular Glues → Targeted Protein Degraders (TPDs) → Small Molecules, Irreversible Covalent Inhibitors → Covalent Small Molecules → Small Molecules
Administration
Oral
01

Overview

Zanubrutinib + lenalidomide is an investigational combination therapy consisting of two small molecule drugs, zanubrutinib and lenalidomide. Zanubrutinib is a next-generation, highly selective Bruton’s tyrosine kinase (BTK) inhibitor that blocks B-cell receptor signaling, leading to inhibition of malignant B-cell proliferation and survival. Lenalidomide is an immunomodulatory agent with direct anti-tumor activity and indirect effects through enhancement of immune responses. The combination has been studied primarily in relapsed/refractory diffuse large B-cell lymphoma (DLBCL) and other lymphoid malignancies, showing promising efficacy and manageable safety profiles in early-phase clinical trials[4][7]. The regimen may be particularly relevant for patients who are unfit for standard chemotherapy or stem cell transplantation.

Other names
ZR²ZR2ZR-2ZR 2
02

Targets

CRBN (Cereblon)BTK (Bruton tyrosine kinase)

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