Drug intelligence / Profile preview

MU-D201

Development stage
Preclinical
Lead developer
MedPacto
Modality
Small Molecules
01

Overview

MU-D201 is a small molecule inhibitor of DAP kinase-related apoptosis-inducing kinase-2 (DRAK2) currently under preclinical development by MedPacto. DRAK2 is a serine/threonine kinase that, when overexpressed, promotes cancer cell growth and metastasis by regulating TGF-β signaling and modulating the activity of the epigenetic regulator enhancer of zeste homolog 2 (EZH2). MU-D201 is specifically being investigated for the treatment of diffuse large B-cell lymphoma (DLBCL), particularly cases involving EZH2 mutations, and gamma delta T-cell leukemia. Preclinical animal studies have demonstrated its ability to suppress tumor growth and metastasis by targeting these signaling and epigenetic pathways.

02

Targets

STK17B (Serine/threonine kinase 17b)

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