Drug intelligence / Profile preview

WX-554

Development stage
Discontinued
Lead developer
Heidelberg Pharma
Modality
Small Molecules
Administration
Oral, Intravenous
01

Overview

WX-554 is an orally available small molecule inhibitor of mitogen-activated protein kinase kinase (MEK, also known as MAP2K or MAPK/ERK kinase). It selectively binds to and inhibits MEK1 and MEK2, thereby preventing the activation of downstream effector proteins such as certain transcription factors. This inhibition disrupts growth factor-mediated cell signaling pathways, leading to reduced tumor cell proliferation. Originally developed by UCB and later by WILEX AG, WX-554 was investigated primarily for the treatment of solid tumors and other cancers. Clinical studies included phase I/II trials in patients with advanced solid tumors to determine safety, pharmacokinetics/pharmacodynamics, optimal biological dose (OBD), and maximum tolerated dose (MTD). The drug demonstrated target inhibition with manageable side effects in early studies but development was discontinued after phase I/II trials[1][3][4][5][7].

02

Targets

MEK2 (Dual specificity mitogen-activated protein kinase kinase 2)MEK1 (Dual specificity mitogen-activated protein kinase kinase 1)

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