Drug intelligence / Profile preview

cicimetinib

Development stage
Unknown
Lead developer
Shanghai Institute of Materia Medica
Modality
Small Molecules
Administration
Oral
01

Overview

Cicimetinib (SIM0235) is an orally bioavailable, highly selective, and potent small molecule inhibitor of the mitogen-activated protein kinase kinases 1 and 2 (MEK1/2). Developed by the Shanghai Institute of Materia Medica (SIMM) in collaboration with Shanghai Runshi Pharmaceutical, cicimetinib targets the MAPK/ERK signaling pathway, which is frequently dysregulated in various human cancers, particularly those harboring RAS or BRAF mutations. By inhibiting MEK1/2, the drug blocks downstream signaling that promotes cell proliferation and survival. Cicimetinib is currently being evaluated in Phase I/II clinical trials in China, both as a monotherapy and in combination with the anti-PD-1 monoclonal antibody SG001, for the treatment of advanced, unresectable, or recurrent solid tumors.

Other names
cicimetinib hydrochloride盐酸希美替尼
02

Targets

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

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