Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
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.
Beyond the preview
Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.
Follow clinical development from study design and recruitment through results.
Explore development by indication, patient population, and geography.
Trace asset ownership, licensing agreements, and commercial partnerships.
Explore the patent landscape and regulatory exclusivity around an asset.
Compare development programs by target, modality, and indication.
Connect source evidence and development news to your research questions.
See how Gosset can support your research on cicimetinib.