Drug intelligence / Profile preview

sorafenib + thalidomide

Development stage
Phase 2
Lead developer
Bayer
Modality
Small Molecules
Administration
Oral
01

Overview

**sorafenib + thalidomide** is an experimental combination therapy involving two small molecule drugs, **sorafenib** and **thalidomide**. Sorafenib is a multikinase inhibitor that targets both serine/threonine and receptor tyrosine kinases involved in tumor cell proliferation and angiogenesis, including RAF kinases, vascular endothelial growth factor receptors (VEGFR-2, VEGFR-3), platelet-derived growth factor receptor beta (PDGFR-β), c-KIT, and FLT-3. Thalidomide is an immunomodulatory and anti-angiogenic agent that inhibits tumor necrosis factor-alpha (TNF-α) production and nuclear factor kappa B (NF-κB) signaling, and blocks angiogenesis via effects on VEGF pathways. This combination has been investigated in early-phase trials for advanced cancers, especially unresectable hepatocellular carcinoma (HCC), to leverage potential dual anti-angiogenic and anti-tumor effects.

02

Targets

BRAF V600ECRBN (Cereblon)FLT3 (Fms related receptor tyrosine kinase 3)KIT (c-KIT proto-oncogene receptor tyrosine kinase)MAPK14 (p38 mitogen-activated protein kinase alpha)PDGFRB (Platelet-derived growth factor receptor beta)RAF1 (c-Raf-1 (Y340D/Y341D))VEGFR-1 (Vascular endothelial growth factor receptor 1)VEGFR2 (Vascular endothelial growth factor receptor 2)VEGFR4 (Vascular endothelial growth factor Receptor-3)NF-κBTNFA (Tumor necrosis factor alpha (soluble))

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