Drug intelligence / Profile preview

nofazinlimab + regorafenib

Development stage
Phase 1
Lead developer
CStone Pharmaceuticals
Modality
Monoclonal Antibodies → Antibody-Based Therapeutics, Small Molecules
Administration
Intravenous, Oral
01

Overview

The **combination of nofazinlimab (formerly known as CS1003) and regorafenib** is an investigational cancer therapy combining a **humanized IgG4 monoclonal antibody targeting PD-1 (programmed cell death protein 1)** with **regorafenib**, a small molecule multi-kinase inhibitor. Nofazinlimab blocks the immune checkpoint PD-1 on T cells, enhancing the anti-tumor immune response, while regorafenib targets and inhibits multiple kinases involved in tumor angiogenesis, tumor growth, and the tumor microenvironment. This combination is being explored in clinical trials for the treatment of solid tumors, particularly in hepatocellular carcinoma and metastatic colorectal cancer, to potentially enhance anti-cancer efficacy through dual immunomodulation and anti-angiogenic effects[2][6][7].

Other names
CS1003 + regorafenibnofazinlimab + regorafenib
02

Targets

ABL2 (ABL proto-oncogene 2, non-receptor tyrosine kinase)BRAF V600ECSF1R (Macrophage colony-stimulating factor receptor)DDR2 (Discoidin domain receptor tyrosine kinase 2)EPHA2 (Ephrin type-A receptor 2)FGFR1 (Fibroblast growth factor receptor 1)FGFR2 (Keratinocyte growth factor receptor)KIT (c-KIT proto-oncogene receptor tyrosine kinase)PDCD1 (Programmed cell death protein 1 receptor)PDGFRA (Platelet-derived growth factor receptor alpha)PDGFRB (Platelet-derived growth factor receptor beta)RAF1 (c-Raf-1 (Y340D/Y341D))RET (Rearranged during transfection receptor tyrosine kinase)TEK (Tie2)NTRK1 (Tropomyosin-related receptor kinase A)VEGFR-1 (Vascular endothelial growth factor receptor 1)VEGFR2 (Vascular endothelial growth factor receptor 2)VEGFR4 (Vascular endothelial growth factor Receptor-3)FGFR3 (Fibroblast growth factor receptor 3)FGFR4 (Fibroblast growth factor receptor 4)

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