Drug intelligence / Profile preview

nofazinlimab + regorafenib

Development stage
Unknown
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

PDCD1 (Programmed cell death protein 1 receptor)BRAF V600ETEK (Tie2)FGFR2 (Keratinocyte growth factor receptor)VEGFR-1 (Vascular endothelial growth factor receptor 1)RET (Rearranged during transfection receptor tyrosine kinase)PDGFRB (Platelet-derived growth factor receptor beta)VEGFR2 (Vascular endothelial growth factor receptor 2)PDGFRA (Platelet-derived growth factor receptor alpha)RAF1 (c-Raf-1 (Y340D/Y341D))FGFR1 (Fibroblast growth factor receptor 1)EPHA2 (Ephrin type-A receptor 2)DDR2 (Discoidin domain receptor tyrosine kinase 2)KIT (c-KIT proto-oncogene receptor tyrosine kinase)NTRK1 (Tropomyosin-related receptor kinase A)CSF1R (Macrophage colony-stimulating factor receptor)ABL2 (ABL proto-oncogene 2, non-receptor tyrosine kinase)VEGFR3 (Vascular endothelial growth factor receptor 3)

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