Drug intelligence / Profile preview

surufatinib + envafolimab

Development stage
Unknown
Lead developer
HUTCHMED
Modality
Monoclonal Antibodies → Antibody-Based Therapeutics, Small Molecules
Administration
Oral, Subcutaneous
01

Overview

Surufatinib + envafolimab is an investigational combination therapy consisting of two agents with complementary mechanisms of action for the treatment of advanced solid tumors, including neuroendocrine neoplasms and biliary tract carcinoma. Surufatinib is an oral small-molecule tyrosine kinase inhibitor that targets vascular endothelial growth factor receptors 1, 2, and 3 (VEGFR1/2/3), fibroblast growth factor receptor 1 (FGFR1), and colony-stimulating factor 1 receptor (CSF-1R). This results in inhibition of tumor angiogenesis and modulation of the tumor immune microenvironment[4][7]. Envafolimab is a humanized single-domain anti-programmed cell death protein 1 (PD-1) monoclonal antibody administered subcutaneously; it blocks PD-1 to enhance T-cell mediated antitumor immunity[9][10]. The combination aims to leverage both antiangiogenic effects and immune checkpoint blockade for synergistic antitumor activity. Early-phase clinical trials are ongoing in indications such as unresectable or metastatic biliary tract cancer, soft tissue sarcoma, and other advanced solid tumors[7].

Brand names
SulandaEnweida
Other names
surufatinib + envafolimab
02

Targets

CD274 (Programmed cell death protein 1 ligand 1)CSF1R (Macrophage colony-stimulating factor receptor)VEGFR3 (Vascular endothelial growth factor receptor 3)VEGFR-1 (Vascular endothelial growth factor receptor 1)VEGFR2 (Vascular endothelial growth factor receptor 2)FGFR1 (Fibroblast growth factor receptor 1)

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