Drug intelligence / Profile preview

donafenib + PD-1

Development stage
Unknown
Lead developer
Suzhou Zelgen Biopharmaceuticals
Modality
Monoclonal Antibodies → Antibody-Based Therapeutics, Small Molecules
Administration
Oral, Intravenous
01

Overview

Donafenib + PD-1 is a combination therapeutic regimen primarily investigated for the treatment of unresectable advanced hepatocellular carcinoma (HCC). Donafenib is an orally administered small molecule multi-kinase inhibitor that targets vascular endothelial growth factor receptors (VEGFR), platelet-derived growth factor receptors (PDGFR), and the Raf/MEK/ERK signaling pathway to inhibit tumor angiogenesis and proliferation. The PD-1 inhibitor component is a monoclonal antibody that blocks the programmed death-1 (PD-1) receptor on T cells, preventing its interaction with ligands PD-L1 and PD-L2, thereby restoring anti-tumor immune responses. This combination is often evaluated alongside Transarterial Chemoembolization (TACE) to enhance local and systemic control of HCC by combining anti-angiogenic effects with immune checkpoint blockade.

Brand names
Zepatinib
Other names
donafenib + PD-1 inhibitordonafenib + anti-PD-1donafenib + programmed cell death-1 inhibitor
02

Targets

PDCD1 (Programmed cell death protein 1 receptor)BRAF (B-Raf proto-oncogene, serine/threonine kinase)VEGFR2 (Vascular endothelial growth factor receptor 2)RAF1 (c-Raf-1 (Y340D/Y341D))PDGFRB (Platelet-derived growth factor receptor beta)VEGFR3 (Vascular endothelial growth factor receptor 3)

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