Drug intelligence / Profile preview

donafenib + PD-1 inhibitor + TACE

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

Overview

This combination therapy regimen is being evaluated as a first-line treatment for patients with unresectable advanced hepatocellular carcinoma (HCC). It consists of donafenib, a programmed cell death protein 1 (PD-1) inhibitor, and transarterial chemoembolization (TACE). Donafenib, developed by Suzhou Zelgen Biopharmaceuticals, is a novel oral small molecule multikinase inhibitor and a deuterated derivative of sorafenib that targets multiple receptor tyrosine kinases, including VEGFR, PDGFR, and various Raf kinases. The PD-1 inhibitor component acts as a checkpoint inhibitor to enhance the immune system's anti-tumor response. TACE is a localized procedure that delivers chemotherapy directly to the liver tumor while simultaneously blocking its blood supply. This triple combination approach aims to improve overall survival and potentially convert unresectable tumors into resectable ones through transformation therapy.

Brand names
Zuniduo
Other names
Donafenib + PD-1 + TACE
02

Targets

PDCD1 (Programmed cell death protein 1 receptor)VEGFR (VEGFR family)KIT (c-KIT proto-oncogene receptor tyrosine kinase)FGFR1 (Fibroblast growth factor receptor 1)RAF1 (c-Raf-1 (Y340D/Y341D))PDGFRB (Platelet-derived growth factor receptor beta)BRAF (B-Raf proto-oncogene, serine/threonine kinase)RET (Rearranged during transfection receptor tyrosine kinase)FLT3 (Fms related receptor tyrosine kinase 3)

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