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DEB-TACE plus Sorafenib

Guangxi Medical University · Phase 3 active Small molecule

DEB-TACE delivers doxorubicin directly to hepatocellular carcinoma via drug-eluting beads, while sorafenib systemically inhibits multiple tyrosine kinases to suppress tumor growth and angiogenesis.

DEB-TACE delivers doxorubicin directly to hepatocellular carcinoma via drug-eluting beads, while sorafenib systemically inhibits multiple tyrosine kinases to suppress tumor growth and angiogenesis. Used for Hepatocellular carcinoma (HCC), intermediate to advanced stage.

At a glance

Generic nameDEB-TACE plus Sorafenib
SponsorGuangxi Medical University
Drug classCombination therapy: locoregional chemoembolization + tyrosine kinase inhibitor
TargetDEB-TACE: topoisomerase II (doxorubicin); Sorafenib: VEGFR, PDGFR, RAF, FLT3
ModalitySmall molecule
Therapeutic areaOncology
PhasePhase 3

Mechanism of action

DEB-TACE (drug-eluting bead transarterial chemoembolization) is a locoregional therapy that uses microspheres loaded with doxorubicin to deliver high drug concentrations directly to the tumor vasculature while occluding blood supply. Sorafenib is a multi-kinase inhibitor targeting VEGFR, PDGFR, RAF, and FLT3, which suppresses angiogenesis and tumor cell proliferation systemically. The combination aims to enhance efficacy through complementary mechanisms: local chemotherapy plus vascular disruption combined with systemic tyrosine kinase inhibition.

Approved indications

Common side effects

Key clinical trials

Primary sources

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SourceUsed for
ClinicalTrials.govTrial enrolment, design, endpoints, results