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Oral Sorafenib

Sun Yat-sen University · Phase 3 active Small molecule

Sorafenib is a multi-kinase inhibitor that blocks RAF, VEGFR, and PDGFR signaling to inhibit tumor cell proliferation and angiogenesis.

Sorafenib is a multi-kinase inhibitor that blocks RAF, VEGFR, and PDGFR signaling to inhibit tumor cell proliferation and angiogenesis. Used for Hepatocellular carcinoma, Renal cell carcinoma, Differentiated thyroid cancer.

At a glance

Generic nameOral Sorafenib
SponsorSun Yat-sen University
Drug classMulti-kinase inhibitor
TargetRAF, VEGFR-2, VEGFR-3, PDGFR-β
ModalitySmall molecule
Therapeutic areaOncology
PhasePhase 3

Mechanism of action

Sorafenib inhibits multiple serine/threonine and receptor tyrosine kinases, including RAF kinase (involved in the MAPK pathway), VEGFR-2 and VEGFR-3 (which promote tumor angiogenesis), and PDGFR-β (which supports tumor vasculature). By blocking these pathways, sorafenib reduces both direct tumor cell growth and the formation of new blood vessels that tumors depend on for survival.

Approved indications

Common side effects

Key clinical trials

Primary sources

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

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