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Pazopanib+Sorafenib

Technical University of Munich · Phase 3 active Small molecule

This combination of two tyrosine kinase inhibitors blocks multiple receptor pathways (VEGFR, PDGFR, RAF kinase) to inhibit tumor angiogenesis and cell proliferation.

This combination of two tyrosine kinase inhibitors blocks multiple receptor pathways (VEGFR, PDGFR, RAF kinase) to inhibit tumor angiogenesis and cell proliferation. Used for Advanced or metastatic renal cell carcinoma, Other solid tumors (under investigation in phase 3).

At a glance

Generic namePazopanib+Sorafenib
SponsorTechnical University of Munich
Drug classMulti-targeted tyrosine kinase inhibitor combination
TargetVEGFR, PDGFR, RAF kinase
ModalitySmall molecule
Therapeutic areaOncology
PhasePhase 3

Mechanism of action

Pazopanib and sorafenib are both multi-targeted receptor tyrosine kinase inhibitors that suppress vascular endothelial growth factor receptor (VEGFR), platelet-derived growth factor receptor (PDGFR), and RAF kinase signaling. By combining these agents, the regimen aims to achieve broader kinase inhibition and potentially overcome resistance mechanisms in cancer cells. This dual approach targets both tumor vasculature and intrinsic oncogenic pathways.

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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