Drug intelligence / Profile preview

cediranib + irinotecan + cetuximab

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

Overview

Cediranib + irinotecan + cetuximab is a three-drug combination therapy evaluated primarily in phase I trials for advanced solid tumors, including metastatic colorectal cancer. **Cediranib** is an oral, potent inhibitor of all three vascular endothelial growth factor receptors (VEGFR-1, -2, -3) and acts as an antiangiogenic agent, reducing tumor blood supply. **Irinotecan** is a topoisomerase I inhibitor (small molecule chemotherapy) that interferes with DNA replication and transcription, leading to cell death. **Cetuximab** is a monoclonal antibody targeting the epidermal growth factor receptor (EGFR), blocking ligand-induced activation and downstream proliferative signaling. When used together, this combination aims to inhibit angiogenesis, disrupt tumor cell proliferation, and overcome resistance to standard chemotherapy, with investigational roles primarily in advanced solid tumors such as colorectal cancer[3].

Brand names
Campto
Other names
cediranib + irinotecan + cetuximab
02

Targets

VEGFR2 (Vascular endothelial growth factor receptor 2)KIT (c-KIT proto-oncogene receptor tyrosine kinase)PDGFRA (Platelet-derived growth factor receptor alpha)TOP1 (DNA Topoisomerase I)EGFR T790M (Epidermal growth factor receptor T790M mutant)PDGFRB (Platelet-derived growth factor receptor beta)VEGFR-1 (Vascular endothelial growth factor receptor 1)VEGFR3 (Vascular endothelial growth factor receptor 3)FGFR1 (Fibroblast growth factor receptor 1)

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