Drug intelligence / Profile preview

irinotecan + sunitinib

Development stage
Phase 1
Lead developer
Pfizer
Modality
Small Molecules
Administration
Intravenous, Oral
01

Overview

Irinotecan + sunitinib is an investigational combination therapy consisting of two small molecule drugs with distinct mechanisms of action, evaluated primarily in advanced or refractory solid tumors, including malignant glioma and metastatic colorectal cancer. Irinotecan is a topoisomerase I inhibitor that interferes with DNA replication in cancer cells, leading to cell death. Sunitinib is a multitargeted tyrosine kinase inhibitor that blocks several receptor tyrosine kinases involved in tumor growth and angiogenesis, notably vascular endothelial growth factor receptors (VEGFRs) and platelet-derived growth factor receptors (PDGFRs). The combination has been studied for potential synergistic antitumor effects but has shown moderate toxicity and limited efficacy in early-phase clinical trials[1][2][4][6]. No unique brand name exists for this combination.

Other names
sunitinib malateirinotecan hydrochloride trihydrate
02

Targets

TOP1 (DNA Topoisomerase I)FLT3 (Fms related receptor tyrosine kinase 3)KIT (c-KIT proto-oncogene receptor tyrosine kinase)PDGFRB (Platelet-derived growth factor receptor beta)VEGFR2 (Vascular endothelial growth factor receptor 2)

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