Drug intelligence / Profile preview

cediranib + paclitaxel + carboplatin

Development stage
Unknown
Lead developer
AstraZeneca
Modality
Small Molecules
Administration
Oral, Intravenous
01

Overview

**Cediranib + paclitaxel + carboplatin** is an investigational combination therapy primarily studied in advanced solid tumors, including non-small cell lung cancer (NSCLC) and metastatic or recurrent cervical cancer. Cediranib is a potent oral small molecule inhibitor of all three vascular endothelial growth factor receptors (VEGFR-1, VEGFR-2, VEGFR-3), blocking angiogenesis required for tumor growth. Paclitaxel, a microtubule inhibitor, and carboplatin, a DNA-damaging platinum agent, are chemotherapeutic agents used to kill or inhibit the proliferation of cancer cells. This combination aims to synergistically inhibit tumor growth by simultaneously blocking tumor angiogenesis and directly killing tumor cells. Clinical trials have shown enhanced tumor responses and progression-free survival compared to chemotherapy alone, but tolerability issues have been noted at some dosing regimens[1][2][3][4][7]. The combination has mainly been investigated in randomized phase II and III studies for advanced NSCLC and recurrent/metastatic cervical cancer, but is not an approved standard of care.

Other names
cediranib maleate + paclitaxel + carboplatin
02

Targets

VEGFR2 (Vascular endothelial growth factor receptor 2)TUBB (Tubulin (alpha and beta subunits))PDGFRA (Platelet-derived growth factor receptor alpha)VEGFR3 (Vascular endothelial growth factor receptor 3)CSF1R (Macrophage colony-stimulating factor receptor)ABL2 (ABL proto-oncogene 2, non-receptor tyrosine kinase)DNAVEGFR-1 (Vascular endothelial growth factor receptor 1)PDGFRB (Platelet-derived growth factor receptor beta)KIT (c-KIT proto-oncogene receptor tyrosine kinase)FGFR1 (Fibroblast growth factor receptor 1)

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