Drug intelligence / Profile preview

bevacizumab + capecitabine + oxaliplatin + vandetanib

Development stage
Preclinical
Lead developer
Roche
Modality
Nucleic Acid-Directed Small Molecules → Small Molecules, Monoclonal Antibodies → Antibody-Based Therapeutics, Covalent Small Molecules → Small Molecules, Classical Binding Small Molecules → Small Molecules
Administration
Intravenous, Oral
01

Overview

This is a combination regimen consisting of four agents: - **Bevacizumab** is a monoclonal antibody that inhibits vascular endothelial growth factor A (VEGF-A), thereby blocking angiogenesis, the process by which tumors develop new blood vessels to sustain their growth. It is used in various cancers, including metastatic colorectal cancer and others[3][4][5]. - **Capecitabine** is an oral prodrug of 5-fluorouracil (5-FU), a pyrimidine analog that interferes with DNA synthesis and inhibits tumor cell proliferation. - **Oxaliplatin** is a platinum-based chemotherapeutic agent that forms DNA crosslinks, leading to apoptosis in rapidly dividing cells. - **Vandetanib** is an oral small molecule tyrosine kinase inhibitor targeting multiple receptors including VEGF receptor, epidermal growth factor receptor (EGFR), and RET proto-oncogene. This combination would be considered an investigational or experimental regimen for cancer treatment. Each component has established use in oncology; however, this specific four-drug combination does not have regulatory approval as a fixed regimen but may be studied in clinical trials for synergistic effects against certain advanced or refractory cancers.

02

Targets

VEGFR2 (Vascular endothelial growth factor receptor 2)TS (Thymidylate synthase)VEGFA (Vascular endothelial growth factor A)DNAEGFR T790M (Epidermal growth factor receptor T790M mutant)VEGFR3 (Vascular endothelial growth factor receptor 3)RET (Rearranged during transfection receptor tyrosine kinase)

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