Drug intelligence / Profile preview

bevacizumab + dasatinib

Development stage
Phase 2
Lead developer
Mayo Clinic
Modality
Monoclonal Antibodies → Antibody-Based Therapeutics, Small Molecules
Administration
Intravenous, Oral
01

Overview

Bevacizumab + dasatinib is an experimental combination therapy consisting of two distinct anticancer agents. Bevacizumab is a humanized IgG1 monoclonal antibody that binds all biologically active isoforms of human vascular endothelial growth factor (VEGF), thereby inhibiting angiogenesis, the process by which new blood vessels form to supply tumors[3][1]. Dasatinib is a small molecule inhibitor targeting multiple tyrosine kinases, including all SRC-family kinases, BCR-ABL, c-KIT, EPH-family kinases, and PDGFβ receptor[3][1]. The rationale for combining these drugs lies in their complementary mechanisms—bevacizumab blocks VEGF-driven angiogenesis while dasatinib inhibits Src-mediated signaling pathways that contribute to tumor growth and metastasis. Preclinical studies suggest this combination may prevent or delay resistance to anti-angiogenic therapy and provide synergistic antitumor effects[5][6]. Both drugs are individually approved for various cancers but their use together remains investigational; clinical trials have focused on advanced solid tumors and glioblastoma multiforme[1][4][7].

02

Targets

ABL1 (ABL proto-oncogene 1, non-receptor tyrosine kinase)EPH (EPH receptor family)PDGFRB (Platelet-derived growth factor receptor beta)SFK (SRC family kinases)VEGFA (Vascular endothelial growth factor A)KIT (c-KIT proto-oncogene receptor tyrosine kinase)

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