Drug intelligence / Profile preview

trebananib + sunitinib

Development stage
Phase 2
Lead developer
Amgen
Modality
Peptide-Protein Conjugates → Peptide Conjugates → Peptides, Small Molecules
Administration
Oral, Intravenous
01

Overview

Trebananib + sunitinib is a **combination therapy** studied primarily in metastatic renal cell carcinoma. **Trebananib** (AMG 386) is an investigational recombinant peptide-Fc fusion protein (peptibody) that blocks the interaction between angiopoietin-1/2 and the Tie2 receptor, thereby inhibiting angiogenesis[1][2][3]. **Sunitinib** is an oral, small molecule tyrosine kinase inhibitor that targets multiple receptor tyrosine kinases, including vascular endothelial growth factor (VEGF) receptors, platelet-derived growth factor (PDGF) receptors, and others, resulting in inhibition of tumor growth and angiogenesis[1][2][3]. The combination was investigated for potential synergistic anti-angiogenic and antitumor activity, with phase I and II studies indicating efficacy but increased toxicity compared to sunitinib alone[1][2][3][4].

Other names
trebananibsunitinib malate
02

Targets

ANGPT1 (Angiopoietin-1)ANGPT2 (Angiopoietin-2)CSF1R (Macrophage colony-stimulating factor receptor)FLT3 (Fms related receptor tyrosine kinase 3)KIT (c-KIT proto-oncogene receptor tyrosine kinase)PDGFRA (Platelet-derived growth factor receptor alpha)PDGFRB (Platelet-derived growth factor receptor beta)RET (Rearranged during transfection receptor tyrosine kinase)VEGFR-1 (Vascular endothelial growth factor receptor 1)VEGFR2 (Vascular endothelial growth factor receptor 2)VEGFR4 (Vascular endothelial growth factor Receptor-3)TEK (Tie2)

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