Drug intelligence / Profile preview

avelumab + axitinib + palbociclib

Development stage
Unknown
Lead developer
Merck
Modality
Monoclonal Antibodies → Antibody-Based Therapeutics, Small Molecules
Administration
Intravenous, Oral
01

Overview

This is a combination drug regimen consisting of three agents used primarily in oncology. - **Avelumab** is a human monoclonal antibody targeting PD-L1 (programmed death-ligand 1), acting as an immune checkpoint inhibitor to enhance anti-tumor immune response. - **Axitinib** is an oral small molecule tyrosine kinase inhibitor that selectively inhibits vascular endothelial growth factor receptors VEGFR-1, VEGFR-2, and VEGFR-3, thereby blocking tumor angiogenesis and growth. - **Palbociclib** is an oral small molecule cyclin-dependent kinase (CDK) 4/6 inhibitor that blocks cell cycle progression from G1 to S phase by inhibiting CDK4 and CDK6 activity leading to cell cycle arrest in cancer cells. This triplet combination has been studied in clinical trials for advanced or metastatic clear cell renal cell carcinoma (ccRCC) and advanced non-small cell lung cancer (NSCLC). The combination aims to leverage immunotherapy with antiangiogenic therapy and targeted CDK inhibition for enhanced antitumor efficacy.

Brand names
Bavencio + Inlyta + Ibrance
Other names
avelumab plus axitinib plus palbociclib
02

Targets

VEGFR2 (Vascular endothelial growth factor receptor 2)CDK6 (Cyclin-dependent kinase 6)PDGFRB (Platelet-derived growth factor receptor beta)KIT (c-KIT proto-oncogene receptor tyrosine kinase)VEGFR-1 (Vascular endothelial growth factor receptor 1)CD274 (Programmed cell death protein 1 ligand 1)VEGFR3 (Vascular endothelial growth factor receptor 3)CDK4 (Cyclin-dependent kinase 4)

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