Drug intelligence / Profile preview

sunitinib + olaparib + tocilizumab

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

Overview

sunitinib + olaparib + tocilizumab is a combination therapy consisting of three distinct pharmacological agents: sunitinib, a multi-targeted tyrosine kinase inhibitor; olaparib, a poly(ADP-ribose) polymerase (PARP) inhibitor; and tocilizumab, an interleukin-6 (IL-6) receptor antagonist. Sunitinib inhibits multiple receptor tyrosine kinases, including VEGFR, PDGFR, and c-KIT, to suppress tumor angiogenesis and proliferation. Olaparib targets PARP1 and PARP2 enzymes to impede DNA repair, particularly in tumors with homologous recombination deficiency (HRD). Tocilizumab is a monoclonal antibody that binds to the IL-6 receptor, blocking pro-inflammatory signaling that can contribute to tumor progression and treatment resistance. While these agents are individually established in oncology and immunology, this specific triple combination is not a recognized clinical program and appears to be a misidentification of a trial evaluating sunitinib and olaparib in combination with the immune checkpoint inhibitors iparomlimab and tuvonralimab for advanced ovarian cancer.

02

Targets

PDGFRA (Platelet-derived growth factor receptor alpha)PARP3 (Poly(adp-ribose) polymerase 3)KIT (c-KIT proto-oncogene receptor tyrosine kinase)VEGFR2 (Vascular endothelial growth factor receptor 2)PDGFRB (Platelet-derived growth factor receptor beta)IL-6R (Interleukin-6 receptor subunit alpha)VEGFR-1 (Vascular endothelial growth factor receptor 1)VEGFR3 (Vascular endothelial growth factor receptor 3)CSF1R (Macrophage colony-stimulating factor receptor)RET (Rearranged during transfection receptor tyrosine kinase)FLT3 (Fms related receptor tyrosine kinase 3)PARP2 (Poly (adp-ribose) polymerase 2)

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