Drug intelligence / Profile preview

capivasertib + sunitinib

Development stage
Preclinical
Lead developer
AstraZeneca
Modality
Small Molecules
Administration
Oral
01

Overview

Capivasertib + sunitinib is an investigational combination of two small molecule kinase inhibitors, each with distinct but potentially complementary mechanisms of action in oncology. Capivasertib is a selective inhibitor of all three isoforms of the serine/threonine kinase AKT (AKT1, AKT2, and AKT3), a key node in the PI3K/AKT signaling pathway that regulates cell proliferation and survival. Sunitinib is a multi-targeted receptor tyrosine kinase inhibitor that blocks several receptors involved in tumor angiogenesis and growth, including vascular endothelial growth factor receptors (VEGFRs), platelet-derived growth factor receptors (PDGFRs), KIT, FLT3, CSF1R, and RET. Both drugs are approved individually for various cancers but there is no evidence from the provided sources or current literature that this specific combination has been approved or widely studied together as a fixed regimen.

Brand names
Truqap (capivasertib)Sutent (sunitinib)
Other names
capivasertib + sunitinib
02

Targets

PDGFRA (Platelet-derived growth factor receptor alpha)KIT (c-KIT proto-oncogene receptor tyrosine kinase)VEGFR2 (Vascular endothelial growth factor receptor 2)PDGFRB (Platelet-derived growth factor receptor beta)CSF1R (Macrophage colony-stimulating factor receptor)AKT2 (Rac-beta serine/threonine-protein kinase)CDK2 (Cyclin-dependent kinase 2)AKT1 (Proto-oncogene serine/threonine-protein kinase Akt1)VEGFR-1 (Vascular endothelial growth factor receptor 1)VEGFR3 (Vascular endothelial growth factor receptor 3)ITK (Interleukin 2-inducible T-cell kinase)FLT3 (Fms related receptor tyrosine kinase 3)

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