Drug intelligence / Profile preview

TT-00420 + atezolizumab

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

Overview

**TT-00420 + atezolizumab** is a combination therapy of two agents: tinengotinib (TT-00420), a novel oral multi-kinase inhibitor, and atezolizumab, an anti-PD-L1 monoclonal antibody. - **Tinengotinib** targets multiple kinases implicated in cancer proliferation and immune regulation, including fibroblast growth factor receptors 1–3 (FGFR1, FGFR2, FGFR3), Janus kinase 1/2 (JAK1, JAK2), vascular endothelial growth factor receptors (VEGFRs), and Aurora kinases A/B. - **Atezolizumab** is a monoclonal antibody that inhibits programmed death-ligand 1 (PD-L1), a crucial immune checkpoint, thereby promoting anti-tumor immune responses. This combination has been investigated primarily in advanced biliary tract carcinoma (BTC) and cholangiocarcinoma, based on preclinical rationale for synergistic anti-tumor effects and observed clinical benefit in patients previously treated with immunotherapies. The combination is under development, notably evaluated in phase Ib/II trials in heavily pretreated solid tumor patients, with results indicating promising efficacy and tolerability[4].

Brand names
Tecentriq
Other names
TT-00420 + Tecentriqtinengotinib + atezolizumab
02

Targets

JAK2 (Janus kinase 2)CD274 (Programmed cell death protein 1 ligand 1)AURKB (Aurora kinase B)VEGFR2 (Vascular endothelial growth factor receptor 2)CSF1R (Macrophage colony-stimulating factor receptor)AURKA (Aurora kinase A)FGFR3 (Fibroblast growth factor receptor 3)FGFR2 (Keratinocyte growth factor receptor)FGFR1 (Fibroblast growth factor receptor 1)

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