Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
**AK112 + tinengotinib** is an investigational combination therapy composed of the bispecific antibody **AK112** (cadonilimab), which targets programmed death-1 (PD-1) and vascular endothelial growth factor (VEGF), and **tinengotinib** (TT-00420), a spectrum-selective, oral multi-kinase inhibitor. AK112 is designed to block both immune checkpoint PD-1 and angiogenic factor VEGF, thereby enhancing anti-tumor immune activity and inhibiting tumor angiogenesis. Tinengotinib targets multiple kinases important in cancer progression, including fibroblast growth factor receptors 1-3 (FGFR1–3), Janus kinase 1/2 (JAK1/2), vascular endothelial growth factor receptors (VEGFRs), and Aurora kinases A/B. The combination is under investigation primarily for advanced solid tumors including cholangiocarcinoma (bile duct cancer) and potentially other cancers, where resistance to other therapies or enhanced efficacy may be achieved by dual checkpoint and multikinase blockade[1][2][3][4][7].
Beyond the preview
Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.
Follow clinical development from study design and recruitment through results.
Explore development by indication, patient population, and geography.
Trace asset ownership, licensing agreements, and commercial partnerships.
Explore the patent landscape and regulatory exclusivity around an asset.
Compare development programs by target, modality, and indication.
Connect source evidence and development news to your research questions.
See how Gosset can support your research on AK112 + tinengotinib.