Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
AB122 + TAS-120 + AB154 is an investigational combination therapy used in oncology clinical trials. AB122 (zimberelimab) is a monoclonal antibody targeting the programmed cell death protein 1 (PD-1) to inhibit immune checkpoint signaling, thereby promoting T-cell-mediated anti-tumor activity. TAS-120 (futibatinib) is an orally available, irreversible FGFR1–4 inhibitor that targets aberrant FGFR signaling pathways in cancers with FGFR genetic alterations. AB154 (domvanalimab) is a humanized monoclonal antibody targeting TIGIT (T cell immunoreceptor with Ig and ITIM domains), an immune checkpoint, to enhance anti-tumor immunity by relieving TIGIT-mediated suppression. This combination is under investigation primarily for advanced or metastatic solid tumors, including but not limited to non-small cell lung cancer, pancreatic ductal adenocarcinoma, and other malignancies[2][4][3]. Clinical studies are evaluating the safety, tolerability, pharmacokinetics, and anti-tumor efficacy of the combination in various cancer populations, typically as intravenous infusions (AB122, AB154) with oral TAS-120 administration[1][2][3][4].
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 AB122 + TAS-120 + AB154.