Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
IPM514 + tislelizumab is an investigational combination therapy being studied primarily for esophageal squamous cell carcinoma. IPM514 is a novel agent (details on its precise modality and mechanism are not yet publicly available), while tislelizumab is a humanized IgG4 monoclonal antibody targeting programmed cell death protein 1 (PD-1). Tislelizumab blocks the interaction between PD-1 and its ligands PD-L1/PD-L2, thereby restoring T-cell function and promoting immune-mediated antitumor activity. The combination is under evaluation in open-label, multicenter clinical trials that include dose escalation (IPM514 monotherapy), dose expansion (IPM514 with anti-PD-1 antibody), and neoadjuvant cohorts (adding cisplatin and paclitaxel). The primary indication under investigation is esophageal squamous cell carcinoma, both in advanced/metastatic settings after failure of first-line therapy and as neoadjuvant treatment for resectable disease[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 IPM514 + tislelizumab.