Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Tislelizumab + S-1 is a combination therapy consisting of tislelizumab, a humanized IgG4 monoclonal antibody targeting programmed death-1 (PD-1), and S-1, an oral fluoropyrimidine-based chemotherapy agent. Tislelizumab blocks the PD-1 receptor on T cells, preventing its interaction with PD-L1 and thereby enhancing anti-tumor immune responses by restoring T cell activity. S-1 combines tegafur (a prodrug of 5-fluorouracil) with two modulators to enhance efficacy and reduce gastrointestinal toxicity. This combination is being investigated primarily for the treatment of locally advanced or recurrent cancers such as esophageal squamous cell carcinoma (ESCC) and intrahepatic cholangiocarcinoma, particularly in elderly or high-risk patients[1][4]. The rationale for combining these agents is to leverage both immunotherapy-mediated tumor recognition and cytotoxic chemotherapy effects.
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 tislelizumab + S-1.