Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Nivolumab + tegafur-gimeracil-oteracil potassium is a **combination therapy** used in the treatment of gastric and gastroesophageal junction cancers. **Nivolumab** is a human monoclonal antibody targeting programmed cell death protein-1 (**PD-1**), functioning as an immune checkpoint inhibitor. **Tegafur-gimeracil-oteracil potassium (S-1)** is an oral fluoropyrimidine prodrug combination that interferes with DNA synthesis and repair by inhibiting thymidylate synthase. The combination exploits both direct cytotoxic chemotherapy and immune-mediated antitumor effects. This combination has primarily been studied as an adjuvant or first-line therapy, including in phase II and III trials such as ATTRACTION-4 and ATTRACTION-5, mainly in East Asian populations. The primary clinical indications under investigation are **gastric cancer** and **esophagogastric junction cancer**, particularly in HER2-negative, advanced, unresectable, or postoperative settings[2][3][5][1][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 nivolumab + tegafur-gimeracil-oteracil potassium.