Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Etoposide + nedaplatin + tislelizumab is a combination regimen consisting of two cytotoxic chemotherapeutic agents (etoposide and nedaplatin) and an immune checkpoint inhibitor (tislelizumab). Etoposide is a topoisomerase II inhibitor that induces DNA strand breaks, leading to apoptosis in rapidly dividing cells. Nedaplatin is a platinum-based chemotherapeutic agent that forms DNA crosslinks, inhibiting DNA replication and transcription. Tislelizumab is a humanized IgG4 monoclonal antibody targeting programmed cell death protein 1 (PD-1) on T cells; it blocks the interaction between PD-1 and its ligands PD-L1/PD-L2, thereby restoring T-cell function and enhancing antitumor immunity[1][2][4]. This combination has been investigated primarily for the treatment of advanced or metastatic esophageal squamous cell carcinoma (ESCC), gastric cancer, or gastroesophageal junction adenocarcinoma as first-line therapy in patients whose tumors express PD-L1[6][8][9].
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 etoposide + nedaplatin + tislelizumab.