Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Tislelizumab + etoposide + cisplatin is a multi-agent regimen primarily investigated as first-line therapy for **extensive-stage small cell lung cancer (ES-SCLC)**. The regimen combines: - **Tislelizumab**, a humanized IgG4 monoclonal antibody targeting the **Programmed Cell Death Protein 1 (PD-1)**, thereby blocking an immune checkpoint and promoting T-cell mediated anticancer activity. - **Etoposide**, a small molecule chemotherapeutic that inhibits **topoisomerase II**, leading to DNA strand breaks and apoptosis in rapidly dividing tumor cells. - **Cisplatin**, a platinum-based chemotherapeutic which causes DNA crosslinks and subsequent apoptosis. Together, this combination delivers a **dual approach**: immune checkpoint blockade and cytotoxic chemotherapy. It is used intravenously, typically in cycles every three weeks. Tislelizumab + etoposide + cisplatin has shown prolonged overall survival and improved response rates in ES-SCLC when compared to chemotherapy alone, leading to regulatory submissions for first-line use in this indication[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 tislelizumab + etoposide + cisplatin.