Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
This is a combination chemotherapy regimen consisting of four distinct drugs: 1. **Docetaxel**: A taxane-based chemotherapeutic agent that inhibits cell division by disrupting microtubule function. 2. **Cisplatin**: A platinum-based chemotherapeutic agent that crosslinks DNA, preventing cell division. 3. **Capecitabine**: An oral fluoropyrimidine prodrug that converts to 5-fluorouracil in tumor tissues, inhibiting DNA synthesis. 4. **Bevacizumab**: A monoclonal antibody that inhibits vascular endothelial growth factor (VEGF), preventing angiogenesis. This combination regimen is used primarily for treating HER2-negative advanced gastric cancer, including locally advanced, recurrent, or metastatic disease. The regimen typically involves docetaxel and cisplatin administered intravenously on day 1, with capecitabine taken orally for 14 days in a 21-day cycle. Bevacizumab is added to enhance anti-angiogenic 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 docetaxel + cisplatin + capecitabine + bevacizumab.