Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Epirubicin + cisplatin + capecitabine (ECX) is a combination chemotherapy regimen used primarily for the treatment of advanced or operable cancers of the stomach (gastric cancer), esophagus (oesophageal cancer), and gastroesophageal junction. - **Epirubicin** is an anthracycline antibiotic that intercalates into DNA and inhibits topoisomerase II, leading to inhibition of DNA replication and transcription. - **Cisplatin** is a platinum-based compound that forms DNA crosslinks, causing apoptosis by inhibiting DNA synthesis and function[6]. - **Capecitabine** is an oral prodrug converted to 5-fluorouracil (5-FU) in the body; it inhibits thymidylate synthase, disrupting DNA synthesis in rapidly dividing cells. The combination works synergistically to destroy rapidly dividing cancer cells through multiple mechanisms affecting DNA structure and function. The regimen typically involves intravenous administration of epirubicin and cisplatin with oral capecitabine taken daily for 21 days per cycle[1][2][4][8].
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 Epirubicin + cisplatin + capecitabine.