Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
The combination of cisplatin, epirubicin, and vinorelbine—often referred to as the PEV regimen—is a multi-agent chemotherapy protocol primarily investigated for use in breast cancer. Each component has a distinct mechanism of action: - Cisplatin is a platinum-based chemotherapeutic that forms DNA crosslinks, leading to apoptosis. - Epirubicin is an anthracycline that intercalates into DNA and inhibits topoisomerase II, disrupting DNA replication and repair. - Vinorelbine is a vinca alkaloid that inhibits microtubule assembly during mitosis. This combination has been studied as primary (neoadjuvant) chemotherapy for locally advanced breast cancer (T2-3 N0-2), showing high rates of tumor reduction and feasibility even in large tumors. The regimen demonstrated good tolerability with manageable hematologic toxicity and no significant cardiac toxicity reported[1][2]. It is not associated with a unique brand name but may be referenced by its acronym "PEV" in clinical literature.
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 cisplatin + epirubicin + vinorelbine.