Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
This refers to an investigational perioperative chemotherapy protocol developed by the **European Institute of Oncology (IEO)** for the treatment of endocrine non-responsive locally advanced breast cancer. The regimen specifically evaluates the efficacy of continuous intravenous infusion of **5-fluorouracil (5-FU)** during the surgical window and for two weeks post-operatively. 5-FU is a pyrimidine analog antimetabolite that inhibits thymidylate synthase, thereby disrupting DNA synthesis. In clinical trials, this perioperative 5-FU infusion was combined with preoperative chemotherapy regimens such as **ViFuP** (vinorelbine, cisplatin, and 5-FU) or **ECF** (epirubicin, cisplatin, and 5-FU). The protocol aims to target micrometastatic disease and reduce the risk of recurrence by maintaining cytotoxic levels of chemotherapy during and immediately following definitive surgery.
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 perioperative chemotherapy-European Institute of Oncology-breast cancer.