Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Genomic-driven chemotherapy refers to a personalized neoadjuvant treatment strategy for patients with HER2-negative breast cancer, evaluated in the Phase 3 NCT01503970 trial. Developed by Gustave Roussy, this regimen assigns specific chemotherapy agents based on tumor genomic markers: the DLD30 (a 30-gene signature predicting docetaxel sensitivity) and TOP2A (Topoisomerase II alpha) expression. Patients with a high DLD30 score receive weekly paclitaxel followed by FEC (fluorouracil, epirubicin, and cyclophosphamide). Patients with high TOP2A expression receive the standard sequence of FEC followed by docetaxel. Patients with low scores for both markers are treated with a combination of docetaxel and capecitabine. This approach aims to improve pathological complete response (pCR) rates by tailoring cytotoxic therapy to the molecular profile of the individual tumor.
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 Genomic-driven chemotherapy.