Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Erlotinib + neoadjuvant chemotherapy is an investigational combination regimen evaluated for the treatment of triple-negative breast cancer (TNBC). Erlotinib is a small molecule tyrosine kinase inhibitor that specifically targets the epidermal growth factor receptor (EGFR), which is frequently overexpressed in TNBC and associated with poor clinical outcomes. In this regimen, erlotinib is administered alongside standard neoadjuvant chemotherapy (typically 4-6 cycles) prior to surgical intervention, followed by a maintenance phase of erlotinib for 12 months. The rationale behind this combination is to exploit the EGFR signaling pathway dependency in TNBC cells to enhance the pathological complete response (pCR) rate. This specific clinical strategy was notably investigated in a Phase II trial led by the University of Kansas Medical Center.
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 erlotinib + neoadjuvant chemotherapy.