Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Icotinib + chemotherapy is a combination regimen developed by Betta Pharmaceuticals for the treatment of non-small cell lung cancer (NSCLC). The regimen consists of icotinib, an orally active, highly selective epidermal growth factor receptor (EGFR) tyrosine kinase inhibitor (TKI), administered alongside standard chemotherapy agents such as docetaxel or pemetrexed. This combination is primarily investigated for patients with locally advanced or metastatic NSCLC who have developed resistance to prior icotinib monotherapy (icotinib-refractory disease). Icotinib works by competitively binding to the adenosine triphosphate (ATP) binding site of the EGFR tyrosine kinase, thereby blocking downstream signaling pathways involved in cell proliferation and survival. The chemotherapy components exert cytotoxic effects through microtubule stabilization (docetaxel) or inhibition of folate-dependent enzymes required for DNA synthesis (pemetrexed).
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 icotinib + chemotherapy (Betta Pharmaceuticals).