Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
This is an investigational combination therapy consisting of the taxane docetaxel, the platinum-based agent cisplatin, and the tyrosine kinase inhibitor imatinib mesylate (STI571). Developed and evaluated by Duke University, this regimen is intended for the treatment of advanced or recurrent non-small cell lung cancer (NSCLC). The rationale behind adding imatinib to standard chemotherapy is its ability to inhibit platelet-derived growth factor receptor beta (PDGFR-β) signaling in the tumor stroma. This inhibition reduces tumor interstitial fluid pressure, which is often elevated in solid tumors and acts as a barrier to the efficient delivery of chemotherapy. By lowering this pressure, imatinib is hypothesized to enhance the uptake and efficacy of docetaxel and cisplatin. The combination was evaluated in a Phase 1/2 clinical trial specifically for patients whose tumors expressed phosphorylated PDGFR-β.
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 docetaxel + cisplatin + imatinib.