Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
A combination chemotherapy regimen consisting of cisplatin, gemcitabine, and lonafarnib. This combination was studied in a phase I clinical trial for patients with advanced solid malignancies. The maximum tolerated dose (MTD) was established as lonafarnib 75 mg BID, gemcitabine 750 mg/m² on days 1, 8, 15, and cisplatin 75 mg/m² on day 1, administered on a 28-day schedule. Despite some observed efficacy, the combination showed substantial toxicity, and there were questions about lonafarnib's contribution to the anti-tumor activity when combined with gemcitabine and cisplatin.
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 cisplatin + gemcitabine + lonafarnib.