Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Gemcitabine + irinotecan is a combination chemotherapy regimen consisting of two cytotoxic small molecule drugs—gemcitabine and irinotecan. Gemcitabine is a nucleoside analog that inhibits DNA synthesis by incorporating into DNA during replication, leading to cell cycle arrest and apoptosis. Irinotecan is a topoisomerase I inhibitor that prevents the religation of single-strand breaks in DNA during replication, resulting in double-strand breaks and cell death. This combination has demonstrated synergistic antitumor activity in preclinical studies and has been evaluated clinically for the treatment of various solid tumors, particularly pancreatic cancer. Phase I/II trials have shown activity with manageable toxicity profiles in advanced or metastatic pancreatic cancer as well as platinum-resistant/refractory ovarian cancer[1][2]. The regimen remains investigational for most indications.
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 gemcitabine + irinotecan.