Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
gemcitabine + cisplatin + ipilimumab is an investigational combination therapy regimen evaluated as a first-line treatment for patients with metastatic urothelial carcinoma. This regimen consists of the standard-of-care chemotherapy doublet, gemcitabine and cisplatin, supplemented with the immune checkpoint inhibitor ipilimumab. Ipilimumab is a recombinant human monoclonal antibody that binds to the cytotoxic T-lymphocyte-associated protein 4 (CTLA-4), an immune checkpoint molecule that downregulates T-cell activation. By blocking CTLA-4, ipilimumab promotes an active immune response against tumor cells. Gemcitabine, a nucleoside analog, and cisplatin, a platinum-based alkylating agent, provide direct cytotoxic effects by interfering with DNA synthesis and repair. The combination was evaluated in the Phase II Hoosier Cancer Research Network GU10-148 trial; while it showed a high objective response rate, it did not meet the primary endpoint of improved 1-year overall survival.
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 + cisplatin + ipilimumab.