Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
This combination therapy comprises **envafolimab** (a subcutaneously administered monoclonal antibody targeting PD-L1), **gemcitabine** (a nucleoside analog DNA synthesis inhibitor), **cisplatin** (a platinum-based DNA crosslinking agent), and **simvastatin** (a statin that inhibits HMG-CoA reductase, primarily used for cholesterol lowering but explored for anticancer synergy). - **Envafolimab** acts as an immune checkpoint inhibitor by blocking PD-L1, thus enhancing T-cell–mediated immune responses against tumors. - **Gemcitabine** and **cisplatin** function as cytotoxic chemotherapies, disrupting DNA synthesis and repair. - **Simvastatin** is being investigated for its potential adjunctive antitumor effects. This four-drug regimen is under clinical investigation as a first-line treatment for advanced biliary tract cancers, aiming to improve antitumor efficacy through combined immunotherapy, chemotherapy, and possible statin-mediated effects[4][5][6].
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 envafolimab + gemcitabine + cisplatin + simvastatin.