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 consists of the PD-1 inhibitor toripalimab administered intravenously in conjunction with a sequential intravesical regimen of gemcitabine and mitomycin C. It is being investigated by the First Affiliated Hospital of Wenzhou Medical University for the treatment of patients with high-risk non-muscle-invasive bladder cancer (HR-NMIBC) who are unresponsive to or intolerant of Bacillus Calmette-Guérin (BCG) therapy. Toripalimab is a humanized IgG4 monoclonal antibody that blocks the interaction between the PD-1 receptor and its ligands (PD-L1 and PD-L2), thereby restoring T-cell mediated anti-tumor immunity. Gemcitabine is a nucleoside analog that inhibits DNA synthesis by acting as an antimetabolite, while mitomycin C is a cytotoxic antibiotic that functions as a DNA alkylating agent to cross-link DNA. This multi-modal approach aims to provide both systemic immune activation and localized cytotoxic eradication of tumor cells within the bladder to prevent recurrence and progression.
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 toripalimab + gemcitabine + mitomycin C.