Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
The GEMCIRAV regimen is a concurrent chemoradiotherapy protocol developed and evaluated by the Institut du Cancer de Montpellier - Val d'Aurelle for the treatment of muscle-invasive bladder cancer (MIBC). This combination therapy consists of gemcitabine hydrochloride, a pyrimidine antimetabolite that inhibits DNA synthesis, and cisplatin, a platinum-based chemotherapy agent that induces DNA cross-linking, administered alongside daily radiotherapy. The regimen is designed as a bladder-preservation strategy for patients with Stage II or III transitional cell carcinoma of the bladder. In the Phase I/II GEMCIRAV clinical trial (NCT00556621), gemcitabine was administered intravenously twice weekly for five weeks, while cisplatin was given as a continuous infusion during the first and fourth weeks of the radiotherapy course. Long-term results from the study demonstrated significant efficacy, with a 5-year overall survival rate of 62%.
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 + radiotherapy.