A Phase 1/2 trial for the use of Intravesical Cabazitaxel, Gemcitabine, and Cisplatin (CGC) in the treatment of BCG-Refractory Non-muscle invasive Urothelial Carcinoma of the Bladder
Study of Intravesical Cabazitaxel, Gemcitabine and Cisplatin (CGC) in the Treatment of Urothelial Carcinoma (Bladder Cancer)
Sponsor: Sanofi-Aventis Pharmaceutials
Enrolling: Male and Female Patients
IRB Number: AAAM8506
U.S. Govt. ID: NCT02202772
Contact: Research Nurse Navigator: 212-342-5162 / cancerclinicaltrials@cumc.columbia.edu
Additional Study Information: We are doing this research to find out the safety, toxicity, and efficacy of intravesical Cabazitaxel, Gemcitabine, and Cisplatin (CGC) in the treatment of non-muscle-invasive urothelial carcinoma of the bladder that has recurred despite BCG use. The purpose of finding the maximum tolerable dose is important for future use of the drug, so as to provide the safest CGC treatment to patients in the future if the treatment is found to be safe, tolerable, and effective. You are being asked to take part in this study because you have bladder cancer, and you may have already failed other treatments or are refusing other treatments.
This study is closed
Investigator
Joel DeCastro, MD, MPH
Do You Qualify?
Are you 18 years of age or older? Yes No
Have you been diagnosed with bladder cancer? Yes No
Are you a pregnant or lactating? Yes No
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For more information, please contact:
Research Nurse Navigator
cancerclinicaltrials@cumc.columbia.edu
212-342-5162