drugset / Trial / NCT01599013

JAVLOR Association Study in CDDP-unfit Patients With Advanced Transitional Cell Carcinoma: Gemcitabine Versus Carboplatin

NCT01599013

Phase 2 Completed 69 enrolled Pierre Fabre Laboratories
RandomizedParallel-groupOpen-labelTreatment

Summary

This study is assessing the combination of well known cytotoxics with a novel anti-cancer agent that could be administered as monotherapy without renal toxicity in patients with renal impairment presenting with advanced or metastatic urothelial carcinoma previously treated with a platinum-based regimen. The intent of this study is to clarify the benefit/risk ratio of the two most promising associations of cytotoxics including the novel therapeutic agent, vinflunine: vinflunine-gemcitabine and vinflunine-carboplatin.

Timeline

Start
2011-02
Primary completion
2013-10
Completion
2014-04

Drugs

EvaluationDrugModalityDoseRoute
Subject Carboplatin Small molecule 4.5 unknown Intravenous
Subject Gemcitabine Small molecule 750 mg/m2 Intravenous
Subject Gemcitabine Small molecule 1000 mg/m2 Intravenous
Background Vinflunine Small molecule 250 mg/m2 Intravenous
Background Vinflunine Small molecule 280 mg/m2 Intravenous