Larotaxel + Cisplatin Versus Gemcitabine + Cisplatin in First Line Treatment of Locally Advanced/Metastatic Urothelial Tract or Bladder Cancer (CILAB)
Status and phase
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Treatments
Details and patient eligibility
About
This is a randomized, open-label, multi-center study comparing the efficacy and safety of XRP9881 plus cisplatin to gemcitabine plus cisplatin in the first line treatment of locally advanced/metastatic urothelial tract or bladder cancer. The primary objective is to compare overall survival. Secondary objectives include comparisons of progression free survival, objective response rate, time to definitive deterioration of performance status, duration of response, time to definitive weight loss, and assessments of overall safety, and pharmacokinetics. Patients are treated until disease progression, death, or unacceptable toxicity and are followed-up until death or the end of the study whichever comes first.
Enrollment
Sex
Ages
Volunteers
Inclusion criteria
- Patients with histology/cytology confirmed Transitional Cell Carcinoma (TCC) with locally advanced (T4b) or metastatic urothelial tract or bladder cancer
- ECOG Performance Status 0 or 1
- No prior palliative chemotherapy
Exclusion criteria
- (Neo)Adjuvant chemotherapy if < 6 months between end of (neo)adjuvant chemotherapy and relapse
- Less than 6 weeks elapsed from prior radiotherapy and less than 3 weeks from surgery to time of randomization
- Prior cisplatin as (neo)adjuvant chemotherapy with cumulative dose > 300 mg/m²
The above information is not intended to contain all considerations relevant to a patient's potential participation in a clinical trial.
Trial design
Primary purpose
Allocation
Interventional model
Masking
337 participants in 2 patient groups
Trial contacts and locations
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Data sourced from clinicaltrials.gov
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