drugset / Trial / NCT00782041

Patients Who Have Failed First Line Treatment for Locally Advanced and/or Metastatic Cervical Cancer

NCT00782041 ↗

Phase 2 Terminated 11 enrolled Sanofi
Non-randomizedSingle-groupOpen-labelTreatment

Summary

Primary: * To assess the overall response rate of oxaliplatin in patients with bidimensionally measurable disease at baseline. Secondary: * To assess the safety and tolerability of oxaliplatin * To assess time to progression and overall survival.

Timeline

Start
2003-01
Primary completion
2003-08
Completion
—

Outcome

Outcome not reported

Stopped: “protocol violation”

Drugs

EvaluationDrugModalityDoseRoute
Subject Oxaliplatin Small molecule 85 mg/m2 —
Background Leucovorin Small molecule 20 mg/m2 —
Background fluorouracil Small molecule 2000 mg/m2 —

Indications