drugset / Trial / NCT00417209

Larotaxel Compared To Continuous Administration of 5-FU in Advanced Pancreatic Cancer Patients Previously Treated With A Gemcitabine-Containing Regimen

NCT00417209 ↗

Phase 3 Completed 408 enrolled Sanofi
RandomizedParallel-groupOpen-labelTreatment

Summary

The purpose of this study is to compare the efficacy and the safety Larotaxel administered as single agent every 3 weeks to continuous administration of 5-FU every 3 weeks, in patients with advanced pancreatic cancer (non operable in a curative intent, locally recurrent or metastatic) previously treated with gemcitabine based therapy.

Timeline

Start
2006-12
Primary completion
2009-07
Completion
2009-11

Drugs

EvaluationDrugModalityDoseRoute
Comparator Capecitabine Small molecule — Oral
Comparator fluorouracil Small molecule — Intravenous
Subject larotaxel Small molecule — Intravenous

Indications