drugset / Trial / NCT00320749

Capecitabine, Docetaxel and Gemcitabine in Patients With Advanced Pancreas Cancer

NCT00320749 ↗

NaSingle-groupOpen-labelTreatment

Summary

The primary purpose of this study is to define the maximum tolerated dose of combination docetaxel, gemcitabine, and capecitabine in patients with pancreatic cancer. Adverse effects will be measured in study participants. In addition, researchers will assess data about preliminary efficacy in patients with this treatment approach.

Timeline

Start
2005-12
Primary completion
2008-10
Completion
2011-01

Drugs

EvaluationDrugModalityDoseRoute
Subject Capecitabine Small molecule 500 mg/m2 Intravenous
Subject Capecitabine Small molecule 650 mg/m2 Intravenous
Subject Docetaxel Small molecule 30 mg/m2 Intravenous
Subject Docetaxel Small molecule 36 mg/m2 Intravenous
Subject Gemcitabine Small molecule 750 mg/m2 Intravenous