drugset / Trial / NCT00320749
Capecitabine, Docetaxel and Gemcitabine in Patients With Advanced Pancreas Cancer
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| 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 |