drugset / Trial / NCT00118755

A Study of Two Different Schedules of Xeloda (Capecitabine) as First Line Therapy in Patients With Metastatic Colorectal Cancer

NCT00118755 ↗

Phase 2 Completed 435 enrolled Hoffmann-La Roche
RandomizedParallel-groupOpen-labelTreatment

Summary

This 2-arm study evaluated the efficacy and safety of 2 different treatment schedules of oral Xeloda with intravenous (IV) Eloxatin (oxaliplatin) and IV bevacizumab (Avastin) as a first-line treatment in patients with locally advanced or metastatic colorectal cancer. Patients were randomized to receive either: 1) Xeloda 850 mg/m\^2 orally twice a day (po bid) on Days 1-14, oxaliplatin 130 mg/m\^2 IV on Day 1, and Avastin 7.5 mg/kg IV on Day 1 of each 3-week cycle; or 2) Xeloda 1500 mg/m\^2 po bid on Days 1-7, oxaliplatin 85 mg/m\^2 IV on Day 1 and Avastin 5 mg/kg IV on Day 1 of each 2-week cycle. The anticipated time on study treatment was 1-2 years, and the target sample size was 100-500 individuals.

Timeline

Start
2005-07
Primary completion
2009-04
Completion
—

Drugs

EvaluationDrugModalityDoseRoute
Comparator Bevacizumab Monoclonal antibody 5 mg/kg Intravenous
Comparator Bevacizumab Monoclonal antibody 7.5 mg/kg Intravenous
Comparator Capecitabine Small molecule 850 mg/m2 Oral
Comparator Capecitabine Small molecule 1500 mg/m2 Oral
Comparator Oxaliplatin Small molecule 85 mg/m2 Intravenous
Comparator Oxaliplatin Small molecule 130 mg/m2 Intravenous

Indications