drugset / Trial / NCT00294385

Study Comparing Concomitant Docetaxel + Gemcitabine to Sequential Therapy of Docetaxel Followed by Gemcitabine

NCT00294385 ↗

Phase 3 Completed 430 enrolled Central European Cooperative Oncology Group
RandomizedParallel-groupOpen-labelTreatment

Summary

The purpose of this study is to compare the Time To Disease Progression (TTDP) between those patients with unresectable, locally recurrent or metastatic breast cancer who are treated with concomitant Docetaxel plus Gemcitabine to those patients treated with sequential therapy of Docetaxel followed by Gemcitabine.

Timeline

Start
2002-06
Primary completion
—
Completion
2005-10

Drugs

EvaluationDrugModalityDoseRoute
Comparator Docetaxel Small molecule 75 mg/m2 —
Comparator Docetaxel Small molecule 100 mg/m2 —
Comparator Gemcitabine Small molecule 1000 mg/m2 Intravenous
Comparator Gemcitabine Small molecule 1250 mg/m2 Intravenous

Indications