drugset / Trial / NCT00140075

Adjuvant Epirubicin/Cytoxan Followed By A Taxane VS. Epirubicin/Taxane As Treatment For Node-Positive Breast Cancer

NCT00140075

Phase 3 Completed 606 enrolled Pfizer
RandomizedParallel-groupOpen-labelTreatment

Summary

The purpose of this study is to compare two combinations of drugs, epirubicin given with a taxane (ET) or epirubicin given with cyclophosphamide (cytoxan) and followed by a taxane to see if one of the combinations is better at preventing or delaying the time for breast cancer recurrence and death after 3 years. The study will also evaluate the side effects of both treatment combinations.

Timeline

Start
2000-11
Primary completion
2006-08
Completion
2006-08

Drugs

EvaluationDrugModalityDoseRoute
Subject Cyclophosphamide Other / unclassified 600 mg/m2
Subject Docetaxel Small molecule 75 mg/m2
Subject Epirubicin Small molecule 75 mg/m2
Subject Epirubicin Small molecule 90 mg/m2
Subject Paclitaxel Small molecule 175 mg/m2

Indications