drugset / Trial / NCT00721747

Taxotere®, Followed by Myocet® and Cyclophosphamide First Line Treatment in HER2 Neg Breast Cancer

NCT00721747 ↗

NaSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to determine how many pathological complete responses are achieved in patients treated with taxotere® (T) followed by Myocet® (M)and Cyclophosphamide (MC) first line treatment in HER2 negative brest cancer patients.

Timeline

Start
2008-01
Primary completion
2011-01
Completion
2015-01

Drugs

EvaluationDrugModalityDoseRoute
Subject Cyclophosphamide Other / unclassified 600 mg/m2 Intravenous
Subject Docetaxel Small molecule 100 mg/m2 Intravenous
Subject Liposomal doxorubicine Unknown 60 mg/m2 Intravenous

Indications