drugset / Trial / NCT00065325

The Evaluation of the Efficacy and Tolerability of FASLODEX (Fulvestrant) and AROMASIN (Exemestane) in Hormone Receptor Positive Postmenopausal Women With Advanced Breast Cancer

NCT00065325

Phase 3 Completed 694 enrolled AstraZeneca
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The purpose of this study is to compare the efficacy of Faslodex (fulvestrant) to Aromasin (exemestane) in hormone receptor positive postmenopausal women with advanced breast cancer. Patients will be treated until disease progression or until the investigator has determined that treatment is not in the best interest of the patient, whichever occurs first.

Timeline

Start
2003-08
Primary completion
2006-06
Completion
2014-09

Drugs

EvaluationDrugModalityDoseRoute
Comparator Exemestane Small molecule Oral
Subject Fulvestrant Small molecule Intramuscular

Indications