drugset / Trial / NCT00328120

Faslodex 500mg Multiple Dose Tolerability Study in BC Patients

NCT00328120

Phase 1 Completed 20 enrolled AstraZeneca
Non-randomizedSingle-groupOpen-labelTreatment

Summary

The primary objective of this study is to assess the tolerability of 500mg fulvestrant in postmenopausal women with hormone receptor positive, advanced or recurrent breast cancer

Timeline

Start
2004-04
Primary completion
2006-04
Completion
2010-06

Drugs

EvaluationDrugModalityDoseRoute
Subject Fulvestrant Small molecule 500 mg Intramuscular