drugset / Trial / NCT00099437

Comparison of Fulvestrant (FASLODEX™) 250 mg and 500 mg in Postmenopausal Women With Oestrogen Receptor Positive Advanced Breast Cancer Progressing or Relapsing After Previous Endocrine Therapy.

NCT00099437

Phase 3 Active not recruiting 736 enrolled AstraZeneca
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The purpose of this study is to evaluate the efficacy of a new dose of 500 mg Fulvestrant with the standard dose of 250 mg in postmenopausal women with oestrogen receptor positive advanced breast cancer who have failed on a previous endocrine treatment.

Timeline

Start
2005-02-13
Primary completion
2009-02-27
Completion
2026-12-31

Drugs

EvaluationDrugModalityDoseRoute
Subject Fulvestrant Small molecule 250 mg Intramuscular
Subject Fulvestrant Small molecule 500 mg Intramuscular

Indications