drugset / Trial / NCT00313170

A Clinical Trial to Compare Efficacy and Tolerability of Fulvestrant 250mg, 250mg Plus 250mg Loading Regimen and 500mg

NCT00313170 ↗

Phase 2 Completed 144 enrolled AstraZeneca
RandomizedParallel-groupQuadruple-blindTreatment

Summary

This study will assess the relationship between fulvestrant dose and efficacy in postmenopausal women with oestrogen receptor positive advanced breast cancer.

Timeline

Start
2006-05-30
Primary completion
2008-06-13
Completion
2019-03-13

Outcome

Missed primary endpoint

paper While there appeared to be a trend toward improved efficacy with HD and LD versus AD, no significant differences could be shown. PMID 20632084 ↗

Drugs

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