CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 10 enrolled
Drug / intervention
Fulvestrantdrug
Likely dose
Fulvestrant 250 mgfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT00476645
NCT00476645Phase 2Completed

Fulvestrant in Hormone-refractory Prostate Cancer

Stanford University·interventional·Posted May 22, 2007·Updated Aug 5, 2014

In Brief

A Phase 2 clinical trial evaluating Fulvestrant for Prostatic Neoplasms and Prostate Cancer. Completed, enrolled 10 participants across 1 site.

Detailed Summary

The purpose of this study is to determine if treatment with fulvestrant leads to a slowing of tumor progression in patients who have developed androgen-independent (AIPC) or hormone-refractory prostate cancer (HRPC) and who have a rising serum prostate specific antigen (PSA).

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesUnited States
CollaboratorsAstraZeneca

Timeline

Phase 2CompletedFinished
200720082009201020112012201320142015201620172018201920202021202220232024202520262027
First PostedMay 22, 2007
Enrollment StartSep 1, 2006
Primary CompletionSep 1, 2009
Study CompletionDec 1, 2009
TodayJul 2, 2026
Enrollment to primary: 3 yearsPosted 19.1 years ago

Interventions

Fulvestrantdrug

Fulvestrant 250 mg IM on Days 1 and 14 in the first month, thereafter 250 mg monthly