ClinicalTrials.gov record
Completed Phase 3 Interventional

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

ClinicalTrials.gov ID: NCT00065325

Public ClinicalTrials.gov record NCT00065325. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced May 17, 2026, 4:52 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Randomized, Double Blind, Multicenter Study to Compare the Efficacy and Tolerability of Fulvestrant (FASLODEX™) vs. Exemestane (AROMASIN™) in Postmenopausal Women With Hormone Receptor Positive Advanced Breast Cancer With Disease Progression After Prior Non-Steroidal Aromatase Inhibitor (AI) Therapy

Study identification

NCT ID
NCT00065325
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
AstraZeneca
Industry
Enrollment
694 participants

Conditions and interventions

Interventions

  • Exemestane Drug
  • Fulvestrant Drug

Drug

Eligibility (public fields only)

Age range
32 Years to 91 Years
Sex
Female
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jul 31, 2003
Primary completion
May 31, 2006
Completion
Aug 31, 2014
Last update posted
Feb 23, 2015

2003 – 2014

United States locations

U.S. sites
51
U.S. states
24
U.S. cities
51
Facility City State ZIP Site status
Research Site Birmingham Alabama
Research Site Arcadia California
Research Site Fountain Valley California
Research Site Laverne California
Research Site Long Beach California
Research Site Santa Rosa California
Research Site Torrington Connecticut
Research Site Washington D.C. District of Columbia
Research Site Boca Raton Florida
Research Site Gainesville Florida
Research Site Jacksonville Florida
Research Site Miami Florida
Research Site New Port Richey Florida
Research Site Pensacola Florida
Research Site Athens Georgia
Research Site Chicago Illinois
Research Site Harvey Illinois
Research Site Springfield Illinois
Research Site Iowa City Iowa
Research Site Overland Park Kansas
Research Site Baton Rouge Louisiana
Research Site Metairie Louisiana
Research Site New Orleans Louisiana
Research Site Shreveport Louisiana
Research Site Bangor Maine
Research Site Baltimore Maryland
Research Site Frederick Maryland
Research Site Kalamazoo Michigan
Research Site Royal Oak Michigan
Research Site Saint Joseph Michigan
Research Site Hooksett New Hampshire
Research Site Livingston New Jersey
Research Site Voorhees Township New Jersey
Research Site Albuquerque New Mexico
Research Site Charlotte North Carolina
Research Site Durham North Carolina
Research Site Canton Ohio
Research Site Hershey Pennsylvania
Research Site Lancaster Pennsylvania
Research Site Langhorne Pennsylvania
Research Site Pittsburgh Pennsylvania
Research Site Providence Rhode Island
Research Site Columbia South Carolina
Research Site Greenville South Carolina
Research Site Spartenburg South Carolina
Research Site Austin Texas
Research Site Dallas Texas
Research Site Houston Texas
Research Site San Antonio Texas
Research Site Burlington Vermont
Research Site Richmond Virginia

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 66 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00065325, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Feb 23, 2015 · Synced May 17, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00065325 live on ClinicalTrials.gov.

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