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Terminated Phase 3 Interventional

To Compare Treatment With Doxorubicin or Capecitabine for Metastatic Breast Cancer in Women 60 Years and Older

ClinicalTrials.gov ID: NCT00082095

Public ClinicalTrials.gov record NCT00082095. 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 Sep 9, 2026, 1:43 AM 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, Open-Label Trial Comparing Treatment With Either Pegylated Liposomal Doxorubicin or Capecitabine as First Line Chemotherapy for Metastatic Breast Cancer in Women 60 Years and Older

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The main purpose of this study is to compare treatment with either pegylated liposomal doxorubicin or capecitabine as first line chemotherapy for metastatic breast cancer in women 60 years and older.

Study identification

NCT ID
NCT00082095
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 3
Enrollment
62 participants

Conditions and interventions

Eligibility (public fields only)

Age range
60 Years and older
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
Mar 31, 2004
Primary completion
Nov 30, 2005
Completion
Nov 30, 2005
Last update posted
Oct 8, 2014

2004 – 2005

United States locations

U.S. sites
27
U.S. states
19
U.S. cities
27
Facility City State ZIP Site status
Not listed Fountain Valley California
Not listed Oxnard California
Not listed Soquel California
Not listed Boca Raton Florida
Not listed New Port Richey Florida
Not listed Plantation Florida
Not listed Atlanta Georgia
Not listed Springfield Illinois
Not listed Hazard Kentucky
Not listed Shreveport Louisiana
Not listed Scarborough Maine
Not listed Baltimore Maryland
Not listed Clinton Township Michigan
Not listed Saint Louis Park Minnesota
Not listed Lebanon New Hampshire
Not listed Voorhees Township New Jersey
Not listed Albuquerque New Mexico
Not listed Armonk New York
Not listed New City New York
Not listed Portland Oregon
Not listed Philadelphia Pennsylvania
Not listed Fort Worth Texas
Not listed Fredericksburg Texas
Not listed Burlington Vermont
Not listed Colchester Vermont
Not listed Everett Washington
Not listed Vancouver Washington

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

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00082095, 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 Oct 8, 2014 · Synced Sep 9, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00082095 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →