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Completed Phase 3 Interventional

Adjuvant Epirubicin/Cytoxan Followed By A Taxane VS. Epirubicin/Taxane As Treatment For Node-Positive Breast Cancer

ClinicalTrials.gov ID: NCT00140075

Public ClinicalTrials.gov record NCT00140075. 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 Oct 18, 2026, 11:03 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

Phase III, Randomized Study Of Epirubicin/Cyclophosphamide Followed By Taxane (Sequential Chemotherapy) Versus Epirubicin/Taxane (Concurrent Chemotherapy) As Adjuvant Treatment For Operable, Node-Positive Breast Cancer

Brief summary

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

The purpose of this study is to compare two combinations of drugs, epirubicin given with a taxane (ET) or epirubicin given with cyclophosphamide (cytoxan) and followed by a taxane to see if one of the combinations is better at preventing or delaying the time for breast cancer recurrence and death after 3 years. The study will also evaluate the side effects of both treatment combinations.

Study identification

NCT ID
NCT00140075
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Pfizer
Industry
Enrollment
606 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 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
Nov 2000 (Type not available)
Primary completion
Aug 2006 (Actual)
Completion
Aug 2006 (Actual)
Last update posted
May 26, 2011

2000 – 2006

United States locations

U.S. sites
54
U.S. states
23
U.S. cities
52
Facility City State ZIP Site status
Pfizer Investigational Site Mobile Alabama 36608 —
Pfizer Investigational Site Tucson Arizona 85712 —
Pfizer Investigational Site Bakersfield California 93309 —
Pfizer Investigational Site Berkeley California 94704 —
Pfizer Investigational Site Fountain Valley California 92708 —
Pfizer Investigational Site Fountian Valley California 92708 —
Pfizer Investigational Site Gilroy California 95020 —
Pfizer Investigational Site Poway California 92064 —
Pfizer Investigational Site Soquel California 95073 —
Pfizer Investigational Site Colorado Springs Colorado 80907 —
Pfizer Investigational Site Jacksonville Florida 32224 —
Pfizer Investigational Site Jacksonville Florida — —
Pfizer Investigational Site Kissimmee Florida 34741 —
Pfizer Investigational Site Lake Worth Florida 33461 —
Pfizer Investigational Site Lecanto Florida 34461 —
Pfizer Investigational Site Miami Florida 33176 —
Pfizer Investigational Site Miami Shores Florida 33138 —
Pfizer Investigational Site Port Saint Lucie Florida 34952 —
Pfizer Investigational Site Tampa Florida 33607 —
Pfizer Investigational Site Atlanta Georgia 30309 —
Pfizer Investigational Site Macon Georgia 31201 —
Pfizer Investigational Site Belleville Illinois 62226 —
Pfizer Investigational Site Skokie Illinois 60076 —
Pfizer Investigational Site Baton Rouge Louisiana 70809 —
Pfizer Investigational Site New Orleans Louisiana — —
Pfizer Investigational Site Baltimore Maryland 21236 —
Pfizer Investigational Site Baltimore Maryland 21237 —
Pfizer Investigational Site Boston Massachusetts 02120 —
Pfizer Investigational Site Harper Woods Michigan — —
Pfizer Investigational Site Hattiesburg Mississippi 39401 —
Pfizer Investigational Site Jackson Mississippi 39202 —
Pfizer Investigational Site Mount Holly New Jersey 08060 —
Pfizer Investigational Site Willingboro New Jersey 08046 —
Pfizer Investigational Site Albuquerque New Mexico 87102 —
Pfizer Investigational Site Brooklyn New York 11235 —
Pfizer Investigational Site Great Neck New York 11021' —
Pfizer Investigational Site Staten Island New York 10310 —
Pfizer Investigational Site Burlington North Carolina 27216 —
Pfizer Investigational Site Greenville North Carolina 27854 —
Pfizer Investigational Site Raleigh North Carolina 27607 —
Pfizer Investigational Site Lawton Oklahoma 73505 —
Pfizer Investigational Site Oklahoma City Oklahoma 73104 —
Pfizer Investigational Site Lemoyne Pennsylvania 17043 —
Pfizer Investigational Site Philadelphia Pennsylvania 19106 —
Pfizer Investigational Site Charleston South Carolina — —
Pfizer Investigational Site Columbia South Carolina 29201 —
Pfizer Investigational Site Germantown Tennessee 38138 —
Pfizer Investigational Site Knoxville Tennessee 37923 —
Pfizer Investigational Site Corpus Christi Texas 78412 —
Pfizer Investigational Site Tyler Texas 11937 —
Pfizer Investigational Site Arlington Virginia 22205 —
Pfizer Investigational Site Portsmouth Virginia 23704 —
Pfizer Investigational Site Richmond Virginia 23226 —
Pfizer Investigational Site Milwaukee Wisconsin 53209 —

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 NCT00140075, 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 May 26, 2011 · Synced Oct 18, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00140075 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →