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Completed Phase 3 Interventional Results available

Safety and Efficacy Comparison of Docetaxel and Ixabepilone in Non Metastatic Poor Prognosis Breast Cancer

ClinicalTrials.gov ID: NCT00630032

Public ClinicalTrials.gov record NCT00630032. 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 Jun 25, 2026, 8:09 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

Randomized, Open Label, Multicentric Phase III Evaluating the Benefit of a Sequential Regimen Associating FEC 100 and Ixabepilone in Adjuvant Treatment of Non Metastatic, Poor Prognosis Breast Cancer Defined as Triple-negative Tumor [HER2 Negative - ER Negative - PR Negative] or [HER2 Negative and PR Negative] Tumor; in Node Positive or Node Negative Patients.

Study identification

NCT ID
NCT00630032
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
UNICANCER
Other
Enrollment
762 participants

Conditions and interventions

Conditions

Interventions

  • cyclophosphamide Drug
  • Docetaxel Drug
  • epirubicin hydrochloride Drug
  • fluorouracil Drug
  • ixabepilone Drug

Drug

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
Aug 31, 2007
Primary completion
May 31, 2017
Completion
Sep 2, 2020
Last update posted
Feb 20, 2024

2007 – 2020

United States locations

U.S. sites
17
U.S. states
13
U.S. cities
17
Facility City State ZIP Site status
Mayo Clinic Scottsdale Scottsdale Arizona 85259-5499
CCOP - Colorado Cancer Research Program Denver Colorado 80224
Mayo Clinic - Jacksonville Jacksonville Florida 32224
CCOP - Northern Indiana CR Consortium South Bend Indiana 46601
CCOP - Cedar Rapids Oncology Project Cedar Rapids Iowa 52403-1206
Siouxland Hematology-Oncology Associates, LLP Sioux City Iowa 51101-1733
Cancer Center of Kansas, PA - Wichita Wichita Kansas 67214-3728
Duluth Clinic Cancer Center - Duluth Duluth Minnesota 55805-1983
Mayo Clinic Cancer Center Rochester Minnesota 55905
CCOP - Metro-Minnesota Saint Louis Park Minnesota 55416
Southeast Nebraska Hematology Oncology Consultants at Southeast Nebraska Cancer Center Lincoln Nebraska 68510
CCOP - Missouri Valley Cancer Consortium Omaha Nebraska 68106
Roger Maris Cancer Center at MeritCare Hospital Fargo North Dakota 58122
CCOP - Dayton Dayton Ohio 45429
CCOP - Geisinger Clinic and Medical Center Danville Pennsylvania 17822-2001
Oncology Associates at Rapid City Regional Hospital Rapid City South Dakota 57701
Green Bay Oncology, Limited at St. Mary's Hospital Green Bay Wisconsin 54303

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 69 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00630032, 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 20, 2024 · Synced Jun 25, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00630032 live on ClinicalTrials.gov.

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