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Completed Phase 3 Interventional Results available

Novel Epothilone Plus Capecitabine Versus Capecitabine Alone in Patients With Advanced Breast Cancer

ClinicalTrials.gov ID: NCT00080301

Public ClinicalTrials.gov record NCT00080301. 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 13, 2026, 10:25 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 Phase III Trial of Novel Epothilone BMS-247550 Plus Capecitabine Versus Capecitabine Alone in Patients With Advanced Breast Cancer Previously Treated With or Resistant to an Anthracycline and Who Are Taxane Resistant

Study identification

NCT ID
NCT00080301
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
R-Pharm
Industry
Enrollment
752 participants

Conditions and interventions

Interventions

  • Capecitabine Drug
  • Ixabepilone + Capecitabine 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, 2003
Primary completion
Oct 31, 2006
Completion
Feb 29, 2008
Last update posted
Nov 1, 2020

2003 – 2008

United States locations

U.S. sites
32
U.S. states
24
U.S. cities
32
Facility City State ZIP Site status
Local Institution Little Rock Arkansas
Local Institution San Francisco California
Local Institution Vallejo California
Local Institution Denver Colorado
Local Institution Hartford Connecticut
Local Institution Washington D.C. District of Columbia
Local Institution Orlando Florida
Local Institution Baltimore Maryland
Local Institution Burlington Massachusetts
Local Institution Jackson Mississippi
Local Institution Columbia Missouri
Local Institution Kansas City Missouri
Local Institution St Louis Missouri
Local Institution Omaha Nebraska
Local Institution Livingston New Jersey
Local Institution New Brunswick New Jersey
Local Institution Albuquerque New Mexico
Local Institution New York New York
Local Institution Columbus Ohio
Local Institution Oklahoma City Oklahoma
Local Institution Tulsa Oklahoma
Local Institution Pittsburgh Pennsylvania
Local Institution Columbia South Carolina
Local Institution Greenville South Carolina
Local Institution Knoxville Tennessee
Local Institution Nashville Tennessee
Local Institution Austin Texas
Local Institution Houston Texas
Local Institution Ogden Utah
Local Institution Burlington Vermont
Local Institution Tacoma Washington
Local Institution Morgantown West 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 95 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00080301, 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 Nov 1, 2020 · Synced May 13, 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 NCT00080301 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →