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Not listed Phase 3 Interventional

Paclitaxel With or Without Carboplatin in Treating Women With Metastatic Breast Cancer

ClinicalTrials.gov ID: NCT00025688

Public ClinicalTrials.gov record NCT00025688. 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 6, 2026, 8:55 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, Phase II Trial of Weekly Taxol (Paclitaxel) Versus Weekly Taxol Plus Paraplatin (Carboplatin) as First-Line Chemotherapy in Patients Age 65 Years or Older With Metastatic Breast Cancer

Study identification

NCT ID
NCT00025688
Recruitment status
Not listed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Theradex
Industry
Enrollment
Not listed

Conditions and interventions

Conditions

Interventions

  • carboplatin Drug
  • paclitaxel 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
Dec 31, 2000
Primary completion
Not listed
Completion
Not listed
Last update posted
Jul 23, 2008

Started 2001

United States locations

U.S. sites
25
U.S. states
17
U.S. cities
25
Facility City State ZIP Site status
Highlands Oncology Group Springdale Arkansas 72764
Monterey Bay Oncology Monterey California 93940
Wilshire Oncology Medical Group, Inc. Pomona California 91767-3021
University of California Davis Cancer Center Sacramento California 95817
New Britain General Hospital New Britain Connecticut 06050
Center for Hematology and Oncology Boca Raton Florida 33486
Cancer Research Network, Inc. Hollywood Florida 33020
Mayo Clinic Jacksonville Florida 32224
MacNeal Cancer Center Berwyn Illinois 60402
Oncology Specialists, SC Park Ridge Illinois 60068
Maine Center for Cancer Medicine and Blood Disorders Scarborough Maine 04074
Maryland Hematology/Oncology Associates Baltimore Maryland 21236
St. John's Mercy Medical Center St Louis Missouri 63141
St. Barnabas Medical Center Livingston New Jersey 07039
Finger Lakes Community Cancer Center Clifton Springs New York 14432
Clinical Hematology & Oncology Service, Inc. Akron Ohio 44302
Scranton Hematology-Oncology Scranton Pennsylvania 18510
East Tennessee Oncology/Hematology, P.C. Knoxville Tennessee 37920
West Clinic Memphis Tennessee 38120
Texas Cancer Care Fort Worth Texas 76104
Oncology Consultants Houston Texas 77024
Scott and White Clinic Temple Texas 76508
Northern Virginia Oncology Group, P.C. Fairfax Virginia 22031
Seattle Cancer Care Alliance Seattle Washington 98109
Dean Medical Center Madison Wisconsin 53715

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 NCT00025688, 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 Jul 23, 2008 · Synced May 6, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00025688 live on ClinicalTrials.gov.

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