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Completed Phase 2 Interventional

Trastuzumab Plus Docetaxel in Treating Women With Recurrent or Metastatic Breast Cancer

ClinicalTrials.gov ID: NCT00006104

Public ClinicalTrials.gov record NCT00006104. 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, 8:49 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 Multi-Institutional Phase II Pilot Trial With Weekly Docetaxel and Herceptin as First or Second Line Therapy for HER2/Neu Overexpressing Metastatic Breast Cancer

Brief summary

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

RATIONALE: Monoclonal antibodies such as trastuzumab can locate tumor cells and either kill them or deliver tumor-killing substances to them without harming normal cells. Drugs used in chemotherapy use different ways to stop tumor cells from dividing so they stop growing or die. Combining chemotherapy with monoclonal antibody therapy may kill more tumor cells. PURPOSE: Phase II trial to study the effectiveness of trastuzumab plus docetaxel in treating women who have recurrent or metastatic breast cancer.

Study identification

NCT ID
NCT00006104
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Enrollment
46 participants

Conditions and interventions

Conditions

Interventions

Biological · 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
Sep 1998 (Type not available)
Primary completion
Jul 2003 (Actual)
Completion
Jul 2003 (Actual)
Last update posted
Aug 14, 2012

1998 – 2003

United States locations

U.S. sites
15
U.S. states
5
U.S. cities
12
Facility City State ZIP Site status
Providence Hospital Mobile Alabama 36608 —
Robert H. Lurie Comprehensive Cancer Center, Northwestern University Chicago Illinois 60611-3013 —
Evanston Hospital Evanston Illinois 60201 —
Owensboro Medical Health System Owensboro Kentucky 42303 —
Fox Chase Cancer Center Philadelphia Pennsylvania 19111 —
Erlanger Health Systems Chattanooga Tennessee 37403 —
Memorial Health Care System Chattanooga Tennessee 37404 —
Williamson Medical Center Franklin Tennessee 37067 —
Jackson-Madison County Hospital Jackson Tennessee 38301 —
Methodist/Thompson Oncology Research Knoxville Tennessee 37916 —
Tennessee Cancer Specialists Knoxville Tennessee 37920 —
Boston Baskin Cancer Group Memphis Tennessee 38104 —
St. Thomas Health Services Nashville Tennessee 37205 —
Vanderbilt-Ingram Cancer Center Nashville Tennessee 37232-6838 —
Methodist Medical Center of Oak Ridge Oak Ridge Tennessee 37831 —

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 NCT00006104, 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 Aug 14, 2012 · 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 NCT00006104 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →