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Completed Phase 2 Interventional Results available

Ixabepilone and Cyclophosphamide as Neoadjuvant Therapy in HER-2 Negative Breast Cancer

ClinicalTrials.gov ID: NCT00866905

Public ClinicalTrials.gov record NCT00866905. 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, 2:48 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 II Study of Ixabepilone and Cyclophosphamide as Neoadjuvant Therapy in HER2-Negative Breast Cancer

Brief summary

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

We propose to evaluate ixabepilone in combination with cyclophosphamide for the neoadjuvant treatment of locally advanced breast cancer. In this regimen, ixabepilone is substituted for docetaxel, since preclinical and clinical studies suggest that ixabepilone is more active than either docetaxel or paclitaxel. The combination of ixabepilone and cyclophosphamide could further improve the efficacy of non-anthracycline neoadjuvant therapy.

Study identification

NCT ID
NCT00866905
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Enrollment
168 participants

Conditions and interventions

Conditions

Interventions

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
Apr 2009 (Type not available)
Primary completion
Jul 2014 (Actual)
Completion
Oct 2014 (Actual)
Last update posted
Nov 22, 2021

2009 – 2014

United States locations

U.S. sites
20
U.S. states
14
U.S. cities
19
Facility City State ZIP Site status
Aventura Medical Center Aventura Florida 33180 —
Florida Cancer Specialists Fort Myers Florida 33901 —
Watson Clinic Center for Cancer Care and Research Lakeland Florida 33805 —
Medical Oncology Associates of Augusta Augusta Georgia 30901 —
Northeast Georgia Medical Center Gainesville Georgia 30501 —
Providence Medical Group Terre Haute Indiana 47802 —
Mercy Hospital Portland Maine 04101 —
Center for Cancer and Blood Disorders Bethesda Maryland 20817 —
National Capital Clinical Research Consortium Bethesda Maryland 20817 —
St. Louis Cancer Care Chesterfield Missouri 63017 —
Methodist Cancer Center Omaha Nebraska 68114 —
Hematology Oncology Associates of Northern NJ Morristown New Jersey 07960 —
Oncology Hematology Care Cincinnati Ohio 45242 —
Cancer Centers of Southwest Oklahoma Lawton Oklahoma 73505 —
South Carolina Oncology Associates, PA Columbia South Carolina 29210 —
Chattanooga Oncology Hematology Associates Chattanooga Tennessee 37404 —
Family Cancer Center Collierville Tennessee 38017 —
Tennessee Oncology Nashville Tennessee 37203 —
South Texas Oncology and Hematology San Antonio Texas 78258 —
Virginia Cancer Institute Richmond Virginia 23235 —

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 NCT00866905, 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 22, 2021 · 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 NCT00866905 live on ClinicalTrials.gov.

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