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Completed Phase 1Phase 2 Interventional Results available

Neoadjuvant Sunitinib With Paclitaxel/Carboplatin in Patients With Triple-Negative Breast Cancer

ClinicalTrials.gov ID: NCT00887575

Public ClinicalTrials.gov record NCT00887575. 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 19, 2026, 8:20 PM 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 I/II Trial of Neoadjuvant Sunitinib Administered With Weekly Paclitaxel/Carboplatin in Patients With Locally Advanced Triple-Negative Breast Cancer

Brief summary

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

This trial will examine the combination of sunitinib plus paclitaxel and carboplatin as neoadjuvant treatment for locally advanced breast cancer.

Study identification

NCT ID
NCT00887575
Recruitment status
Completed
Study type
Interventional
Phase
Phase 1, Phase 2
Enrollment
54 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
Jun 2009 (Type not available)
Primary completion
Jul 2013 (Actual)
Completion
Sep 2014 (Actual)
Last update posted
Sep 7, 2016

2009 – 2014

United States locations

U.S. sites
14
U.S. states
10
U.S. cities
12
Facility City State ZIP Site status
Holy Cross Hospital Fort Lauderdale Florida 33308 —
Florida Cancer Specialists North Fort Myers Florida 33916 —
Florida Cancer Specialists South Fort Myers Florida 33916 —
Northeast Georgia Medical Center Gainesville Georgia 30501 —
Providence Medical Group Terre Haute Indiana 47802 —
Baptist Hospital East Louisville Kentucky 40207 —
Center for Cancer and Blood Disorders Bethesda Maryland 20817 —
National Capital Clinical Research Consortium Bethesda Maryland 20817 —
St. Louis Cancer Care Chesterfield Missouri 63017 —
Nebraska Methodist Cancer Center Omaha Nebraska 68114 —
Hematology Oncology Associates of Northern NJ Morristown New Jersey 07960 —
Cancer Centers of Southwest Oklahoma Lawton Oklahoma 73505 —
Family Cancer Center Collierville Tennessee 38017 —
Tennessee Oncology, PLLC Nashville Tennessee 37023 —

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 NCT00887575, 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 Sep 7, 2016 · Synced Oct 19, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00887575 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →