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Completed Phase 2 Interventional Results available

Therapy With Bevacizumab (BEV), Epirubicin, and Cyclophosphamide Followed by Docetaxel Plus Trastuzumab and BEV Given as Neoadjuvant or Adjuvant Therapy for Women With Locally Advanced HER2 Positive Invasive Breast Cancer

ClinicalTrials.gov ID: NCT00464646

Public ClinicalTrials.gov record NCT00464646. 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 22, 2026, 10:59 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

A Phase II Clinical Trial of Epirubicin Plus Cyclophosphamide Followed by Docetaxel Plus Trastuzumab and Bevacizumab Given as Neoadjuvant Therapy for HER2-Positive Locally Advanced Breast Cancer or Given as Adjuvant Therapy for HER2-Positive Pathologic Stage III Breast Cancer

Brief summary

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

The main purpose is to learn if adding bevacizumab to standard chemotherapy and trastuzumab to treat HER2-positive breast cancer will affect heart function. This study will evaluate: * How bevacizumab, given with chemotherapy, and then bevacizumab given with trastuzumab after surgery, will affect breast tumors * Side effects from adding bevacizumab to chemotherapy and trastuzumab * Whether adding bevacizumab to chemotherapy and trastuzumab for breast cancer will affect the heart * If receiving bevacizumab will have any effect on how patients recover from surgery

Study identification

NCT ID
NCT00464646
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
NSABP Foundation Inc
Network
Enrollment
105 participants

Conditions and interventions

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
May 2007 (Type not available)
Primary completion
Dec 2009 (Actual)
Completion
May 2014 (Actual)
Last update posted
Oct 25, 2021

2007 – 2014

United States locations

U.S. sites
35
U.S. states
21
U.S. cities
32
Facility City State ZIP Site status
Clearview Cancer Institute- Huntsville Huntsville Alabama 35801 —
Kaiser Permanente-San Diego San Diego California 92120 —
Kaiser Permanente-Vallejo Vallejo California 94589 —
CCOP, Colorado Cancer Research Program, Inc. Denver Colorado 80224 —
Baptist Regional Cancer Institute Jacksonville Florida 32207 —
Rush University Medical Center Chicago Illinois 60612 —
CCOP, Central Illinois Springfield Illinois 62526 —
CCOP, Northern Indiana Cancer Research Consortium South Bend Indiana 46601 —
University of Iowa Iowa City Iowa 52242 —
NortonHealtcare Inc. Louisville Kentucky 40202 —
CCOP, Grand Rapids Clnical Oncology Program Grand Rapids Michigan 49503 —
CCOP, Michigan Cancer Research Consortium Grosse Pointe Woods Michigan 48236 —
CCOP, Kalamazoo, MI Kalamazoo Michigan 49007 —
Michigan State University - Breslin Cancer Center Lansing Michigan 48910 —
CCOP, Metro-Minnesota Minneapolis Minnesota 55416 —
CCOP, Cancer Research for the Ozarks Springfield Missouri 65804 —
Cancer Institute of New Jersey New Brunswick New Jersey 08901 —
University Hospital and Medical Center - SUNY Stony Brook New York 11794 —
CCOP, Southeast Cancer Control Consortium Charlotte North Carolina 28203 —
East Carolina University Greenville North Carolina 27834 —
Aultman Hospital Canton Ohio 44710 —
Case Western Reserve/University Hospitals-Ireland Cancer Cntr. Cleveland Ohio 44106 —
CCOP, Dayton, OH Dayton Ohio 45429 —
CCOP, Columbia River Oncology Portland Oregon 97225 —
Kimmel Cancer Center at Jefferson Philadelphia Pennsylvania 19107 —
Albert Einstein Healthcare Network Philadelphia Pennsylvania 19141-3098 —
Allegheny General Hospital/Allegheny-Singer Research Institute Pittsburgh Pennsylvania 15212 —
NSABP Foundation, Inc. Pittsburgh Pennsylvania 15212 —
University of Pittsburgh Pittsburgh Pennsylvania 15213 —
Mercy Hospital Scranton Pennsylvania 18501 —
CCOP, Upstate Carolina Spartanburg South Carolina 29303 —
Joe Arrington Cancer Research & Treatment Center Lubbock Texas 79410 —
CCOP, Scott and White Memorial Hospital Temple Texas 76508 —
MBCCOP, Virginia Commonwealth University Richmond Virginia 23298 —
CCOP, Marshfield Clinic Marshfield Wisconsin 54449 —

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 1 non-U.S. site.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00464646, 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 Oct 25, 2021 · Synced Oct 22, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00464646 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →