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Completed Phase 3 Interventional Results available

BEATRICE Study: A Study of Bevacizumab (Avastin) Adjuvant Therapy in Triple Negative Breast Cancer

ClinicalTrials.gov ID: NCT00528567

Public ClinicalTrials.gov record NCT00528567. 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 Sep 17, 2026, 12:58 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

An International Multi-centre Open-label 2-arm Phase III Trial of Adjuvant Bevacizumab in "Triple Negative" Breast Cancer.

Brief summary

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

The main objective of the trial is to compare Invasive Disease-Free Survival (IDFS) of patients randomised to treatment with adjuvant chemotherapy alone or to adjuvant chemotherapy with 1 year of bevacizumab. The secondary objectives of this trial are to: * compare Overall Survival (OS), Breast Cancer-Free Interval (BCFI), Disease- Free Survival (DFS) and Distant Disease-Free Survival (DDFS) of patients randomised to treatment with adjuvant chemotherapy alone or to adjuvant chemotherapy in combination with 1 year of bevacizumab * evaluate the safety and tolerability of bevacizumab An exploratory sub-study (not reported here) was to identify biomarkers (from tumour or serum) predictive of toxicity and for the level of benefit from the addition of bevacizumab to standard adjuvant systemic treatment.

Study identification

NCT ID
NCT00528567
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Hoffmann-La Roche
Industry
Enrollment
2,591 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
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
Nov 30, 2007
Primary completion
Jan 31, 2012
Completion
May 31, 2014
Last update posted
Sep 3, 2015

2007 – 2014

United States locations

U.S. sites
44
U.S. states
21
U.S. cities
43
Facility City State ZIP Site status
Not listed Huntsville Alabama 35805
Not listed Mobile Alabama 36604
Not listed Fayetteville Arkansas 72703
Not listed Bakersfield California 93309
Not listed Fountain Valley California 92708
Not listed Greenbrae California 94904
Not listed Los Angeles California 90057
Not listed Pleasant Hill California 94523
Not listed Fairfield Connecticut 06824
Not listed Stamford Connecticut 06902
Not listed Washington D.C. District of Columbia 20010
Not listed Gainesville Florida 32605
Not listed Orlando Florida 32806
Not listed Tamarac Florida 33321
Not listed Atlanta Georgia 30318
Not listed Augusta Georgia 30901
Not listed Lawrenceville Georgia 30046
Not listed Niles Illinois 60714
Not listed Iowa City Iowa 52242
Not listed Waterloo Iowa 50702
Not listed Baltimore Maryland 21215
Not listed Baltimore Maryland 21237
Not listed Rockville Maryland 20850-3348
Not listed Brownstown Michigan 48183
Not listed Kalamazoo Michigan 49007
Not listed Southfield Michigan 48075-3707
Not listed Kansas City Missouri 64111
Not listed St Louis Missouri 63141
Not listed Long Branch New Jersey 07740
Not listed The Bronx New York 10469
Not listed Hickory North Carolina 28602
Not listed Winston-Salem North Carolina 27103
Not listed Cincinnati Ohio 45242
Not listed Columbus Ohio 43235
Not listed Middletown Ohio 45042
Not listed Columbia South Carolina 29210
Not listed Chattanooga Tennessee 37404
Not listed Germantown Tennessee 38138
Not listed Nashville Tennessee 37203
Not listed Austin Texas 78759
Not listed Dallas Texas 75234
Not listed Rutland Vermont 05701
Not listed Abingdon Virginia 24211
Not listed Richmond Virginia 23230

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 359 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00528567, 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 3, 2015 · Synced Sep 17, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00528567 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →