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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 Nov 7, 2026, 2:33 AM EST

All trial information on this site comes from the official ClinicalTrials.gov public API (clinicaltrials.gov/api/v2), run by the U.S. National Library of Medicine. We only display that public information; we do not add opinions, endorsements, or any other intent. 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
Dec 2007 (Type not available)
Primary completion
Feb 2012 (Actual)
Completion
Jun 2014 (Actual)
Last update posted
Sep 4, 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 4, 2015 · Synced Nov 7, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00528567 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →