Independent directory Public ClinicalTrials.gov records United States
ClinicalTrials.gov record
Completed Phase 2 Interventional

Bevacizumab Plus Fluorouracil and Leucovorin in Treating Patients With Locally Advanced or Metastatic Stage IV Colorectal Cancer That Has Progressed After Standard Chemotherapy

ClinicalTrials.gov ID: NCT00066846

Public ClinicalTrials.gov record NCT00066846. 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 8, 2026, 9:54 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

A Multicenter Study of the Anti-VEGF Monoclonal Antibody Bevacizumab (Avastin®) Plus 5-Fluorouracil/Leucovorin in Patients With Metastatic Colorectal Cancers That Have Progressed After Standard Chemotherapy

Brief summary

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

RATIONALE: Bevacizumab may stop the growth of tumor cells by blocking the enzymes necessary for cancer cell growth. Drugs used in chemotherapy such as fluorouracil and leucovorin use different ways to stop tumor cells from dividing so they stop growing or die. Combining bevacizumab with fluorouracil and leucovorin may kill more tumor cells. PURPOSE: Phase II trial to study the effectiveness of combining bevacizumab with fluorouracil and leucovorin in treating patients who have locally advanced or metastatic stage IV colorectal cancer that has progressed after standard chemotherapy.

Study identification

NCT ID
NCT00066846
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Enrollment
Not listed

Conditions and interventions

Interventions

Biological · Drug

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
Aug 2003 (Type not available)
Primary completion
Not listed
Completion
Jul 2007 (Actual)
Last update posted
Jun 20, 2013

2003 – 2007

United States locations

U.S. sites
33
U.S. states
26
U.S. cities
30
Facility City State ZIP Site status
Providence Alaska Medical Center Anchorage Alaska 99519-6604 —
Jonsson Comprehensive Cancer Center, UCLA Los Angeles California 90024 —
USC/Norris Comprehensive Cancer Center and Hospital Los Angeles California 90033-0804 —
University of Colorado Cancer Center at University of Colorado Health Sciences Center Aurora Colorado 80010 —
Yale Comprehensive Cancer Center New Haven Connecticut 06520-8028 —
Lombardi Cancer Center Washington D.C. District of Columbia 20007 —
CCOP - Atlanta Regional Atlanta Georgia 30342-1701 —
Robert H. Lurie Comprehensive Cancer Center, Northwestern University Chicago Illinois 60611 —
Loyola University Medical Center Maywood Illinois 60153 —
Holden Comprehensive Cancer Center Iowa City Iowa 52242-1009 —
Siouxland Hematology-Oncology Sioux City Iowa 51101-1733 —
CCOP - Wichita Wichita Kansas 67214-3882 —
Cancer Care of Maine Bangor Maine 04401 —
Saint Joseph Mercy Health System Ann Arbor Michigan 48106 —
St. Mary's/Duluth Clinic Cancer Center Duluth Minnesota 55805 —
University of Mississippi Medical Center Jackson Mississippi 39216-4505 —
CCOP - Montana Cancer Consortium Billings Montana 59101 —
Southern Nevada Cancer Research Foundation Las Vegas Nevada 89106 —
Norris Cotton Cancer Center Lebanon New Hampshire 03756-0002 —
Roswell Park Cancer Institute Buffalo New York 14263-0001 —
New York Weill Cornell Cancer Center at Cornell University New York New York 10021 —
Duke Comprehensive Cancer Center Durham North Carolina 27710 —
Comprehensive Cancer Center at Wake Forest University Winston-Salem North Carolina 27157-1082 —
Meritcare Roger Maris Cancer Center Fargo North Dakota 58122 —
Ireland Cancer Center Cleveland Ohio 44106-5065 —
University of Oklahoma Health Sciences Center Oklahoma City Oklahoma 73104 —
Abramson Cancer Center of the University of Pennsylvania Philadelphia Pennsylvania 19104 —
Kimmel Cancer Center of Thomas Jefferson University - Philadelphia Philadelphia Pennsylvania 19107-5541 —
Sioux Valley Clinics - Oncology Sioux Falls South Dakota 57104 —
Fletcher Allen Health Care - University Health Center Campus Burlington Vermont 05401 —
Massey Cancer Center Richmond Virginia 23298-0037 —
CCOP - Virginia Mason Research Center Seattle Washington 98101 —
Seattle Cancer Care Alliance Seattle Washington 98109 —

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 NCT00066846, 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 Jun 20, 2013 · Synced Nov 8, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00066846 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →