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Completed Phase 2 Interventional

Ph II Trial of a Novel Anti-angiogenic Agent in Combination With Chemotherapy for the Second-line Treatment of Metastatic Colorectal Cancer

ClinicalTrials.gov ID: NCT00851045

Public ClinicalTrials.gov record NCT00851045. 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 Apr 29, 2026, 12:17 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 Randomized, Double-Blind, Phase II Trial of CT-322 (BMS-844203) Plus Irinotecan, 5-FU and Leucovorin (FOLFIRI) Versus Bevacizumab Plus FOLFIRI as Second-Line Treatment for Metastatic Colorectal Cancer

Study identification

NCT ID
NCT00851045
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Bristol-Myers Squibb
Industry
Enrollment
17 participants

Conditions and interventions

Interventions

  • 5-Fluorouracil (bolus) Drug
  • 5-Fluorouracil (infusional) Drug
  • Bevacizumab Drug
  • Bevacizumab Placebo (saline solution) Drug
  • CT-322 Drug
  • Irinotecan Drug
  • Leucovorin calcium Drug

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
Sep 30, 2009
Primary completion
Aug 31, 2011
Completion
Sep 30, 2011
Last update posted
Oct 11, 2015

2009 – 2011

United States locations

U.S. sites
12
U.S. states
10
U.S. cities
12
Facility City State ZIP Site status
Acrc/Arizona Clinical Research Center, Inc. Tucson Arizona 85715
Compassionate Cancer Care Medical Group Inc Fountain Valley California 92708
Compassionate Cancer Care Medical Group, Inc Riverside California 92501
Sharp Memorial Hospital San Diego California 92123
Florida Cancer Specialists Fort Myers Florida 33916
Midwest Center For Hematology/Oncology Joliet Illinois 60432
Cancer Center Of Kansas Wichita Kansas 67214
Gurtler, Jayne Metairie Louisiana 70006
Guthrie Clinic, Ltd Sayre Pennsylvania 18840
Pharma Resource East Providence Rhode Island 02915
Sarah Cannon Research Institute Nashville Tennessee 37203
University Of Texas M.D. Anderson Cancer Center Houston Texas 77030

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 3 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00851045, 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 11, 2015 · Synced Apr 29, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00851045 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →