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Completed Phase 1Phase 2 Interventional

Phase 1b/2 Study of AMG 655 With mFOLFOX6 and Bevacizumab for First-Line Metastatic Colorectal Cancer

ClinicalTrials.gov ID: NCT00625651

Public ClinicalTrials.gov record NCT00625651. 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 23, 2026, 3:11 AM 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 1b/2 Study of AMG 655 in Combination With Modified FOLFOX6 and Bevacizumab for the First-Line Treatment of Subjects With Metastatic Colorectal Cancer

Brief summary

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

This phase 1/2, multi-center, randomized, double-blind, placebo-controlled trial is designed to evaluate the efficacy and safety of AMG 655 when combined with mFOLFOX6 and bevacizumab compared with mFOLFOX6 and bevacizumab alone in subjects with previously untreated metastatic colorectal cancer (CRC). The clinical benefit of AMG 655 in combination with mFOLFOX6 and bevacizumab will be measured by progression-free survival, objective response rate, time to response, duration of response, and overall survival. This study is also designed to evaluate the safety and tolerability of AMG 655 in combination with mFOLFOX6 and bevacizumab and to evaluate anti-AMG 655 antibody formation and the pharmacokinetics of AMG 655.

Study identification

NCT ID
NCT00625651
Recruitment status
Completed
Study type
Interventional
Phase
Phase 1, Phase 2
Lead sponsor
Amgen
Industry
Enrollment
202 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
Oct 2007 (Type not available)
Primary completion
Aug 2010 (Actual)
Completion
Sep 2011 (Actual)
Last update posted
Apr 25, 2014

2007 – 2011

United States locations

U.S. sites
61
U.S. states
30
U.S. cities
59
Facility City State ZIP Site status
Research Site Hot Springs Arkansas 71913 —
Research Site Downey California 90241 —
Research Site La Jolla California 92093-0957 —
Research Site Loma Linda California 92354 —
Research Site Orange California 92868 —
Research Site Rancho Mirage California 92270 —
Research Site San Diego California 92123 —
Research Site Denver Colorado 80218 —
Research Site Newark Delaware 19718 —
Research Site Washington D.C. District of Columbia 20007 —
Research Site Boca Raton Florida 33486 —
Research Site Kissimmee Florida 34741 —
Research Site Leesburg Florida 34788 —
Research Site Miami Florida 33136 —
Research Site Miami Florida 33176 —
Research Site Atlanta Georgia 30309 —
Research Site Lawrenceville Georgia 30045 —
Research Site Harvey Illinois 60426 —
Research Site Maywood Illinois 60153 —
Research Site Indianapolis Indiana 46227 —
Research Site Overland Park Kansas 66210 —
Research Site Louisville Kentucky 40202 —
Research Site Baltimore Maryland 21215 —
Research Site Baltimore Maryland 21237 —
Research Site Boston Massachusetts 02115 —
Research Site Ann Arbor Michigan 48106-0995 —
Research Site Saint Joseph Michigan 49085 —
Research Site Rochester Minnesota 55905 —
Research Site St Louis Missouri 63136 —
Research Site Great Falls Montana 59405 —
Research Site Long Branch New Jersey 07740 —
Research Site Albuquerque New Mexico 87109-4397 —
Research Site Buffalo New York 14263 —
Research Site Hudson New York 12534 —
Research Site New York New York 10021 —
Research Site The Bronx New York 10469 —
Research Site Asheville North Carolina 28801 —
Research Site Burlington North Carolina 27215 —
Research Site Gastonia North Carolina 28054 —
Research Site Raleigh North Carolina 27607 —
Research Site Winston-Salem North Carolina 27103 —
Research Site Cincinnati Ohio 45226 —
Research Site Columbus Ohio 43219 —
Research Site Middletown Ohio 45042 —
Research Site Portland Oregon 97227 —
Research Site Harrisburg Pennsylvania 17109 —
Research Site Philadelphia Pennsylvania 19107 —
Research Site Pottsville Pennsylvania 17901 —
Research Site Greenville South Carolina 29605 —
Research Site Memphis Tennessee 38120 —
Research Site Nashville Tennessee 37203 —
Research Site Austin Texas 78731 —
Research Site Richardson Texas 75080 —
Research Site Tyler Texas 75702 —
Research Site Wichita Falls Texas 76310 —
Research Site Ogden Utah 84403 —
Research Site Fairfax Virginia 22031 —
Research Site Norfolk Virginia 23502 —
Research Site Richmond Virginia 23235 —
Research Site Tacoma Washington 98405 —
Research Site Vancouver Washington 98684 —

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 NCT00625651, 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 Apr 25, 2014 · Synced Oct 23, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00625651 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →