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Completed Phase 2 Interventional Results available

Irinotecan and Cetuximab With or Without Bevacizumab in Treating Patients With RAS Wild-Type Locally Advanced or Metastatic Colorectal Cancer That Cannot Be Removed by Surgery

ClinicalTrials.gov ID: NCT02292758

Public ClinicalTrials.gov record NCT02292758. 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 6, 2026, 12:17 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

BOND-3: A Randomized, Double-Blind, Placebo-Controlled Phase II Trial of Irinotecan, Cetuximab, and Bevacizumab Compared With Irinotecan, Cetuximab, and Placebo in RAS-Wildtype, Irinotecan-Refractory, Metastatic Colorectal Cancer

Brief summary

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

This randomized phase II trial studies how well irinotecan and cetuximab with or without bevacizumab work in treating patients with RAS wild-type colorectal cancer that has spread to other places in the body (locally advanced/metastatic) and cannot be removed by surgery. Irinotecan may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. Immunotherapy with monoclonal antibodies, such as cetuximab and bevacizumab, may help the body?s immune system attack the cancer, and may interfere with the ability of tumor cells to grow and spread. Giving irinotecan and cetuximab with or without bevacizumab may work betting in treating patients with colorectal cancer.

Study identification

NCT ID
NCT02292758
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Enrollment
36 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 11, 2014
Primary completion
Mar 19, 2019
Completion
Sep 26, 2019
Last update posted
Jan 30, 2022

2014 – 2019

United States locations

U.S. sites
13
U.S. states
12
U.S. cities
13
Facility City State ZIP Site status
Mayo Clinic in Arizona Scottsdale Arizona 85259
Saint Luke's Mountain States Tumor Institute Boise Idaho 83712
Siouxland Regional Cancer Center Sioux City Iowa 51101
Cancer Center of Kansas - Wichita Wichita Kansas 67214
Ochsner Medical Center Jefferson New Orleans Louisiana 70121
Dana-Farber Cancer Institute Boston Massachusetts 02215
Michigan Cancer Research Consortium NCORP Ann Arbor Michigan 48106
Mayo Clinic Rochester Minnesota 55905
Heartland Regional Medical Center Saint Joseph Missouri 64507
Missouri Baptist Medical Center St Louis Missouri 63131
New Hampshire Oncology Hematology PA-Hooksett Hooksett New Hampshire 03106
State University of New York Upstate Medical University Syracuse New York 13210
Saint Vincent Regional Cancer Center CCOP Green Bay Wisconsin 54301

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 NCT02292758, 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 Jan 30, 2022 · Synced Sep 6, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02292758 live on ClinicalTrials.gov.

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