ClinicalTrials.gov record
Completed Phase 2 Interventional Results available

Lower or Standard Dose Regorafenib in Treating Patients With Refractory Metastatic Colorectal Cancer

ClinicalTrials.gov ID: NCT02368886

Public ClinicalTrials.gov record NCT02368886. 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 May 21, 2026, 12:56 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

Regorafenib Dose Optimization Study (ReDOS): A Phase II Randomized Study of Lower Dose Regorafenib Compared to Standard Dose Regorafenib in Patients With Refractory Metastatic Colorectal Cancer (mCRC)

Study identification

NCT ID
NCT02368886
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Academic and Community Cancer Research United
Other
Enrollment
123 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
Mar 26, 2015
Primary completion
Aug 31, 2017
Completion
Mar 1, 2023
Last update posted
Jun 17, 2025

2015 – 2023

United States locations

U.S. sites
22
U.S. states
16
U.S. cities
21
Facility City State ZIP Site status
Mayo Clinic Hospital Phoenix Arizona 85054
Mayo Clinic in Arizona Scottsdale Arizona 85259
USC / Norris Comprehensive Cancer Center Los Angeles California 90033
Illinois CancerCare-Peoria Peoria Illinois 61615
Northern Indiana Cancer Research Consortium South Bend Indiana 46628
Siouxland Regional Cancer Center Sioux City Iowa 51101
Dana-Farber Cancer Institute Boston Massachusetts 02215
Mayo Clinic Rochester Minnesota 55905
Metro Minnesota Community Oncology Research Consortium Saint Louis Park Minnesota 55416
Washington University School of Medicine St Louis Missouri 63110
Missouri Valley Cancer Consortium Omaha Nebraska 68106
University of Nebraska Medical Center Omaha Nebraska 68198
Roswell Park Cancer Institute Buffalo New York 14263
Hematology Oncology Associates of Central New York-East Syracuse East Syracuse New York 13057
Wake Forest University Health Sciences Winston-Salem North Carolina 27157
Ohio State University Comprehensive Cancer Center Columbus Ohio 43210
Toledo Clinic Cancer Centers-Toledo Toledo Ohio 43623
Geisinger Medical Center Danville Pennsylvania 17822
Wellmont Medical Associates Oncology and Hematology-Kingsport Kingsport Tennessee 37660
University of Washington Medical Center Seattle Washington 98195
Saint Vincent Hospital Cancer Center Green Bay Green Bay Wisconsin 54301
Marshfield Clinic Marshfield Wisconsin 54449

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 NCT02368886, 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 17, 2025 · Synced May 21, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02368886 live on ClinicalTrials.gov.

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