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Terminated Phase 3 Interventional Results available

Colorectal Cancer Treated With Adjuvant Regorafenib Versus Placebo After Curative Treatment of Liver Metastases in a Randomized, Double-blind, Placebo-Controlled Phase-III STudy

ClinicalTrials.gov ID: NCT01939223

Public ClinicalTrials.gov record NCT01939223. 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 6, 2026, 8:45 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, Placebo-controlled Phase-III Study of Adjuvant Regorafenib Versus Placebo for Patients With Stage IV Colorectal Cancer After Curative Treatment of Liver Metastases

Study identification

NCT ID
NCT01939223
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 3
Lead sponsor
Bayer
Industry
Enrollment
25 participants

Conditions and interventions

Interventions

  • Placebo Drug
  • Regorafenib (Stivarga, BAY73-4506) 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
Dec 1, 2013
Primary completion
Aug 28, 2016
Completion
Aug 28, 2016
Last update posted
Oct 19, 2017

2013 – 2016

United States locations

U.S. sites
23
U.S. states
15
U.S. cities
20
Facility City State ZIP Site status
Not listed Laguna Hills California 92653
Not listed Los Angeles California 90033
Not listed Los Angeles California 90089
Not listed Los Angeles California 90095
Not listed New Haven Connecticut 06520-8064
Not listed New Orleans Louisiana 70121
Not listed Baltimore Maryland 21201-1595
Not listed Detroit Michigan 48202
Not listed Rochester Minnesota 55905
Not listed Omaha Nebraska 68106
Not listed New Brunswick New Jersey 08903-2681
Not listed Buffalo New York 14263-0001
Not listed New York New York 10021
Not listed Syracuse New York 13210
Duke University Medical Center Durham North Carolina 27710
Not listed Philadelphia Pennsylvania 19104
Not listed Chattanooga Tennessee 37421
Not listed Germantown Tennessee 38138
Not listed Dallas Texas 75390
Not listed Richmond Virginia 23298-0037
Not listed Kirkland Washington 98034
Not listed Seattle Washington 98101
Not listed 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.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 98 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01939223, 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 19, 2017 · Synced May 6, 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 protocol, eligibility criteria, and contact information for NCT01939223 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →