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Completed Phase 3 Interventional Results available

Nintedanib (BIBF 1120) vs Placebo in Refractory Metastatic Colorectal Cancer (LUME-Colon 1)

ClinicalTrials.gov ID: NCT02149108

Public ClinicalTrials.gov record NCT02149108. 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 2, 2026, 4:15 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 Double-blind, Randomised, Placebo Controlled Phase III Study of Nintedanib Plus Best Supportive Care (BSC) Versus Placebo Plus BSC in Patients With Metastatic Colorectal Cancer Refractory to Standard Therapies.

Brief summary

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

The objective of this Phase III study is to evaluate the efficacy of nintedanib in patients with metastatic colorectal cancer (mCRC) after failure of previous treatment with standard chemotherapy and biological agents.

Study identification

NCT ID
NCT02149108
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Boehringer Ingelheim
Industry
Enrollment
768 participants

Conditions and interventions

Interventions

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 24, 2014
Primary completion
May 12, 2016
Completion
Aug 24, 2016
Last update posted
Jul 20, 2017

2014 – 2016

United States locations

U.S. sites
14
U.S. states
12
U.S. cities
14
Facility City State ZIP Site status
1199.52.0108 Boehringer Ingelheim Investigational Site Los Angeles California
1199.52.0105 Boehringer Ingelheim Investigational Site New Haven Connecticut
1199.52.0101 Boehringer Ingelheim Investigational Site Plainville Connecticut
1199.52.0121 Boehringer Ingelheim Investigational Site Arlington Heights Illinois
1199.52.0123 Boehringer Ingelheim Investigational Site Sioux City Iowa
1199.52.0104 Boehringer Ingelheim Investigational Site Topeka Kansas
1199.52.0114 Boehringer Ingelheim Investigational Site New Orleans Louisiana
1199.52.0113 Boehringer Ingelheim Investigational Site Detroit Michigan
1199.52.0125 Boehringer Ingelheim Investigational Site Omaha Nebraska
1199.52.0119 Boehringer Ingelheim Investigational Site Johnson City New York
1199.52.0115 Boehringer Ingelheim Investigational Site Canton Ohio
1199.52.0106 Boehringer Ingelheim Investigational Site Sylvania Ohio
1199.52.0102 Boehringer Ingelheim Investigational Site Nashville Tennessee
1199.52.0120 Boehringer Ingelheim Investigational Site Fort Worth Texas

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 115 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02149108, 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 Jul 20, 2017 · Synced Sep 2, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02149108 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →