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Terminated Phase 3 Interventional Results available

LUME-Columbus: Nintedanib Plus Docetaxel in Advanced Non-small Cell Lung Cancer With Translational Research

ClinicalTrials.gov ID: NCT02231164

Public ClinicalTrials.gov record NCT02231164. 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 20, 2026, 3:58 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

Multicentre, Randomised, Double-blind, Phase III Trial to Investigate the Efficacy and Safety of Oral Nintedanib Plus Docetaxel Therapy Compared to Placebo Plus Docetaxel Therapy in Patients With Stage IIIB/IV or Recurrent, Adenocarcinoma Subtype Non-small Cell Lung Cancer After Failure of First Line Chemotherapy

Brief summary

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

The present trial will investigate the efficacy and safety of nintedanib in combination with docetaxel as compared to placebo in combination with docetaxel in patients with stage IIIB/IV or recurrent NSCLC of adenocarcinoma histology after failure of first-line platinum-based chemotherapy.

Study identification

NCT ID
NCT02231164
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 3
Lead sponsor
Boehringer Ingelheim
Industry
Enrollment
12 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 14, 2014 (Actual)
Primary completion
Dec 24, 2015 (Actual)
Completion
Dec 24, 2015 (Actual)
Last update posted
Feb 13, 2025

2014 – 2015

United States locations

U.S. sites
9
U.S. states
8
U.S. cities
9
Facility City State ZIP Site status
1199.128.10032 Boehringer Ingelheim Investigational Site Chandler Arizona — —
1199.128.10041 Boehringer Ingelheim Investigational Site Fayetteville Arkansas — —
1199.128.10010 Boehringer Ingelheim Investigational Site Highland California — —
1199.128.10044 Boehringer Ingelheim Investigational Site Rancho Mirage California — —
1199.128.10080 Boehringer Ingelheim Investigational Site Paducah Kentucky — —
1199.128.10016 Boehringer Ingelheim Investigational Site Farmington New Mexico — —
1199.128.10013 Boehringer Ingelheim Investigational Site Minot North Dakota — —
1199.128.10077 Boehringer Ingelheim Investigational Site Blacksburg Virginia — —
1199.128.10011 Boehringer Ingelheim Investigational Site Kennewick Washington — —

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 4 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02231164, 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 Feb 13, 2025 · Synced Oct 20, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT02231164 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →