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Completed Phase 3 Interventional Results available

Lume Lung 2 : BIBF 1120 Plus Pemetrexed Compared to Placebo Plus Pemetrexed in 2nd Line Nonsquamous NSCLC

ClinicalTrials.gov ID: NCT00806819

Public ClinicalTrials.gov record NCT00806819. 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 11, 2026, 1:17 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

Multicenter, Randomized, Double-blind, Phase III Trial to Investigate the Efficacy and Safety of Oral BIBF 1120 Plus Standard Pemetrexed Therapy Compared to Placebo Plus Standard Pemetrexed Therapy in Patients With Stage IIIB/IV or Recurrent 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 trial will be performed to evaluate if BIBF 1120 in combination with standard pemetrexed therapy is more effective than placebo (inactive capsule) plus standard pemetrexed therapy in patients with stage IIIB, IV or recurrent NSCLC. Safety information about BIBF1120/pemetrexed will be obtained.

Study identification

NCT ID
NCT00806819
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Boehringer Ingelheim
Industry
Enrollment
718 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
Nov 30, 2008
Primary completion
May 31, 2011
Completion
Nov 30, 2015
Last update posted
Feb 1, 2017

2008 – 2015

United States locations

U.S. sites
40
U.S. states
19
U.S. cities
40
Facility City State ZIP Site status
Boehringer Ingelheim Investigational Site Downy California
Boehringer Ingelheim Investigational Site Fountain Valley California
Boehringer Ingelheim Investigational Site Fullerton California
Boehringer Ingelheim Investigational Site Long Beach California
Boehringer Ingelheim Investigational Site Meriden Connecticut
Boehringer Ingelheim Investigational Site Aventura Florida
Boehringer Ingelheim Investigational Site Boynton Beach Florida
Boehringer Ingelheim Investigational Site Jacksonville Florida
Boehringer Ingelheim Investigational Site Miami Florida
Boehringer Ingelheim Investigational Site New Port Richey Florida
Boehringer Ingelheim Investigational Site Port Saint Lucie Florida
Boehringer Ingelheim Investigational Site Stuart Florida
Boehringer Ingelheim Investigational Site Galesburg Illinois
Boehringer Ingelheim Investigational Site Skokie Illinois
Boehringer Ingelheim Investigational Site Indianapolis Indiana
Boehringer Ingelheim Investigational Site New Albany Indiana
Boehringer Ingelheim Investigational Site Witchita Kansas
Boehringer Ingelheim Investigational Site Ashland Kentucky
Boehringer Ingelheim Investigational Site Louisville Kentucky
Boehringer Ingelheim Investigational Site Burlington Massachusetts
Boehringer Ingelheim Investigational Site Springfield Massachusetts
Boehringer Ingelheim Investigational Site Saint Louis Park Minnesota
Boehringer Ingelheim Investigational Site Grand Island Nebraska
Boehringer Ingelheim Investigational Site Farmington New Mexico
Boehringer Ingelheim Investigational Site Dunkirk New York
Boehringer Ingelheim Investigational Site Goshen New York
Boehringer Ingelheim Investigational Site Lake Success New York
Boehringer Ingelheim Investigational Site Nyack New York
Boehringer Ingelheim Investigational Site Asheville North Carolina
Boehringer Ingelheim Investigational Site Canton Ohio
Boehringer Ingelheim Investigational Site Sandusky Ohio
Boehringer Ingelheim Investigational Site Ephrata Pennsylvania
Boehringer Ingelheim Investigational Site Langhorne Pennsylvania
Boehringer Ingelheim Investigational Site Philadelphia Pennsylvania
Boehringer Ingelheim Investigational Site Germantown Tennessee
Boehringer Ingelheim Investigational Site Amarillo Texas
Boehringer Ingelheim Investigational Site Seattle Washington
Boehringer Ingelheim Investigational Site Spokane Washington
Boehringer Ingelheim Investigational Site Madison Wisconsin
Boehringer Ingelheim Investigational Site Milwaukee Wisconsin

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 123 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00806819, 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 1, 2017 · Synced Sep 11, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00806819 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →