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Completed Phase 3 Interventional Results available

Safety and Efficacy of BIBF 1120 at High Dose in Idiopathic Pulmonary Fibrosis Patients II

ClinicalTrials.gov ID: NCT01335477

Public ClinicalTrials.gov record NCT01335477. 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 Jul 23, 2026, 1:09 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 52 Weeks, Double Blind, Randomized, Placebo-controlled Trial Evaluating the Effect of Oral BIBF 1120, 150 mg Twice Daily, on Annual Forced Vital Capacity Decline, in Patients With Idiopathic Pulmonary Fibrosis (IPF)

Study identification

NCT ID
NCT01335477
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Boehringer Ingelheim
Industry
Enrollment
551 participants

Conditions and interventions

Interventions

  • placebo Drug
  • BIBF 1120 Drug

Drug

Eligibility (public fields only)

Age range
40 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
Apr 30, 2011
Primary completion
Sep 30, 2013
Completion
Sep 30, 2013
Last update posted
Jul 24, 2016

2011 – 2013

United States locations

U.S. sites
27
U.S. states
21
U.S. cities
26
Facility City State ZIP Site status
1199.34.10078 Boehringer Ingelheim Investigational Site Scottsdale Arizona
1199.34.10086 Boehringer Ingelheim Investigational Site San Francisco California
1199.34.10093 Boehringer Ingelheim Investigational Site Santa Barbara California
1199.34.10077 Boehringer Ingelheim Investigational Site Stanford California
1199.34.10083 Boehringer Ingelheim Investigational Site Torrance California
1199.34.10080 Boehringer Ingelheim Investigational Site Stamford Connecticut
1199.34.10087 Boehringer Ingelheim Investigational Site South Miami Florida
1199.34.10100 Boehringer Ingelheim Investigational Site Austell Georgia
1199.34.10075 Boehringer Ingelheim Investigational Site Chicago Illinois
1199.34.10069 Boehringer Ingelheim Investigational Site Olathe Kansas
1199.34.10090 Boehringer Ingelheim Investigational Site Lexington Kentucky
1199.34.10079 Boehringer Ingelheim Investigational Site Rochester Minnesota
1199.34.10067 Boehringer Ingelheim Investigational Site Chesterfield Missouri
1199.34.10066 Boehringer Ingelheim Investigational Site Lebanon New Hampshire
1199.34.10085 Boehringer Ingelheim Investigational Site Albany New York
1199.34.10092 Boehringer Ingelheim Investigational Site Jamaica New York
1199.34.10074 Boehringer Ingelheim Investigational Site Durham North Carolina
1199.34.10088 Boehringer Ingelheim Investigational Site Toledo Ohio
1199.34.10070 Boehringer Ingelheim Investigational Site Portland Oregon
1199.34.10064 Boehringer Ingelheim Investigational Site Philadelphia Pennsylvania
1199.34.10089 Boehringer Ingelheim Investigational Site Philadelphia Pennsylvania
1199.34.10082 Boehringer Ingelheim Investigational Site Charleston South Carolina
1199.34.10095 Boehringer Ingelheim Investigational Site Longview Texas
1199.34.10060 Boehringer Ingelheim Investigational Site San Antonio Texas
1199.34.10084 Boehringer Ingelheim Investigational Site Salt Lake City Utah
1199.34.10101 Boehringer Ingelheim Investigational Site Colchester Vermont
1199.34.10073 Boehringer Ingelheim Investigational Site Madison 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 81 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01335477, 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 24, 2016 · Synced Jul 23, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01335477 live on ClinicalTrials.gov.

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