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Withdrawn Phase 2 Interventional

Safety and Efficacy of 4-weeks Treatment of BIBW 2948 BS in Patients With Chronic Obstructive Bronchitis

ClinicalTrials.gov ID: NCT00726479

Public ClinicalTrials.gov record NCT00726479. 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, 10:54 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 Phase II, Randomised, Double-blind, Placebo-controlled and Parallel Group Study to Evaluate the Safety and Efficacy of Four Weeks Treatment of 7.5 mg b.i.d, 15 mg q.d and 15 mg b.i.d. BIBW 2948 BS (Inhalation Powder, Hard Capsule for HandiHaler®) in Patients With COPD Associated With Chronic Bronchitis.

Study identification

NCT ID
NCT00726479
Recruitment status
Withdrawn
Study type
Interventional
Phase
Phase 2
Lead sponsor
Boehringer Ingelheim
Industry
Enrollment
Not listed

Conditions and interventions

Interventions

  • BIBW 2948 BS 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
Jul 31, 2008
Primary completion
Aug 31, 2008
Completion
Not listed
Last update posted
Mar 26, 2014

Started 2008

United States locations

U.S. sites
8
U.S. states
6
U.S. cities
8
Facility City State ZIP Site status
1219.4.01001 Boehringer Ingelheim Investigational Site Birmingham Alabama
1219.4.01007 Boehringer Ingelheim Investigational Site Phoenix Arizona
1219.4.01006 Boehringer Ingelheim Investigational Site Fort Collins Colorado
1219.4.01002 Boehringer Ingelheim Investigational Site Stamford Connecticut
1219.4.01008 Boehringer Ingelheim Investigational Site Rincon Georgia
1219.4.01003 Boehringer Ingelheim Investigational Site Greenville South Carolina
1219.4.01004 Boehringer Ingelheim Investigational Site Spartanburg South Carolina
1219.4.01005 Boehringer Ingelheim Investigational Site Union South Carolina

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 16 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00726479, 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 Mar 26, 2014 · Synced Jul 23, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00726479 live on ClinicalTrials.gov.

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