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Completed Phase 2 Interventional Results available

An Efficacy and Safety Study to Compare Three Doses of BEA 2180 BR to Tiotropium and Placebo in the Respimat Inhaler.

ClinicalTrials.gov ID: NCT00528996

Public ClinicalTrials.gov record NCT00528996. 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 19, 2026, 3:13 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 Multinational, Randomised, Double-blind, Placebo- and Active-controlled, Parallel Group Efficacy and Safety Comparison Over 24 Weeks of Three Doses (50µg, 100µg, 200µg) of BEA 2180 BR to Tiotropium 5µg, Delivered by the Respimat Inhaler and Placebo in Patients With Chronic Obstructive Pulmonary Disease (COPD)

Brief summary

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

The primary objective of this study is to compare the bronchodilator efficacy of three doses (50 µg, 100 µg and 200 µg) of BEA 2180 delivered by the Respimat® once daily to placebo and tiotropium bromide delivered by the Respimat® in patients with COPD. Additional objectives include comparing the effects on dyspnea and health status.

Study identification

NCT ID
NCT00528996
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Boehringer Ingelheim
Industry
Enrollment
2,080 participants

Conditions and interventions

Eligibility (public fields only)

Age range
40 Years to 100 Years
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 6, 2007 (Actual)
Primary completion
May 5, 2009 (Actual)
Completion
May 5, 2009 (Actual)
Last update posted
Aug 24, 2021

2007 – 2009

United States locations

U.S. sites
56
U.S. states
25
U.S. cities
53
Facility City State ZIP Site status
1205.14.061 Boehringer Ingelheim Investigational Site Jasper Alabama — —
1205.14.054 Boehringer Ingelheim Investigational Site Mobile Alabama — —
1205.14.042 Boehringer Ingelheim Investigational Site Berkeley California — —
1205.14.017 Boehringer Ingelheim Investigational Site La Jolla California — —
1205.14.022 Boehringer Ingelheim Investigational Site Lakewood California — —
1205.14.046 Boehringer Ingelheim Investigational Site Riverside California — —
1205.14.008 Boehringer Ingelheim Investigational Site San Diego California — —
1205.14.047 Boehringer Ingelheim Investigational Site San Diego California — —
1205.14.037 Boehringer Ingelheim Investigational Site Sepulveda California — —
1205.14.041 Boehringer Ingelheim Investigational Site Denver Colorado — —
1205.14.027 Boehringer Ingelheim Investigational Site Fort Collins Colorado — —
1205.14.034 Boehringer Ingelheim Investigational Site Wheat Ridge Colorado — —
1205.14.050 Boehringer Ingelheim Investigational Site Stamford Connecticut — —
1205.14.013 Boehringer Ingelheim Investigational Site Bay Pines Florida — —
1205.14.016 Boehringer Ingelheim Investigational Site Clearwater Florida — —
1205.14.048 Boehringer Ingelheim Investigational Site DeLand Florida — —
1205.14.043 Boehringer Ingelheim Investigational Site Panama City Florida — —
1205.14.040 Boehringer Ingelheim Investigational Site Tampa Florida — —
1205.14.007 Boehringer Ingelheim Investigational Site Atlanta Georgia — —
1205.14.053 Boehringer Ingelheim Investigational Site Stockbridge Georgia — —
1205.14.014 Boehringer Ingelheim Investigational Site Coeur d'Alene Idaho — —
1205.14.035 Boehringer Ingelheim Investigational Site Olathe Kansas — —
1205.14.057 Boehringer Ingelheim Investigational Site New Orleans Louisiana — —
1205.14.052 Boehringer Ingelheim Investigational Site Shreveport Louisiana — —
1205.14.036 Boehringer Ingelheim Investigational Site Ann Arbor Michigan — —
1205.14.019 Boehringer Ingelheim Investigational Site Livonia Michigan — —
1205.14.018 Boehringer Ingelheim Investigational Site Chesterfield Missouri — —
1205.14.032 Boehringer Ingelheim Investigational Site St Louis Missouri — —
1205.14.033 Boehringer Ingelheim Investigational Site Reno Nevada — —
1205.14.044 Boehringer Ingelheim Investigational Site Brick New Jersey — —
1205.14.056 Boehringer Ingelheim Investigational Site Cherry Hill New Jersey — —
1205.14.058 Boehringer Ingelheim Investigational Site Summit New Jersey — —
1205.14.010 Boehringer Ingelheim Investigational Site Albuquerque New Mexico — —
1205.14.062 Boehringer Ingelheim Investigational Site Larchmont New York — —
1205.14.028 Boehringer Ingelheim Investigational Site Mineola New York — —
1205.14.030 Boehringer Ingelheim Investigational Site New Hyde Park New York — —
1205.14.021 Boehringer Ingelheim Investigational Site New York New York — —
1205.14.059 Boehringer Ingelheim Investigational Site Toledo Ohio — —
1205.14.012 Boehringer Ingelheim Investigational Site Oklahoma City Oklahoma — —
1205.14.031 Boehringer Ingelheim Investigational Site Medford Oregon — —
1205.14.003 Boehringer Ingelheim Investigational Site Philadelphia Pennsylvania — —
1205.14.004 Boehringer Ingelheim Investigational Site Pittsburgh Pennsylvania — —
1205.14.005 Boehringer Ingelheim Investigational Site Johnston Rhode Island — —
1205.14.029 Boehringer Ingelheim Investigational Site Charleston South Carolina — —
1205.14.055 Boehringer Ingelheim Investigational Site Greer South Carolina — —
1205.14.020 Boehringer Ingelheim Investigational Site Spartanburg South Carolina — —
1205.14.045 Boehringer Ingelheim Investigational Site Fort Worth Texas — —
1205.14.025 Boehringer Ingelheim Investigational Site Houston Texas — —
1205.14.060 Boehringer Ingelheim Investigational Site Killeen Texas — —
1205.14.002 Boehringer Ingelheim Investigational Site San Antonio Texas — —
1205.14.023 Boehringer Ingelheim Investigational Site Richmond Virginia — —
1205.14.024 Boehringer Ingelheim Investigational Site Richmond Virginia — —
1205.14.026 Boehringer Ingelheim Investigational Site Roanoke Virginia — —
1205.14.009 Boehringer Ingelheim Investigational Site Spokane Washington — —
1205.14.039 Boehringer Ingelheim Investigational Site Spokane Washington — —
1205.14.001 Boehringer Ingelheim Investigational Site Morgantown West Virginia — —

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 122 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00528996, 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 Aug 24, 2021 · Synced Oct 19, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00528996 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →