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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 Sep 3, 2026, 2:28 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 5, 2007
Primary completion
May 4, 2009
Completion
May 4, 2009
Last update posted
Aug 23, 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 23, 2021 · Synced Sep 3, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00528996 live on ClinicalTrials.gov.

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