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Characterization of 24 Hour Spirometry Profiles of Inhaled BI 1744 CL and Inhaled Foradil in Patients With Chronic Obstructive Pulmonary Disease

Boehringer Ingelheim logo

Boehringer Ingelheim

Status and phase

Completed
Phase 3

Conditions

Pulmonary Disease, Chronic Obstructive

Treatments

Drug: Placebo
Drug: bi1744
Drug: BI 1744
Drug: Foradil

Study type

Interventional

Funder types

Industry

Identifiers

NCT00931385
1222.24

Details and patient eligibility

About

The study is intended to characterize the lung function profile of BI1744 in COPD patients where patients will perform pulmonary function tests at regular intervals for 24 hours at the end of a 6 week treatment period. Each patient will receive all four treatments.

Enrollment

99 patients

Sex

All

Ages

40+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients willing to participate with confirmed diagnosis of COPD
  • 40 years of age or older
  • having a 10 pack year smoking history
  • able to perform serial pulmonary function tests
  • able to use both a DPI and Respimat device

Exclusion criteria

  • Significant other disease
  • clinically relevant abnormal hematology, chemistry, or urinalysis
  • history of asthma
  • diagnosis of thyrotoxicosis
  • paroxysmal tachycardia related to beta agonists
  • history of MI within 1 year, cardiac arrhythmia, hospitalization for heart failure within 1 year
  • active tuberculosis, cystic fibrosis, clinically evident bronchiectasis
  • significant alcohol or drug use
  • pulmonary resection
  • taking oral beta adrenergics
  • taking unstable oral steroids
  • daytime oxygen
  • enrolled in rehabilitation program
  • enrolled in another study or taking investigational products
  • pregnant or nursing women, women of child bearing potential not willing to use two methods of birth control
  • those who are not willing to comply with pulmonary medication washouts

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

Double Blind

99 participants in 4 patient groups, including a placebo group

BI 1744 (Olodaterol) Low Dose
Experimental group
Description:
BI1744 Low Dose once daily
Treatment:
Drug: bi1744
BI 1744 (Olodaterol) Med Dose
Experimental group
Description:
BI 1744 Med Dose once daily
Treatment:
Drug: BI 1744
Placebo
Placebo Comparator group
Description:
Placebo once daily
Treatment:
Drug: Placebo
Foradil
Active Comparator group
Description:
Foradil 12 mcg twice daily
Treatment:
Drug: Foradil

Trial contacts and locations

11

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Data sourced from clinicaltrials.gov

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