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Tiotropium Once Daily 18 Mcg Versus Salmeterol Twice Daily 50 Mcg on Time to First Exacerbation in COPD Patients.

Primary Purpose

Pulmonary Disease, Chronic Obstructive

Status
Completed
Phase
Phase 4
Locations
International
Study Type
Interventional
Intervention
Tiotropium bromide
Salmeterol
Placebo Salmeterol
Placebo Tiotropium
Sponsored by
Boehringer Ingelheim
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Pulmonary Disease, Chronic Obstructive

Eligibility Criteria

40 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. All patients must have a diagnosis of chronic obstructive pulmonary disease (COPD) and must meet the following criteria at Visit 1:

    Patients must have relatively stable, moderate to very severe airway obstruction with a post-bronchodilator FEV1 <=70% of predicted normal and FEV1 <=70% of FVC post-bronchodilator (i.e. 30 minutes after inhalation of 4 puffs of 100 µg salbutamol or equivalent SABA). Predicted normal values will be calculated according to ECSC.

    For Height measured in inches Males: FEV1 predicted (L) = 4.30 x (height (inches) / 39.37)-0.029 x age (yrs) - 2.49 Females:FEV1 predicted (L) = 3.95 x (height (inches) / 39.37)-0.025 x age (yrs) - 2.60 For Height measured in metres Males: FEV1 predicted (L) = 4.30 x (height (metres)) - 0.029 x age (years) - 2.49 Females: FEV1 predicted (L) = 3.95 x (height (metres)) - 0.025 x age (years) - 2.60

  2. All patients must sign an informed consent consistent with ICH-GCP guidelines prior to participation in the trial.
  3. Male or female patients 40 years of age or older.
  4. Patients with a history of at least one exacerbation within the past year requiring treatment with either antibiotics and/or systemic steroids and/or hospitalisation.
  5. Patients must be current or ex-smokers with a smoking history of >= 10 pack-years. (Patients who have never smoked cigarettes must be excluded.)
  6. Patients must be able to perform all study-related procedures including technically acceptable pulmonary function tests (PFTs).
  7. Patients must be able to inhale medication in a competent manner from the HandiHaler and a metered dose inhaler (MDI).
  8. Patients must be able to maintain records (patient daily diary card) during the study period as required in the protocol.

Exclusion Criteria:

  1. Significant diseases other than COPD. A significant disease is defined as a disease or condition which, in the opinion of the investigator, may put the patient at risk because of participation in the study or may influence either the results of the study or the patients' ability to participate in the study.
  2. Patients with a diagnosis of asthma.
  3. Patients with a life-threatening pulmonary obstruction, or a history of cystic fibrosis.
  4. Patients with known active tuberculosis.
  5. Patients with a known symptomatic prostatic hyperplasia or bladder neck obstruction. Patients with symptomatically-controlled prostatic hyperplasia on medication may be included and should continue their medication.
  6. Patients with known narrow-angle glaucoma.
  7. Patients with a history of myocardial infarction within the year prior to Visit 1.
  8. Patients with a history of hospital admission for heart failure within the year prior to Visit 1.
  9. Patients with cardiac arrhythmia requiring medical or surgical treatment.
  10. Patients with severe cardiovascular disorders.
  11. Patients with a known hypersensitivity to anticholinergic drugs, beta-adrenergics, lactose or any other component of the medication delivery system.
  12. Patients with known moderate or severe renal insufficiency (known creatinine clearance of <= 50 mL/min).
  13. Patients with untreated known hypokalaemia.
  14. Patients with untreated known thyrotoxicosis.
  15. Patients with brittle/unstable diabetes mellitus.
  16. Patients with a history of and/or active significant alcohol or drug abuse. See exclusion criterion 1.
  17. Patients who have taken an investigational drug within 30 days or six half-lives (whichever is greater) prior to Screening Visit (Visit 1).
  18. Use of systemic corticosteroid medication at unstable doses (i.e less than six weeks on stable dose) or at doses in excess of the equivalent of 10 mg prednisolone per day or 20 mg every other day.
  19. Pregnant or nursing women or women of childbearing potential not using a medically approved means of contraception (i.e oral contraceptives, intrauterine devices, diaphragm or subdermal implants e.g Norplant) for at least three months prior to, and for the duration of the trial.
  20. Previous participation (receipt of randomised treatment) in this study.
  21. Patients who are currently participating in another study.
  22. Patients with any respiratory infection or COPD exacerbation in the four weeks prior to the Screening Visit (Visit 1) or during the run-in period should be postponed. In the case of a respiratory infection or COPD exacerbation during the run-in period, the latter may be extended up to four weeks.

Sites / Locations

  • 205.389.1020 Boehringer Ingelheim Investigational Site
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Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

Tiotropium + Placebo

Salmeterol + Placebo

Arm Description

patients inhale Tiotropium 18mcg once daily via HandiHaler and Placebo MDI twice daily

patients inhale Salmeterol 50mcg twice daily via MDI and Placebo HandiHaler once daily

Outcomes

Primary Outcome Measures

First Occurrence of (Moderate or Severe) COPD Exacerbation
First occurrence analysed by Cox regression as time to first exacerbation and reported as hazard ratio. An exacerbation was defined as an increase or new onset of more than 1 symptom (cough, sputum, wheezing, dyspnoea, chest tightness), with at least 1 symptom lasting at least 3 days and requiring treatment with systemic steroids and/or antibiotics (moderate exacerbation) or hospitalisation (severe exacerbation).

Secondary Outcome Measures

COPD Exacerbations Per Patient-year Leading to Hospitalisation
An exacerbation was defined as an increase or new onset of more than 1 symptom (cough, sputum, wheezing, dyspnoea, chest tightness), with at least 1 symptom lasting at least 3 days and requiring treatment with systemic steroids and/or antibiotics (moderate exacerbation) or hospitalisation (severe exacerbation).
Number of Participants With at Least One COPD Exacerbation
An exacerbation was defined as an increase or new onset of more than 1 symptom (cough, sputum, wheezing, dyspnoea, chest tightness), with at least 1 symptom lasting at least 3 days and requiring treatment with systemic steroids and/or antibiotics (moderate exacerbation) or hospitalisation (severe exacerbation).
COPD Exacerbations Per Patient-year
First Occurrence of COPD Exacerbation Leading to Hospitalization
First occurrence analysed by Cox regression as time to first exacerbation leading to hospitalisation and reported as hazard ratio. An exacerbation was defined as an increase or new onset of more than 1 symptom (cough, sputum, wheezing, dyspnoea, chest tightness), with at least 1 symptom lasting at least 3 days and requiring treatment with systemic steroids and/or antibiotics (moderate exacerbation) or hospitalisation (severe exacerbation).
Number of Participants With at Least One COPD Exacerbation Leading to Hospitalisation
An exacerbation was defined as an increase or new onset of more than 1 symptom (cough, sputum, wheezing, dyspnoea, chest tightness), with at least 1 symptom lasting at least 3 days and requiring treatment with systemic steroids and/or antibiotics (moderate exacerbation) or hospitalisation (severe exacerbation).
Occurrence of Premature Discontinuation of Trial Medication
Occurrence analysed by Cox regression as time to premature discontinuation of trial medication and reported as hazard ratio
Number of Participants With Premature Discontinuation of Trial Medication
First Occurrence of COPD Exacerbation or Discontinuation of Trial Medication Because of Worsening of Underlying Disease, Whichever Comes First
First occurrence analysed by Cox regression as time to first exacerbation or discontinuation of trial medication because of worsening of underlying disease, whichever comes first and reported as hazard ratio. An exacerbation was defined as an increase or new onset of more than 1 symptom (cough, sputum, wheezing, dyspnoea, chest tightness), with at least 1 symptom lasting at least 3 days and requiring treatment with systemic steroids and/or antibiotics (moderate exacerbation) or hospitalisation (severe exacerbation).
First Occurrence of COPD Exacerbations Treated With Systemic Steroids
First occurrence analysed by Cox regression as time to first exacerbation treated with systemic steroids and reported as hazard ratio. An exacerbation was defined as an increase or new onset of more than 1 symptom (cough, sputum, wheezing, dyspnoea, chest tightness), with at least 1 symptom lasting at least 3 days and requiring treatment with systemic steroids and/or antibiotics (moderate exacerbation) or hospitalisation (severe exacerbation).
First Occurrence of COPD Exacerbations Treated With Antibiotics
First occurrence analysed by Cox regression as time to first exacerbation treated with antibiotics and reported as hazard ratio. An exacerbation was defined as an increase or new onset of more than 1 symptom (cough, sputum, wheezing, dyspnoea, chest tightness), with at least 1 symptom lasting at least 3 days and requiring treatment with systemic steroids and/or antibiotics (moderate exacerbation) or hospitalisation (severe exacerbation).
First Occurrence of COPD Exacerbations Treated With Systemic Steroids and Antibiotics
First occurrence analysed by Cox regression as time to first exacerbation treated with systemic steroids and antibiotics and reported as hazard ratio. An exacerbation was defined as an increase or new onset of more than 1 symptom (cough, sputum, wheezing, dyspnoea, chest tightness), with at least 1 symptom lasting at least 3 days and requiring treatment with systemic steroids and/or antibiotics (moderate exacerbation) or hospitalisation (severe exacerbation).
COPD Exacerbations Treated With Systemic Steroids Per Patient-year
An exacerbation was defined as an increase or new onset of more than 1 symptom (cough, sputum, wheezing, dyspnoea, chest tightness), with at least 1 symptom lasting at least 3 days and requiring treatment with systemic steroids and/or antibiotics (moderate exacerbation) or hospitalisation (severe exacerbation).
COPD Exacerbations Treated With Antibiotics Per Patient-year
An exacerbation was defined as an increase or new onset of more than 1 symptom (cough, sputum, wheezing, dyspnoea, chest tightness), with at least 1 symptom lasting at least 3 days and requiring treatment with systemic steroids and/or antibiotics (moderate exacerbation) or hospitalisation (severe exacerbation).
COPD Exacerbations Treated With Systemic Steroids and Antibiotics Per Patient-year
An exacerbation was defined as an increase or new onset of more than 1 symptom (cough, sputum, wheezing, dyspnoea, chest tightness), with at least 1 symptom lasting at least 3 days and requiring treatment with systemic steroids and/or antibiotics (moderate exacerbation) or hospitalisation (severe exacerbation).
Pre-dose Morning PEFR Measured by Patients at Home During the First Four Months of Randomised Treatment (Weekly Means Will be Calculated), Week 1
PEFR means peak expiratory flow rate and is measured in liter per minute
Pre-dose Morning PEFR Measured by Patients at Home During the First Four Months of Randomised Treatment (Weekly Means Will be Calculated), Week 2
PEFR means peak expiratory flow rate and is measured in liter per minute
Pre-dose Morning PEFR Measured by Patients at Home During the First Four Months of Randomised Treatment (Weekly Means Will be Calculated), Week 3
PEFR means peak expiratory flow rate and is measured in liter per minute
Pre-dose Morning PEFR Measured by Patients at Home During the First Four Months of Randomised Treatment (Weekly Means Will be Calculated), Week 4
PEFR means peak expiratory flow rate and is measured in liter per minute
Pre-dose Morning PEFR Measured by Patients at Home During the First Four Months of Randomised Treatment (Weekly Means Will be Calculated), Week 5
PEFR means peak expiratory flow rate and is measured in liter per minute
Pre-dose Morning PEFR Measured by Patients at Home During the First Four Months of Randomised Treatment (Weekly Means Will be Calculated), Week 6
PEFR means peak expiratory flow rate and is measured in liter per minute
Pre-dose Morning PEFR Measured by Patients at Home During the First Four Months of Randomised Treatment (Weekly Means Will be Calculated), Week 7
PEFR means peak expiratory flow rate and is measured in liter per minute
Pre-dose Morning PEFR Measured by Patients at Home During the First Four Months of Randomised Treatment (Weekly Means Will be Calculated), Week 8
PEFR means peak expiratory flow rate and is measured in liter per minute
Pre-dose Morning PEFR Measured by Patients at Home During the First Four Months of Randomised Treatment (Weekly Means Will be Calculated), Week 9
PEFR means peak expiratory flow rate and is measured in liter per minute
Pre-dose Morning PEFR Measured by Patients at Home During the First Four Months of Randomised Treatment (Weekly Means Will be Calculated), Week 10
PEFR means peak expiratory flow rate and is measured in liter per minute
Pre-dose Morning PEFR Measured by Patients at Home During the First Four Months of Randomised Treatment (Weekly Means Will be Calculated), Week 11
PEFR means peak expiratory flow rate and is measured in liter per minute
Pre-dose Morning PEFR Measured by Patients at Home During the First Four Months of Randomised Treatment (Weekly Means Will be Calculated), Week 12
PEFR means peak expiratory flow rate and is measured in liter per minute
Pre-dose Morning PEFR Measured by Patients at Home During the First Four Months of Randomised Treatment (Weekly Means Will be Calculated), Week 13
PEFR means peak expiratory flow rate and is measured in liter per minute
Pre-dose Morning PEFR Measured by Patients at Home During the First Four Months of Randomised Treatment (Weekly Means Will be Calculated), Week 14
PEFR means peak expiratory flow rate and is measured in liter per minute
Pre-dose Morning PEFR Measured by Patients at Home During the First Four Months of Randomised Treatment (Weekly Means Will be Calculated), Week 15
PEFR means peak expiratory flow rate and is measured in liter per minute
Pre-dose Morning PEFR Measured by Patients at Home During the First Four Months of Randomised Treatment (Weekly Means Will be Calculated), Week 16
PEFR means peak expiratory flow rate and is measured in liter per minute

Full Information

First Posted
November 22, 2007
Last Updated
November 27, 2013
Sponsor
Boehringer Ingelheim
Collaborators
Pfizer
search

1. Study Identification

Unique Protocol Identification Number
NCT00563381
Brief Title
Tiotropium Once Daily 18 Mcg Versus Salmeterol Twice Daily 50 Mcg on Time to First Exacerbation in COPD Patients.
Official Title
Effect of Inhalation of Tiotropium Once Daily 18 Mcg Versus Salmeterol Twice Daily 50 Mcg on Time to First Exacerbation in COPD Patients (a Randomised, Double-blind, Double-dummy, Parallel Group, One-year Study).
Study Type
Interventional

2. Study Status

Record Verification Date
July 2012
Overall Recruitment Status
Completed
Study Start Date
January 2008 (undefined)
Primary Completion Date
April 2010 (Actual)
Study Completion Date
undefined (undefined)

3. Sponsor/Collaborators

Name of the Sponsor
Boehringer Ingelheim
Collaborators
Pfizer

4. Oversight

5. Study Description

Brief Summary
This is a randomised, double-blind, double-dummy, multinational, multicentre, parallel group trial comparing tiotropium (18 mcg) inhalation capsule via HandiHaler and salmeterol (50 mcg) via MDI in patients with COPD. There will be a two-week run-in period followed by a 52-week randomised treatment phase. Patients who withdraw prematurely from trial medication will be encouraged to remain in the trial and participate in follow-up telephone contacts until their predicted normal exit date from the trial (i.e. 52 weeks after taking the first dose of randomised treatment). The phone calls will be made at all scheduled visits. The primary objective of this study is to compare the effect of tiotropium (18 mcg) inhalation capsule via HandiHaler with that of salmeterol (50 mcg) via MDI on COPD exacerbations. The primary endpoint is time to first COPD exacerbation during the 52 week randomised treatment period. A COPD exacerbation will be defined as a complex of respiratory events / symptoms (increase or new onset) of more than one of the following: cough, sputum, wheezing, dyspnoea or chest tightness with at least one symptom lasting at least three days requiring treatment with antibiotics and/or systemic steroids and/or hospitalisation. The onset of an exacerbation is defined as the onset of the first new or increased reported symptom. The end of the exacerbation should be recorded as defined by the investigator. Only COPD exacerbations with onset during randomised treatment will be included in the analysis.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Pulmonary Disease, Chronic Obstructive

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
Double
Allocation
Randomized
Enrollment
7376 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Tiotropium + Placebo
Arm Type
Active Comparator
Arm Description
patients inhale Tiotropium 18mcg once daily via HandiHaler and Placebo MDI twice daily
Arm Title
Salmeterol + Placebo
Arm Type
Active Comparator
Arm Description
patients inhale Salmeterol 50mcg twice daily via MDI and Placebo HandiHaler once daily
Intervention Type
Drug
Intervention Name(s)
Tiotropium bromide
Intervention Description
18 mcg/daily
Intervention Type
Drug
Intervention Name(s)
Salmeterol
Intervention Description
100 mcg/daily
Intervention Type
Drug
Intervention Name(s)
Placebo Salmeterol
Intervention Description
Placebo identical to Salmeterol device
Intervention Type
Drug
Intervention Name(s)
Placebo Tiotropium
Intervention Description
Placebo identical to Tiotropium device
Primary Outcome Measure Information:
Title
First Occurrence of (Moderate or Severe) COPD Exacerbation
Description
First occurrence analysed by Cox regression as time to first exacerbation and reported as hazard ratio. An exacerbation was defined as an increase or new onset of more than 1 symptom (cough, sputum, wheezing, dyspnoea, chest tightness), with at least 1 symptom lasting at least 3 days and requiring treatment with systemic steroids and/or antibiotics (moderate exacerbation) or hospitalisation (severe exacerbation).
Time Frame
52 weeks
Secondary Outcome Measure Information:
Title
COPD Exacerbations Per Patient-year Leading to Hospitalisation
Description
An exacerbation was defined as an increase or new onset of more than 1 symptom (cough, sputum, wheezing, dyspnoea, chest tightness), with at least 1 symptom lasting at least 3 days and requiring treatment with systemic steroids and/or antibiotics (moderate exacerbation) or hospitalisation (severe exacerbation).
Time Frame
52 weeks
Title
Number of Participants With at Least One COPD Exacerbation
Description
An exacerbation was defined as an increase or new onset of more than 1 symptom (cough, sputum, wheezing, dyspnoea, chest tightness), with at least 1 symptom lasting at least 3 days and requiring treatment with systemic steroids and/or antibiotics (moderate exacerbation) or hospitalisation (severe exacerbation).
Time Frame
52 weeks
Title
COPD Exacerbations Per Patient-year
Time Frame
52 weeks
Title
First Occurrence of COPD Exacerbation Leading to Hospitalization
Description
First occurrence analysed by Cox regression as time to first exacerbation leading to hospitalisation and reported as hazard ratio. An exacerbation was defined as an increase or new onset of more than 1 symptom (cough, sputum, wheezing, dyspnoea, chest tightness), with at least 1 symptom lasting at least 3 days and requiring treatment with systemic steroids and/or antibiotics (moderate exacerbation) or hospitalisation (severe exacerbation).
Time Frame
52 weeks
Title
Number of Participants With at Least One COPD Exacerbation Leading to Hospitalisation
Description
An exacerbation was defined as an increase or new onset of more than 1 symptom (cough, sputum, wheezing, dyspnoea, chest tightness), with at least 1 symptom lasting at least 3 days and requiring treatment with systemic steroids and/or antibiotics (moderate exacerbation) or hospitalisation (severe exacerbation).
Time Frame
52 weeks
Title
Occurrence of Premature Discontinuation of Trial Medication
Description
Occurrence analysed by Cox regression as time to premature discontinuation of trial medication and reported as hazard ratio
Time Frame
52 weeks
Title
Number of Participants With Premature Discontinuation of Trial Medication
Time Frame
52 weeks
Title
First Occurrence of COPD Exacerbation or Discontinuation of Trial Medication Because of Worsening of Underlying Disease, Whichever Comes First
Description
First occurrence analysed by Cox regression as time to first exacerbation or discontinuation of trial medication because of worsening of underlying disease, whichever comes first and reported as hazard ratio. An exacerbation was defined as an increase or new onset of more than 1 symptom (cough, sputum, wheezing, dyspnoea, chest tightness), with at least 1 symptom lasting at least 3 days and requiring treatment with systemic steroids and/or antibiotics (moderate exacerbation) or hospitalisation (severe exacerbation).
Time Frame
52 weeks
Title
First Occurrence of COPD Exacerbations Treated With Systemic Steroids
Description
First occurrence analysed by Cox regression as time to first exacerbation treated with systemic steroids and reported as hazard ratio. An exacerbation was defined as an increase or new onset of more than 1 symptom (cough, sputum, wheezing, dyspnoea, chest tightness), with at least 1 symptom lasting at least 3 days and requiring treatment with systemic steroids and/or antibiotics (moderate exacerbation) or hospitalisation (severe exacerbation).
Time Frame
52 weeks
Title
First Occurrence of COPD Exacerbations Treated With Antibiotics
Description
First occurrence analysed by Cox regression as time to first exacerbation treated with antibiotics and reported as hazard ratio. An exacerbation was defined as an increase or new onset of more than 1 symptom (cough, sputum, wheezing, dyspnoea, chest tightness), with at least 1 symptom lasting at least 3 days and requiring treatment with systemic steroids and/or antibiotics (moderate exacerbation) or hospitalisation (severe exacerbation).
Time Frame
52 weeks
Title
First Occurrence of COPD Exacerbations Treated With Systemic Steroids and Antibiotics
Description
First occurrence analysed by Cox regression as time to first exacerbation treated with systemic steroids and antibiotics and reported as hazard ratio. An exacerbation was defined as an increase or new onset of more than 1 symptom (cough, sputum, wheezing, dyspnoea, chest tightness), with at least 1 symptom lasting at least 3 days and requiring treatment with systemic steroids and/or antibiotics (moderate exacerbation) or hospitalisation (severe exacerbation).
Time Frame
52 weeks
Title
COPD Exacerbations Treated With Systemic Steroids Per Patient-year
Description
An exacerbation was defined as an increase or new onset of more than 1 symptom (cough, sputum, wheezing, dyspnoea, chest tightness), with at least 1 symptom lasting at least 3 days and requiring treatment with systemic steroids and/or antibiotics (moderate exacerbation) or hospitalisation (severe exacerbation).
Time Frame
52 weeks
Title
COPD Exacerbations Treated With Antibiotics Per Patient-year
Description
An exacerbation was defined as an increase or new onset of more than 1 symptom (cough, sputum, wheezing, dyspnoea, chest tightness), with at least 1 symptom lasting at least 3 days and requiring treatment with systemic steroids and/or antibiotics (moderate exacerbation) or hospitalisation (severe exacerbation).
Time Frame
52 weeks
Title
COPD Exacerbations Treated With Systemic Steroids and Antibiotics Per Patient-year
Description
An exacerbation was defined as an increase or new onset of more than 1 symptom (cough, sputum, wheezing, dyspnoea, chest tightness), with at least 1 symptom lasting at least 3 days and requiring treatment with systemic steroids and/or antibiotics (moderate exacerbation) or hospitalisation (severe exacerbation).
Time Frame
52 weeks
Title
Pre-dose Morning PEFR Measured by Patients at Home During the First Four Months of Randomised Treatment (Weekly Means Will be Calculated), Week 1
Description
PEFR means peak expiratory flow rate and is measured in liter per minute
Time Frame
16 weeks
Title
Pre-dose Morning PEFR Measured by Patients at Home During the First Four Months of Randomised Treatment (Weekly Means Will be Calculated), Week 2
Description
PEFR means peak expiratory flow rate and is measured in liter per minute
Time Frame
16 weeks
Title
Pre-dose Morning PEFR Measured by Patients at Home During the First Four Months of Randomised Treatment (Weekly Means Will be Calculated), Week 3
Description
PEFR means peak expiratory flow rate and is measured in liter per minute
Time Frame
16 weeks
Title
Pre-dose Morning PEFR Measured by Patients at Home During the First Four Months of Randomised Treatment (Weekly Means Will be Calculated), Week 4
Description
PEFR means peak expiratory flow rate and is measured in liter per minute
Time Frame
16 weeks
Title
Pre-dose Morning PEFR Measured by Patients at Home During the First Four Months of Randomised Treatment (Weekly Means Will be Calculated), Week 5
Description
PEFR means peak expiratory flow rate and is measured in liter per minute
Time Frame
16 weeks
Title
Pre-dose Morning PEFR Measured by Patients at Home During the First Four Months of Randomised Treatment (Weekly Means Will be Calculated), Week 6
Description
PEFR means peak expiratory flow rate and is measured in liter per minute
Time Frame
16 weeks
Title
Pre-dose Morning PEFR Measured by Patients at Home During the First Four Months of Randomised Treatment (Weekly Means Will be Calculated), Week 7
Description
PEFR means peak expiratory flow rate and is measured in liter per minute
Time Frame
16 weeks
Title
Pre-dose Morning PEFR Measured by Patients at Home During the First Four Months of Randomised Treatment (Weekly Means Will be Calculated), Week 8
Description
PEFR means peak expiratory flow rate and is measured in liter per minute
Time Frame
16 weeks
Title
Pre-dose Morning PEFR Measured by Patients at Home During the First Four Months of Randomised Treatment (Weekly Means Will be Calculated), Week 9
Description
PEFR means peak expiratory flow rate and is measured in liter per minute
Time Frame
16 weeks
Title
Pre-dose Morning PEFR Measured by Patients at Home During the First Four Months of Randomised Treatment (Weekly Means Will be Calculated), Week 10
Description
PEFR means peak expiratory flow rate and is measured in liter per minute
Time Frame
16 weeks
Title
Pre-dose Morning PEFR Measured by Patients at Home During the First Four Months of Randomised Treatment (Weekly Means Will be Calculated), Week 11
Description
PEFR means peak expiratory flow rate and is measured in liter per minute
Time Frame
16 weeks
Title
Pre-dose Morning PEFR Measured by Patients at Home During the First Four Months of Randomised Treatment (Weekly Means Will be Calculated), Week 12
Description
PEFR means peak expiratory flow rate and is measured in liter per minute
Time Frame
16 weeks
Title
Pre-dose Morning PEFR Measured by Patients at Home During the First Four Months of Randomised Treatment (Weekly Means Will be Calculated), Week 13
Description
PEFR means peak expiratory flow rate and is measured in liter per minute
Time Frame
16 weeks
Title
Pre-dose Morning PEFR Measured by Patients at Home During the First Four Months of Randomised Treatment (Weekly Means Will be Calculated), Week 14
Description
PEFR means peak expiratory flow rate and is measured in liter per minute
Time Frame
16 weeks
Title
Pre-dose Morning PEFR Measured by Patients at Home During the First Four Months of Randomised Treatment (Weekly Means Will be Calculated), Week 15
Description
PEFR means peak expiratory flow rate and is measured in liter per minute
Time Frame
16 weeks
Title
Pre-dose Morning PEFR Measured by Patients at Home During the First Four Months of Randomised Treatment (Weekly Means Will be Calculated), Week 16
Description
PEFR means peak expiratory flow rate and is measured in liter per minute
Time Frame
16 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
40 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: All patients must have a diagnosis of chronic obstructive pulmonary disease (COPD) and must meet the following criteria at Visit 1: Patients must have relatively stable, moderate to very severe airway obstruction with a post-bronchodilator FEV1 <=70% of predicted normal and FEV1 <=70% of FVC post-bronchodilator (i.e. 30 minutes after inhalation of 4 puffs of 100 µg salbutamol or equivalent SABA). Predicted normal values will be calculated according to ECSC. For Height measured in inches Males: FEV1 predicted (L) = 4.30 x (height (inches) / 39.37)-0.029 x age (yrs) - 2.49 Females:FEV1 predicted (L) = 3.95 x (height (inches) / 39.37)-0.025 x age (yrs) - 2.60 For Height measured in metres Males: FEV1 predicted (L) = 4.30 x (height (metres)) - 0.029 x age (years) - 2.49 Females: FEV1 predicted (L) = 3.95 x (height (metres)) - 0.025 x age (years) - 2.60 All patients must sign an informed consent consistent with ICH-GCP guidelines prior to participation in the trial. Male or female patients 40 years of age or older. Patients with a history of at least one exacerbation within the past year requiring treatment with either antibiotics and/or systemic steroids and/or hospitalisation. Patients must be current or ex-smokers with a smoking history of >= 10 pack-years. (Patients who have never smoked cigarettes must be excluded.) Patients must be able to perform all study-related procedures including technically acceptable pulmonary function tests (PFTs). Patients must be able to inhale medication in a competent manner from the HandiHaler and a metered dose inhaler (MDI). Patients must be able to maintain records (patient daily diary card) during the study period as required in the protocol. Exclusion Criteria: Significant diseases other than COPD. A significant disease is defined as a disease or condition which, in the opinion of the investigator, may put the patient at risk because of participation in the study or may influence either the results of the study or the patients' ability to participate in the study. Patients with a diagnosis of asthma. Patients with a life-threatening pulmonary obstruction, or a history of cystic fibrosis. Patients with known active tuberculosis. Patients with a known symptomatic prostatic hyperplasia or bladder neck obstruction. Patients with symptomatically-controlled prostatic hyperplasia on medication may be included and should continue their medication. Patients with known narrow-angle glaucoma. Patients with a history of myocardial infarction within the year prior to Visit 1. Patients with a history of hospital admission for heart failure within the year prior to Visit 1. Patients with cardiac arrhythmia requiring medical or surgical treatment. Patients with severe cardiovascular disorders. Patients with a known hypersensitivity to anticholinergic drugs, beta-adrenergics, lactose or any other component of the medication delivery system. Patients with known moderate or severe renal insufficiency (known creatinine clearance of <= 50 mL/min). Patients with untreated known hypokalaemia. Patients with untreated known thyrotoxicosis. Patients with brittle/unstable diabetes mellitus. Patients with a history of and/or active significant alcohol or drug abuse. See exclusion criterion 1. Patients who have taken an investigational drug within 30 days or six half-lives (whichever is greater) prior to Screening Visit (Visit 1). Use of systemic corticosteroid medication at unstable doses (i.e less than six weeks on stable dose) or at doses in excess of the equivalent of 10 mg prednisolone per day or 20 mg every other day. Pregnant or nursing women or women of childbearing potential not using a medically approved means of contraception (i.e oral contraceptives, intrauterine devices, diaphragm or subdermal implants e.g Norplant) for at least three months prior to, and for the duration of the trial. Previous participation (receipt of randomised treatment) in this study. Patients who are currently participating in another study. Patients with any respiratory infection or COPD exacerbation in the four weeks prior to the Screening Visit (Visit 1) or during the run-in period should be postponed. In the case of a respiratory infection or COPD exacerbation during the run-in period, the latter may be extended up to four weeks.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Boehringer Ingelheim
Organizational Affiliation
Boehringer Ingelheim
Official's Role
Study Chair
Facility Information:
Facility Name
205.389.1020 Boehringer Ingelheim Investigational Site
City
Feldbach
Country
Austria
Facility Name
205.389.1010 Boehringer Ingelheim Investigational Site
City
Feldkirch
Country
Austria
Facility Name
205.389.1011 Boehringer Ingelheim Investigational Site
City
Grimmenstein/Hochegg
Country
Austria
Facility Name
205.389.1003 Boehringer Ingelheim Investigational Site
City
Gänserndorf
Country
Austria
Facility Name
205.389.1005 Boehringer Ingelheim Investigational Site
City
Hallein
Country
Austria
Facility Name
205.389.1023 Boehringer Ingelheim Investigational Site
City
Linz
Country
Austria
Facility Name
205.389.1001 Boehringer Ingelheim Investigational Site
City
Mittersill
Country
Austria
Facility Name
205.389.1027 Boehringer Ingelheim Investigational Site
City
Salzburg
Country
Austria
Facility Name
205.389.1026 Boehringer Ingelheim Investigational Site
City
Schlüßlberg
Country
Austria
Facility Name
205.389.1016 Boehringer Ingelheim Investigational Site
City
Spittal/Drau
Country
Austria
Facility Name
205.389.1022 Boehringer Ingelheim Investigational Site
City
Steyr
Country
Austria
Facility Name
205.389.1002 Boehringer Ingelheim Investigational Site
City
Wien
Country
Austria
Facility Name
205.389.1006 Boehringer Ingelheim Investigational Site
City
Wien
Country
Austria
Facility Name
205.389.1014 Boehringer Ingelheim Investigational Site
City
Wien
Country
Austria
Facility Name
205.389.1018 Boehringer Ingelheim Investigational Site
City
Wien
Country
Austria
Facility Name
205.389.1021 Boehringer Ingelheim Investigational Site
City
Wien
Country
Austria
Facility Name
205.389.1029 Boehringer Ingelheim Investigational Site
City
Wien
Country
Austria
Facility Name
205.389.1017 Boehringer Ingelheim Investigational Site
City
Zwettl
Country
Austria
Facility Name
205.389.1120 Boehringer Ingelheim Investigational Site
City
Buizingen
Country
Belgium
Facility Name
205.389.1124 Boehringer Ingelheim Investigational Site
City
Cerexhe Heuseux
Country
Belgium
Facility Name
205.389.1116 Boehringer Ingelheim Investigational Site
City
Chenée (Liége)
Country
Belgium
Facility Name
205.389.1121 Boehringer Ingelheim Investigational Site
City
Dour
Country
Belgium
Facility Name
205.389.1113 Boehringer Ingelheim Investigational Site
City
Gembloux
Country
Belgium
Facility Name
205.389.1117 Boehringer Ingelheim Investigational Site
City
Gozée
Country
Belgium
Facility Name
205.389.1126 Boehringer Ingelheim Investigational Site
City
Hasselt
Country
Belgium
Facility Name
205.389.1129 Boehringer Ingelheim Investigational Site
City
Natoye
Country
Belgium
Facility Name
205.389.1130 Boehringer Ingelheim Investigational Site
City
Quaregnon
Country
Belgium
Facility Name
205.389.1115 Boehringer Ingelheim Investigational Site
City
Thuillies
Country
Belgium
Facility Name
205.389.1107 Boehringer Ingelheim Investigational Site
City
Wetteren
Country
Belgium
Facility Name
205.389.3911 Boehringer Ingelheim Investigational Site
City
Pazardjik
Country
Bulgaria
Facility Name
205.389.3903 Boehringer Ingelheim Investigational Site
City
Plovdiv
Country
Bulgaria
Facility Name
205.389.3915 Boehringer Ingelheim Investigational Site
City
Plovdiv
Country
Bulgaria
Facility Name
205.389.3918 Boehringer Ingelheim Investigational Site
City
Rousse
Country
Bulgaria
Facility Name
205.389.3914 Boehringer Ingelheim Investigational Site
City
Sliven
Country
Bulgaria
Facility Name
205.389.3902 Boehringer Ingelheim Investigational Site
City
Sofia
Country
Bulgaria
Facility Name
205.389.3906 Boehringer Ingelheim Investigational Site
City
Sofia
Country
Bulgaria
Facility Name
205.389.3907 Boehringer Ingelheim Investigational Site
City
Sofia
Country
Bulgaria
Facility Name
205.389.3908 Boehringer Ingelheim Investigational Site
City
Stara Zagora
Country
Bulgaria
Facility Name
205.389.3916 Boehringer Ingelheim Investigational Site
City
Troyan
Country
Bulgaria
Facility Name
205.389.3912 Boehringer Ingelheim Investigational Site
City
Varna
Country
Bulgaria
Facility Name
205.389.3901 Boehringer Ingelheim Investigational Site
City
Veliko Turnovo
Country
Bulgaria
Facility Name
205.389.1211 Boehringer Ingelheim Investigational Site
City
Benesov
Country
Czech Republic
Facility Name
205.389.1213 Boehringer Ingelheim Investigational Site
City
Beroun
Country
Czech Republic
Facility Name
205.389.1220 Boehringer Ingelheim Investigational Site
City
Beroun
Country
Czech Republic
Facility Name
205.389.1204 Boehringer Ingelheim Investigational Site
City
Brno-Kralovo Pole
Country
Czech Republic
Facility Name
205.389.1212 Boehringer Ingelheim Investigational Site
City
Cheb
Country
Czech Republic
Facility Name
205.389.1205 Boehringer Ingelheim Investigational Site
City
Havlickuv Brod
Country
Czech Republic
Facility Name
205.389.1230 Boehringer Ingelheim Investigational Site
City
Humpolec
Country
Czech Republic
Facility Name
205.389.1208 Boehringer Ingelheim Investigational Site
City
Jaromer
Country
Czech Republic
Facility Name
205.389.1219 Boehringer Ingelheim Investigational Site
City
Kyjov
Country
Czech Republic
Facility Name
205.389.1225 Boehringer Ingelheim Investigational Site
City
Liberec
Country
Czech Republic
Facility Name
205.389.1218 Boehringer Ingelheim Investigational Site
City
Litomerice
Country
Czech Republic
Facility Name
205.389.1214 Boehringer Ingelheim Investigational Site
City
Lovosice
Country
Czech Republic
Facility Name
205.389.1207 Boehringer Ingelheim Investigational Site
City
Neratovice
Country
Czech Republic
Facility Name
205.389.1222 Boehringer Ingelheim Investigational Site
City
Ostrava
Country
Czech Republic
Facility Name
205.389.1209 Boehringer Ingelheim Investigational Site
City
Plzen
Country
Czech Republic
Facility Name
205.389.1216 Boehringer Ingelheim Investigational Site
City
Plzen
Country
Czech Republic
Facility Name
205.389.1217 Boehringer Ingelheim Investigational Site
City
Praha 13
Country
Czech Republic
Facility Name
205.389.1215 Boehringer Ingelheim Investigational Site
City
Praha 17
Country
Czech Republic
Facility Name
205.389.1232 Boehringer Ingelheim Investigational Site
City
Praha 3
Country
Czech Republic
Facility Name
205.389.1229 Boehringer Ingelheim Investigational Site
City
Praha 4
Country
Czech Republic
Facility Name
205.389.1223 Boehringer Ingelheim Investigational Site
City
Praha 5
Country
Czech Republic
Facility Name
205.389.1227 Boehringer Ingelheim Investigational Site
City
Praha 5
Country
Czech Republic
Facility Name
205.389.1224 Boehringer Ingelheim Investigational Site
City
Praha 6 - Brevnov
Country
Czech Republic
Facility Name
205.389.1228 Boehringer Ingelheim Investigational Site
City
Prerov
Country
Czech Republic
Facility Name
205.389.1231 Boehringer Ingelheim Investigational Site
City
Rokycany
Country
Czech Republic
Facility Name
205.389.1221 Boehringer Ingelheim Investigational Site
City
Strakonice
Country
Czech Republic
Facility Name
205.389.1206 Boehringer Ingelheim Investigational Site
City
Tremosna
Country
Czech Republic
Facility Name
205.389.1201 Boehringer Ingelheim Investigational Site
City
Zatec
Country
Czech Republic
Facility Name
205.389.1210 Boehringer Ingelheim Investigational Site
City
Znojmo
Country
Czech Republic
Facility Name
205.389.1304 Boehringer Ingelheim Investigational Site
City
Copenhagen
Country
Denmark
Facility Name
205.389.1309 Boehringer Ingelheim Investigational Site
City
Frederikssund
Country
Denmark
Facility Name
205.389.1301 Boehringer Ingelheim Investigational Site
City
Helsingor
Country
Denmark
Facility Name
205.389.1308 Boehringer Ingelheim Investigational Site
City
Helsingør
Country
Denmark
Facility Name
205.389.1311 Boehringer Ingelheim Investigational Site
City
Holstebro
Country
Denmark
Facility Name
205.389.1302 Boehringer Ingelheim Investigational Site
City
Næstved
Country
Denmark
Facility Name
205.389.1303 Boehringer Ingelheim Investigational Site
City
Roskilde
Country
Denmark
Facility Name
205.389.1310 Boehringer Ingelheim Investigational Site
City
Skive
Country
Denmark
Facility Name
205.389.1312 Boehringer Ingelheim Investigational Site
City
Sonderborg
Country
Denmark
Facility Name
205.389.1307 Boehringer Ingelheim Investigational Site
City
Værløse
Country
Denmark
Facility Name
205.389.1402 Boehringer Ingelheim Investigational Site
City
Helsinki
Country
Finland
Facility Name
205.389.1416 Boehringer Ingelheim Investigational Site
City
Hyvinkää
Country
Finland
Facility Name
205.389.1410 Boehringer Ingelheim Investigational Site
City
Jyväskylä
Country
Finland
Facility Name
205.389.1404 Boehringer Ingelheim Investigational Site
City
Lahti
Country
Finland
Facility Name
205.389.1417 Boehringer Ingelheim Investigational Site
City
Lappeenranta
Country
Finland
Facility Name
205.389.1415 Boehringer Ingelheim Investigational Site
City
Lohja
Country
Finland
Facility Name
205.389.1411 Boehringer Ingelheim Investigational Site
City
Mikkeli
Country
Finland
Facility Name
205.389.1409 Boehringer Ingelheim Investigational Site
City
Pori
Country
Finland
Facility Name
205.389.1412 Boehringer Ingelheim Investigational Site
City
Preitilä Paimio
Country
Finland
Facility Name
205.389.1407 Boehringer Ingelheim Investigational Site
City
Turku
Country
Finland
Facility Name
205.389.1607 Boehringer Ingelheim Investigational Site
City
Bauge
Country
France
Facility Name
205.389.1525 Boehringer Ingelheim Investigational Site
City
Beauvais
Country
France
Facility Name
205.389.1523 Boehringer Ingelheim Investigational Site
City
Bethune
Country
France
Facility Name
205.389.1571 Boehringer Ingelheim Investigational Site
City
Cestas
Country
France
Facility Name
205.389.1561 Boehringer Ingelheim Investigational Site
City
Charry le Rouet
Country
France
Facility Name
205.389.1507 Boehringer Ingelheim Investigational Site
City
Cholet
Country
France
Facility Name
205.389.1606 Boehringer Ingelheim Investigational Site
City
Ecouflant
Country
France
Facility Name
205.389.1554 Boehringer Ingelheim Investigational Site
City
Ermont
Country
France
Facility Name
205.389.1597 Boehringer Ingelheim Investigational Site
City
La Barre de Monts
Country
France
Facility Name
205.389.1581 Boehringer Ingelheim Investigational Site
City
La Jubaudière
Country
France
Facility Name
205.389.1536 Boehringer Ingelheim Investigational Site
City
La Roche Sur Yon
Country
France
Facility Name
205.389.1598 Boehringer Ingelheim Investigational Site
City
La Roche sur Yon
Country
France
Facility Name
205.389.1501 Boehringer Ingelheim Investigational Site
City
Le Kremlin Bicetre
Country
France
Facility Name
205.389.1503 Boehringer Ingelheim Investigational Site
City
Le Mans Cedex
Country
France
Facility Name
205.389.1586 Boehringer Ingelheim Investigational Site
City
Le Pradet
Country
France
Facility Name
205.389.1528 Boehringer Ingelheim Investigational Site
City
Marseille
Country
France
Facility Name
205.389.1530 Boehringer Ingelheim Investigational Site
City
Marseille
Country
France
Facility Name
205.389.1558 Boehringer Ingelheim Investigational Site
City
Marseille
Country
France
Facility Name
205.389.1564 Boehringer Ingelheim Investigational Site
City
Marseille
Country
France
Facility Name
205.389.1565 Boehringer Ingelheim Investigational Site
City
Marseille
Country
France
Facility Name
205.389.1539 Boehringer Ingelheim Investigational Site
City
Montfermeil
Country
France
Facility Name
205.389.1608 Boehringer Ingelheim Investigational Site
City
Nantes
Country
France
Facility Name
205.389.1526 Boehringer Ingelheim Investigational Site
City
Nice
Country
France
Facility Name
205.389.1504 Boehringer Ingelheim Investigational Site
City
Nimes
Country
France
Facility Name
205.389.1502 Boehringer Ingelheim Investigational Site
City
Ollioules
Country
France
Facility Name
205.389.1541 Boehringer Ingelheim Investigational Site
City
Orleans
Country
France
Facility Name
205.389.1527 Boehringer Ingelheim Investigational Site
City
Perpignan
Country
France
Facility Name
205.389.1532 Boehringer Ingelheim Investigational Site
City
PIERRE BENITE cédex
Country
France
Facility Name
205.389.1553 Boehringer Ingelheim Investigational Site
City
Rennes cedex 9
Country
France
Facility Name
205.389.1555 Boehringer Ingelheim Investigational Site
City
Saint Dié des Vosges
Country
France
Facility Name
205.389.1575 Boehringer Ingelheim Investigational Site
City
Saint Germain du Puch
Country
France
Facility Name
205.389.1547 Boehringer Ingelheim Investigational Site
City
Saint Laurent du Var
Country
France
Facility Name
205.389.1572 Boehringer Ingelheim Investigational Site
City
Saint Laurent
Country
France
Facility Name
205.389.1567 Boehringer Ingelheim Investigational Site
City
Saint Orens de Cameville
Country
France
Facility Name
205.389.1577 Boehringer Ingelheim Investigational Site
City
Saint Pierre Montlimard
Country
France
Facility Name
205.389.1531 Boehringer Ingelheim Investigational Site
City
Saint Quentin
Country
France
Facility Name
205.389.1569 Boehringer Ingelheim Investigational Site
City
Seysses
Country
France
Facility Name
205.389.1514 Boehringer Ingelheim Investigational Site
City
St-Etienne
Country
France
Facility Name
205.389.1510 Boehringer Ingelheim Investigational Site
City
Strasbourg
Country
France
Facility Name
205.389.1522 Boehringer Ingelheim Investigational Site
City
Strasbourg
Country
France
Facility Name
205.389.1520 Boehringer Ingelheim Investigational Site
City
Sélestat
Country
France
Facility Name
205.389.1512 Boehringer Ingelheim Investigational Site
City
Toulon
Country
France
Facility Name
205.389.1515 Boehringer Ingelheim Investigational Site
City
Toulon
Country
France
Facility Name
205.389.1519 Boehringer Ingelheim Investigational Site
City
Toulon
Country
France
Facility Name
205.389.1588 Boehringer Ingelheim Investigational Site
City
Toulon
Country
France
Facility Name
205.389.1589 Boehringer Ingelheim Investigational Site
City
Toulon
Country
France
Facility Name
205.389.1590 Boehringer Ingelheim Investigational Site
City
Toulon
Country
France
Facility Name
205.389.1595 Boehringer Ingelheim Investigational Site
City
Toulon
Country
France
Facility Name
205.389.1542 Boehringer Ingelheim Investigational Site
City
Toulouse
Country
France
Facility Name
205.389.1574 Boehringer Ingelheim Investigational Site
City
Villenave D'ornon
Country
France
Facility Name
205.389.1741 Boehringer Ingelheim Investigational Site
City
Aachen
Country
Germany
Facility Name
205.389.1857 Boehringer Ingelheim Investigational Site
City
Aalen
Country
Germany
Facility Name
205.389.1934 Boehringer Ingelheim Investigational Site
City
Auerbach
Country
Germany
Facility Name
205.389.1868 Boehringer Ingelheim Investigational Site
City
Augsburg
Country
Germany
Facility Name
205.389.1887 Boehringer Ingelheim Investigational Site
City
Augsburg
Country
Germany
Facility Name
205.389.1707 Boehringer Ingelheim Investigational Site
City
Bad Lippspringe
Country
Germany
Facility Name
205.389.1722 Boehringer Ingelheim Investigational Site
City
Bad Pymont
Country
Germany
Facility Name
205.389.1850 Boehringer Ingelheim Investigational Site
City
Bad Wörishofen
Country
Germany
Facility Name
205.389.1765 Boehringer Ingelheim Investigational Site
City
Bahrdorf
Country
Germany
Facility Name
205.389.1792 Boehringer Ingelheim Investigational Site
City
Beckum
Country
Germany
Facility Name
205.389.1801 Boehringer Ingelheim Investigational Site
City
Bensheim
Country
Germany
Facility Name
205.389.1946 Boehringer Ingelheim Investigational Site
City
Bensheim
Country
Germany
Facility Name
205.389.1824 Boehringer Ingelheim Investigational Site
City
Bergisch Gladbach
Country
Germany
Facility Name
205.389.1709 Boehringer Ingelheim Investigational Site
City
Bergkamen
Country
Germany
Facility Name
205.389.1750 Boehringer Ingelheim Investigational Site
City
Berkatal-Frankershausen
Country
Germany
Facility Name
205.389.1701 Boehringer Ingelheim Investigational Site
City
Berlin
Country
Germany
Facility Name
205.389.1743 Boehringer Ingelheim Investigational Site
City
Berlin
Country
Germany
Facility Name
205.389.1769 Boehringer Ingelheim Investigational Site
City
Berlin
Country
Germany
Facility Name
205.389.1789 Boehringer Ingelheim Investigational Site
City
Berlin
Country
Germany
Facility Name
205.389.1790 Boehringer Ingelheim Investigational Site
City
Berlin
Country
Germany
Facility Name
205.389.1847 Boehringer Ingelheim Investigational Site
City
Berlin
Country
Germany
Facility Name
205.389.1855 Boehringer Ingelheim Investigational Site
City
Berlin
Country
Germany
Facility Name
205.389.1861 Boehringer Ingelheim Investigational Site
City
Berlin
Country
Germany
Facility Name
205.389.1862 Boehringer Ingelheim Investigational Site
City
Berlin
Country
Germany
Facility Name
205.389.1867 Boehringer Ingelheim Investigational Site
City
Berlin
Country
Germany
Facility Name
205.389.1903 Boehringer Ingelheim Investigational Site
City
Berlin
Country
Germany
Facility Name
205.389.1931 Boehringer Ingelheim Investigational Site
City
Berlin
Country
Germany
Facility Name
205.389.1932 Boehringer Ingelheim Investigational Site
City
Berlin
Country
Germany
Facility Name
205.389.1937 Boehringer Ingelheim Investigational Site
City
Berlin
Country
Germany
Facility Name
205.389.1960 Boehringer Ingelheim Investigational Site
City
Berlin
Country
Germany
Facility Name
205.389.1969 Boehringer Ingelheim Investigational Site
City
Berlin
Country
Germany
Facility Name
205.389.1981 Boehringer Ingelheim Investigational Site
City
Berlin
Country
Germany
Facility Name
205.389.1983 Boehringer Ingelheim Investigational Site
City
Berlin
Country
Germany
Facility Name
205.389.1984 Boehringer Ingelheim Investigational Site
City
Berlin
Country
Germany
Facility Name
205.389.1747 Boehringer Ingelheim Investigational Site
City
Bocholt
Country
Germany
Facility Name
205.389.1808 Boehringer Ingelheim Investigational Site
City
Bochum
Country
Germany
Facility Name
205.389.1811 Boehringer Ingelheim Investigational Site
City
Bochum
Country
Germany
Facility Name
205.389.1828 Boehringer Ingelheim Investigational Site
City
Bonn
Country
Germany
Facility Name
205.389.1870 Boehringer Ingelheim Investigational Site
City
Bonn
Country
Germany
Facility Name
205.389.1705 Boehringer Ingelheim Investigational Site
City
Borna
Country
Germany
Facility Name
205.389.1809 Boehringer Ingelheim Investigational Site
City
Brandenburg/Havel
Country
Germany
Facility Name
205.389.1859 Boehringer Ingelheim Investigational Site
City
Bruchsal
Country
Germany
Facility Name
205.389.1734 Boehringer Ingelheim Investigational Site
City
Camburg
Country
Germany
Facility Name
205.389.1923 Boehringer Ingelheim Investigational Site
City
Celle
Country
Germany
Facility Name
205.389.1901 Boehringer Ingelheim Investigational Site
City
Coswig
Country
Germany
Facility Name
205.389.1891 Boehringer Ingelheim Investigational Site
City
Cottbus
Country
Germany
Facility Name
205.389.1858 Boehringer Ingelheim Investigational Site
City
Deggendorf
Country
Germany
Facility Name
205.389.1784 Boehringer Ingelheim Investigational Site
City
Donaueschingen
Country
Germany
Facility Name
205.389.1713 Boehringer Ingelheim Investigational Site
City
Dortmund
Country
Germany
Facility Name
205.389.1706 Boehringer Ingelheim Investigational Site
City
Dresden
Country
Germany
Facility Name
205.389.1967 Boehringer Ingelheim Investigational Site
City
Düren
Country
Germany
Facility Name
205.389.1814 Boehringer Ingelheim Investigational Site
City
Engelskirchen
Country
Germany
Facility Name
205.389.1773 Boehringer Ingelheim Investigational Site
City
Ense
Country
Germany
Facility Name
205.389.1727 Boehringer Ingelheim Investigational Site
City
Eppelborn-Bubach
Country
Germany
Facility Name
205.389.1864 Boehringer Ingelheim Investigational Site
City
Erfurt
Country
Germany
Facility Name
205.389.1940 Boehringer Ingelheim Investigational Site
City
Erlangen
Country
Germany
Facility Name
205.389.1900 Boehringer Ingelheim Investigational Site
City
Eschwege
Country
Germany
Facility Name
205.389.1758 Boehringer Ingelheim Investigational Site
City
Essen
Country
Germany
Facility Name
205.389.1975 Boehringer Ingelheim Investigational Site
City
Essen
Country
Germany
Facility Name
205.389.1982 Boehringer Ingelheim Investigational Site
City
Essen
Country
Germany
Facility Name
205.389.1724 Boehringer Ingelheim Investigational Site
City
Ettlingen
Country
Germany
Facility Name
205.389.1806 Boehringer Ingelheim Investigational Site
City
Feldkirchen-Westerham
Country
Germany
Facility Name
205.389.1976 Boehringer Ingelheim Investigational Site
City
Forchheim
Country
Germany
Facility Name
205.389.1795 Boehringer Ingelheim Investigational Site
City
Frankenberg
Country
Germany
Facility Name
205.389.1905 Boehringer Ingelheim Investigational Site
City
Frankfurt/Main
Country
Germany
Facility Name
205.389.1752 Boehringer Ingelheim Investigational Site
City
Fuldatal-Ihringshausen
Country
Germany
Facility Name
205.389.1943 Boehringer Ingelheim Investigational Site
City
Föhren
Country
Germany
Facility Name
205.389.1971 Boehringer Ingelheim Investigational Site
City
Fürth
Country
Germany
Facility Name
205.389.1766 Boehringer Ingelheim Investigational Site
City
Gars
Country
Germany
Facility Name
205.389.1977 Boehringer Ingelheim Investigational Site
City
Gelsenkirchen
Country
Germany
Facility Name
205.389.1744 Boehringer Ingelheim Investigational Site
City
Georgensgmünd
Country
Germany
Facility Name
205.389.1875 Boehringer Ingelheim Investigational Site
City
Gießen
Country
Germany
Facility Name
205.389.1836 Boehringer Ingelheim Investigational Site
City
Gifhorn
Country
Germany
Facility Name
205.389.1914 Boehringer Ingelheim Investigational Site
City
Goch
Country
Germany
Facility Name
205.389.1886 Boehringer Ingelheim Investigational Site
City
Greiz
Country
Germany
Facility Name
205.389.1768 Boehringer Ingelheim Investigational Site
City
Grünberg
Country
Germany
Facility Name
205.389.1751 Boehringer Ingelheim Investigational Site
City
Göttingen
Country
Germany
Facility Name
205.389.1831 Boehringer Ingelheim Investigational Site
City
Hagen
Country
Germany
Facility Name
205.389.1827 Boehringer Ingelheim Investigational Site
City
Halle
Country
Germany
Facility Name
205.389.1917 Boehringer Ingelheim Investigational Site
City
Hamburg
Country
Germany
Facility Name
205.389.1924 Boehringer Ingelheim Investigational Site
City
Hamburg
Country
Germany
Facility Name
205.389.1925 Boehringer Ingelheim Investigational Site
City
Hamburg
Country
Germany
Facility Name
205.389.1980 Boehringer Ingelheim Investigational Site
City
Hamburg
Country
Germany
Facility Name
205.389.1716 Boehringer Ingelheim Investigational Site
City
Hammah
Country
Germany
Facility Name
205.389.1702 Boehringer Ingelheim Investigational Site
City
Hammelburg
Country
Germany
Facility Name
205.389.1802 Boehringer Ingelheim Investigational Site
City
Hannover
Country
Germany
Facility Name
205.389.1712 Boehringer Ingelheim Investigational Site
City
Harsewinkel
Country
Germany
Facility Name
205.389.1738 Boehringer Ingelheim Investigational Site
City
Hauzenberg
Country
Germany
Facility Name
205.389.1860 Boehringer Ingelheim Investigational Site
City
Hemmingen
Country
Germany
Facility Name
205.389.1949 Boehringer Ingelheim Investigational Site
City
Höchstädt
Country
Germany
Facility Name
205.389.1726 Boehringer Ingelheim Investigational Site
City
Ingelheim
Country
Germany
Facility Name
205.389.1873 Boehringer Ingelheim Investigational Site
City
Karlsruhe
Country
Germany
Facility Name
205.389.1838 Boehringer Ingelheim Investigational Site
City
Kaufbeuren
Country
Germany
Facility Name
205.389.1839 Boehringer Ingelheim Investigational Site
City
Koblenz
Country
Germany
Facility Name
205.389.1881 Boehringer Ingelheim Investigational Site
City
Krefeld
Country
Germany
Facility Name
205.389.1786 Boehringer Ingelheim Investigational Site
City
Krumpa
Country
Germany
Facility Name
205.389.1704 Boehringer Ingelheim Investigational Site
City
Käbschütztal-Krögis
Country
Germany
Facility Name
205.389.1892 Boehringer Ingelheim Investigational Site
City
Köln
Country
Germany
Facility Name
205.389.1974 Boehringer Ingelheim Investigational Site
City
Köln
Country
Germany
Facility Name
205.389.1813 Boehringer Ingelheim Investigational Site
City
Köthen
Country
Germany
Facility Name
205.389.1902 Boehringer Ingelheim Investigational Site
City
Landsberg
Country
Germany
Facility Name
205.389.1837 Boehringer Ingelheim Investigational Site
City
Leipzig
Country
Germany
Facility Name
205.389.1841 Boehringer Ingelheim Investigational Site
City
Leipzig
Country
Germany
Facility Name
205.389.1894 Boehringer Ingelheim Investigational Site
City
Leipzig
Country
Germany
Facility Name
205.389.1908 Boehringer Ingelheim Investigational Site
City
Leipzig
Country
Germany
Facility Name
205.389.1874 Boehringer Ingelheim Investigational Site
City
Leonberg
Country
Germany
Facility Name
205.389.1955 Boehringer Ingelheim Investigational Site
City
Limburg
Country
Germany
Facility Name
205.389.1904 Boehringer Ingelheim Investigational Site
City
Lorch
Country
Germany
Facility Name
205.389.1877 Boehringer Ingelheim Investigational Site
City
Lübeck
Country
Germany
Facility Name
205.389.1823 Boehringer Ingelheim Investigational Site
City
Lützen
Country
Germany
Facility Name
205.389.1879 Boehringer Ingelheim Investigational Site
City
Magdeburg
Country
Germany
Facility Name
205.389.1840 Boehringer Ingelheim Investigational Site
City
Mannheim
Country
Germany
Facility Name
205.389.1978 Boehringer Ingelheim Investigational Site
City
Mannheim
Country
Germany
Facility Name
205.389.1866 Boehringer Ingelheim Investigational Site
City
Marburg
Country
Germany
Facility Name
205.389.1871 Boehringer Ingelheim Investigational Site
City
Marburg
Country
Germany
Facility Name
205.389.1926 Boehringer Ingelheim Investigational Site
City
Marburg
Country
Germany
Facility Name
205.389.1776 Boehringer Ingelheim Investigational Site
City
Marl
Country
Germany
Facility Name
205.389.1779 Boehringer Ingelheim Investigational Site
City
Merrbusch
Country
Germany
Facility Name
205.389.1799 Boehringer Ingelheim Investigational Site
City
München
Country
Germany
Facility Name
205.389.1815 Boehringer Ingelheim Investigational Site
City
München
Country
Germany
Facility Name
205.389.1817 Boehringer Ingelheim Investigational Site
City
München
Country
Germany
Facility Name
205.389.1843 Boehringer Ingelheim Investigational Site
City
München
Country
Germany
Facility Name
205.389.1952 Boehringer Ingelheim Investigational Site
City
Neubrandenburg
Country
Germany
Facility Name
205.389.1948 Boehringer Ingelheim Investigational Site
City
Neuss
Country
Germany
Facility Name
205.389.1958 Boehringer Ingelheim Investigational Site
City
Neuwied
Country
Germany
Facility Name
205.389.1805 Boehringer Ingelheim Investigational Site
City
Neuötting
Country
Germany
Facility Name
205.389.1830 Boehringer Ingelheim Investigational Site
City
Niesky
Country
Germany
Facility Name
205.389.1711 Boehringer Ingelheim Investigational Site
City
Nussbach
Country
Germany
Facility Name
205.389.1781 Boehringer Ingelheim Investigational Site
City
Oberdorla
Country
Germany
Facility Name
205.389.1753 Boehringer Ingelheim Investigational Site
City
Paderborn
Country
Germany
Facility Name
205.389.1810 Boehringer Ingelheim Investigational Site
City
Paderborn
Country
Germany
Facility Name
205.389.1854 Boehringer Ingelheim Investigational Site
City
Paderborn
Country
Germany
Facility Name
205.389.1756 Boehringer Ingelheim Investigational Site
City
Pirmasens
Country
Germany
Facility Name
205.389.1794 Boehringer Ingelheim Investigational Site
City
Potsdam
Country
Germany
Facility Name
205.389.1899 Boehringer Ingelheim Investigational Site
City
Potsdam
Country
Germany
Facility Name
205.389.1842 Boehringer Ingelheim Investigational Site
City
Radebeul
Country
Germany
Facility Name
205.389.1897 Boehringer Ingelheim Investigational Site
City
Rathenow
Country
Germany
Facility Name
205.389.1950 Boehringer Ingelheim Investigational Site
City
Raubach
Country
Germany
Facility Name
205.389.1783 Boehringer Ingelheim Investigational Site
City
Riesa
Country
Germany
Facility Name
205.389.1826 Boehringer Ingelheim Investigational Site
City
Riesa
Country
Germany
Facility Name
205.389.1742 Boehringer Ingelheim Investigational Site
City
Rostock
Country
Germany
Facility Name
205.389.1816 Boehringer Ingelheim Investigational Site
City
Rüdersdorf
Country
Germany
Facility Name
205.389.1883 Boehringer Ingelheim Investigational Site
City
Rüsselsheim
Country
Germany
Facility Name
205.389.1878 Boehringer Ingelheim Investigational Site
City
Saarlouis
Country
Germany
Facility Name
205.389.1833 Boehringer Ingelheim Investigational Site
City
Schmallenberg-Grafschaft
Country
Germany
Facility Name
205.389.1973 Boehringer Ingelheim Investigational Site
City
Schmölln
Country
Germany
Facility Name
205.389.1979 Boehringer Ingelheim Investigational Site
City
Schwetzingen
Country
Germany
Facility Name
205.389.1856 Boehringer Ingelheim Investigational Site
City
Simmern
Country
Germany
Facility Name
205.389.1918 Boehringer Ingelheim Investigational Site
City
Solingen
Country
Germany
Facility Name
205.389.1822 Boehringer Ingelheim Investigational Site
City
Steinfurt
Country
Germany
Facility Name
205.389.1728 Boehringer Ingelheim Investigational Site
City
Sulzbach
Country
Germany
Facility Name
205.389.1717 Boehringer Ingelheim Investigational Site
City
Templin
Country
Germany
Facility Name
205.389.1882 Boehringer Ingelheim Investigational Site
City
Treuenbrietzen
Country
Germany
Facility Name
205.389.1745 Boehringer Ingelheim Investigational Site
City
Wallerfing
Country
Germany
Facility Name
205.389.1800 Boehringer Ingelheim Investigational Site
City
Wardenburg
Country
Germany
Facility Name
205.389.1885 Boehringer Ingelheim Investigational Site
City
Weißenhorn
Country
Germany
Facility Name
205.389.1927 Boehringer Ingelheim Investigational Site
City
Westerstede
Country
Germany
Facility Name
205.389.1825 Boehringer Ingelheim Investigational Site
City
Weyhe
Country
Germany
Facility Name
205.389.1863 Boehringer Ingelheim Investigational Site
City
Wiesbaden
Country
Germany
Facility Name
205.389.1968 Boehringer Ingelheim Investigational Site
City
Wilhelmshaven
Country
Germany
Facility Name
205.389.1807 Boehringer Ingelheim Investigational Site
City
Wilster
Country
Germany
Facility Name
205.389.1754 Boehringer Ingelheim Investigational Site
City
Wolfsburg
Country
Germany
Facility Name
205.389.1919 Boehringer Ingelheim Investigational Site
City
Wuppertal
Country
Germany
Facility Name
205.389.1898 Boehringer Ingelheim Investigational Site
City
Zerbst
Country
Germany
Facility Name
205.389.2001 Boehringer Ingelheim Investigational Site
City
Budapest
Country
Hungary
Facility Name
205.389.2005 Boehringer Ingelheim Investigational Site
City
Budapest
Country
Hungary
Facility Name
205.389.2006 Boehringer Ingelheim Investigational Site
City
Budapest
Country
Hungary
Facility Name
205.389.2009 Boehringer Ingelheim Investigational Site
City
Budapest
Country
Hungary
Facility Name
205.389.2016 Boehringer Ingelheim Investigational Site
City
Budapest
Country
Hungary
Facility Name
205.389.2018 Boehringer Ingelheim Investigational Site
City
Budapest
Country
Hungary
Facility Name
205.389.2027 Boehringer Ingelheim Investigational Site
City
Budapest
Country
Hungary
Facility Name
205.389.2007 Boehringer Ingelheim Investigational Site
City
Debrecen
Country
Hungary
Facility Name
205.389.2035 Boehringer Ingelheim Investigational Site
City
Deszk
Country
Hungary
Facility Name
205.389.2015 Boehringer Ingelheim Investigational Site
City
Dunaújváros
Country
Hungary
Facility Name
205.389.2011 Boehringer Ingelheim Investigational Site
City
Füzesabony
Country
Hungary
Facility Name
205.389.2013 Boehringer Ingelheim Investigational Site
City
Gyor
Country
Hungary
Facility Name
205.389.2028 Boehringer Ingelheim Investigational Site
City
Gyula
Country
Hungary
Facility Name
205.389.2014 Boehringer Ingelheim Investigational Site
City
Jászberény
Country
Hungary
Facility Name
205.389.2021 Boehringer Ingelheim Investigational Site
City
Kecskemét
Country
Hungary
Facility Name
205.389.2025 Boehringer Ingelheim Investigational Site
City
Komárom
Country
Hungary
Facility Name
205.389.2024 Boehringer Ingelheim Investigational Site
City
Mosdós
Country
Hungary
Facility Name
205.389.2026 Boehringer Ingelheim Investigational Site
City
Mosonmagyaróvár
Country
Hungary
Facility Name
205.389.2031 Boehringer Ingelheim Investigational Site
City
Nyíregyháza
Country
Hungary
Facility Name
205.389.2002 Boehringer Ingelheim Investigational Site
City
Pécs
Country
Hungary
Facility Name
205.389.2017 Boehringer Ingelheim Investigational Site
City
Ráckeve
Country
Hungary
Facility Name
205.389.2003 Boehringer Ingelheim Investigational Site
City
Siófok
Country
Hungary
Facility Name
205.389.2010 Boehringer Ingelheim Investigational Site
City
Szarvas
Country
Hungary
Facility Name
205.389.2019 Boehringer Ingelheim Investigational Site
City
Szentendre
Country
Hungary
Facility Name
205.389.2022 Boehringer Ingelheim Investigational Site
City
Százhalombatta
Country
Hungary
Facility Name
205.389.2030 Boehringer Ingelheim Investigational Site
City
Tatabánya
Country
Hungary
Facility Name
205.389.2029 Boehringer Ingelheim Investigational Site
City
Törökbálint
Country
Hungary
Facility Name
205.389.2020 Boehringer Ingelheim Investigational Site
City
Veszprém
Country
Hungary
Facility Name
205.389.2008 Boehringer Ingelheim Investigational Site
City
Érd
Country
Hungary
Facility Name
205.389.2101 Boehringer Ingelheim Investigational Site
City
Afula
Country
Israel
Facility Name
205.389.2110 Boehringer Ingelheim Investigational Site
City
Ashkelon
Country
Israel
Facility Name
205.389.2106 Boehringer Ingelheim Investigational Site
City
Be'er-Sheva
Country
Israel
Facility Name
205.389.2112 Boehringer Ingelheim Investigational Site
City
Hadera
Country
Israel
Facility Name
205.389.2107 Boehringer Ingelheim Investigational Site
City
Haifa
Country
Israel
Facility Name
205.389.2111 Boehringer Ingelheim Investigational Site
City
Haifa
Country
Israel
Facility Name
205.389.2108 Boehringer Ingelheim Investigational Site
City
Holon
Country
Israel
Facility Name
205.389.2104 Boehringer Ingelheim Investigational Site
City
Jerusalem
Country
Israel
Facility Name
205.389.2114 Boehringer Ingelheim Investigational Site
City
Jerusalem
Country
Israel
Facility Name
205.389.2116 Boehringer Ingelheim Investigational Site
City
Nahariya
Country
Israel
Facility Name
205.389.2102 Boehringer Ingelheim Investigational Site
City
Petah Tiqwa
Country
Israel
Facility Name
205.389.2105 Boehringer Ingelheim Investigational Site
City
Rehovot
Country
Israel
Facility Name
205.389.2103 Boehringer Ingelheim Investigational Site
City
Tel Hashomer
Country
Israel
Facility Name
205.389.2117 Boehringer Ingelheim Investigational Site
City
Zerifin
Country
Israel
Facility Name
205.389.2211 Boehringer Ingelheim Investigational Site
City
Brescia
Country
Italy
Facility Name
205.389.2206 Boehringer Ingelheim Investigational Site
City
Cagliari
Country
Italy
Facility Name
205.389.2223 Boehringer Ingelheim Investigational Site
City
Catania
Country
Italy
Facility Name
205.389.2209 Boehringer Ingelheim Investigational Site
City
Ferrara
Country
Italy
Facility Name
205.389.2214 Boehringer Ingelheim Investigational Site
City
Genova
Country
Italy
Facility Name
205.389.2215 Boehringer Ingelheim Investigational Site
City
Lecco
Country
Italy
Facility Name
205.389.2221 Boehringer Ingelheim Investigational Site
City
Milano
Country
Italy
Facility Name
205.389.2226 Boehringer Ingelheim Investigational Site
City
Milano
Country
Italy
Facility Name
205.389.2224 Boehringer Ingelheim Investigational Site
City
Modena
Country
Italy
Facility Name
205.389.2203 Boehringer Ingelheim Investigational Site
City
Montescano (PV)
Country
Italy
Facility Name
205.389.2230 Boehringer Ingelheim Investigational Site
City
Napoli
Country
Italy
Facility Name
205.389.2201 Boehringer Ingelheim Investigational Site
City
Novara
Country
Italy
Facility Name
205.389.2229 Boehringer Ingelheim Investigational Site
City
Pavia
Country
Italy
Facility Name
205.389.2227 Boehringer Ingelheim Investigational Site
City
Pisa
Country
Italy
Facility Name
205.389.2205 Boehringer Ingelheim Investigational Site
City
Roma
Country
Italy
Facility Name
205.389.2228 Boehringer Ingelheim Investigational Site
City
Roma
Country
Italy
Facility Name
205.389.2210 Boehringer Ingelheim Investigational Site
City
Sassari
Country
Italy
Facility Name
205.389.2232 Boehringer Ingelheim Investigational Site
City
Treviso
Country
Italy
Facility Name
205.389.2315 Boehringer Ingelheim Investigational Site
City
Balvi
Country
Latvia
Facility Name
205.389.2305 Boehringer Ingelheim Investigational Site
City
Daugavpils
Country
Latvia
Facility Name
205.389.2313 Boehringer Ingelheim Investigational Site
City
Jelgava
Country
Latvia
Facility Name
205.389.2311 Boehringer Ingelheim Investigational Site
City
Kraslava
Country
Latvia
Facility Name
205.389.2312 Boehringer Ingelheim Investigational Site
City
Kuldiga
Country
Latvia
Facility Name
205.389.2301 Boehringer Ingelheim Investigational Site
City
Riga
Country
Latvia
Facility Name
205.389.2303 Boehringer Ingelheim Investigational Site
City
Riga
Country
Latvia
Facility Name
205.389.2307 Boehringer Ingelheim Investigational Site
City
Riga
Country
Latvia
Facility Name
205.389.2310 Boehringer Ingelheim Investigational Site
City
Riga
Country
Latvia
Facility Name
205.389.2306 Boehringer Ingelheim Investigational Site
City
Talsi
Country
Latvia
Facility Name
205.389.2314 Boehringer Ingelheim Investigational Site
City
Tukums
Country
Latvia
Facility Name
205.389.2304 Boehringer Ingelheim Investigational Site
City
Valmiera
Country
Latvia
Facility Name
205.389.2302 Boehringer Ingelheim Investigational Site
City
Ventspils
Country
Latvia
Facility Name
205.389.2401 Boehringer Ingelheim Investigational Site
City
Alytus
Country
Lithuania
Facility Name
205.389.2402 Boehringer Ingelheim Investigational Site
City
Kaunas
Country
Lithuania
Facility Name
205.389.2403 Boehringer Ingelheim Investigational Site
City
Kaunas
Country
Lithuania
Facility Name
205.389.2404 Boehringer Ingelheim Investigational Site
City
Kaunas
Country
Lithuania
Facility Name
205.389.2406 Boehringer Ingelheim Investigational Site
City
Kaunas
Country
Lithuania
Facility Name
205.389.2409 Boehringer Ingelheim Investigational Site
City
Kaunas
Country
Lithuania
Facility Name
205.389.2407 Boehringer Ingelheim Investigational Site
City
Klaipeda
Country
Lithuania
Facility Name
205.389.2411 Boehringer Ingelheim Investigational Site
City
Klaipeda
Country
Lithuania
Facility Name
205.389.2408 Boehringer Ingelheim Investigational Site
City
Siauliai
Country
Lithuania
Facility Name
205.389.2410 Boehringer Ingelheim Investigational Site
City
Utena
Country
Lithuania
Facility Name
205.389.2405 Boehringer Ingelheim Investigational Site
City
Vilnius
Country
Lithuania
Facility Name
205.389.2412 Boehringer Ingelheim Investigational Site
City
Vilnius
Country
Lithuania
Facility Name
205.389.2413 Boehringer Ingelheim Investigational Site
City
Vilnius
Country
Lithuania
Facility Name
205.389.2414 Boehringer Ingelheim Investigational Site
City
Vilnius
Country
Lithuania
Facility Name
205.389.2504 Boehringer Ingelheim Investigational Site
City
Rotterdam
Country
Netherlands
Facility Name
205.389.2508 Boehringer Ingelheim Investigational Site
City
te Leiderdrop
Country
Netherlands
Facility Name
205.389.2510 Boehringer Ingelheim Investigational Site
City
Velp
Country
Netherlands
Facility Name
205.389.2511 Boehringer Ingelheim Investigational Site
City
Zoetermeer
Country
Netherlands
Facility Name
205.389.2614 Boehringer Ingelheim Investigational Site
City
Alesund
Country
Norway
Facility Name
205.389.2604 Boehringer Ingelheim Investigational Site
City
Bekkestua
Country
Norway
Facility Name
205.389.2601 Boehringer Ingelheim Investigational Site
City
Elverum
Country
Norway
Facility Name
205.389.2611 Boehringer Ingelheim Investigational Site
City
Follebu
Country
Norway
Facility Name
205.389.2602 Boehringer Ingelheim Investigational Site
City
Hamar
Country
Norway
Facility Name
205.389.2610 Boehringer Ingelheim Investigational Site
City
Harstad
Country
Norway
Facility Name
205.389.2613 Boehringer Ingelheim Investigational Site
City
Harstad
Country
Norway
Facility Name
205.389.2609 Boehringer Ingelheim Investigational Site
City
Hønefoss
Country
Norway
Facility Name
205.389.2608 Boehringer Ingelheim Investigational Site
City
Lørenskog
Country
Norway
Facility Name
205.389.2605 Boehringer Ingelheim Investigational Site
City
Oslo
Country
Norway
Facility Name
205.389.2612 Boehringer Ingelheim Investigational Site
City
Oslo
Country
Norway
Facility Name
205.389.2616 Boehringer Ingelheim Investigational Site
City
Stavanger
Country
Norway
Facility Name
205.389.2708 Boehringer Ingelheim Investigational Site
City
Bialystok
Country
Poland
Facility Name
205.389.2744 Boehringer Ingelheim Investigational Site
City
Bialystok
Country
Poland
Facility Name
205.389.2762 Boehringer Ingelheim Investigational Site
City
Bialystok
Country
Poland
Facility Name
205.389.2765 Boehringer Ingelheim Investigational Site
City
Bialystok
Country
Poland
Facility Name
205.389.2778 Boehringer Ingelheim Investigational Site
City
Bielsko-Biala
Country
Poland
Facility Name
205.389.2706 Boehringer Ingelheim Investigational Site
City
Bienkowka 410
Country
Poland
Facility Name
205.389.2750 Boehringer Ingelheim Investigational Site
City
Brzesko
Country
Poland
Facility Name
205.389.2758 Boehringer Ingelheim Investigational Site
City
Bydgoszcz
Country
Poland
Facility Name
205.389.2773 Boehringer Ingelheim Investigational Site
City
Bystra
Country
Poland
Facility Name
205.389.2800 Boehringer Ingelheim Investigational Site
City
Chodziez
Country
Poland
Facility Name
205.389.2712 Boehringer Ingelheim Investigational Site
City
Czestochowa
Country
Poland
Facility Name
205.389.2774 Boehringer Ingelheim Investigational Site
City
Czestochowa
Country
Poland
Facility Name
205.389.2815 Boehringer Ingelheim Investigational Site
City
Dzialdowo
Country
Poland
Facility Name
205.389.2787 Boehringer Ingelheim Investigational Site
City
Elblag
Country
Poland
Facility Name
205.389.2715 Boehringer Ingelheim Investigational Site
City
Gdansk
Country
Poland
Facility Name
205.389.2723 Boehringer Ingelheim Investigational Site
City
Gdansk
Country
Poland
Facility Name
205.389.2743 Boehringer Ingelheim Investigational Site
City
Gdansk
Country
Poland
Facility Name
205.389.2764 Boehringer Ingelheim Investigational Site
City
Gdansk
Country
Poland
Facility Name
205.389.2802 Boehringer Ingelheim Investigational Site
City
Gdansk
Country
Poland
Facility Name
205.389.2801 Boehringer Ingelheim Investigational Site
City
Gorzow Wlkp
Country
Poland
Facility Name
205.389.2805 Boehringer Ingelheim Investigational Site
City
Ilawa
Country
Poland
Facility Name
205.389.2791 Boehringer Ingelheim Investigational Site
City
Inowroclaw
Country
Poland
Facility Name
205.389.2705 Boehringer Ingelheim Investigational Site
City
Katowice
Country
Poland
Facility Name
205.389.2749 Boehringer Ingelheim Investigational Site
City
Katowice
Country
Poland
Facility Name
205.389.2771 Boehringer Ingelheim Investigational Site
City
Katowice
Country
Poland
Facility Name
205.389.2759 Boehringer Ingelheim Investigational Site
City
Koszalin
Country
Poland
Facility Name
205.389.2711 Boehringer Ingelheim Investigational Site
City
Krakow
Country
Poland
Facility Name
205.389.2722 Boehringer Ingelheim Investigational Site
City
Krakow
Country
Poland
Facility Name
205.389.2747 Boehringer Ingelheim Investigational Site
City
Krakow
Country
Poland
Facility Name
205.389.2753 Boehringer Ingelheim Investigational Site
City
Krakow
Country
Poland
Facility Name
205.389.2798 Boehringer Ingelheim Investigational Site
City
Krakow
Country
Poland
Facility Name
205.389.2748 Boehringer Ingelheim Investigational Site
City
Kraków
Country
Poland
Facility Name
205.389.2757 Boehringer Ingelheim Investigational Site
City
Kutno
Country
Poland
Facility Name
205.389.2727 Boehringer Ingelheim Investigational Site
City
Leszno
Country
Poland
Facility Name
205.389.2701 Boehringer Ingelheim Investigational Site
City
Lodz
Country
Poland
Facility Name
205.389.2709 Boehringer Ingelheim Investigational Site
City
Lodz
Country
Poland
Facility Name
205.389.2716 Boehringer Ingelheim Investigational Site
City
Lodz
Country
Poland
Facility Name
205.389.2724 Boehringer Ingelheim Investigational Site
City
Lodz
Country
Poland
Facility Name
205.389.2732 Boehringer Ingelheim Investigational Site
City
Lodz
Country
Poland
Facility Name
205.389.2746 Boehringer Ingelheim Investigational Site
City
Lodz
Country
Poland
Facility Name
205.389.2751 Boehringer Ingelheim Investigational Site
City
Lodz
Country
Poland
Facility Name
205.389.2804 Boehringer Ingelheim Investigational Site
City
Lomza
Country
Poland
Facility Name
205.389.2741 Boehringer Ingelheim Investigational Site
City
Lublin
Country
Poland
Facility Name
205.389.2776 Boehringer Ingelheim Investigational Site
City
Lublin
Country
Poland
Facility Name
205.389.2817 Boehringer Ingelheim Investigational Site
City
Lublin
Country
Poland
Facility Name
205.389.2760 Boehringer Ingelheim Investigational Site
City
Olawa
Country
Poland
Facility Name
205.389.2756 Boehringer Ingelheim Investigational Site
City
Olsztyn
Country
Poland
Facility Name
205.389.2816 Boehringer Ingelheim Investigational Site
City
Olsztyn
Country
Poland
Facility Name
205.389.2702 Boehringer Ingelheim Investigational Site
City
Ostrow Wielkopolska
Country
Poland
Facility Name
205.389.2726 Boehringer Ingelheim Investigational Site
City
Pabianice
Country
Poland
Facility Name
205.389.2795 Boehringer Ingelheim Investigational Site
City
Plawno
Country
Poland
Facility Name
205.389.2730 Boehringer Ingelheim Investigational Site
City
Plock
Country
Poland
Facility Name
205.389.2703 Boehringer Ingelheim Investigational Site
City
Poznan
Country
Poland
Facility Name
205.389.2719 Boehringer Ingelheim Investigational Site
City
Poznan
Country
Poland
Facility Name
205.389.2737 Boehringer Ingelheim Investigational Site
City
Poznan
Country
Poland
Facility Name
205.389.2766 Boehringer Ingelheim Investigational Site
City
Poznan
Country
Poland
Facility Name
205.389.2769 Boehringer Ingelheim Investigational Site
City
Poznan
Country
Poland
Facility Name
205.389.2813 Boehringer Ingelheim Investigational Site
City
Poznan
Country
Poland
Facility Name
205.389.2763 Boehringer Ingelheim Investigational Site
City
Proszowice
Country
Poland
Facility Name
205.389.2767 Boehringer Ingelheim Investigational Site
City
Pruszkow
Country
Poland
Facility Name
205.389.2768 Boehringer Ingelheim Investigational Site
City
Radom
Country
Poland
Facility Name
205.389.2792 Boehringer Ingelheim Investigational Site
City
Sandomierz
Country
Poland
Facility Name
205.389.2781 Boehringer Ingelheim Investigational Site
City
Sieradz
Country
Poland
Facility Name
205.389.2725 Boehringer Ingelheim Investigational Site
City
Skierniewice
Country
Poland
Facility Name
205.389.2777 Boehringer Ingelheim Investigational Site
City
Szczecin - Zdunowo
Country
Poland
Facility Name
205.389.2782 Boehringer Ingelheim Investigational Site
City
Szczecin - Zdunowo
Country
Poland
Facility Name
205.389.2718 Boehringer Ingelheim Investigational Site
City
Szczecin
Country
Poland
Facility Name
205.389.2739 Boehringer Ingelheim Investigational Site
City
Szczecin
Country
Poland
Facility Name
205.389.2772 Boehringer Ingelheim Investigational Site
City
Szczecin
Country
Poland
Facility Name
205.389.2738 Boehringer Ingelheim Investigational Site
City
Tarnow
Country
Poland
Facility Name
205.389.2799 Boehringer Ingelheim Investigational Site
City
Tarnow
Country
Poland
Facility Name
205.389.2810 Boehringer Ingelheim Investigational Site
City
Tczew
Country
Poland
Facility Name
205.389.2775 Boehringer Ingelheim Investigational Site
City
Torun
Country
Poland
Facility Name
205.389.2754 Boehringer Ingelheim Investigational Site
City
Tranow
Country
Poland
Facility Name
205.389.2806 Boehringer Ingelheim Investigational Site
City
Turek
Country
Poland
Facility Name
205.389.2803 Boehringer Ingelheim Investigational Site
City
Wabrzenzo
Country
Poland
Facility Name
205.389.2707 Boehringer Ingelheim Investigational Site
City
Warsaw
Country
Poland
Facility Name
205.389.2714 Boehringer Ingelheim Investigational Site
City
Warsaw
Country
Poland
Facility Name
205.389.2728 Boehringer Ingelheim Investigational Site
City
Warsaw
Country
Poland
Facility Name
205.389.2734 Boehringer Ingelheim Investigational Site
City
Warszawa
Country
Poland
Facility Name
205.389.2812 Boehringer Ingelheim Investigational Site
City
Warszawa
Country
Poland
Facility Name
205.389.2818 Boehringer Ingelheim Investigational Site
City
Warszawa
Country
Poland
Facility Name
205.389.2710 Boehringer Ingelheim Investigational Site
City
Wodzislaw Slaski
Country
Poland
Facility Name
205.389.2721 Boehringer Ingelheim Investigational Site
City
Wroclaw
Country
Poland
Facility Name
205.389.2731 Boehringer Ingelheim Investigational Site
City
Wroclaw
Country
Poland
Facility Name
205.389.2736 Boehringer Ingelheim Investigational Site
City
Wroclaw
Country
Poland
Facility Name
205.389.2752 Boehringer Ingelheim Investigational Site
City
Wroclaw
Country
Poland
Facility Name
205.389.2761 Boehringer Ingelheim Investigational Site
City
Wroclaw
Country
Poland
Facility Name
205.389.2780 Boehringer Ingelheim Investigational Site
City
Wroclaw
Country
Poland
Facility Name
205.389.2793 Boehringer Ingelheim Investigational Site
City
Wroclaw
Country
Poland
Facility Name
205.389.2783 Boehringer Ingelheim Investigational Site
City
Zabrze
Country
Poland
Facility Name
205.389.2735 Boehringer Ingelheim Investigational Site
City
Zakopane
Country
Poland
Facility Name
205.389.2770 Boehringer Ingelheim Investigational Site
City
Zgierz
Country
Poland
Facility Name
205.389.2912 Boehringer Ingelheim Investigational Site
City
Angra do Heroísmo
Country
Portugal
Facility Name
205.389.2911 Boehringer Ingelheim Investigational Site
City
Barreiro
Country
Portugal
Facility Name
205.389.2904 Boehringer Ingelheim Investigational Site
City
Faro
Country
Portugal
Facility Name
205.389.2910 Boehringer Ingelheim Investigational Site
City
Figueira da Foz
Country
Portugal
Facility Name
205.389.2907 Boehringer Ingelheim Investigational Site
City
Guarda
Country
Portugal
Facility Name
205.389.2914 Boehringer Ingelheim Investigational Site
City
Lisboa
Country
Portugal
Facility Name
205.389.2917 Boehringer Ingelheim Investigational Site
City
Lisboa
Country
Portugal
Facility Name
205.389.2905 Boehringer Ingelheim Investigational Site
City
Santa Maria da Feira
Country
Portugal
Facility Name
205.389.2909 Boehringer Ingelheim Investigational Site
City
Santiago do Cacem
Country
Portugal
Facility Name
205.389.2903 Boehringer Ingelheim Investigational Site
City
Torres Vedras
Country
Portugal
Facility Name
205.389.3009 Boehringer Ingelheim Investigational Site
City
Brasov
Country
Romania
Facility Name
205.389.3018 Boehringer Ingelheim Investigational Site
City
Brasov
Country
Romania
Facility Name
205.389.3023 Boehringer Ingelheim Investigational Site
City
Brasov
Country
Romania
Facility Name
205.389.3025 Boehringer Ingelheim Investigational Site
City
Bucharest
Country
Romania
Facility Name
205.389.3001 Boehringer Ingelheim Investigational Site
City
Bucuresti
Country
Romania
Facility Name
205.389.3002 Boehringer Ingelheim Investigational Site
City
Bucuresti
Country
Romania
Facility Name
205.389.3004 Boehringer Ingelheim Investigational Site
City
Bucuresti
Country
Romania
Facility Name
205.389.3006 Boehringer Ingelheim Investigational Site
City
Bucuresti
Country
Romania
Facility Name
205.389.3007 Boehringer Ingelheim Investigational Site
City
Bucuresti
Country
Romania
Facility Name
205.389.3012 Boehringer Ingelheim Investigational Site
City
Bucuresti
Country
Romania
Facility Name
205.389.3013 Boehringer Ingelheim Investigational Site
City
Bucuresti
Country
Romania
Facility Name
205.389.3016 Boehringer Ingelheim Investigational Site
City
Constanta
Country
Romania
Facility Name
205.389.3019 Boehringer Ingelheim Investigational Site
City
Constanta
Country
Romania
Facility Name
205.389.3015 Boehringer Ingelheim Investigational Site
City
Craiova
Country
Romania
Facility Name
205.389.3008 Boehringer Ingelheim Investigational Site
City
Iasi
Country
Romania
Facility Name
205.389.3014 Boehringer Ingelheim Investigational Site
City
Iasi
Country
Romania
Facility Name
205.389.3022 Boehringer Ingelheim Investigational Site
City
Iasi
Country
Romania
Facility Name
205.389.3024 Boehringer Ingelheim Investigational Site
City
Iasi
Country
Romania
Facility Name
205.389.3005 Boehringer Ingelheim Investigational Site
City
Oradea
Country
Romania
Facility Name
205.389.3017 Boehringer Ingelheim Investigational Site
City
Tg. Mures
Country
Romania
Facility Name
205.389.3021 Boehringer Ingelheim Investigational Site
City
Timisoara
Country
Romania
Facility Name
205.389.3174 Boehringer Ingelheim Investigational Site
City
Arkhangelsk
Country
Russian Federation
Facility Name
205.389.3113 Boehringer Ingelheim Investigational Site
City
Barnaul
Country
Russian Federation
Facility Name
205.389.3131 Boehringer Ingelheim Investigational Site
City
Barnaul
Country
Russian Federation
Facility Name
205.389.3105 Boehringer Ingelheim Investigational Site
City
Chelyabinsk
Country
Russian Federation
Facility Name
205.389.3182 Boehringer Ingelheim Investigational Site
City
Chelyabinsk
Country
Russian Federation
Facility Name
205.389.3183 Boehringer Ingelheim Investigational Site
City
Chelyabinsk
Country
Russian Federation
Facility Name
205.389.3184 Boehringer Ingelheim Investigational Site
City
Chelyabinsk
Country
Russian Federation
Facility Name
205.389.3116 Boehringer Ingelheim Investigational Site
City
Ekaterinburg
Country
Russian Federation
Facility Name
205.389.3138 Boehringer Ingelheim Investigational Site
City
Ekaterinburg
Country
Russian Federation
Facility Name
205.389.3148 Boehringer Ingelheim Investigational Site
City
Ekaterinburg
Country
Russian Federation
Facility Name
205.389.3166 Boehringer Ingelheim Investigational Site
City
Ekaterinburg
Country
Russian Federation
Facility Name
205.389.3186 Boehringer Ingelheim Investigational Site
City
Gatchina (Leningradskaya oblast)
Country
Russian Federation
Facility Name
205.389.3193 Boehringer Ingelheim Investigational Site
City
Kaliningrad
Country
Russian Federation
Facility Name
205.389.3104 Boehringer Ingelheim Investigational Site
City
Kazan
Country
Russian Federation
Facility Name
205.389.3111 Boehringer Ingelheim Investigational Site
City
Kemerovo
Country
Russian Federation
Facility Name
205.389.3120 Boehringer Ingelheim Investigational Site
City
Kirov
Country
Russian Federation
Facility Name
205.389.3170 Boehringer Ingelheim Investigational Site
City
Krasnodar
Country
Russian Federation
Facility Name
205.389.3132 Boehringer Ingelheim Investigational Site
City
Krasnoyarsk
Country
Russian Federation
Facility Name
205.389.3103 Boehringer Ingelheim Investigational Site
City
Moscow
Country
Russian Federation
Facility Name
205.389.3106 Boehringer Ingelheim Investigational Site
City
Moscow
Country
Russian Federation
Facility Name
205.389.3107 Boehringer Ingelheim Investigational Site
City
Moscow
Country
Russian Federation
Facility Name
205.389.3108 Boehringer Ingelheim Investigational Site
City
Moscow
Country
Russian Federation
Facility Name
205.389.3109 Boehringer Ingelheim Investigational Site
City
Moscow
Country
Russian Federation
Facility Name
205.389.3125 Boehringer Ingelheim Investigational Site
City
Moscow
Country
Russian Federation
Facility Name
205.389.3127 Boehringer Ingelheim Investigational Site
City
Moscow
Country
Russian Federation
Facility Name
205.389.3128 Boehringer Ingelheim Investigational Site
City
Moscow
Country
Russian Federation
Facility Name
205.389.3130 Boehringer Ingelheim Investigational Site
City
Moscow
Country
Russian Federation
Facility Name
205.389.3134 Boehringer Ingelheim Investigational Site
City
Moscow
Country
Russian Federation
Facility Name
205.389.3136 Boehringer Ingelheim Investigational Site
City
Moscow
Country
Russian Federation
Facility Name
205.389.3139 Boehringer Ingelheim Investigational Site
City
Moscow
Country
Russian Federation
Facility Name
205.389.3140 Boehringer Ingelheim Investigational Site
City
Moscow
Country
Russian Federation
Facility Name
205.389.3143 Boehringer Ingelheim Investigational Site
City
Moscow
Country
Russian Federation
Facility Name
205.389.3149 Boehringer Ingelheim Investigational Site
City
Moscow
Country
Russian Federation
Facility Name
205.389.3151 Boehringer Ingelheim Investigational Site
City
Moscow
Country
Russian Federation
Facility Name
205.389.3156 Boehringer Ingelheim Investigational Site
City
Moscow
Country
Russian Federation
Facility Name
205.389.3157 Boehringer Ingelheim Investigational Site
City
Moscow
Country
Russian Federation
Facility Name
205.389.3163 Boehringer Ingelheim Investigational Site
City
Moscow
Country
Russian Federation
Facility Name
205.389.3164 Boehringer Ingelheim Investigational Site
City
Moscow
Country
Russian Federation
Facility Name
205.389.3167 Boehringer Ingelheim Investigational Site
City
Moscow
Country
Russian Federation
Facility Name
205.389.3168 Boehringer Ingelheim Investigational Site
City
Moscow
Country
Russian Federation
Facility Name
205.389.3171 Boehringer Ingelheim Investigational Site
City
Moscow
Country
Russian Federation
Facility Name
205.389.3196 Boehringer Ingelheim Investigational Site
City
Moscow
Country
Russian Federation
Facility Name
205.389.3188 Boehringer Ingelheim Investigational Site
City
Murmansk
Country
Russian Federation
Facility Name
205.389.3953 Boehringer Ingelheim Investigational Site
City
Nizhniy Novgorod
Country
Russian Federation
Facility Name
205.389.3169 Boehringer Ingelheim Investigational Site
City
Nizhny Novgorod
Country
Russian Federation
Facility Name
205.389.3112 Boehringer Ingelheim Investigational Site
City
Novosibirsk
Country
Russian Federation
Facility Name
205.389.3114 Boehringer Ingelheim Investigational Site
City
Novosibirsk
Country
Russian Federation
Facility Name
205.389.3129 Boehringer Ingelheim Investigational Site
City
Novosibirsk
Country
Russian Federation
Facility Name
205.389.3141 Boehringer Ingelheim Investigational Site
City
Novosibirsk
Country
Russian Federation
Facility Name
205.389.3153 Boehringer Ingelheim Investigational Site
City
Novosibirsk
Country
Russian Federation
Facility Name
205.389.3175 Boehringer Ingelheim Investigational Site
City
Novosibirsk
Country
Russian Federation
Facility Name
205.389.3126 Boehringer Ingelheim Investigational Site
City
Orenburg
Country
Russian Federation
Facility Name
205.389.3185 Boehringer Ingelheim Investigational Site
City
Perm
Country
Russian Federation
Facility Name
205.389.3192 Boehringer Ingelheim Investigational Site
City
Petrozavodsk
Country
Russian Federation
Facility Name
205.389.3179 Boehringer Ingelheim Investigational Site
City
Pskov
Country
Russian Federation
Facility Name
205.389.3190 Boehringer Ingelheim Investigational Site
City
Pskov
Country
Russian Federation
Facility Name
205.389.3199 Boehringer Ingelheim Investigational Site
City
Pyatigorsk,
Country
Russian Federation
Facility Name
205.389.3159 Boehringer Ingelheim Investigational Site
City
Rostov-on-Don
Country
Russian Federation
Facility Name
205.389.3197 Boehringer Ingelheim Investigational Site
City
Ryazan
Country
Russian Federation
Facility Name
205.389.3198 Boehringer Ingelheim Investigational Site
City
Saint Petersburg
Country
Russian Federation
Facility Name
205.389.3110 Boehringer Ingelheim Investigational Site
City
Saratov
Country
Russian Federation
Facility Name
205.389.3951 Boehringer Ingelheim Investigational Site
City
Saratov
Country
Russian Federation
Facility Name
205.389.3191 Boehringer Ingelheim Investigational Site
City
St-Petersburg
Country
Russian Federation
Facility Name
205.389.3119 Boehringer Ingelheim Investigational Site
City
St. Petersburg
Country
Russian Federation
Facility Name
205.389.3121 Boehringer Ingelheim Investigational Site
City
St. Petersburg
Country
Russian Federation
Facility Name
205.389.3122 Boehringer Ingelheim Investigational Site
City
St. Petersburg
Country
Russian Federation
Facility Name
205.389.3123 Boehringer Ingelheim Investigational Site
City
St. Petersburg
Country
Russian Federation
Facility Name
205.389.3135 Boehringer Ingelheim Investigational Site
City
St. Petersburg
Country
Russian Federation
Facility Name
205.389.3137 Boehringer Ingelheim Investigational Site
City
St. Petersburg
Country
Russian Federation
Facility Name
205.389.3145 Boehringer Ingelheim Investigational Site
City
St. Petersburg
Country
Russian Federation
Facility Name
205.389.3146 Boehringer Ingelheim Investigational Site
City
St. Petersburg
Country
Russian Federation
Facility Name
205.389.3160 Boehringer Ingelheim Investigational Site
City
St. Petersburg
Country
Russian Federation
Facility Name
205.389.3161 Boehringer Ingelheim Investigational Site
City
St. Petersburg
Country
Russian Federation
Facility Name
205.389.3176 Boehringer Ingelheim Investigational Site
City
St. Petersburg
Country
Russian Federation
Facility Name
205.389.3177 Boehringer Ingelheim Investigational Site
City
St. Petersburg
Country
Russian Federation
Facility Name
205.389.3178 Boehringer Ingelheim Investigational Site
City
St. Petersburg
Country
Russian Federation
Facility Name
205.389.3180 Boehringer Ingelheim Investigational Site
City
St. Petersburg
Country
Russian Federation
Facility Name
205.389.3181 Boehringer Ingelheim Investigational Site
City
St. Petersburg
Country
Russian Federation
Facility Name
205.389.3189 Boehringer Ingelheim Investigational Site
City
St. Petersburg
Country
Russian Federation
Facility Name
205.389.3195 Boehringer Ingelheim Investigational Site
City
St. Petersburg
Country
Russian Federation
Facility Name
205.389.3950 Boehringer Ingelheim Investigational Site
City
St. Petersburg
Country
Russian Federation
Facility Name
205.389.3165 Boehringer Ingelheim Investigational Site
City
St.Peterburg
Country
Russian Federation
Facility Name
205.389.3117 Boehringer Ingelheim Investigational Site
City
St.Petersburg
Country
Russian Federation
Facility Name
205.389.3147 Boehringer Ingelheim Investigational Site
City
St.Petersburg
Country
Russian Federation
Facility Name
205.389.3152 Boehringer Ingelheim Investigational Site
City
St.Petersburg
Country
Russian Federation
Facility Name
205.389.3101 Boehringer Ingelheim Investigational Site
City
Tomsk
Country
Russian Federation
Facility Name
205.389.3102 Boehringer Ingelheim Investigational Site
City
Tomsk
Country
Russian Federation
Facility Name
205.389.3133 Boehringer Ingelheim Investigational Site
City
Tomsk
Country
Russian Federation
Facility Name
205.389.3144 Boehringer Ingelheim Investigational Site
City
Tomsk
Country
Russian Federation
Facility Name
205.389.3194 Boehringer Ingelheim Investigational Site
City
Velikiy Novgorod
Country
Russian Federation
Facility Name
205.389.3118 Boehringer Ingelheim Investigational Site
City
Yaroslavl
Country
Russian Federation
Facility Name
205.389.3155 Boehringer Ingelheim Investigational Site
City
Yaroslavl
Country
Russian Federation
Facility Name
205.389.3208 Boehringer Ingelheim Investigational Site
City
Bratislava
Country
Slovakia
Facility Name
205.389.3204 Boehringer Ingelheim Investigational Site
City
Kosice
Country
Slovakia
Facility Name
205.389.3209 Boehringer Ingelheim Investigational Site
City
Kosice
Country
Slovakia
Facility Name
205.389.3205 Boehringer Ingelheim Investigational Site
City
Prievidza
Country
Slovakia
Facility Name
205.389.3210 Boehringer Ingelheim Investigational Site
City
Revuca
Country
Slovakia
Facility Name
205.389.3203 Boehringer Ingelheim Investigational Site
City
Spisska Nova Ves
Country
Slovakia
Facility Name
205.389.3202 Boehringer Ingelheim Investigational Site
City
Trnava
Country
Slovakia
Facility Name
205.389.3207 Boehringer Ingelheim Investigational Site
City
Vrable
Country
Slovakia
Facility Name
205.389.3301 Boehringer Ingelheim Investigational Site
City
Golnik
Country
Slovenia
Facility Name
205.389.3308 Boehringer Ingelheim Investigational Site
City
Grosuplje
Country
Slovenia
Facility Name
205.389.3304 Boehringer Ingelheim Investigational Site
City
Jesenice
Country
Slovenia
Facility Name
205.389.3302 Boehringer Ingelheim Investigational Site
City
Kamnik
Country
Slovenia
Facility Name
205.389.3303 Boehringer Ingelheim Investigational Site
City
Ljubljana
Country
Slovenia
Facility Name
205.389.3306 Boehringer Ingelheim Investigational Site
City
Topolsica
Country
Slovenia
Facility Name
205.389.3410 Boehringer Ingelheim Investigational Site
City
Badajoz
Country
Spain
Facility Name
205.389.3403 Boehringer Ingelheim Investigational Site
City
Badalona (Barcelona)
Country
Spain
Facility Name
205.389.3401 Boehringer Ingelheim Investigational Site
City
Barcelona
Country
Spain
Facility Name
205.389.3402 Boehringer Ingelheim Investigational Site
City
Barcelona
Country
Spain
Facility Name
205.389.3428 Boehringer Ingelheim Investigational Site
City
Barcelona
Country
Spain
Facility Name
205.389.3430 Boehringer Ingelheim Investigational Site
City
Cartagena
Country
Spain
Facility Name
205.389.3416 Boehringer Ingelheim Investigational Site
City
Cáceres
Country
Spain
Facility Name
205.389.3425 Boehringer Ingelheim Investigational Site
City
Elche
Country
Spain
Facility Name
205.389.3408 Boehringer Ingelheim Investigational Site
City
Las Palmas de Gran Canarias
Country
Spain
Facility Name
205.389.3405 Boehringer Ingelheim Investigational Site
City
Lleida
Country
Spain
Facility Name
205.389.3404 Boehringer Ingelheim Investigational Site
City
Madrid
Country
Spain
Facility Name
205.389.3406 Boehringer Ingelheim Investigational Site
City
Madrid
Country
Spain
Facility Name
205.389.3414 Boehringer Ingelheim Investigational Site
City
Málaga
Country
Spain
Facility Name
205.389.3431 Boehringer Ingelheim Investigational Site
City
Pontevedra
Country
Spain
Facility Name
205.389.3419 Boehringer Ingelheim Investigational Site
City
Requena
Country
Spain
Facility Name
205.389.3427 Boehringer Ingelheim Investigational Site
City
Reus
Country
Spain
Facility Name
205.389.3422 Boehringer Ingelheim Investigational Site
City
Sagunto
Country
Spain
Facility Name
205.389.3420 Boehringer Ingelheim Investigational Site
City
San Juan
Country
Spain
Facility Name
205.389.3415 Boehringer Ingelheim Investigational Site
City
Santander
Country
Spain
Facility Name
205.389.3421 Boehringer Ingelheim Investigational Site
City
Santiago de Compostela
Country
Spain
Facility Name
205.389.3407 Boehringer Ingelheim Investigational Site
City
Terrasa (Barcelona)
Country
Spain
Facility Name
205.389.3413 Boehringer Ingelheim Investigational Site
City
Valencia
Country
Spain
Facility Name
205.389.3426 Boehringer Ingelheim Investigational Site
City
Valencia
Country
Spain
Facility Name
205.389.3417 Boehringer Ingelheim Investigational Site
City
Valladolid
Country
Spain
Facility Name
205.389.3821 Boehringer Ingelheim Investigational Site
City
Adana
Country
Turkey
Facility Name
205.389.3808 Boehringer Ingelheim Investigational Site
City
Ankara
Country
Turkey
Facility Name
205.389.3810 Boehringer Ingelheim Investigational Site
City
Ankara
Country
Turkey
Facility Name
205.389.3817 Boehringer Ingelheim Investigational Site
City
Bursa
Country
Turkey
Facility Name
205.389.3819 Boehringer Ingelheim Investigational Site
City
Erzurum
Country
Turkey
Facility Name
205.389.3812 Boehringer Ingelheim Investigational Site
City
Istanbul
Country
Turkey
Facility Name
205.389.3827 Boehringer Ingelheim Investigational Site
City
Izmir
Country
Turkey
Facility Name
205.389.3813 Boehringer Ingelheim Investigational Site
City
Izmit
Country
Turkey
Facility Name
205.389.3820 Boehringer Ingelheim Investigational Site
City
Kahramanmaras
Country
Turkey
Facility Name
205.389.3825 Boehringer Ingelheim Investigational Site
City
Malatya
Country
Turkey
Facility Name
205.389.3809 Boehringer Ingelheim Investigational Site
City
Sihhiye Ankara
Country
Turkey
Facility Name
205.389.3807 Boehringer Ingelheim Investigational Site
City
Yenisehir-IZMIR
Country
Turkey
Facility Name
205.389.3521 Boehringer Ingelheim Investigational Site
City
AR Crimea
Country
Ukraine
Facility Name
205.389.3516 Boehringer Ingelheim Investigational Site
City
Cherkassy
Country
Ukraine
Facility Name
205.389.3549 Boehringer Ingelheim Investigational Site
City
Chernivtsi
Country
Ukraine
Facility Name
205.389.3509 Boehringer Ingelheim Investigational Site
City
Dnipropetrovsk
Country
Ukraine
Facility Name
205.389.3510 Boehringer Ingelheim Investigational Site
City
Dnipropetrovsk
Country
Ukraine
Facility Name
205.389.3511 Boehringer Ingelheim Investigational Site
City
Dnipropetrovsk
Country
Ukraine
Facility Name
205.389.3523 Boehringer Ingelheim Investigational Site
City
Dnipropetrovsk
Country
Ukraine
Facility Name
205.389.3514 Boehringer Ingelheim Investigational Site
City
Donetsk
Country
Ukraine
Facility Name
205.389.3524 Boehringer Ingelheim Investigational Site
City
Donetsk
Country
Ukraine
Facility Name
205.389.3533 Boehringer Ingelheim Investigational Site
City
Ivano-Frankivsk
Country
Ukraine
Facility Name
205.389.3506 Boehringer Ingelheim Investigational Site
City
Kharkiv
Country
Ukraine
Facility Name
205.389.3507 Boehringer Ingelheim Investigational Site
City
Kharkiv
Country
Ukraine
Facility Name
205.389.3508 Boehringer Ingelheim Investigational Site
City
Kharkiv
Country
Ukraine
Facility Name
205.389.3520 Boehringer Ingelheim Investigational Site
City
Kharkiv
Country
Ukraine
Facility Name
205.389.3522 Boehringer Ingelheim Investigational Site
City
Kharkiv
Country
Ukraine
Facility Name
205.389.3532 Boehringer Ingelheim Investigational Site
City
Kharkiv
Country
Ukraine
Facility Name
205.389.3539 Boehringer Ingelheim Investigational Site
City
Kharkiv
Country
Ukraine
Facility Name
205.389.3541 Boehringer Ingelheim Investigational Site
City
Kharkiv
Country
Ukraine
Facility Name
205.389.3543 Boehringer Ingelheim Investigational Site
City
Kharkiv
Country
Ukraine
Facility Name
205.389.3555 Boehringer Ingelheim Investigational Site
City
Kharkiv
Country
Ukraine
Facility Name
205.389.3501 Boehringer Ingelheim Investigational Site
City
Kiev
Country
Ukraine
Facility Name
205.389.3502 Boehringer Ingelheim Investigational Site
City
Kiev
Country
Ukraine
Facility Name
205.389.3503 Boehringer Ingelheim Investigational Site
City
Kiev
Country
Ukraine
Facility Name
205.389.3550 Boehringer Ingelheim Investigational Site
City
Kiev
Country
Ukraine
Facility Name
205.389.3552 Boehringer Ingelheim Investigational Site
City
Kiev
Country
Ukraine
Facility Name
205.389.3553 Boehringer Ingelheim Investigational Site
City
Kiev
Country
Ukraine
Facility Name
205.389.3504 Boehringer Ingelheim Investigational Site
City
Kyiv
Country
Ukraine
Facility Name
205.389.3525 Boehringer Ingelheim Investigational Site
City
Kyiv
Country
Ukraine
Facility Name
205.389.3526 Boehringer Ingelheim Investigational Site
City
Kyiv
Country
Ukraine
Facility Name
205.389.3528 Boehringer Ingelheim Investigational Site
City
Kyiv
Country
Ukraine
Facility Name
205.389.3534 Boehringer Ingelheim Investigational Site
City
Kyiv
Country
Ukraine
Facility Name
205.389.3535 Boehringer Ingelheim Investigational Site
City
Kyiv
Country
Ukraine
Facility Name
205.389.3536 Boehringer Ingelheim Investigational Site
City
Kyiv
Country
Ukraine
Facility Name
205.389.3538 Boehringer Ingelheim Investigational Site
City
Kyiv
Country
Ukraine
Facility Name
205.389.3551 Boehringer Ingelheim Investigational Site
City
Kyiv
Country
Ukraine
Facility Name
205.389.3545 Boehringer Ingelheim Investigational Site
City
Lugansk
Country
Ukraine
Facility Name
205.389.3512 Boehringer Ingelheim Investigational Site
City
Lviv
Country
Ukraine
Facility Name
205.389.3530 Boehringer Ingelheim Investigational Site
City
Lviv
Country
Ukraine
Facility Name
205.389.3540 Boehringer Ingelheim Investigational Site
City
Lviv
Country
Ukraine
Facility Name
205.389.3554 Boehringer Ingelheim Investigational Site
City
Lviv
Country
Ukraine
Facility Name
205.389.3556 Boehringer Ingelheim Investigational Site
City
m.Donetsk
Country
Ukraine
Facility Name
205.389.3513 Boehringer Ingelheim Investigational Site
City
m.Odesa
Country
Ukraine
Facility Name
205.389.3519 Boehringer Ingelheim Investigational Site
City
Odesa
Country
Ukraine
Facility Name
205.389.3542 Boehringer Ingelheim Investigational Site
City
Odesa
Country
Ukraine
Facility Name
205.389.3527 Boehringer Ingelheim Investigational Site
City
Odessa
Country
Ukraine
Facility Name
205.389.3531 Boehringer Ingelheim Investigational Site
City
Poltava
Country
Ukraine
Facility Name
205.389.3517 Boehringer Ingelheim Investigational Site
City
Simferopil
Country
Ukraine
Facility Name
205.389.3518 Boehringer Ingelheim Investigational Site
City
Ternopil
Country
Ukraine
Facility Name
205.389.3529 Boehringer Ingelheim Investigational Site
City
Vinnitsa
Country
Ukraine
Facility Name
205.389.3515 Boehringer Ingelheim Investigational Site
City
Zaporizhzhya
Country
Ukraine
Facility Name
205.389.3547 Boehringer Ingelheim Investigational Site
City
Zaporizhzhya
Country
Ukraine
Facility Name
205.389.3548 Boehringer Ingelheim Investigational Site
City
Zaporizhzhya
Country
Ukraine
Facility Name
205.389.3601 Boehringer Ingelheim Investigational Site
City
Bath
Country
United Kingdom
Facility Name
205.389.3630 Boehringer Ingelheim Investigational Site
City
Bexhill on Sea
Country
United Kingdom
Facility Name
205.389.3636 Boehringer Ingelheim Investigational Site
City
Bexhill-on-Sea
Country
United Kingdom
Facility Name
205.389.3608 Boehringer Ingelheim Investigational Site
City
Birmingham
Country
United Kingdom
Facility Name
205.389.3605 Boehringer Ingelheim Investigational Site
City
Blackburn
Country
United Kingdom
Facility Name
205.389.3609 Boehringer Ingelheim Investigational Site
City
Bolton
Country
United Kingdom
Facility Name
205.389.3640 Boehringer Ingelheim Investigational Site
City
Burbage
Country
United Kingdom
Facility Name
205.389.3643 Boehringer Ingelheim Investigational Site
City
Chesterfield
Country
United Kingdom
Facility Name
205.389.3627 Boehringer Ingelheim Investigational Site
City
Corsham
Country
United Kingdom
Facility Name
205.389.3606 Boehringer Ingelheim Investigational Site
City
Coventry
Country
United Kingdom
Facility Name
205.389.3633 Boehringer Ingelheim Investigational Site
City
Coventry
Country
United Kingdom
Facility Name
205.389.3639 Boehringer Ingelheim Investigational Site
City
Frome
Country
United Kingdom
Facility Name
205.389.3602 Boehringer Ingelheim Investigational Site
City
Glasgow
Country
United Kingdom
Facility Name
205.389.3632 Boehringer Ingelheim Investigational Site
City
Irvine
Country
United Kingdom
Facility Name
205.389.3623 Boehringer Ingelheim Investigational Site
City
London
Country
United Kingdom
Facility Name
205.389.3638 Boehringer Ingelheim Investigational Site
City
Middlesex
Country
United Kingdom
Facility Name
205.389.3616 Boehringer Ingelheim Investigational Site
City
Newcastle upon Tyne
Country
United Kingdom
Facility Name
205.389.3618 Boehringer Ingelheim Investigational Site
City
Paisley
Country
United Kingdom
Facility Name
205.389.3622 Boehringer Ingelheim Investigational Site
City
Radstock
Country
United Kingdom
Facility Name
205.389.3626 Boehringer Ingelheim Investigational Site
City
Randalstown
Country
United Kingdom
Facility Name
205.389.3604 Boehringer Ingelheim Investigational Site
City
Soham
Country
United Kingdom
Facility Name
205.389.3613 Boehringer Ingelheim Investigational Site
City
St Just, Penzance
Country
United Kingdom
Facility Name
205.389.3624 Boehringer Ingelheim Investigational Site
City
Sunderland
Country
United Kingdom
Facility Name
205.389.3635 Boehringer Ingelheim Investigational Site
City
Wansford, Peterborough
Country
United Kingdom
Facility Name
205.389.3631 Boehringer Ingelheim Investigational Site
City
Windsor
Country
United Kingdom
Facility Name
205.389.3612 Boehringer Ingelheim Investigational Site
City
Wrexham
Country
United Kingdom

12. IPD Sharing Statement

Citations:
PubMed Identifier
26100349
Citation
Vogelmeier CF, Asijee GM, Kupas K, Beeh KM. Tiotropium and Salmeterol in COPD Patients at Risk of Exacerbations: A Post Hoc Analysis from POET-COPD((R)). Adv Ther. 2015 Jun;32(6):537-47. doi: 10.1007/s12325-015-0216-2. Epub 2015 Jun 23.
Results Reference
derived
PubMed Identifier
24461901
Citation
Rabe KF, Fabbri LM, Israel E, Kogler H, Riemann K, Schmidt H, Glaab T, Vogelmeier CF. Effect of ADRB2 polymorphisms on the efficacy of salmeterol and tiotropium in preventing COPD exacerbations: a prespecified substudy of the POET-COPD trial. Lancet Respir Med. 2014 Jan;2(1):44-53. doi: 10.1016/S2213-2600(13)70248-0. Epub 2013 Dec 5.
Results Reference
derived
PubMed Identifier
24168767
Citation
Beeh KM, Glaab T, Stowasser S, Schmidt H, Fabbri LM, Rabe KF, Vogelmeier CF. Characterisation of exacerbation risk and exacerbator phenotypes in the POET-COPD trial. Respir Res. 2013 Oct 29;14(1):116. doi: 10.1186/1465-9921-14-116.
Results Reference
derived
PubMed Identifier
23188489
Citation
Rabe KF, Fabbri LM, Vogelmeier C, Kogler H, Schmidt H, Beeh KM, Glaab T. Seasonal distribution of COPD exacerbations in the Prevention of Exacerbations with Tiotropium in COPD trial. Chest. 2013 Mar;143(3):711-719. doi: 10.1378/chest.12-1277.
Results Reference
derived
PubMed Identifier
21428765
Citation
Vogelmeier C, Hederer B, Glaab T, Schmidt H, Rutten-van Molken MP, Beeh KM, Rabe KF, Fabbri LM; POET-COPD Investigators. Tiotropium versus salmeterol for the prevention of exacerbations of COPD. N Engl J Med. 2011 Mar 24;364(12):1093-1103. doi: 10.1056/NEJMoa1008378.
Results Reference
derived
PubMed Identifier
19436693
Citation
Beeh KM, Hederer B, Glaab T, Muller A, Rutten-van Moelken M, Kesten S, Vogelmeier C. Study design considerations in a large COPD trial comparing effects of tiotropium with salmeterol on exacerbations. Int J Chron Obstruct Pulmon Dis. 2009;4:119-25. Epub 2009 Apr 15.
Results Reference
derived
Links:
URL
http://trials.boehringer-ingelheim.com/content/dam/internet/opu/clinicaltrial/com_EN/results/205/205.389_U10-2159.pdf
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Tiotropium Once Daily 18 Mcg Versus Salmeterol Twice Daily 50 Mcg on Time to First Exacerbation in COPD Patients.

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