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Comparison of Tiotropium Inhalation Capsules and Oxitropium Metered Dose Inhalator (MDI) in Patients With Chronic Obstructive Pulmonary Disease (COPD)

Primary Purpose

Pulmonary Disease, Chronic Obstructive

Status
Completed
Phase
Phase 3
Locations
Study Type
Interventional
Intervention
Tiotropium powder inhalation capsules
Tersigan®
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:

The patients with COPD (chronic bronchitis, emphysema) whose symptoms are stable and who satisfy the following criteria

  1. Patients with FEV1.0 of <=70% of predicted normal and FEV1.0/FVC of <=70% in the screening test (The FEV1.0 value should also be <=70% of predicted normal on the starting day of administration (visit 2).)
  2. Patients with a smoking history (<number of cigarettes smoked a day x number of smoking years> is >=200.)
  3. Male or female patients aged >=40 years old

Exclusion Criteria:

  1. Patients complicated with bronchial asthma, making the assessment of drug efficacy against COPD difficult
  2. Patients using oral corticosteroid medication at a dose in excess of the equivalent 10 mg/day of prednisolon
  3. Patients with glaucoma
  4. Patients with symptomatic prostatic hypertrophy
  5. Patients with hypersensitivity to anticholinergic drugs or powder inhalants
  6. Patients with serious complication who are judged by the investigator to be inappropriate as the subjects of study
  7. Patients demonstrating clinically problematic abnormal laboratory test values (general blood test, biochemical test, urinalysis). Those showing Glutamic Oxaloacetic Transaminase (GOT) and Glutamic PyruvicTransaminase (GPT) twice the upper limit of the normal range, bilirubin 1.25 times or creatinine 1.25 times of the upper limit of normal range are excluded.
  8. Patients with a recent history of myocardial infarction or heart failure (i.e. within 3 months before the screening test)
  9. Patients with arrhythmia requiring the treatment with drugs
  10. Patients for whom the concomitant use of beta-blocker cannot be prohibited.
  11. Patients who began treatment with an ACE inhibitor within 1 month before the screening test
  12. Patients with tuberculosis (currently active) or with definite sequela of tuberculosis
  13. Patients with a recent history of carcinoma (excluding basal cell carcinoma) (i.e. within the past 5 years)
  14. Patients with a history of cystic fibrosis and bronchiectasis
  15. Patients with recent onset of upper airway infection (i.e. within 1 month before the screening test)
  16. Patients who have taken an investigational drug within one month or within period six times of half-lives of that drug (whichever is longer) before the screening test.
  17. Women who are pregnant or who may become pregnant, or those breast feeding
  18. Other than above, those who are judged by the investigator to be inappropriate as the subjects of study

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Experimental

    Active Comparator

    Arm Label

    Tiotropium

    Oxitropium bromide

    Arm Description

    Outcomes

    Primary Outcome Measures

    Occurrence of Adverse Events
    Changes from baseline in Blood Pressure / Heart Rate
    Changes from baseline in ECG
    Changes from baseline in laboratory tests

    Secondary Outcome Measures

    Changes from baseline in Trough Forced expiratory volume in one second (FEV1.0) response
    Changes from baseline in FEV1.0 at 1 hr post-dosing
    Changes from baseline in Trough Forced vital capacity (FVC) response
    Changes from baseline in FVC at 1 hr post-dosing
    Changes from baseline COPD clinical symptoms (Cough frequency, sputum amount, severity of short breath, nocturnal sleep)
    Frequency of rescue use of β2 stimulants
    Changes from baseline in Quality of Life QOL (St George's Respiratory Questionnaire (SGRQ) and Airways Questionnaire-20 (AQ20), if possible)
    Patient's impression
    Physician's global evaluation

    Full Information

    First Posted
    June 20, 2014
    Last Updated
    August 29, 2018
    Sponsor
    Boehringer Ingelheim
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    1. Study Identification

    Unique Protocol Identification Number
    NCT02172430
    Brief Title
    Comparison of Tiotropium Inhalation Capsules and Oxitropium Metered Dose Inhalator (MDI) in Patients With Chronic Obstructive Pulmonary Disease (COPD)
    Official Title
    A Multiple Dose Comparison of Tiotropium 18 μg Inhalation Capsules and Oxitropium MDI (2 Puffs of 100 μg) in a One-year, Open-Label, Safety and Efficacy Study in Patients With COPD
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    August 2018
    Overall Recruitment Status
    Completed
    Study Start Date
    September 2000 (undefined)
    Primary Completion Date
    May 2002 (Actual)
    Study Completion Date
    undefined (undefined)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Sponsor
    Name of the Sponsor
    Boehringer Ingelheim

    4. Oversight

    5. Study Description

    Brief Summary
    The objective of this study is to investigate the long-term safety of Ba 79 BR (tiotropium) powder inhalation in patients with COPD using oxitropium bromide (Tersigan) as a comparator. Secondarily, the long-term efficacy of Ba 679 BR is also investigated

    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 3
    Interventional Study Model
    Parallel Assignment
    Masking
    None (Open Label)
    Allocation
    Randomized
    Enrollment
    161 (Actual)

    8. Arms, Groups, and Interventions

    Arm Title
    Tiotropium
    Arm Type
    Experimental
    Arm Title
    Oxitropium bromide
    Arm Type
    Active Comparator
    Intervention Type
    Drug
    Intervention Name(s)
    Tiotropium powder inhalation capsules
    Intervention Description
    Powder inhalation via the HandiHaler® once daily
    Intervention Type
    Drug
    Intervention Name(s)
    Tersigan®
    Intervention Description
    2 puffs of oxitropium three times daily via MDI
    Primary Outcome Measure Information:
    Title
    Occurrence of Adverse Events
    Time Frame
    up to 52 weeks
    Title
    Changes from baseline in Blood Pressure / Heart Rate
    Time Frame
    up to 52 weeks
    Title
    Changes from baseline in ECG
    Time Frame
    up to 52 weeks
    Title
    Changes from baseline in laboratory tests
    Time Frame
    up to 52 weeks
    Secondary Outcome Measure Information:
    Title
    Changes from baseline in Trough Forced expiratory volume in one second (FEV1.0) response
    Time Frame
    week 24 and 52
    Title
    Changes from baseline in FEV1.0 at 1 hr post-dosing
    Time Frame
    week 24 and 52
    Title
    Changes from baseline in Trough Forced vital capacity (FVC) response
    Time Frame
    week 24 and 52
    Title
    Changes from baseline in FVC at 1 hr post-dosing
    Time Frame
    week 24 and 52
    Title
    Changes from baseline COPD clinical symptoms (Cough frequency, sputum amount, severity of short breath, nocturnal sleep)
    Time Frame
    up to 52 weeks
    Title
    Frequency of rescue use of β2 stimulants
    Time Frame
    up to 2 weeks
    Title
    Changes from baseline in Quality of Life QOL (St George's Respiratory Questionnaire (SGRQ) and Airways Questionnaire-20 (AQ20), if possible)
    Time Frame
    week 24 and 52
    Title
    Patient's impression
    Time Frame
    week 24 and 52
    Title
    Physician's global evaluation
    Time Frame
    week 24 and 52

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    40 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: The patients with COPD (chronic bronchitis, emphysema) whose symptoms are stable and who satisfy the following criteria Patients with FEV1.0 of <=70% of predicted normal and FEV1.0/FVC of <=70% in the screening test (The FEV1.0 value should also be <=70% of predicted normal on the starting day of administration (visit 2).) Patients with a smoking history (<number of cigarettes smoked a day x number of smoking years> is >=200.) Male or female patients aged >=40 years old Exclusion Criteria: Patients complicated with bronchial asthma, making the assessment of drug efficacy against COPD difficult Patients using oral corticosteroid medication at a dose in excess of the equivalent 10 mg/day of prednisolon Patients with glaucoma Patients with symptomatic prostatic hypertrophy Patients with hypersensitivity to anticholinergic drugs or powder inhalants Patients with serious complication who are judged by the investigator to be inappropriate as the subjects of study Patients demonstrating clinically problematic abnormal laboratory test values (general blood test, biochemical test, urinalysis). Those showing Glutamic Oxaloacetic Transaminase (GOT) and Glutamic PyruvicTransaminase (GPT) twice the upper limit of the normal range, bilirubin 1.25 times or creatinine 1.25 times of the upper limit of normal range are excluded. Patients with a recent history of myocardial infarction or heart failure (i.e. within 3 months before the screening test) Patients with arrhythmia requiring the treatment with drugs Patients for whom the concomitant use of beta-blocker cannot be prohibited. Patients who began treatment with an ACE inhibitor within 1 month before the screening test Patients with tuberculosis (currently active) or with definite sequela of tuberculosis Patients with a recent history of carcinoma (excluding basal cell carcinoma) (i.e. within the past 5 years) Patients with a history of cystic fibrosis and bronchiectasis Patients with recent onset of upper airway infection (i.e. within 1 month before the screening test) Patients who have taken an investigational drug within one month or within period six times of half-lives of that drug (whichever is longer) before the screening test. Women who are pregnant or who may become pregnant, or those breast feeding Other than above, those who are judged by the investigator to be inappropriate as the subjects of study

    12. IPD Sharing Statement

    Links:
    URL
    http://trials.boehringer-ingelheim.com/content/dam/internet/opu/clinicaltrial/com_EN/results/205/205.227.pdf
    Description
    Related Info
    URL
    http://trials.boehringer-ingelheim.com/content/dam/internet/opu/clinicaltrial/com_EN/results/205/205.227_literature.pdf
    Description
    Related Info

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    Comparison of Tiotropium Inhalation Capsules and Oxitropium Metered Dose Inhalator (MDI) in Patients With Chronic Obstructive Pulmonary Disease (COPD)

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