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Dose Ranging Study of Ba 679 BR Inhalation Powder in Chronic Obstructive Pulmonary Disease (COPD) Patients

Primary Purpose

Pulmonary Disease, Chronic Obstructive

Status
Completed
Phase
Phase 2
Locations
Study Type
Interventional
Intervention
Ba 679 BR low dose
Ba 679 BR middle dose
Ba 679 BR high dose
Placebo inhalation powder
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. In a pulmonary function test of Screening Test II, FEV1.0 was less than 70% of predict normal and FEV1.0 was less than 70% of FVC.
  2. In the reversibility test of Screening Test II, FEV1.0 was improved by 10% or more at 1 hour after inhalation of 2 puffs of an anticholinergic agent (Tersigan ® Aerozol)
  3. History of smoking (< no. of cigarettes a day x no. of years of smoking > = 200 or more)
  4. 40 years of age or older
  5. Regardless of sex and the length of disease period

Exclusion Criteria:

  1. A history of bronchial asthma
  2. A history of atopic disease, such as allergic rhinitis
  3. Blood eosinophil of 440/µl or more
  4. Continuous use of steroid drugs (oral administration, inhalation or injection) at a dose equivalent to over 5 mg daily of prednisolone
  5. A history of respiratory infection, including virus infection within 1 month before study initiation
  6. Tuberculosis, lung cancer or a history of pneumonectomy
  7. Glaucoma
  8. Under treatment of benign prostatic hypertrophy
  9. Hypersensitivity to anticholinergic agents or sympathomimetics
  10. Difficulty in expectoration of sputum
  11. Serious heart disease, renal disease, hepatic disease, endocrine disease or metabolic disease
  12. Use of any β blockers
  13. A history of myocardial infarction within the past 1 year
  14. A history of heart failure, cor pulmonale or arrhythmia requiring medication within the past 3 years
  15. A history of drug abuse or alcoholism
  16. Treatment of psychotic disease
  17. Pregnancy, possible pregnancy or lactation
  18. A history of participation in any other clinical studies within the past 6 months
  19. Judgment by the investigator that the patient is ineligible for inclusion in the present study

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm 3

    Arm 4

    Arm Type

    Experimental

    Placebo Comparator

    Experimental

    Experimental

    Arm Label

    Ba 679 BR low dose

    Placebo inhalation powder

    Ba 679 BR middle dose

    Ba 679 BR high dose

    Arm Description

    Outcomes

    Primary Outcome Measures

    FEV1.0 max (maximum forced expiratory volume in one second)

    Secondary Outcome Measures

    FEV1.0 AUC 0-24 (forced expiratory volume in one second as area under the curve 0 to 24 hours after administration)
    FEV1.0 time to response
    FEV1.0 Tmax (time to FEV1.0 max)
    FEV1.0 at measuring time points up to 24 hours after administration of study drug
    FVC AUC 0-24 (forced vital capacity as area under the curve 0 to 24 hours after administration)
    FVC max
    FVC at measuring time points up to 24 hours after administration of study drug
    Occurrence of adverse events
    Changes in blood pressure
    Changes in pulse rate
    Changes in transdermal O2 saturation
    Abnormal findings in electrocardiogram (ECG)
    Abnormal changes in laboratory measurements
    Urinary excretion rate
    MMEF AUC 0-24 (maximal midexpiratory flow as area under the curve 0 to 24 hours after administration)
    MMEF max
    MMEF at measuring time points up to 24 hours after administration of study drug

    Full Information

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

    Unique Protocol Identification Number
    NCT02172352
    Brief Title
    Dose Ranging Study of Ba 679 BR Inhalation Powder in Chronic Obstructive Pulmonary Disease (COPD) Patients
    Official Title
    Dose Ranging Study of Ba 679 BR Inhalation Powder Following Single Inhalation in COPD Patients - Double-blind, Placebo-controlled, 4 Treatment, 4 Period Crossover Study-
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    June 2014
    Overall Recruitment Status
    Completed
    Study Start Date
    July 1998 (undefined)
    Primary Completion Date
    May 1999 (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
    To investigate the dose response following single inhalation of Ba 679 BR inhalation powder in COPD patients using pulmonary functions as indicators, and to compare data obtained with overseas study findings

    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 2
    Interventional Study Model
    Crossover Assignment
    Masking
    Double
    Allocation
    Randomized
    Enrollment
    28 (Actual)

    8. Arms, Groups, and Interventions

    Arm Title
    Ba 679 BR low dose
    Arm Type
    Experimental
    Arm Title
    Placebo inhalation powder
    Arm Type
    Placebo Comparator
    Arm Title
    Ba 679 BR middle dose
    Arm Type
    Experimental
    Arm Title
    Ba 679 BR high dose
    Arm Type
    Experimental
    Intervention Type
    Drug
    Intervention Name(s)
    Ba 679 BR low dose
    Intervention Type
    Drug
    Intervention Name(s)
    Ba 679 BR middle dose
    Intervention Type
    Drug
    Intervention Name(s)
    Ba 679 BR high dose
    Intervention Type
    Drug
    Intervention Name(s)
    Placebo inhalation powder
    Primary Outcome Measure Information:
    Title
    FEV1.0 max (maximum forced expiratory volume in one second)
    Time Frame
    before and up to 24 hours after each study drug administration
    Secondary Outcome Measure Information:
    Title
    FEV1.0 AUC 0-24 (forced expiratory volume in one second as area under the curve 0 to 24 hours after administration)
    Time Frame
    before and up to 24 hours after each study drug administration
    Title
    FEV1.0 time to response
    Time Frame
    before and up to 24 hours after each study drug administration
    Title
    FEV1.0 Tmax (time to FEV1.0 max)
    Time Frame
    before and up to 24 hours after each study drug administration
    Title
    FEV1.0 at measuring time points up to 24 hours after administration of study drug
    Time Frame
    before and up to 24 hours after each study drug administration
    Title
    FVC AUC 0-24 (forced vital capacity as area under the curve 0 to 24 hours after administration)
    Time Frame
    before and up to 24 hours after each study drug administration
    Title
    FVC max
    Time Frame
    before and up to 24 hours after each study drug administration
    Title
    FVC at measuring time points up to 24 hours after administration of study drug
    Time Frame
    before and up to 24 hours after each study drug administration
    Title
    Occurrence of adverse events
    Time Frame
    up to 29 days
    Title
    Changes in blood pressure
    Time Frame
    before and up to 24 hours after each study drug administration
    Title
    Changes in pulse rate
    Time Frame
    before and up to 24 hours after each study drug administration
    Title
    Changes in transdermal O2 saturation
    Time Frame
    before and up to 24 hours after each study drug administration
    Title
    Abnormal findings in electrocardiogram (ECG)
    Time Frame
    before and 1.5 and 24 hours after each administration of study drug
    Title
    Abnormal changes in laboratory measurements
    Time Frame
    at 24 hours after last study drug administration
    Title
    Urinary excretion rate
    Time Frame
    before (from 4 hours pre-dosing until immediately before dosing) and 0-2, 2-4, 4-8, 8-12 and 12-24 hours after drug administration
    Title
    MMEF AUC 0-24 (maximal midexpiratory flow as area under the curve 0 to 24 hours after administration)
    Time Frame
    before and up to 24 hours after each study drug administration
    Title
    MMEF max
    Time Frame
    before and up to 24 hours after each study drug administration
    Title
    MMEF at measuring time points up to 24 hours after administration of study drug
    Time Frame
    before and up to 24 hours after each study drug administration

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    40 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: In a pulmonary function test of Screening Test II, FEV1.0 was less than 70% of predict normal and FEV1.0 was less than 70% of FVC. In the reversibility test of Screening Test II, FEV1.0 was improved by 10% or more at 1 hour after inhalation of 2 puffs of an anticholinergic agent (Tersigan ® Aerozol) History of smoking (< no. of cigarettes a day x no. of years of smoking > = 200 or more) 40 years of age or older Regardless of sex and the length of disease period Exclusion Criteria: A history of bronchial asthma A history of atopic disease, such as allergic rhinitis Blood eosinophil of 440/µl or more Continuous use of steroid drugs (oral administration, inhalation or injection) at a dose equivalent to over 5 mg daily of prednisolone A history of respiratory infection, including virus infection within 1 month before study initiation Tuberculosis, lung cancer or a history of pneumonectomy Glaucoma Under treatment of benign prostatic hypertrophy Hypersensitivity to anticholinergic agents or sympathomimetics Difficulty in expectoration of sputum Serious heart disease, renal disease, hepatic disease, endocrine disease or metabolic disease Use of any β blockers A history of myocardial infarction within the past 1 year A history of heart failure, cor pulmonale or arrhythmia requiring medication within the past 3 years A history of drug abuse or alcoholism Treatment of psychotic disease Pregnancy, possible pregnancy or lactation A history of participation in any other clinical studies within the past 6 months Judgment by the investigator that the patient is ineligible for inclusion in the present study

    12. IPD Sharing Statement

    Links:
    URL
    http://trials.boehringer-ingelheim.com/content/dam/internet/opu/clinicaltrial/com_EN/results/205/205.139_U00-0156.pdf
    Description
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    Dose Ranging Study of Ba 679 BR Inhalation Powder in Chronic Obstructive Pulmonary Disease (COPD) Patients

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