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Assessment of the Safety and Ability of a Once-a-day Dose of an Orally Inhaled Medicine [ie, Glycopyrrolate Inhalation Solution = GIS] to Improve Airflow in the Lungs When Delivered With an Electronic eFlow Nebulizer System in Patients With Chronic Obstructive Pulmonary Disease (COPD)

Primary Purpose

Chronic Obstructive Pulmonary Disease

Status
Completed
Phase
Phase 2
Locations
Study Type
Interventional
Intervention
Glycopyrrolate Inhalation Solution 25mg
Glycopyrrolate Inhalation Solution 75mg
Glycopyrrolate Inhalation Solution 200mg
Glycopyrrolate Inhalation Solution 200mg Jet
Glycopyrrolate Inhalation Solution 500mg
Glycopyrrolate Inhalation Solution1000mg
Placebo
Sponsored by
Sunovion Respiratory Development Inc.
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Chronic Obstructive Pulmonary Disease focused on measuring Emphysema, Chronic bronchitis, COPD, Chronic Obstructive Pulmonary Disease

Eligibility Criteria

40 Years - 75 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Male and female patients aged 40 through 75 years, inclusive
  2. A clinical diagnosis of COPD according to the GOLD guidelines
  3. Current smokers or ex-smokers with at least 10 pack-year smoking history (e.g., at least 1 pack/day for 10 years, or 10 packs/day for 1 year)
  4. Post-bronchodilator FEV1 40-80% of predicted normal
  5. Post-bronchodilator FEV1/FVC ratio < 0.70
  6. Improvement in FEV1 >12% (minimum 150 mL) following inhalation of ipratropium bromide
  7. Ability to perform reproducible spirometry according to the ATS/ERS guidelines
  8. If female and of childbearing potential, must have had a negative pregnancy test and was not lactating at the Screening Visit, and was using one of the following acceptable means of birth control throughout the study:

    • Post-menopausal for at least two years
    • Surgically sterile
    • Oral contraceptives (taken for at least one month prior to the Screening Visit)
    • Approved implantable or injectable contraceptives (e.g., Norplant®, Depo-Provera® or equivalent)
    • Barrier methods (e.g., condoms with spermicide)
    • Intrauterine device (i.e., IUD)
    • Vasectomy of male partner
    • Non-heterosexual life style
  9. Willing and able to provide written informed consent

Exclusion Criteria:

  1. Current evidence or recent history of any clinically significant disease (other than COPD) or abnormality in the opinion of the Investigator that would put the patients at risk or which would compromise the quality of the study data; including but not limited to cardiovascular disease, myocardial infraction, hypertension, arrhythmia, diabetes, neurological or neuromuscular disease, liver disease, gastrointestinal disease or electrolyte abnormalities.
  2. Recent history of an exacerbation of airway disease within 3 months or need for increased treatments for COPD within 6 weeks prior to the Screening Visit.
  3. Regular use of daily oxygen therapy.
  4. Use of systemic (e.g., intramuscular or intravenous) steroids within 3 months prior to the Screening Visit
  5. Respiratory tract infection within 6 weeks prior to the Screening Visit
  6. History of tuberculosis, bronchiectasis or other non-specific pulmonary disease
  7. History of urinary retention or bladder neck obstruction type symptoms
  8. History of narrow-angle glaucoma
  9. Current or recent history (previous 12 months) of excessive use or abuse of alcohol
  10. Current evidence or history of abusing legal drugs or the use of illegal drugs or substances
  11. History of hypersensitivity or intolerance to aerosol medications
  12. Participation in another investigational drug study where drug was received within 30 days prior to the Screening Visit

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm 3

    Arm 4

    Arm 5

    Arm 6

    Arm 7

    Arm Type

    Experimental

    Experimental

    Experimental

    Experimental

    Experimental

    Experimental

    Placebo Comparator

    Arm Label

    Glycopyrrolate Inhalation Solution 25mg

    Glycopyrrolate Inhalation Solution 75mg

    Glycopyrrolate Inhalation Solution 200mg

    Glycopyrrolate Inhalation Solution 200mg Jet

    Glycopyrrolate Inhalation Solution 500mg

    Glycopyrrolate Inhalation Solution1000mg

    Placebo 0.5 mL

    Arm Description

    Glycopyrrolate Inhalation Solution 25 μg via eFlow nebulizer, once daily

    Glycopyrrolate Inhalation Solution 75 μg via eFlow nebulizer, once daily

    Glycopyrrolate Inhalation Solution 200 μg via eFlow nebulizer, once daily

    Glycopyrrolate Inhalation Solution 200 μg via jet nebulizer, once daily

    Glycopyrrolate Inhalation Solution 500 μg via eFlow nebulizer, once daily

    Glycopyrrolate Inhalation Solution 1000 μg via eFlow nebulizer, once daily

    Placebo 0.5 mL via jet nebulizer, once daily

    Outcomes

    Primary Outcome Measures

    Number of Subjects Who Died
    Number of Subjects With Treatment Emergent SAEs
    AEs are defined as existing conditions which worsen or events which occur during the course of the clinical trial after treatment.AEs are defined as existing conditions which worsen or events which occur during the course of the clinical trial after treatment. SAEs are AEs that result in the following outcomes: death, are life-threatening, persistent or significant disability/incapacity, congenital anomaly/birth defect, or important medical events that may have been considered a SAE when, based upon appropriate medical judgment, they may have jeopardized the subject and may have required medical or surgical intervention to prevent one of the outcomes listed in the definition.
    Number of Subjects Who Discontinued Due to AE
    AEs are defined as existing conditions which worsen or events which occur during the course of the clinical trial after treatment.
    Percentage of Subjects With Treatment Emergent AEs
    AEs are defined as existing conditions which worsen or events which occur during the course of the clinical trial after treatment.
    Number of Subjects With Clinically Significant Abnormal Vital Signs Reported During the Study
    Vital signs were measured at screening, during the study (pre-dose, and 30 and 60 minutes and 2, 4, 8, 12, 24 and 30 hours post-dose) and at post study assessment. The clinical significance of each out of normal range vital sign parameter was determined by the investigator during the study.
    Number of Subjects With Clinically Significant Abnormal Laboratory Results Reported During the Study
    Clinical safety lab parameters were collected at screening and at the post study follow-up assessment. The clinical significance of each out of normal range laboratory parameter was determined by the investigator during the study.
    Number of Subjects With Clinically Significant ECG Parameters Reported During the Study
    ECGs were measured at screening, during the study (pre-dose, and 30 and 60 minutes and 2, 4, 8, 12, 24 and 30 hours post-dose) and at post study follow-up assessment.
    Number of Subjects With Clinically Significant Abnormal Laboratory Results Reported During the Study
    Clinical safety lab parameters were collected at screening and at the post study follow-up assessment. The clinical significance of each out of normal range laboratory parameter was determined by the investigator during the study.
    Number of Subjects With Treatment Emergent AEs
    AEs are defined as existing conditions which worsen or events which occur during the course of the clinical trial after treatment. SAEs are AEs that result in the following outcomes: death, are life-threatening, persistent or significant disability/incapacity, congenital anomaly/birth defect, or important medical events that may have been considered a SAE when, based upon appropriate medical judgment, they may have jeopardized the subject and may have required medical or surgical intervention to prevent one of the outcomes listed in the definition.

    Secondary Outcome Measures

    Trough FEV1 (Change From Baseline)
    Spirometry measurements were conducted in accordance with the current ATS/ERS 2005 guidelines. Trough FEV1 was defined as the spirometry value collected at 24 hours post dose within each Treatment Period.
    Peak FEV1 (Percent Change)
    Spirometry measurements were conducted in accordance with the current ATS/ERS 2005 guidelines.
    Peak FEV1 (Change From Baseline )
    Spirometry measurements were conducted in accordance with the current ATS/ERS 2005 guidelines.
    FEV1 AUC0-24 Area Under the FEV1 Over Time Curve (Change From Baseline)
    Spirometry measurements were conducted in accordance with the current ATS/ERS 2005 guidelines.
    Cmax Maximum Observed Plasma Concentration
    Pk parameters are calculated from glycopyrrolate plasma concentration analysed from serial blood samples collected between 0 and 12 hr
    Tmax Time to Maximum Observed Plasma Concentration
    Pk parameters are calculated from glycopyrrolate plasma concentration analysed from serial blood samples collected between 0 and 12 hr
    AUC0-t Area Under the Plasma Concentration-time Curve From Time Zero to the Last Quantifiable Concentration
    Pk parameters are calculated from glycopyrrolate plasma concentration analysed from serial blood samples collected between 0 and 12 hr
    AUC0-inf Area Under the Plasma Concentration-time Curve From Time Zero to Infinity
    Pk parameters are calculated from glycopyrrolate plasma concentration analysed from serial blood samples collected between 0 and 12 hr
    t1/2 Plasma Half-life
    Pk parameters are calculated from glycopyrrolate plasma concentration analysed from serial blood samples collected between 0 and 12 hr.

    Full Information

    First Posted
    October 26, 2016
    Last Updated
    March 28, 2018
    Sponsor
    Sunovion Respiratory Development Inc.
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    1. Study Identification

    Unique Protocol Identification Number
    NCT02951312
    Brief Title
    Assessment of the Safety and Ability of a Once-a-day Dose of an Orally Inhaled Medicine [ie, Glycopyrrolate Inhalation Solution = GIS] to Improve Airflow in the Lungs When Delivered With an Electronic eFlow Nebulizer System in Patients With Chronic Obstructive Pulmonary Disease (COPD)
    Official Title
    Single-dose, Dose Escalation Study to Assess the Safety, Tolerability, Pharmacokinetics and Bronchodilatory Effects of Glycopyrrolate Inhalation Solution (GIS) Using a High Efficiency Nebulizer in Patients With COPD
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    March 2018
    Overall Recruitment Status
    Completed
    Study Start Date
    May 2009 (undefined)
    Primary Completion Date
    July 2009 (Actual)
    Study Completion Date
    July 2009 (Actual)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Sponsor
    Name of the Sponsor
    Sunovion Respiratory Development Inc.

    4. Oversight

    Data Monitoring Committee
    No

    5. Study Description

    Brief Summary
    The study assessed the safety and ability of several doses of an orally inhaled medicine [ie, Glycopyrrolate Inhalation Solution = GIS] to improve airflow in the lungs when delivered with an electronic eFlow nebulizer system in patients with Chronic Obstructive Pulmonary Disease (COPD). The study was conducted in 12 patients in 2 parts. Part 1 was designed to find the once-a- day GIS dose that produced the highest improvement in lung airflow. Part 2 tested the GIS dose with the highest improvement in lung airflow and a placebo (ie, no drug) delivered by a general purpose nebulizer. The airflow improvements of the same GIS dose were compared between the two nebulizer systems to determine what effect the device had on GIS delivery.
    Detailed Description
    In Part I, 12 subjects were randomly allocated to one of 2 cohorts, running in parallel. The 6 cohort 1 subjects received 25 mg and then 200 mg during their treatment periods 1 and 2, respectively. The 6 cohort 2 subjects received 75mg, 500mg, and 1000 mg during their treatment periods 1, 2, and 3, respectively. During Part II of the study, the same 12 subjects from Part I were randomized to receive either 200 mg jet or placebo in a 1:1 ratio.

    6. Conditions and Keywords

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

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Phase 2
    Interventional Study Model
    Parallel Assignment
    Masking
    ParticipantCare ProviderOutcomes Assessor
    Allocation
    Randomized
    Enrollment
    12 (Actual)

    8. Arms, Groups, and Interventions

    Arm Title
    Glycopyrrolate Inhalation Solution 25mg
    Arm Type
    Experimental
    Arm Description
    Glycopyrrolate Inhalation Solution 25 μg via eFlow nebulizer, once daily
    Arm Title
    Glycopyrrolate Inhalation Solution 75mg
    Arm Type
    Experimental
    Arm Description
    Glycopyrrolate Inhalation Solution 75 μg via eFlow nebulizer, once daily
    Arm Title
    Glycopyrrolate Inhalation Solution 200mg
    Arm Type
    Experimental
    Arm Description
    Glycopyrrolate Inhalation Solution 200 μg via eFlow nebulizer, once daily
    Arm Title
    Glycopyrrolate Inhalation Solution 200mg Jet
    Arm Type
    Experimental
    Arm Description
    Glycopyrrolate Inhalation Solution 200 μg via jet nebulizer, once daily
    Arm Title
    Glycopyrrolate Inhalation Solution 500mg
    Arm Type
    Experimental
    Arm Description
    Glycopyrrolate Inhalation Solution 500 μg via eFlow nebulizer, once daily
    Arm Title
    Glycopyrrolate Inhalation Solution1000mg
    Arm Type
    Experimental
    Arm Description
    Glycopyrrolate Inhalation Solution 1000 μg via eFlow nebulizer, once daily
    Arm Title
    Placebo 0.5 mL
    Arm Type
    Placebo Comparator
    Arm Description
    Placebo 0.5 mL via jet nebulizer, once daily
    Intervention Type
    Drug
    Intervention Name(s)
    Glycopyrrolate Inhalation Solution 25mg
    Other Intervention Name(s)
    GIS
    Intervention Description
    25 μg oral inhalation via eFlow Nebulizer, once daily
    Intervention Type
    Drug
    Intervention Name(s)
    Glycopyrrolate Inhalation Solution 75mg
    Other Intervention Name(s)
    GIS
    Intervention Description
    75 μg oral inhalation via eFlow Nebulizer, once daily
    Intervention Type
    Drug
    Intervention Name(s)
    Glycopyrrolate Inhalation Solution 200mg
    Other Intervention Name(s)
    GIS
    Intervention Description
    200 μg oral inhalation via eFlow Nebulizer, once daily
    Intervention Type
    Drug
    Intervention Name(s)
    Glycopyrrolate Inhalation Solution 200mg Jet
    Other Intervention Name(s)
    GIS
    Intervention Description
    200 μg oral inhalation via inhalation via jet nebulizer, once daily
    Intervention Type
    Drug
    Intervention Name(s)
    Glycopyrrolate Inhalation Solution 500mg
    Other Intervention Name(s)
    GIS
    Intervention Description
    500 μg oral inhalation via eFlow nebulizer, once daily
    Intervention Type
    Drug
    Intervention Name(s)
    Glycopyrrolate Inhalation Solution1000mg
    Other Intervention Name(s)
    GIS
    Intervention Description
    1000 μg oral inhalation via eFlow nebulizer, once daily
    Intervention Type
    Drug
    Intervention Name(s)
    Placebo
    Intervention Description
    Placebo 0.5 mL oral inhalation via jet nebulizer, once daily
    Primary Outcome Measure Information:
    Title
    Number of Subjects Who Died
    Time Frame
    0-47 days
    Title
    Number of Subjects With Treatment Emergent SAEs
    Description
    AEs are defined as existing conditions which worsen or events which occur during the course of the clinical trial after treatment.AEs are defined as existing conditions which worsen or events which occur during the course of the clinical trial after treatment. SAEs are AEs that result in the following outcomes: death, are life-threatening, persistent or significant disability/incapacity, congenital anomaly/birth defect, or important medical events that may have been considered a SAE when, based upon appropriate medical judgment, they may have jeopardized the subject and may have required medical or surgical intervention to prevent one of the outcomes listed in the definition.
    Time Frame
    0-47 days
    Title
    Number of Subjects Who Discontinued Due to AE
    Description
    AEs are defined as existing conditions which worsen or events which occur during the course of the clinical trial after treatment.
    Time Frame
    0-47 days
    Title
    Percentage of Subjects With Treatment Emergent AEs
    Description
    AEs are defined as existing conditions which worsen or events which occur during the course of the clinical trial after treatment.
    Time Frame
    0-47 days
    Title
    Number of Subjects With Clinically Significant Abnormal Vital Signs Reported During the Study
    Description
    Vital signs were measured at screening, during the study (pre-dose, and 30 and 60 minutes and 2, 4, 8, 12, 24 and 30 hours post-dose) and at post study assessment. The clinical significance of each out of normal range vital sign parameter was determined by the investigator during the study.
    Time Frame
    30 hrs post dose
    Title
    Number of Subjects With Clinically Significant Abnormal Laboratory Results Reported During the Study
    Description
    Clinical safety lab parameters were collected at screening and at the post study follow-up assessment. The clinical significance of each out of normal range laboratory parameter was determined by the investigator during the study.
    Time Frame
    day 47 (post studyfollow-up assessment)
    Title
    Number of Subjects With Clinically Significant ECG Parameters Reported During the Study
    Description
    ECGs were measured at screening, during the study (pre-dose, and 30 and 60 minutes and 2, 4, 8, 12, 24 and 30 hours post-dose) and at post study follow-up assessment.
    Time Frame
    30hr post dose
    Title
    Number of Subjects With Clinically Significant Abnormal Laboratory Results Reported During the Study
    Description
    Clinical safety lab parameters were collected at screening and at the post study follow-up assessment. The clinical significance of each out of normal range laboratory parameter was determined by the investigator during the study.
    Time Frame
    post study follow-up assessment (Day 47)
    Title
    Number of Subjects With Treatment Emergent AEs
    Description
    AEs are defined as existing conditions which worsen or events which occur during the course of the clinical trial after treatment. SAEs are AEs that result in the following outcomes: death, are life-threatening, persistent or significant disability/incapacity, congenital anomaly/birth defect, or important medical events that may have been considered a SAE when, based upon appropriate medical judgment, they may have jeopardized the subject and may have required medical or surgical intervention to prevent one of the outcomes listed in the definition.
    Time Frame
    0-47 days
    Secondary Outcome Measure Information:
    Title
    Trough FEV1 (Change From Baseline)
    Description
    Spirometry measurements were conducted in accordance with the current ATS/ERS 2005 guidelines. Trough FEV1 was defined as the spirometry value collected at 24 hours post dose within each Treatment Period.
    Time Frame
    24hr post dose
    Title
    Peak FEV1 (Percent Change)
    Description
    Spirometry measurements were conducted in accordance with the current ATS/ERS 2005 guidelines.
    Time Frame
    0 to 4hr
    Title
    Peak FEV1 (Change From Baseline )
    Description
    Spirometry measurements were conducted in accordance with the current ATS/ERS 2005 guidelines.
    Time Frame
    0 to 4hr
    Title
    FEV1 AUC0-24 Area Under the FEV1 Over Time Curve (Change From Baseline)
    Description
    Spirometry measurements were conducted in accordance with the current ATS/ERS 2005 guidelines.
    Time Frame
    0 to 24hr post dose
    Title
    Cmax Maximum Observed Plasma Concentration
    Description
    Pk parameters are calculated from glycopyrrolate plasma concentration analysed from serial blood samples collected between 0 and 12 hr
    Time Frame
    0 to 12 hours post dose
    Title
    Tmax Time to Maximum Observed Plasma Concentration
    Description
    Pk parameters are calculated from glycopyrrolate plasma concentration analysed from serial blood samples collected between 0 and 12 hr
    Time Frame
    0 to 12 hours post dose
    Title
    AUC0-t Area Under the Plasma Concentration-time Curve From Time Zero to the Last Quantifiable Concentration
    Description
    Pk parameters are calculated from glycopyrrolate plasma concentration analysed from serial blood samples collected between 0 and 12 hr
    Time Frame
    0 to 12 hourr post dose
    Title
    AUC0-inf Area Under the Plasma Concentration-time Curve From Time Zero to Infinity
    Description
    Pk parameters are calculated from glycopyrrolate plasma concentration analysed from serial blood samples collected between 0 and 12 hr
    Time Frame
    0 to 12 hours post dose
    Title
    t1/2 Plasma Half-life
    Description
    Pk parameters are calculated from glycopyrrolate plasma concentration analysed from serial blood samples collected between 0 and 12 hr.
    Time Frame
    0 to 12 hours post-dose

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    40 Years
    Maximum Age & Unit of Time
    75 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Male and female patients aged 40 through 75 years, inclusive A clinical diagnosis of COPD according to the GOLD guidelines Current smokers or ex-smokers with at least 10 pack-year smoking history (e.g., at least 1 pack/day for 10 years, or 10 packs/day for 1 year) Post-bronchodilator FEV1 40-80% of predicted normal Post-bronchodilator FEV1/FVC ratio < 0.70 Improvement in FEV1 >12% (minimum 150 mL) following inhalation of ipratropium bromide Ability to perform reproducible spirometry according to the ATS/ERS guidelines If female and of childbearing potential, must have had a negative pregnancy test and was not lactating at the Screening Visit, and was using one of the following acceptable means of birth control throughout the study: Post-menopausal for at least two years Surgically sterile Oral contraceptives (taken for at least one month prior to the Screening Visit) Approved implantable or injectable contraceptives (e.g., Norplant®, Depo-Provera® or equivalent) Barrier methods (e.g., condoms with spermicide) Intrauterine device (i.e., IUD) Vasectomy of male partner Non-heterosexual life style Willing and able to provide written informed consent Exclusion Criteria: Current evidence or recent history of any clinically significant disease (other than COPD) or abnormality in the opinion of the Investigator that would put the patients at risk or which would compromise the quality of the study data; including but not limited to cardiovascular disease, myocardial infraction, hypertension, arrhythmia, diabetes, neurological or neuromuscular disease, liver disease, gastrointestinal disease or electrolyte abnormalities. Recent history of an exacerbation of airway disease within 3 months or need for increased treatments for COPD within 6 weeks prior to the Screening Visit. Regular use of daily oxygen therapy. Use of systemic (e.g., intramuscular or intravenous) steroids within 3 months prior to the Screening Visit Respiratory tract infection within 6 weeks prior to the Screening Visit History of tuberculosis, bronchiectasis or other non-specific pulmonary disease History of urinary retention or bladder neck obstruction type symptoms History of narrow-angle glaucoma Current or recent history (previous 12 months) of excessive use or abuse of alcohol Current evidence or history of abusing legal drugs or the use of illegal drugs or substances History of hypersensitivity or intolerance to aerosol medications Participation in another investigational drug study where drug was received within 30 days prior to the Screening Visit
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Ahmet Tutuncu, MD, PhD
    Organizational Affiliation
    Elevation Pharmaceuticals, Inc.(now known as Sunovion Respiratory Development Inc.)
    Official's Role
    Study Chair

    12. IPD Sharing Statement

    Learn more about this trial

    Assessment of the Safety and Ability of a Once-a-day Dose of an Orally Inhaled Medicine [ie, Glycopyrrolate Inhalation Solution = GIS] to Improve Airflow in the Lungs When Delivered With an Electronic eFlow Nebulizer System in Patients With Chronic Obstructive Pulmonary Disease (COPD)

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