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Study of Mometasone Furoate/Formoterol Combination and Fluticasone/Salmeterol in Persistent Asthmatics Previously Treated With Inhaled Glucocorticosteroids (P04139)

Primary Purpose

Asthma

Status
Completed
Phase
Phase 3
Locations
Study Type
Interventional
Intervention
mometasone furoate combination MDI 200/10 mcg BID
mometasone furoate combination MDI 400/10 mcg BID
Fluticasone/Salmeterol 250/50 mcg BID
Fluticasone/Salmeterol 500/50 mcg BID
Sponsored by
Organon and Co
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Asthma

Eligibility Criteria

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

Inclusion Criteria:

  • Subjects of either sex and any race, at least 12 years of age, with a diagnosis of asthma of at least 12 months.
  • Use of medium or high daily dose of ICS (alone or in combination with long-acting beta-agonist [LABA]) for at least 12 weeks prior to Screening and have been on a stable regimen for at least 2 weeks prior to Screening.

    • Medium daily doses of ICS:

      • > 500 to 1000 mcg beclomethasone chlorofluorocarbon (CFC)
      • > 250 to 500 mcg beclomethasone hydrofluoroalkane (HFA)
      • > 600 to 1000 mcg budesonide dry powder inhaler (DPI)
      • > 1000 to 2000 mcg flunisolide
      • > 250 to 500 mcg fluticasone
      • 400 mcg MF
      • > 1000 to 2000 mcg triamcinolone acetonide
    • High daily doses of ICS:

      • > 1000 mcg beclomethasone CFC
      • > 500 mcg beclomethasone HFA
      • > 1000 mcg budesonide DPI
      • > 2000 mcg flunisolide
      • > 500 mcg fluticasone
      • > 400 mcg MF
      • > 2000 mcg triamcinolone acetonide
  • If there is no inherent harm in changing the subject's current asthma therapy, the subject must discontinue prescribed ICS or ICS/LABA combination at Baseline.
  • Must show evidence of reversibility within the last 12 months or during the Screening Period. Historical reversibility defined as an increase in absolute forced expiratory volume in 1 second (FEV1) of >= 12% and >= 200 mL will qualify if performed within 12 months of Screening. If no historical reversibility, subject must demonstrate an absolute FEV1 of >= 12% and >= 200 mL within 10 to 15 minutes after four puffs of salbutamol at Visit 1 or anytime prior to Baseline.
  • At Screening and Baseline, FEV1 must be >= 50% predicted, when restricted medications are withheld for the appropriate intervals.
  • Complete blood count, blood chemistries, urinalysis, and electrocardiogram (ECG) conducted at Screening must be within normal limits or clinically acceptable to the investigator/sponsor. A chest x-ray performed at Screening or within 12 months prior must be clinically acceptable.
  • A female of childbearing potential must be using a medically acceptable, adequate form of birth control:

    • prescribed hormonal contraceptives;
    • medically prescribed intrauterine device (IUD);
    • medically prescribed transdermal contraceptive;
    • condom in combination with spermicide;
    • monogamous relationship with a male partner who has had a vasectomy.

Birth control must have started at least 3 months prior to Screening. Subject must agree to continue its use for the duration of the study. A subject of childbearing potential who is not currently sexually active must agree to use a medically acceptable method should she become sexually active during the study. Women who have been surgically sterilized or are at least 1 year postmenopausal are not considered to be of childbearing potential. A subject of childbearing potential must have a negative serum pregnancy test at Screening.

Key Exclusion Criteria:

  • A change (increase or decrease) in absolute FEV1 of > 20% at any time from the Screening Visit up to, and including, the Baseline Visit.
  • A subject who requires the use of > 12 inhalations per day of short-acting beta-agonist (SABA) MDI or > 2 nebulized treatments per day of 2.5 mg salbutamol, on any 2 consecutive days from the Screening Visit up to, and including, the Baseline Visit.
  • A subject who experiences a clinical asthma exacerbation (defined as a deterioration of asthma that results in emergency treatment, hospitalization due to asthma, or treatment with additional, excluded asthma medication [other than SABA]) at any time from the Screening Visit up to, and including, the Baseline Visit.
  • A subject who has ever required ventilator support for respiratory failure secondary to asthma.
  • A subject who is a smoker or ex-smoker and has smoked within the previous year or has had a cumulative smoking history > 10 pack-years.

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm 3

    Arm 4

    Arm Type

    Experimental

    Experimental

    Active Comparator

    Active Comparator

    Arm Label

    MF/F 200/10 mcg BID

    MF/F 400/10 mcg BID

    F/SC 250/50 mcg BID

    F/SC 500/50 mcg BID

    Arm Description

    Outcomes

    Primary Outcome Measures

    The Number of All Randomized Subjects Reporting Adverse Events (AEs).
    AEs that are considered Related, Severe, and Serious, as determined by the investigator and using specific criteria defined in the protocol, are included in the primary results.

    Secondary Outcome Measures

    Full Information

    First Posted
    September 19, 2006
    Last Updated
    February 7, 2022
    Sponsor
    Organon and Co
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    1. Study Identification

    Unique Protocol Identification Number
    NCT00379288
    Brief Title
    Study of Mometasone Furoate/Formoterol Combination and Fluticasone/Salmeterol in Persistent Asthmatics Previously Treated With Inhaled Glucocorticosteroids (P04139)
    Official Title
    A 1-Year Safety Study of Medium and High Doses of Mometasone Furoate/Formoterol Combination Formulation and Medium and High Doses of Fluticasone/Salmeterol in Persistent Asthmatics Previously Treated With Medium to High Doses of Inhaled Glucocorticosteroids
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    February 2022
    Overall Recruitment Status
    Completed
    Study Start Date
    June 2006 (undefined)
    Primary Completion Date
    November 2007 (Actual)
    Study Completion Date
    November 2007 (Actual)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Sponsor
    Name of the Sponsor
    Organon and Co

    4. Oversight

    Data Monitoring Committee
    No

    5. Study Description

    Brief Summary
    The purpose of this study is to evaluate the long-term safety of mometasone furoate/formoterol (MF/F) metered dose inhaler (MDI) 200/10 mcg twice-a-day (BID) and MF/F MDI 400/10 mcg BID and two doses of fluticasone/salmeterol combination (F/SC) (250/50 mcg BID and 500/50 mcg BID) in subjects with persistent asthma who require maintenance treatment on inhaled glucocorticosteroids (ICS); evaluator-blind. In addition, the extrapulmonary effects on 24-hour plasma cortisol area under curve (AUC), of MF/F MDI 200/10 mcg BID, MF/F MDI 400/10 mcg BID, F/SC MDI 250/50 mcg BID, and F/SC MDI 500/50 mcg BID will be evaluated.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Asthma

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Phase 3
    Interventional Study Model
    Parallel Assignment
    Masking
    None (Open Label)
    Allocation
    Randomized
    Enrollment
    404 (Actual)

    8. Arms, Groups, and Interventions

    Arm Title
    MF/F 200/10 mcg BID
    Arm Type
    Experimental
    Arm Title
    MF/F 400/10 mcg BID
    Arm Type
    Experimental
    Arm Title
    F/SC 250/50 mcg BID
    Arm Type
    Active Comparator
    Arm Title
    F/SC 500/50 mcg BID
    Arm Type
    Active Comparator
    Intervention Type
    Drug
    Intervention Name(s)
    mometasone furoate combination MDI 200/10 mcg BID
    Other Intervention Name(s)
    SCH 418131
    Intervention Description
    MF/F 200/10 mcg via a metered dose inhaler (MDI) twice daily for 1 year
    Intervention Type
    Drug
    Intervention Name(s)
    mometasone furoate combination MDI 400/10 mcg BID
    Other Intervention Name(s)
    SCH 418131
    Intervention Description
    MF/F 400/10 mcg via a metered dose inhaler (MDI) twice daily for 1 year
    Intervention Type
    Drug
    Intervention Name(s)
    Fluticasone/Salmeterol 250/50 mcg BID
    Other Intervention Name(s)
    Seretide
    Intervention Description
    F/SC 250/50 twice daily for 1 year
    Intervention Type
    Drug
    Intervention Name(s)
    Fluticasone/Salmeterol 500/50 mcg BID
    Other Intervention Name(s)
    Seretide
    Intervention Description
    F/SC 500/50 twice daily for 1 year
    Primary Outcome Measure Information:
    Title
    The Number of All Randomized Subjects Reporting Adverse Events (AEs).
    Description
    AEs that are considered Related, Severe, and Serious, as determined by the investigator and using specific criteria defined in the protocol, are included in the primary results.
    Time Frame
    1 year

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    12 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Subjects of either sex and any race, at least 12 years of age, with a diagnosis of asthma of at least 12 months. Use of medium or high daily dose of ICS (alone or in combination with long-acting beta-agonist [LABA]) for at least 12 weeks prior to Screening and have been on a stable regimen for at least 2 weeks prior to Screening. Medium daily doses of ICS: > 500 to 1000 mcg beclomethasone chlorofluorocarbon (CFC) > 250 to 500 mcg beclomethasone hydrofluoroalkane (HFA) > 600 to 1000 mcg budesonide dry powder inhaler (DPI) > 1000 to 2000 mcg flunisolide > 250 to 500 mcg fluticasone 400 mcg MF > 1000 to 2000 mcg triamcinolone acetonide High daily doses of ICS: > 1000 mcg beclomethasone CFC > 500 mcg beclomethasone HFA > 1000 mcg budesonide DPI > 2000 mcg flunisolide > 500 mcg fluticasone > 400 mcg MF > 2000 mcg triamcinolone acetonide If there is no inherent harm in changing the subject's current asthma therapy, the subject must discontinue prescribed ICS or ICS/LABA combination at Baseline. Must show evidence of reversibility within the last 12 months or during the Screening Period. Historical reversibility defined as an increase in absolute forced expiratory volume in 1 second (FEV1) of >= 12% and >= 200 mL will qualify if performed within 12 months of Screening. If no historical reversibility, subject must demonstrate an absolute FEV1 of >= 12% and >= 200 mL within 10 to 15 minutes after four puffs of salbutamol at Visit 1 or anytime prior to Baseline. At Screening and Baseline, FEV1 must be >= 50% predicted, when restricted medications are withheld for the appropriate intervals. Complete blood count, blood chemistries, urinalysis, and electrocardiogram (ECG) conducted at Screening must be within normal limits or clinically acceptable to the investigator/sponsor. A chest x-ray performed at Screening or within 12 months prior must be clinically acceptable. A female of childbearing potential must be using a medically acceptable, adequate form of birth control: prescribed hormonal contraceptives; medically prescribed intrauterine device (IUD); medically prescribed transdermal contraceptive; condom in combination with spermicide; monogamous relationship with a male partner who has had a vasectomy. Birth control must have started at least 3 months prior to Screening. Subject must agree to continue its use for the duration of the study. A subject of childbearing potential who is not currently sexually active must agree to use a medically acceptable method should she become sexually active during the study. Women who have been surgically sterilized or are at least 1 year postmenopausal are not considered to be of childbearing potential. A subject of childbearing potential must have a negative serum pregnancy test at Screening. Key Exclusion Criteria: A change (increase or decrease) in absolute FEV1 of > 20% at any time from the Screening Visit up to, and including, the Baseline Visit. A subject who requires the use of > 12 inhalations per day of short-acting beta-agonist (SABA) MDI or > 2 nebulized treatments per day of 2.5 mg salbutamol, on any 2 consecutive days from the Screening Visit up to, and including, the Baseline Visit. A subject who experiences a clinical asthma exacerbation (defined as a deterioration of asthma that results in emergency treatment, hospitalization due to asthma, or treatment with additional, excluded asthma medication [other than SABA]) at any time from the Screening Visit up to, and including, the Baseline Visit. A subject who has ever required ventilator support for respiratory failure secondary to asthma. A subject who is a smoker or ex-smoker and has smoked within the previous year or has had a cumulative smoking history > 10 pack-years.

    12. IPD Sharing Statement

    Plan to Share IPD
    Yes
    IPD Sharing Plan Description
    http://www.merck.com/clinical-trials/pdf/Merck%20Procedure%20on%20Clinical%20Trial%20Data%20Access%20Final_Updated%20July_9_2014.pdf http://engagezone.msd.com/ds_documentation.php
    Citations:
    PubMed Identifier
    20874458
    Citation
    Maspero JF, Nolte H, Cherrez-Ojeda I; P04139 Study Group. Long-term safety of mometasone furoate/formoterol combination for treatment of patients with persistent asthma. J Asthma. 2010 Dec;47(10):1106-15. doi: 10.3109/02770903.2010.514634. Epub 2010 Nov 1. Erratum In: J Asthma. 2011 Feb;48(1):114.
    Results Reference
    result
    PubMed Identifier
    25044280
    Citation
    Maspero J, Cherrez I, Doherty DE, Tashkin DP, Kuna P, Kuo WL, Gates D, Nolte H, Chylack LT Jr. Appraisal of lens opacity with mometasone furoate/formoterol fumarate combination in patients with COPD or asthma. Respir Med. 2014 Sep;108(9):1355-62. doi: 10.1016/j.rmed.2014.04.015. Epub 2014 May 2.
    Results Reference
    derived

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    Study of Mometasone Furoate/Formoterol Combination and Fluticasone/Salmeterol in Persistent Asthmatics Previously Treated With Inhaled Glucocorticosteroids (P04139)

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