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A Study of Montelukast (MK-0476) Compared With Fluticasone in Pediatric Participants With Chronic Asthma (MK-0476-303)

Primary Purpose

Asthma, Bronchial

Status
Withdrawn
Phase
Phase 3
Locations
Study Type
Interventional
Intervention
Montelukast sodium
Placebo to montelukast
Fluticasone propionate
Placebo to fluticasone
Sponsored by
Organon and Co
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Asthma, Bronchial

Eligibility Criteria

6 Months - 5 Years (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Between 6 months and 5 years, 4 months of age
  • Diagnosed with asthma by a doctor
  • At least 3 episodes of asthma symptoms within the last 6 months

Exclusion Criteria:

  • Active or chronic breathing disease, other than asthma
  • Required insertion of a breathing tube for asthma
  • Major surgery within the last 4 weeks
  • Currently in the hospital
  • Allergic to certain drugs, and for children under 2 years of age, apples, applesauce and formula

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Experimental

    Active Comparator

    Arm Label

    Montelukast

    Fluticasone

    Arm Description

    Participants receive montelukast 4 mg oral granules (OG) or 4 mg chewable tablets (CT) once daily (QD) for 24 weeks and placebo to fluticasone 50 mcg inhalation aerosol twice daily (BID) for 24 weeks. Participants aged >6 months to <2 years receive montelukast 4 mg packet of OG QD for 24 weeks. Participants aged >2 years to <64 months receive montelukast 4 mg CT QD for 24 weeks.

    Participants receive fluticasone 50 mcg inhalation aerosol twice daily (BID) for 24 weeks and placebo to montelukast 4 mg QD for 24 weeks. Participants aged >6 months to <2 years receive placebo packet of OG QD for 24 weeks. Participants aged >2 years to <64 months receive placebo CT QD for 24 weeks.

    Outcomes

    Primary Outcome Measures

    Percentage of days without asthma
    A day without asthma is defined as a day with all of the following: no daytime symptoms, no nighttime cough, no β-agonist use, and no asthma attack (defined as a visit to a doctor, urgent care clinic, emergency room, or hospital for asthma [other than a scheduled visit to a doctor], or treatment with systemic corticosteroid during the previous 24 hours).
    Number of participants who experience at least one adverse event (AE)
    Number of participants who discontinue study drug due to an AE

    Secondary Outcome Measures

    Percentage of days without daytime symptoms
    Percentage of days without nighttime cough
    Percentage of days without β-agonist use

    Full Information

    First Posted
    October 4, 2007
    Last Updated
    January 31, 2022
    Sponsor
    Organon and Co
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    1. Study Identification

    Unique Protocol Identification Number
    NCT00540839
    Brief Title
    A Study of Montelukast (MK-0476) Compared With Fluticasone in Pediatric Participants With Chronic Asthma (MK-0476-303)
    Official Title
    A Phase III Double-Blind, Randomized, Placebo-Controlled Clinical Trial to Prospectively Evaluate Efficacy of Montelukast in Patients Aged 6 Months to 5 Years With Chronic Asthma
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    January 2022
    Overall Recruitment Status
    Withdrawn
    Why Stopped
    Based on input from regulatory agencies, it is not necessary to conduct this study. An ongoing study was sufficient for regulatory purposes.
    Study Start Date
    November 2007 (undefined)
    Primary Completion Date
    March 2008 (Actual)
    Study Completion Date
    undefined (undefined)

    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
    A study to determine the effects of montelukast (MK-0476) on pediatric participants with chronic asthma compared with fluticasone. The primary hypotheses are that, over 24 weeks of treatment, montelukast will provide at least the same level of asthma control as inhaled fluticasone as measured by the percentage of days without asthma and that, over 24 weeks of treatment, daily administration of montelukast will be safe and well tolerated in children aged 6 months to 5 years with chronic asthma. This trial was stopped at a time before any participants had actually entered the trial. Based on input from regulatory agencies, it is not necessary to conduct this study; a separate ongoing study was sufficient for regulatory purposes.
    Detailed Description
    This study consists of a 4-week placebo run-in period followed by a 24-week double-blind treatment period.

    6. Conditions and Keywords

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

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Phase 3
    Interventional Study Model
    Parallel Assignment
    Masking
    ParticipantCare ProviderInvestigator
    Allocation
    Randomized
    Enrollment
    0 (Actual)

    8. Arms, Groups, and Interventions

    Arm Title
    Montelukast
    Arm Type
    Experimental
    Arm Description
    Participants receive montelukast 4 mg oral granules (OG) or 4 mg chewable tablets (CT) once daily (QD) for 24 weeks and placebo to fluticasone 50 mcg inhalation aerosol twice daily (BID) for 24 weeks. Participants aged >6 months to <2 years receive montelukast 4 mg packet of OG QD for 24 weeks. Participants aged >2 years to <64 months receive montelukast 4 mg CT QD for 24 weeks.
    Arm Title
    Fluticasone
    Arm Type
    Active Comparator
    Arm Description
    Participants receive fluticasone 50 mcg inhalation aerosol twice daily (BID) for 24 weeks and placebo to montelukast 4 mg QD for 24 weeks. Participants aged >6 months to <2 years receive placebo packet of OG QD for 24 weeks. Participants aged >2 years to <64 months receive placebo CT QD for 24 weeks.
    Intervention Type
    Drug
    Intervention Name(s)
    Montelukast sodium
    Other Intervention Name(s)
    MK-0476, Singulair®
    Intervention Description
    Montelukast 4 mg OG or montelukast 4 mg CT
    Intervention Type
    Drug
    Intervention Name(s)
    Placebo to montelukast
    Intervention Description
    Placebo OG or CT
    Intervention Type
    Drug
    Intervention Name(s)
    Fluticasone propionate
    Intervention Description
    Fluticasone 50 mcg inhalation aerosol metered dose inhaler
    Intervention Type
    Drug
    Intervention Name(s)
    Placebo to fluticasone
    Intervention Description
    Placebo inhalation aerosol metered dose inhaler
    Primary Outcome Measure Information:
    Title
    Percentage of days without asthma
    Description
    A day without asthma is defined as a day with all of the following: no daytime symptoms, no nighttime cough, no β-agonist use, and no asthma attack (defined as a visit to a doctor, urgent care clinic, emergency room, or hospital for asthma [other than a scheduled visit to a doctor], or treatment with systemic corticosteroid during the previous 24 hours).
    Time Frame
    24 weeks
    Title
    Number of participants who experience at least one adverse event (AE)
    Time Frame
    Up to 26 weeks
    Title
    Number of participants who discontinue study drug due to an AE
    Time Frame
    Up to 24 weeks
    Secondary Outcome Measure Information:
    Title
    Percentage of days without daytime symptoms
    Time Frame
    24 weeks
    Title
    Percentage of days without nighttime cough
    Time Frame
    24 weeks
    Title
    Percentage of days without β-agonist use
    Time Frame
    24 weeks
    Other Pre-specified Outcome Measures:
    Title
    Percentage of participants without asthma attacks
    Time Frame
    24 weeks
    Title
    Percentage of participants without corticosteroid rescues
    Time Frame
    24 weeks
    Title
    Caregiver global evaluation
    Time Frame
    Week 24
    Title
    Physician global evaluation
    Time Frame
    Week 24
    Title
    Percentage of days without individual daytime asthma symptoms (cough, wheeze, trouble breathing, and activity limitation)
    Time Frame
    24 weeks

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    6 Months
    Maximum Age & Unit of Time
    5 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Between 6 months and 5 years, 4 months of age Diagnosed with asthma by a doctor At least 3 episodes of asthma symptoms within the last 6 months Exclusion Criteria: Active or chronic breathing disease, other than asthma Required insertion of a breathing tube for asthma Major surgery within the last 4 weeks Currently in the hospital Allergic to certain drugs, and for children under 2 years of age, apples, applesauce and formula
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Medical Director
    Organizational Affiliation
    Merck Sharp & Dohme LLC
    Official's Role
    Study Director

    12. IPD Sharing Statement

    Learn more about this trial

    A Study of Montelukast (MK-0476) Compared With Fluticasone in Pediatric Participants With Chronic Asthma (MK-0476-303)

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