Clincosm LogoSign in Get a demo

A Randomized Trial Assessing Once Daily Administration of Mometasone Furoate DPI in Asthmatics (Study P02177)

Sponsor
Organon and Co (Industry)
Overall Status
Completed
CT.gov ID
NCT00835094
Collaborator
(none)
216
Enrollment
2
Arms
9
Actual Duration (Months)

Study Details

Study Description

Brief Summary

This will be an open-label, randomized, parallel-group comparison of mometasone furoate dry powder inhaler (MF-DPI) 400 mcg once daily administered in the morning vs. the evening for 12 weeks in subjects with asthma.

Condition or Disease Intervention/Treatment Phase
  • Device: Mometasone furoate
  • Device: Mometasone furoate
 Phase 4

Study Design

Study Type:
Interventional
Actual Enrollment :
216 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
A Randomized Trial Assessing the Chronobiology of Once Daily Administration of Mometasone Furoate DPI in Patients With Asthma
Actual Study Start Date :
Oct 1, 2002
Actual Primary Completion Date :
Jul 1, 2003
Actual Study Completion Date :
Jul 1, 2003

Arms and Interventions

Arm Intervention/Treatment
Experimental: Morning

Device: Mometasone furoate
MF-DPI 400 mcg once daily in the morning for 12 weeks
Other Names:
  • Asmanex
  • SCH 32088

    		•
    Experimental: Evening

    Device: Mometasone furoate
    MF-DPI 400 mcg once daily in the evening for 12 weeks
    Other Names:
  • Asmanex
  • SCH 32088

    		•

    Outcome Measures

    Primary Outcome Measures

    1. Between-treatment group comparisons (MF-DPI 400 mcg once daily in the morning compared to the evening) of daytime and nocturnal symptoms based on a 4 point scale. [12 weeks]

    2. To compare the incidence of adverse events of MF-DPI 400 mcg once daily administered in the morning compared to the evening. [12 weeks]

    Secondary Outcome Measures

    1. To assess morning vs. evening compliance with therapy. [12 weeks]

    2. To assess subject satisfaction with the Twisthaler^TM device. [12 weeks]

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    12 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:

    • Subjects (and their parent/guardian if the subject is <18) must demonstrate their willingness to participate in the study and comply with its procedures by signing a written informed consent.

    • Subjects must be >=12 years of age (unless restricted to an older age by local ethical committees or national health authorities), of either gender and any race.

    • Subjects must have had a history of asthma for >=6 months.

    • If the subject is taking inhaled corticosteroids, the daily dose must be <= the upper limit defined below:

    • budesonide <=800 mcg/day

    • triamcinolone acetonide <=800 mcg/day

    • beclomethasone dipropionate <=1000 mcg/day

    • fluticasone propionate <=500 mcg/day

    • flunisolide <=1000 mcg/day

    • Women of childbearing potential must have a negative urine (hCG) pregnancy test on the day of randomization (Baseline visit).

    • Women of childbearing potential (includes women who are <1 year postmenopausal) must be using an acceptable method of birth control (eg, hormonal contraceptive, medically prescribed IUD, condom in combination with spermicide) or be surgically sterilized (eg, hysterectomy or tubal ligation).

    • Subjects must agree to inform their usual treating physician (if other than the study investigator) of their participation in this study.

    Exclusion Criteria:

    • Female subjects who are pregnant, breast-feeding, or are premenarcheal.

    • Subjects who have required daily or alternate day oral corticosteroid treatment for more than a total of 14 days during the 6 months immediately prior to Visit 1, and/or subjects who have required a course of systemic corticosteroids within the previous month.

    • Subjects who have had either an asthma exacerbation or a clinically relevant change in asthma medication within the last 4 weeks.

    • Subjects who have been admitted to the hospital for asthma control within the previous 3 months or more than once within the previous 6 months.

    • Subjects who have required ventilator support for respiratory failure secondary to their asthma within the last 5 years.

    • Subjects who have used any investigational drug in the 30 days prior to Baseline, or subjects who have been treated with any investigational antibody for asthma in the 90 days prior to Baseline.

    • Subjects who are allergic or have had an idiosyncratic reaction to corticosteroids.

    • Subjects with any clinically significant disorder of the cardiovascular, neurologic, hematologic, gastrointestinal, cerebrovascular, or immunologic system, or respiratory disease other than asthma (eg, COPD), or any other disorder which may interfere with the study evaluations or affect subject safety.

    • Subjects with a history of drug abuse, poor motivation, hypochondriasis, or any other emotional or intellectual problems that are likely to limit the validity of consent to participate in the study.

    Contacts and Locations

    Locations

    No locations specified.

    Sponsors and Collaborators

    • Organon and Co

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Organon and Co
    ClinicalTrials.gov Identifier:
    NCT00835094
    Other Study ID Numbers:
    • P02177
    First Posted:
    Feb 3, 2009
    Last Update Posted:
    Feb 17, 2022
    Last Verified:
    Feb 1, 2022
    Additional relevant MeSH terms:
    Asthma
    Mometasone Furoate

    Study Results

    No Results Posted as of Feb 17, 2022