Comparison of Combination Therapy: Montelukast and Inhaled Steroid on Exercise Induced Bronchoconstriction

Asthma Clinical Trial

Official title:

A Randomised Double Blind, Placebo Controlled 4-way Cross Over Study Comparing Montelukast, Inhaled Budesonide and Their Combination on Exercise-induced Bronchoconstriction

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT00462592
• Other study ID #: monbud8035
• Status: Completed
• Phase: Phase 3
• First received: April 18, 2007
• Last updated: October 20, 2009
• Start date: March 2007
• Est. completion date: June 2009

Study information

• Verified date: October 2009
• Source: McMaster University
• Contact: n/a
• Is FDA regulated: No
• Health authority: Canada: Health Canada
• Study type: Interventional

Clinical Trial Summary

The purpose of this study is to compare the effects of 2 weeks therapy of montelukast, budesonide, their combination on exercise induced bronchoconstriction (EIB) and airway inflammation in children and young adults, not on regular controller therapy.

Inhaled corticosteroids (ICS) are potent anti-inflammatory agents, which are effective in controlling and improving all aspects of asthma including the attenuation of EIB. However, the effect of ICS monotherapy on EIB is comparable if not inferior to the effect of CysLTs modifiers alone. This may be due to the lack of effect of ICS on the CysLT pathway. As a consequence, the investigators hypothesize that the combination of ICS and CysLT modifiers will offer a greater protection against EIB than either therapy alone. The different classes of drugs may act on complementary pathways believed to be important in the pathophysiology of EIB.

Description:

The study will be a 2 centre randomised, double blind, placebo controlled 4-way cross over study comparing montelukast, budesonide and their combination on exercise-induced bronchoconstriction (EIB). Subjects with stable mild to moderate asthma, between the ages of 8-35 years, not on controller asthma therapy will be screened. A maxFEV1% ≥15% following a standardized dry air exercise challenge at screening (SC) and following a 1 week run-in (V-1) is required to qualify. Once qualified, subjects will return the following day (V0) for a skin prick test and a methacholine inhalation test before being randomised to 1 of 4 treatment sequences. Each treatment will be given for a total of 14 days with a 4 weeks washout. During each period, subjects will attend the laboratory on 2 occasions, at the beginning and end of each period. Baseline spirometry; eNO; EBC will be performed, followed by an exercise challenge with serial FEV1 and eNO measurements up to 30 minutes post exercise and post-exercise EBC and sputum induction at each evaluation visit. There will be a total of 10 visits and the duration of study will be approximately 148 days (21 weeks). All visits will be scheduled within 2 hours of the post-run visit (V1) and at least 8 hours after the last dose of trial medications.

Investigational Product, Dose and Administration:

Montelukast 5mg (<15 years) or 10mg (and matching placebo) will be taken 1 tablet in the evening together with inhaled budesonide turbuhalers 200ug (and matching placebo) taken 1 puff in the morning and 1 puff in the evening.

Efficacy on EIB:

The changes between pre and post treatment exercise-induced maxFEV1% and area under the curve (AUC0-30) will be compared between the 4 periods. MaxFEV1% will be calculated as pre-exercise FEV1 minus post exercise lowest FEV1 divided by pre-exercise FEV1 multiplied by 100; AUC will be calculated using the trapezoidal rule. The protection provided by the active treatments will be defined as the pre-treatment maxFEV1% minus post-treatment maxFEV1% divided by pre-treatment maxFEV1% x 100. The proportions of subjects attaining ≥50% protection will be compared between the 4 arms.

Efficacy on eNO and inflammatory parameters measured in sputum and EBC Changes in % and absolute counts of sputum differential cells, eNO and inflammatory mediators (in EBC/ sputum) at baseline and in response to exercise will be compared between the 4 arms.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 18
• Est. completion date: June 2009
• Est. primary completion date: June 2009
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 8 Years to 35 Years

Eligibility

Inclusion Criteria:

• Males or females ages 8-35 years with stable mild-to-moderate asthma (ATS criteria) not on regular controller therapy

• Prebronchodilator FEV1 predicted = 70%

• No other medical co-morbidity

• Demonstrate maxFEV1% =15% on exercise challenge at screening and 1 week post run-in.

Exclusion Criteria:

• Asthma exacerbations or respiratory infection within 4 weeks of screening

• Recent use of inhaled or systemic steroids

• Immunosuppressives

• Antihistamines, NSAIDs and investigational drugs within 30 days

• Unable to reliably perform spirometry and exercise challenge

• Current or ex-smokers = 10 pack-years and less than 1 month abstinence

• Contra-indications to inhaled steroids or montelukast use.

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Crossover Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Treatment

Related Conditions & MeSH terms

• Asthma

Intervention

Drug:
• budesonide
inhaled budesonide turbuhaler 200ug taken 1 puff morning & 1 puff evening.
• montelukast
montelukast 5 mg ( < 15 years) or 10 mg (and matching placebo)will be taken 1 tab in the evening

Other:
• placebo
placebo

Locations

Country	Name	City	State
Canada	Hamilton Health Sciences-McMaster University	Hamilton	Ontario
Canada	Hospital for Sick Children	Toronto	Ontario

Sponsors (2)

Lead Sponsor	Collaborator
Hamilton Health Sciences Corporation	Merck Sharp & Dohme Corp.

Country where clinical trial is conducted

Canada, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	The magnitude of protection and the number of subjects with =50% protection (considered to be clinically relevant) following treatment		Before and after 2 weeks of treatment in each 4 arm	No
Secondary	Change in sputum cell counts and fluid phase inflammatory mediators		Before and after 2 weeks of treatment in each 4 arm	No
Secondary	Change in baseline exhaled nitric oxide (eNO) and response to exercise challenge		Before and after 2 weeks of treatment in each 4 arm	No
Secondary	Change in EBC (exhaled breath condensate) inflammatory mediators from baseline		Before and after 2 weeks of treatment in each 4 arm	No
Secondary	The change in exercise induced maximal percent fall in FEV1 (maxFEV1%) and area under the curve (AUC0-30) relative to pre-exercise FEV1 up to 30 minutes following exercise challenge		Before and after 2 weeks of treatment in each 4 arm	No