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Clinical Trials/NCT02040779
NCT02040779
Completed
Phase 3

A Randomized, Double-Blind, Placebo-Controlled, Parallel-Group, 12-Week Clinical Study to Assess the Efficacy and Safety of Beclomethasone Dipropionate (80 and 160 mcg/Day) Delivered Via Breath-Actuated Inhaler (BAI) in Adolescent and Adult Patients 12 Years of Age and Older With Persistent Asthma

Teva Branded Pharmaceutical Products R&D, Inc.47 sites in 1 country273 target enrollmentDecember 26, 2013

Overview

Phase
Phase 3
Intervention
Beclomethasone dipropionate breath-actuated inhaler
Conditions
Persistent Asthma
Sponsor
Teva Branded Pharmaceutical Products R&D, Inc.
Enrollment
273
Locations
47
Primary Endpoint
Standardized Baseline-Adjusted Trough Morning Forced Expiratory Volume in One Minute (FEV1) Area Under the Effect Curve From Time Zero to 12 Weeks (AUEC(0-12wk)) by Actual Treatment Received
Status
Completed
Last Updated
4 years ago

Overview

Brief Summary

This is a randomized, double-blind, placebo-controlled parallel-group study. Participants will be randomly assigned to receive treatment with beclomethasone dipropionate at a dosage of 80 or 160 mcg/day delivered via a Breath-Actuated Inhaler (BAI); or a matching BAI placebo, in a 1:1:1 ratio after a 14- to 21-day run-in period. Participants and investigators will remain blinded to randomized treatment assignment during the study

Registry
clinicaltrials.gov
Start Date
December 26, 2013
End Date
December 24, 2014
Last Updated
4 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Severity of Disease: The patient has persistent asthma, with an forced expiratory volume in 1 second (FEV1) 40%-85% of the value predicted for age, height, sex, and race as per the National Health and Nutrition Examination Survey (NHANES III) reference values at screening visit (SV) (Hankinson et al 1999).
  • Current asthma therapy: The patient is currently being treated with 1 of the following:
  • inhaled corticosteroids (ICSs) at a stable daily dose of less than or equal to 220 mcg/day fluticasone propionate via metered dose inhaler (MDI) or equivalent for a minimum of 4 weeks (28 days) before screening visit, or 2) a stable daily dosage of non-corticosteroid therapy, including leukotriene modifiers, theophylline, chromones, or short-acting beta-2 agonists (SABAs) alone or in combination for a minimum of 4 weeks (28 days) before screening visit (SV).
  • Reversibility of disease: The patient has demonstrated at least 15% and at least 200 mL increase from baseline FEV1 (patients age 18 and older) within 30 minutes after 2-4 inhalations of albuterol/salbutamol hydrofluoroalkane (HFA) MDI (90 mcg ex-actuator) or equivalent at SV or on retesting. - Other criteria apply, please contact the investigator for more information

Exclusion Criteria

  • The patient has a history of life-threatening asthma, defined for this protocol as an asthma episode that required intubation and/or was associated with hypercapnea, respiratory arrest, or hypoxic seizures.
  • The patient is a pregnant or lactating female or plans to become pregnant.
  • The patient has a known hypersensitivity to any corticosteroid or any of the excipients in the study drug or rescue medication formulation.
  • The patient currently smokes or has a smoking history of 10 pack-years or more (a pack-year is defined as smoking 1 pack of cigarettes/day for 1 year). The patient may not have used tobacco products within the past year.
  • The patient has had an asthma exacerbation requiring oral corticosteroids within 1 month before SV, or has had any hospitalization for asthma within 2 months before SV.
  • The patient has historical or current evidence of a clinically significant disease. Significant disease is defined as any disease that in the medical judgment of the investigator would put the safety of the patient at risk through participation or that could affect the efficacy or safety analysis if the disease/condition worsened during the study.
  • Other criteria apply, please contact the investigator for more information

Arms & Interventions

BDP 80 mcg BAI

40 mcg beclomethasone dipropionate (BDP) via breath-actuated inhaler (BAI) twice daily for a total of 80 mcg/day.

Intervention: Beclomethasone dipropionate breath-actuated inhaler

BDP 80 mcg BAI

40 mcg beclomethasone dipropionate (BDP) via breath-actuated inhaler (BAI) twice daily for a total of 80 mcg/day.

Intervention: albuterol/salbutamol

BDP 160 mcg BAI

80 mcg beclomethasone dipropionate (BDP) via breath-actuated inhaler (BAI) twice daily for a total of 160 mcg/day.

Intervention: Beclomethasone dipropionate breath-actuated inhaler

BDP 160 mcg BAI

80 mcg beclomethasone dipropionate (BDP) via breath-actuated inhaler (BAI) twice daily for a total of 160 mcg/day.

Intervention: albuterol/salbutamol

Placebo BAI

Placebo breath-actuated inhaler (BAI) twice daily.

Intervention: Placebo breath-actuated inhaler

Placebo BAI

Placebo breath-actuated inhaler (BAI) twice daily.

Intervention: albuterol/salbutamol

Outcomes

Primary Outcomes

Standardized Baseline-Adjusted Trough Morning Forced Expiratory Volume in One Minute (FEV1) Area Under the Effect Curve From Time Zero to 12 Weeks (AUEC(0-12wk)) by Actual Treatment Received

Time Frame: Baseline (Day 1 predose), weeks 2, 4, 8 and 12

The primary efficacy variable was the standardized baseline-adjusted trough morning (pre-dose and pre-rescue bronchodilator) FEV1 AUEC(0-12wk). Pulmonary function measurements such as FEV1 were obtained electronically by spirometry at the randomization visit (Day 1), each treatment visit (Weeks 2, 4, 8 and 12) and any unscheduled visit (such as the early termination visit). This summary is based on observed values recorded as 'best attempt'. The least-square (LS) means, difference of LS means and its 95% confidence interval (CI), and p-value represent the results obtained from the analysis of covariance with covariate adjustment for baseline, sex, age, current asthma therapy, and treatment.

Secondary Outcomes

  • Participants With Treatment-Emergent Adverse Events (TEAEs)(Day 1 up to Week 12)
  • Number of Participants Withdrawn From Study Due to Meeting Stopping Criteria for Worsening Asthma During the 12-Week Treatment Period(Treatment period: Day 1 up to Week 12)
  • Change From Baseline in Weekly Average of Daily Trough Morning Peak Expiratory Flow (PEF) Rate Over the 12-Week Treatment Period(Baseline (Days -6 to Day 1 pre-dose), daily up to Week 12)
  • Change From Baseline in Weekly Average of Daily Evening Peak Expiratory Flow (PEF) Over the 12-Week Treatment Period(Baseline (Days -6 to Day 1 pre-dose), daily up to Week 12)
  • Change From Baseline in Weekly Average of Total Daily Use of Albuterol/Salbutamol Inhalation Aerosol Over Weeks 1-12(Baseline (Days -6 to Day 1 pre-dose), daily up to Week 12)
  • Change From Baseline in Weekly Average of Total Daily Asthma Symptom Score Over the 12-Week Treatment Period(Baseline (Days -6 to Day 1 pre-dose), daily up to Week 12)
  • Kaplan-Meier Estimates of Time to Study Drug Treatment Withdrawal Due to Meeting Stopping Criteria for Worsening Asthma During the 12-Week Treatment Period(Treatment period: daily from Day 1 up to Week 12)
  • Participants With Potentially Clinically Relevant Abnormal Vital Sign Results During the Treatment Period(Baseline (Day 1 predose), Visits at weeks 2, 4, 8, 12)
  • Participants With Findings During Oropharyngeal Examination During Treatment(Visits at weeks 2, 4, 8, 12)

Study Sites (47)

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