Study on BI 54903 (Inhaled Corticosteroid) Administered Once Daily or Twice Daily Via Respimat Inhaler in Patients With Asthma Inadequately Controlled on Short Acting Beta-2 Agonist (SABA) Therapy Alone

NCT01458886 | Withdrawn Phase 2

• 2 other identifiers: 1248.22010-023165-22
• Study Type: interventional
• Target: N/A
• Locations: 0 countries
• Sites: N/A

Brief Summary

The aim of this study is to assess and compare efficacy and safety of BI 54903 at doses of very low dose twice daily (b.i.d) and low dose once daily (evening dosing) and placebo over an 12-week treatment period in asthmatic patients aged 12 to 65 years inadequately controlled on short acting beta-2 agonist (SABA) therapy alone as demonstrated by a decrease in forced expiratory volume in 1 second (FEV1) (not less than 10 %, and equal to or less than 25%) and an Asthma Control Questionnaire (ACQ-6) of not less than 1.5 at time of randomisation.

Conditions

Asthma

Outcome Measures

Primary Outcomes (1)

• Mean change from randomisation baseline to the end of the 12-week treatment period in evening trough (pre-dose and pre-rescue bronchodilator) FEV1

  12 weeks

Secondary Outcomes (9)

• Mean change from randomisation baseline to the end of the 12-week treatment period in morning and evening trough (pre-dose and pre-rescue bronchodilator) FVC

  12 weeks

• Mean change from randomisation baseline in morning and evening trough (pre-dose and pre-rescue bronchodilator) FEV1 and FVC after 2, 4 and 8-week treatment periods, and in morning trough FEV1 after 12 week treatment period

  12 weeks

• Mean pre-dose (and pre-rescue) PEF as assessed via AM2+ device (in the morning and evening) of the last week of the 12-week treatment period

  12 weeks

• Mean rescue medication use (daytime and night-time) as assessed via AM2+ device (in the morning and evening) of the last week of the 12-week treatment period

  12 weeks

• Asthma control questionnaire (ACQ-6)

  12 weeks

Study Arms (3)

BI 54903 LD b.i.d.

EXPERIMENTAL

Patients receive 2 puffs b.i.d. via Respimat inhaler

Drug: BI 54903

BI 54903 MD q.d.

EXPERIMENTAL

Patients receive 2 puffs q.d. via Respimat inhaler (p.m.) combined with 2 puffs placebo (a.m.)

Drug: BI 54903 MD; Drug: Placebo matching Respimat

Placebo

PLACEBO COMPARATOR

Patients receive 2 puffs b.i.d. via Respimat inhaler

Drug: Placebo matching Respimat

Interventions

BI 54903 MD DRUG

2 puffs b.i.d. via Respimat inhaler

BI 54903 MD q.d.

Placebo matching Respimat DRUG

2 puffs a.m. via Respimat inhaler

BI 54903 MD q.d.

BI 54903 DRUG

2 puffs LD b.i.d. via Respimat inhaler

BI 54903 LD b.i.d.

Eligibility Criteria

• Age: 12 Years - 65 Years
• Sex: all
• Healthy Volunteers: No
• Age Groups: Child (0-17), Adult (18-64), Older Adult (65+)

You may qualify if:

• To enter run-in following completion of pre-screening period:
• All patients must sign and date an Informed Consent Form (ICF) at Visit 0 consistent with International Conference on Harmonisation - Good Clinical Practice (ICH-GCP) guidelines and local legislation prior to participation in trial, which includes medication washout and restrictions
• Male and female patients aged at least 12 to 65 years.
• All patients must have a history of asthma diagnosed by a physician for at least three months at the time of enrolment into the trial according to the 2009 Global Initiative for Asthma (GINA) Guidelines. The initial diagnosis of asthma must have been made before the age of 40 years.
• All patients must be on a maintenance treatment with either medium-dose inhaled corticosteroids (ICS) plus long acting beta-2 agonist (LABA) or high-dose ICS without LABA, stable for at least six weeks prior to Visit 1.
• All patients must have a pre-bronchodilator forced expiratory volume in 1 second (FEV1) of not less than 60 to 90% of predicted normal and an Asthma Control Questionnaire (ACQ-6) mean score of less than 1.5 at the pre-screening Visit 1.
• Patients must be never-smokers or ex-smokers with a smoking history of less than10 pack-years and smoking cessation at least one year prior to screening .
• Patients must be able to use Respimat® inhaler and metered dosed inhaler (MDI) correctly
• Patients must be able to perform all trial-related procedures including technically acceptable pulmonary function tests and electronic pear expiratory flow (PEF) measurements, and must be able to maintain records during the study period as required in the protocol.
• To enter treatment period following additional criteria have to be met (at randomisation visit):
• All patients must have an improvement in FEV1 not less than 12 % above baseline and an absolute change of at least 200 mL within 15-30 min after administration of 400 mcg salbutamol/albuterol hydroflouroalkane (HFA) MDI., as demonstrated at Visit 1 or during one of the visits during the run-in period.
• During the run-in period (at the same clinic visit) all patients must be both symptomatic (ACQ-6 mean score equal to or greater than 1.5) and have shown a decrease in morning pre-bronchodilator FEV1 not less than 10% and less than or equal to 25% from pre-screening baseline FEV1 at Visit 2.

You may not qualify if:

• Patients with significant pulmonary disease other than asthma or other significant medical conditions (as determined by medical history, examination and clinical investigations at screening) that may, in the opinion of the investigator, result in any of the following: (i) put the patient at risk because of participation in this trial or (ii) influence the results of the trial or (iii) cause concern regarding the patient's ability to participate in the trial.
• Patients with a history of upper or lower respiratory tract infection (URTI/LRTI) in the past four weeks prior to the pre-screening Visit 1, and during pre-screening and run-in periods.
• Patients with any exacerbation of their underlying asthma during the eight weeks prior to the pre-screening Visit 1.
• Patients with active allergic rhinitis requiring treatment with systemic corticosteroids.
• Any of the following criteria are met during the pre-screening / run-in period (Visits 1 - 6):
• in clinic pre-bronchodilator FEV1 % predicted less than 40%,
• more than 12 puffs rescue salbutamol/albuterol HFA MDI per day for \> 2 consecutive days,
• exacerbation of asthma.
• Patients with a history of pneumonectomy or who are planning to undergo thoracotomy for any reason.
• Patients who are currently in a pulmonary rehabilitation program or have completed a pulmonary rehabilitation program in the six weeks prior to the first screening visit 1.
• Patients with two or more hospitalizations for asthma within the previous 12 months.
• Patients with a recent history of myocardial infarction during the last twelve months or known coronary heart disease that requires treatment
• Patients with a history of hospitalisation due to heart failure in the past twelve months
• Patients with myocarditis or any unstable or life-threatening cardiac arrhythmia or cardiac arrhythmia requiring intervention or a change in drug therapy within the past year
• Patients with significant alcohol or drug abuse in the opinion of the investigator within the past two years

Sponsors & Collaborators

• Boehringer Ingelheim: lead

MeSH Terms

Conditions

Asthma

Condition Hierarchy (Ancestors)

Bronchial Diseases; Respiratory Tract Diseases; Lung Diseases, Obstructive; Lung Diseases; Respiratory Hypersensitivity; Hypersensitivity, Immediate; Hypersensitivity; Immune System Diseases

Study Officials

• Boehringer Ingelheim

  Boehringer Ingelheim

  STUDY CHAIR

Study Design

• Study Type: interventional
• Phase: phase 2
• Allocation: RANDOMIZED
• Masking: DOUBLE
• Purpose: TREATMENT
• Intervention Model: PARALLEL
• Sponsor Type: INDUSTRY
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: October 24, 2011
• First Posted: October 25, 2011
• Study Start: November 1, 2011
• Primary Completion: May 1, 2013
• Last Updated: October 31, 2013

Record last verified: 2013-10