Study on BI 54903 (Inhaled Corticosteroid) Administered Once Daily or Twice Daily Via Respimat Inhaler in Patients With Asthma Inadequately Controlled on Low Dose Inhaled Corticosteroids

This study has been withdrawn prior to enrollment.
Sponsor:
Information provided by (Responsible Party):
Boehringer Ingelheim
ClinicalTrials.gov Identifier:
NCT01458912
First received: October 24, 2011
Last updated: November 21, 2011
Last verified: November 2011
  Purpose

The aim of this study is to assess and compare efficacy and safety of BI 54903 at medium doses twice daily and high doses once daily (evening dosing) and placebo over an 12-week treatment period in asthmatic patients aged 12 to 65 years inadequately controlled on low dose inhaled corticosteroid (ICS) therapy as demonstrated by a decrease in Forced Expiratory Volume in one second (FEV1) (not less than 10 %, and equal to or less than 25%) and an Asthma Control Questionnaire (ACQ)-6 score of not less than 1.5 at time of randomisation.


Condition Intervention Phase
Asthma
Drug: Placebo matching Respimat
Drug: BI 54903 MD
Drug: BI 54903 HD
Phase 2

Study Type: Interventional
Study Design: Allocation: Randomized
Endpoint Classification: Safety/Efficacy Study
Intervention Model: Parallel Assignment
Masking: Double-Blind
Primary Purpose: Treatment
Official Title: A Randomised, Double-blind, Placebo-controlled, Parallel-group Study to Assess and Compare Efficacy and Safety of a 12-week Treatment With BI 54903 at Doses of 181.8 Mcg b.i.d. and 363.6 Mcg q.d. (p.m. Dosing) Administered Via Respimat® Inhaler in Patients With Asthma Inadequately Controlled on Low Dose ICS Therapy

Resource links provided by NLM:


Further study details as provided by Boehringer Ingelheim:

Primary Outcome Measures:
  • Mean change from randomisation baseline to the end of the 12-week treatment period in evening trough (pre-dose and pre-rescue bronchodilator) FEV1 [ Time Frame: 12 weeks ] [ Designated as safety issue: No ]

Secondary Outcome Measures:
  • 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) Forced Vital Capacity (FVC) [ Time Frame: 12 weeks ] [ Designated as safety issue: No ]
  • 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 [ Time Frame: 12 weeks ] [ Designated as safety issue: No ]
  • Mean pre-dose (and pre-rescue) Peak Expiratory Flow (PEF) as assessed via Asthma Monitor2+ (AM2+) device (in the morning and evening) of the last week of the 12-week treatment period [ Time Frame: 12 weeks ] [ Designated as safety issue: No ]
  • 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 [ Time Frame: 12 weeks ] [ Designated as safety issue: No ]
  • Asthma control questionnaire (ACQ-6). [ Time Frame: 12 weeks ] [ Designated as safety issue: No ]
  • Asthma quality of life questionnaire (AQLQ(S)+12) [ Time Frame: 12 weeks ] [ Designated as safety issue: No ]
  • Time to withdrawal due to first asthma exacerbation [ Time Frame: 12 weeks ] [ Designated as safety issue: No ]
  • Daytime 12-h FEV1 profiles after 12-week treatment period (FEV1 Area Under Curve (AUC) 0-12h) [ Time Frame: 12 weeks ] [ Designated as safety issue: No ]

Enrollment: 0
Study Start Date: November 2011
Estimated Primary Completion Date: May 2013 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Experimental: BI 54903 HD q.d.
Patients receive 2 puffs BI 54903 HD q.d. via Respimat inhaler (p.m.) combined with 2 puffs placebo (a.m.)
Drug: Placebo matching Respimat
2 puffs a.m. via Respimat inhaler
Drug: BI 54903 HD
2 puffs HD p.m. via Respimat inhaler
Placebo Comparator: Placebo
Patients receive 2 puffs Placebo b.i.d. via Respimat inhaler
Drug: Placebo matching Respimat
2 puffs a.m. via Respimat inhaler
Experimental: BI 54903 MD b.i.d.
Patients receive 2 puffs BI 54903 MD b.i.d.via Respimat inhaler
Drug: BI 54903 MD
2 puffs MD b.i.d. via Respimat inhaler

  Eligibility

Ages Eligible for Study:   12 Years to 65 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion criteria:

  • 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 ICS plus Long-acting beta agonist (LABA) or high-dose ICS without LABA, stable for at least six weeks prior to Visit 1 (see also Section 3.3.1 and Appendix 10.3).
  • All patients must have a pre-bronchodilator FEV1 of not less than 60 to 90% of predicted normal and an ACQ-6 mean score of less than 1.5 at the pre-screening Visit 1.
  • 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 Hydrofluoroalkane (HFA) Metered Dose Inhaler (MDI). When the reversibility is not achieved at Visit 1, there will be the option to repeat reversibility test at any visit during the run-in period.
  • Variation of absolute pre-bronchodilator FEV1 values at Visit 2 as compared to Visit 1 must be within plus/minus 20 %.
  • 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 MDI correctly
  • Patients must be able to perform all trial-related procedures including technically acceptable pulmonary function tests and electronic 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 HFA MDI. When the reversibility is not achieved at Visit 1, there will be the option to repeat reversibility test at any visit 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.

Exclusion criteria:

  • 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 clinically relevant, abnormal screening haematology and/or blood chemistry finding, if the abnormality indicates a significant disease as defined in exclusion criterion no. 1.
  • 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
  • Patients with rheumatoid arthritis or other systemic diseases that require immune system modulating treatment
  • Patients suffering from or with a history of glaucoma, increased intraocular pressure, and/or cataracts
  • Pregnant or nursing women
  • Women of childbearing potential not using a highly effective method of birth control.
  • Patients who have been treated with anti-IgE-antibodies (e.g. omalizumab - Xolair®) or other immune system modulating antibodies such as TNF-alpha blockers within six months prior to Visit 1.
  • Patients who have been treated with the following drugs during the past four weeks prior to Visit 1 or are foreseen to need this during the study:
  • Non-selective ß-blockers (topical cardio-selective beta-blocker eye medications for non-narrow angle glaucoma are allowed),
  • Oral or other systemic corticosteroids,
  • Oral beta-agonists,
  • Changes in allergen desensitisation therapy in last 6 months,
  • Immune system modulating agents such as methotrexate or cyclosporine,
  • Inhibitors of cytochrome P450 3A4 such as antifungals (e.g. ketoconazole, itraconazole), antibiotics (e.g. erythromycin) or antiretroviral drugs.
  • Patients who have been treated with leukotriene modifiers, cromones or theophylline within two weeks prior to Visit 1.
  • Patients who have been treated with tiotropium within 3 weeks prior to Visit 1.
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT01458912

Sponsors and Collaborators
Boehringer Ingelheim
Investigators
Study Chair: Boehringer Ingelheim Boehringer Ingelheim
  More Information

No publications provided

Responsible Party: Boehringer Ingelheim
ClinicalTrials.gov Identifier: NCT01458912     History of Changes
Other Study ID Numbers: 1248.3, 2010-023166-51
Study First Received: October 24, 2011
Last Updated: November 21, 2011
Health Authority: United States: Food and Drug Administration

Additional relevant MeSH terms:
Asthma
Bronchial Diseases
Hypersensitivity
Hypersensitivity, Immediate
Immune System Diseases
Lung Diseases
Lung Diseases, Obstructive
Respiratory Hypersensitivity
Respiratory Tract Diseases

ClinicalTrials.gov processed this record on October 21, 2014