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

NCT01397201 | Terminated Phase 2 Results

• 2 other identifiers: 1248.62010-023168-41
• Study Type: interventional
• Target: 30
• Locations: 1 country
• Sites: 41

Brief Summary

The aim of the study is to assess and compare efficacy and safety of BI 54903 at 3 doses twice daily (b.i.d.), fluticasone propionate hydrofluoroalkane metered dose inhaler (HFA MDI) at a dose of 220 mcg b.i.d. and placebo b.i.d. over an 8-week treatment period in asthmatic patients aged 12 to 65 years inadequately controlled on low dose Inhaled corticosteroid (ICS) as demonstrated by a decrease in forced expiratory volume in one second (FEV1 (range 10-25%) and an asthma control questionnaire (ACQ-6) greater or equal 1.5 at time of randomisation

Conditions

Asthma

Outcome Measures

Primary Outcomes (1)

• Mean Change From Randomisation Baseline to the End of the 8-week Treatment Period in Trough (Pre-dose and Pre-rescue Bronchodilator) Forced Expiratory Volume in One Second (FEV1)

  Mean change from randomisation baseline to the end of the 8-week treatment period in trough (pre-dose and pre-rescue bronchodilator) forced expiratory volume in one second (FEV1).

  At baseline and at week 8.

Secondary Outcomes (8)

• Mean Changes From Randomisation Baseline in Trough (Pre-dose and Pre-rescue Bronchodilator) Forced Vital Capacity (FVC) After 2, 4 and 8-week Treatment Periods

  At baseline and at week 2, 4 and 8.

• Mean Changes From Randomisation Baseline in Trough (Pre-dose and Pre-rescue Bronchodilator) Forced Expiratory Volume in One Second (FEV1) After 2 and 4-week Treatment Periods

  At baseline and at week 2 and 4.

• Mean Changes From Randomisation Baseline in Trough (Morning Pre-dose and Pre-rescue Bronchodilator) FEF25-75 After 2, 4 and 8-week Treatment Periods

  At baseline and at week 2, 4 and 8.

• Mean Pre-dose (and Pre-rescue) Peak Expiratory Flow (PEF) as Assessed Via Asthma Monitor (AM2+) in the Morning and Evening, of the Last Week of the 8-week Treatment Period

  8 weeks

• Mean Rescue Medication Use (Daytime and Night-time) as Assessed Via Asthma Monitor (AM2+) in the Morning and Evening, of the Last Week of the 8-week Treatment Period

  At week 8.

Study Arms (5)

BI 54903 - low dose

EXPERIMENTAL

Respimat inhaler containing low dose BI 54903 plus placebo matching hydrofluoralkane (HFA) metered dose inhaler (MDI)

Drug: Placebo; Drug: BI 54903

BI 54903 - medium dose

EXPERIMENTAL

Respimat inhaler containing medium dose BI 54903 plus placebo matching HFA MDI

Drug: Placebo; Drug: BI 54903

BI 54903 - high dose

EXPERIMENTAL

Respimat inhaler containing high dose BI 54903 plus placebo matching HFA MDI

Drug: Placebo; Drug: BI 54903

Fluticasone propionate

ACTIVE COMPARATOR

Fluticasone HFA MDI containing ICS plus placebo matching Respimat inhaler

Drug: Fluticasone propionate

Placebo

PLACEBO COMPARATOR

Placebo matching Respimat inhaler plus placebo matching HFA MDI

Drug: Placebo

Interventions

Placebo DRUG

Placebo matching fluticasone propionate HFA MDI

BI 54903 - high dose; BI 54903 - low dose; BI 54903 - medium dose; Placebo

BI 54903 DRUG

BI 54903

BI 54903 - high dose; BI 54903 - low dose; BI 54903 - medium dose

Fluticasone propionate DRUG

Fluticasone propionate

Fluticasone propionate

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:

• Must be willing and able to give informed consent
• 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 corticosteroid (ICS) plus long acting beta agonist (LABA) or high-dose inhaled corticosteroid (ICS) without long acting beta agonist (LABA), stable for at least six weeks prior to Visit 1
• All patients must have a pre-bronchodilator forced expiratory volume in one 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
• 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 metered dose inhaler (HFA MDI)
• Patients must be never-smokers or ex-smokers with a smoking history of less than 10 pack-years and smoking cessation at least one year prior to screening
• Patients must be able to use Respimat® inhaler and metered dose inhaler (MDI) correctly
• Patients must be able to perform all trial-related procedures including technically acceptable pulmonary function tests and electronic peak 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):
• 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)
• Patients with a clinically relevant, abnormal screening haematology and/or blood chemistry finding
• Patients with a history of upper or lower respiratory tract infection 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 forced expiratory volume in one second (FEV1 %) predicted less than 40%,
• more than 12 puffs rescue salbutamol/albuterol hydrofluoroalkane metered dose inhaler (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 twelve 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

Sponsors & Collaborators

• Boehringer Ingelheim: lead

Study Sites (41)

1248.6.01047 Boehringer Ingelheim Investigational Site

Fountain Valley, California, United States

Location

1248.6.01023 Boehringer Ingelheim Investigational Site

Fullerton, California, United States

Location

1248.6.01041 Boehringer Ingelheim Investigational Site

Huntington Beach, California, United States

Location

1248.6.01038 Boehringer Ingelheim Investigational Site

Long Beach, California, United States

Location

1248.6.01004 Boehringer Ingelheim Investigational Site

Mission Viejo, California, United States

Location

1248.6.01028 Boehringer Ingelheim Investigational Site

Palmdale, California, United States

Location

1248.6.01044 Boehringer Ingelheim Investigational Site

Stockton, California, United States

Location

1248.6.01034 Boehringer Ingelheim Investigational Site

Walnut Creek, California, United States

Location

1248.6.01015 Boehringer Ingelheim Investigational Site

Centennial, Colorado, United States

Location

1248.6.01035 Boehringer Ingelheim Investigational Site

Aventura, Florida, United States

Location

1248.6.01022 Boehringer Ingelheim Investigational Site

Miami, Florida, United States

Location

1248.6.01042 Boehringer Ingelheim Investigational Site

Sarasota, Florida, United States

Location

1248.6.01051 Boehringer Ingelheim Investigational Site

Columbus, Georgia, United States

Location

1248.6.01052 Boehringer Ingelheim Investigational Site

Savannah, Georgia, United States

Location

1248.6.01011 Boehringer Ingelheim Investigational Site

Eagle, Idaho, United States

Location

1248.6.01055 Boehringer Ingelheim Investigational Site

Oak Lawn, Illinois, United States

Location

1248.6.01019 Boehringer Ingelheim Investigational Site

Baltimore, Maryland, United States

Location

1248.6.01039 Boehringer Ingelheim Investigational Site

North Dartmouth, Massachusetts, United States

Location

1248.6.01037 Boehringer Ingelheim Investigational Site

Ypsilanti, Michigan, United States

Location

1248.6.01056 Boehringer Ingelheim Investigational Site

Rolla, Missouri, United States

Location

1248.6.01036 Boehringer Ingelheim Investigational Site

Warrensburg, Missouri, United States

Location

1248.6.01020 Boehringer Ingelheim Investigational Site

Omaha, Nebraska, United States

Location

1248.6.01049 Boehringer Ingelheim Investigational Site

Berlin, New Jersey, United States

Location

1248.6.01054 Boehringer Ingelheim Investigational Site

Trenton, New Jersey, United States

Location

1248.6.01010 Boehringer Ingelheim Investigational Site

Verona, New Jersey, United States

Location

1248.6.01006 Boehringer Ingelheim Investigational Site

Rochester, New York, United States

Location

1248.6.01031 Boehringer Ingelheim Investigational Site

High Point, North Carolina, United States

Location

1248.6.01045 Boehringer Ingelheim Investigational Site

Cincinnati, Ohio, United States

Location

1248.6.01005 Boehringer Ingelheim Investigational Site

Gresham, Oregon, United States

Location

1248.6.01021 Boehringer Ingelheim Investigational Site

Portland, Oregon, United States

Location

1248.6.01013 Boehringer Ingelheim Investigational Site

Philadelphia, Pennsylvania, United States

Location

1248.6.01040 Boehringer Ingelheim Investigational Site

Pittsburgh, Pennsylvania, United States

Location

1248.6.01012 Boehringer Ingelheim Investigational Site

Upland, Pennsylvania, United States

Location

1248.6.01048 Boehringer Ingelheim Investigational Site

Charleston, South Carolina, United States

Location

1248.6.01050 Boehringer Ingelheim Investigational Site

Austin, Texas, United States

Location

1248.6.01002 Boehringer Ingelheim Investigational Site

Live Oak, Texas, United States

Location

1248.6.01046 Boehringer Ingelheim Investigational Site

San Antonio, Texas, United States

Location

1248.6.01001 Boehringer Ingelheim Investigational Site

Waco, Texas, United States

Location

1248.6.01025 Boehringer Ingelheim Investigational Site

Murray, Utah, United States

Location

1248.6.01053 Boehringer Ingelheim Investigational Site

Alexandria, Virginia, United States

Location

1248.6.01030 Boehringer Ingelheim Investigational Site

Tacoma, Washington, United States

Location

Related Links

• Related Info

MeSH Terms

Conditions

Asthma

Interventions

Fluticasone

Condition Hierarchy (Ancestors)

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

Intervention Hierarchy (Ancestors)

Androstadienes; Androstenes; Androstanes; Steroids; Fused-Ring Compounds; Polycyclic Compounds

Limitations and Caveats

Study was terminated by the decision of the sponsor. As limited data were collected due to early termination and only limited number of patients completed the 8-week treatment period, no analysis of primary and secondary endpoint were conducted.

Results Point of Contact

• Title: Boehringer Ingelheim Call Center
• Organization: Boehringer Ingelheim

clintriage.rdg@boehringer-ingelheim.com

1-800-243-0127

Study Officials

• Boehringer Ingelheim

  Boehringer Ingelheim

  STUDY CHAIR

Publication Agreements

• PI is Sponsor Employee: No
• Restriction Type: OTHER
• Restrictive Agreement: Yes

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: July 18, 2011
• First Posted: July 19, 2011
• Study Start: July 1, 2011
• Primary Completion: December 23, 2011
• Study Completion: December 23, 2011
• Last Updated: June 23, 2022
• Results First Posted: June 23, 2022

Record last verified: 2022-05

Locations

US (41)