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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01092143
Other study ID # 1268.17
Secondary ID
Status Completed
Phase Phase 2
First received
Last updated
Start date March 18, 2010
Est. completion date March 26, 2011

Study information

Verified date May 2022
Source Boehringer Ingelheim
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This is a 6 week study to investigate the effectiveness and safety of BI 671800 ED in patients with asthma who do not take inhaled corticosteroids.


Recruitment information / eligibility

Status Completed
Enrollment 389
Est. completion date March 26, 2011
Est. primary completion date March 26, 2011
Accepts healthy volunteers No
Gender All
Age group 18 Years to 65 Years
Eligibility Inclusion criteria: 1. Signed informed consent consistent with ICH-GCP 2. Three month history of reversible (12% with 200 mL) asthma (according to GINA) with following spirometry at randomization: FEV1 60%-85%. 3. No ICS previous 3 months prior to screening. 4. Diagnosis of asthma prior to 40 years. 5. ACQ at least 1.5 at randomization. 6. Male or female, 18 to 65 years. 7. Non-smokers or ex-smokers ( less than 10 pack year history) with negative cotinine screen. 8. Able to perform PFT Exclusion criteria: 1. Significant diseases other than asthma or allergic rhinitis. 2. Hepatic transaminases or total bilirubin greater than 1.5 ULN. 3. Hospitalizations for asthma or asthma related intubation within 3 months. 4. Uncontrolled asthma. 5. Respiratory tract infection or exacerbation within 4 weeks. 6. FEV1 less than 40%, more than 12 puffs of SABA on more than two consecutive days or asthma exacerbation during the run-in period. 7. Participation in another interventional study. 8. Pregnant or nursing women. 9. Women of child bearing potential nor using appropriate methods of birth control as defined by protocol

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
BI 671800
BI 671800
Fluticasone propionate placebo
Placebo matching Fluticasone propionate
Fluticasone propionate
Fluticasone propionate
BI 671800 Placebo
Placebo matching BI 671800

Locations

Country Name City State
Australia 1268.17.61001 Boehringer Ingelheim Investigational Site Adelaide South Australia
Canada 1268.17.02012 Boehringer Ingelheim Investigational Site Hawkesbury Ontario
Canada 1268.17.02010 Boehringer Ingelheim Investigational Site Mississauga Ontario
Canada 1268.17.02014 Boehringer Ingelheim Investigational Site Newmarket Ontario
Canada 1268.17.02001 Boehringer Ingelheim Investigational Site Quebec
Canada 1268.17.02004 Boehringer Ingelheim Investigational Site Quebec
Canada 1268.17.02015 Boehringer Ingelheim Investigational Site Sudbury Ontario
Canada 1268.17.02003 Boehringer Ingelheim Investigational Site Toronto Ontario
Canada 1268.17.02013 Boehringer Ingelheim Investigational Site Toronto Ontario
Colombia 1268.17.57003 Boehringer Ingelheim Investigational Site Bogotá
Colombia 1268.17.57004 Boehringer Ingelheim Investigational Site Bogotá
Colombia 1268.17.57002 Boehringer Ingelheim Investigational Site Medellín
Korea, Republic of 1268.17.82007 Boehringer Ingelheim Investigational Site Cheongju
Korea, Republic of 1268.17.82001 Boehringer Ingelheim Investigational Site Seoul
Korea, Republic of 1268.17.82002 Boehringer Ingelheim Investigational Site Seoul
Korea, Republic of 1268.17.82004 Boehringer Ingelheim Investigational Site Seoul
Korea, Republic of 1268.17.82005 Boehringer Ingelheim Investigational Site Seoul
Korea, Republic of 1268.17.82006 Boehringer Ingelheim Investigational Site Seoul
Korea, Republic of 1268.17.82003 Boehringer Ingelheim Investigational Site Suwon
Korea, Republic of 1268.17.82008 Boehringer Ingelheim Investigational Site Wonju
Mexico 1268.17.52002 Boehringer Ingelheim Investigational Site Cuernavaca
Mexico 1268.17.52001 Boehringer Ingelheim Investigational Site Monterrey
Mexico 1268.17.52004 Boehringer Ingelheim Investigational Site Toriello Guerra
Mexico 1268.17.52003 Boehringer Ingelheim Investigational Site Zona Río
New Zealand 1268.17.64001 Boehringer Ingelheim Investigational Site Christchurch
New Zealand 1268.17.64003 Boehringer Ingelheim Investigational Site Greenlane East Auckland
New Zealand 1268.17.64002 Boehringer Ingelheim Investigational Site Newtown Wellington NZ
Peru 1268.17.51003 Boehringer Ingelheim Investigational Site Jesús María
Peru 1268.17.51002 Boehringer Ingelheim Investigational Site Lima
Peru 1268.17.51006 Boehringer Ingelheim Investigational Site San Borja
Peru 1268.17.51004 Boehringer Ingelheim Investigational Site San Isidro.
Peru 1268.17.51005 Boehringer Ingelheim Investigational Site Santiago de Surco
Peru 1268.17.51001 Boehringer Ingelheim Investigational Site Urb. Ingeniería
Philippines 1268.17.63007 Boehringer Ingelheim Investigational Site Caloocan City
Philippines 1268.17.63002 Boehringer Ingelheim Investigational Site Manila
Philippines 1268.17.63001 Boehringer Ingelheim Investigational Site Quezon City
Philippines 1268.17.63003 Boehringer Ingelheim Investigational Site Quezon City
Philippines 1268.17.63004 Boehringer Ingelheim Investigational Site Quezon City
Philippines 1268.17.63005 Boehringer Ingelheim Investigational Site Quezon City
Philippines 1268.17.63006 Boehringer Ingelheim Investigational Site Quezon City
Taiwan 1268.17.86210 Boehringer Ingelheim Investigational Site Chiayi City
Taiwan 1268.17.86211 Boehringer Ingelheim Investigational Site Kaohsiung City
Taiwan 1268.17.86207 Boehringer Ingelheim Investigational Site Taichung
Taiwan 1268.17.86208 Boehringer Ingelheim Investigational Site Taichung
Taiwan 1268.17.86209 Boehringer Ingelheim Investigational Site Taichung
Taiwan 1268.17.86201 Boehringer Ingelheim Investigational Site Taipei
Taiwan 1268.17.86202 Boehringer Ingelheim Investigational Site Taipei
Taiwan 1268.17.86203 Boehringer Ingelheim Investigational Site Taipei
Taiwan 1268.17.86204 Boehringer Ingelheim Investigational Site Taipei
Taiwan 1268.17.86205 Boehringer Ingelheim Investigational Site Taipei
Taiwan 1268.17.86206 Boehringer Ingelheim Investigational Site Taipei
Taiwan 1268.17.86200 Boehringer Ingelheim Investigational Site Taoyuan County
United States 1268.17.01034 Boehringer Ingelheim Investigational Site Baltimore Maryland
United States 1268.17.01008 Boehringer Ingelheim Investigational Site Bellevue Nebraska
United States 1268.17.01022 Boehringer Ingelheim Investigational Site Bozeman Montana
United States 1268.17.01007 Boehringer Ingelheim Investigational Site Charleston South Carolina
United States 1268.17.01004 Boehringer Ingelheim Investigational Site Cincinnati Ohio
United States 1268.17.01015 Boehringer Ingelheim Investigational Site Colorado Springs Colorado
United States 1268.17.01009 Boehringer Ingelheim Investigational Site Cypress California
United States 1268.17.01019 Boehringer Ingelheim Investigational Site Dallas Texas
United States 1268.17.01045 Boehringer Ingelheim Investigational Site DeLand Florida
United States 1268.17.01001 Boehringer Ingelheim Investigational Site Denver Colorado
United States 1268.17.01031 Boehringer Ingelheim Investigational Site Easley South Carolina
United States 1268.17.01012 Boehringer Ingelheim Investigational Site El Paso Texas
United States 1268.17.01039 Boehringer Ingelheim Investigational Site Fort Mill South Carolina
United States 1268.17.01026 Boehringer Ingelheim Investigational Site Greenville South Carolina
United States 1268.17.01029 Boehringer Ingelheim Investigational Site Greenville South Carolina
United States 1268.17.01023 Boehringer Ingelheim Investigational Site Houston Texas
United States 1268.17.01005 Boehringer Ingelheim Investigational Site Iowa City Iowa
United States 1268.17.01048 Boehringer Ingelheim Investigational Site Killeen Texas
United States 1268.17.01016 Boehringer Ingelheim Investigational Site Lakewood Colorado
United States 1268.17.01006 Boehringer Ingelheim Investigational Site Los Angeles California
United States 1268.17.01032 Boehringer Ingelheim Investigational Site Minneapolis Minnesota
United States 1268.17.01028 Boehringer Ingelheim Investigational Site New Braunfels Texas
United States 1268.17.01036 Boehringer Ingelheim Investigational Site Normal Illinois
United States 1268.17.01014 Boehringer Ingelheim Investigational Site North Dartmouth Massachusetts
United States 1268.17.01030 Boehringer Ingelheim Investigational Site North Dartmouth Massachusetts
United States 1268.17.01027 Boehringer Ingelheim Investigational Site Novi Michigan
United States 1268.17.01038 Boehringer Ingelheim Investigational Site Oklahoma City Oklahoma
United States 1268.17.01040 Boehringer Ingelheim Investigational Site Palmdale California
United States 1268.17.01042 Boehringer Ingelheim Investigational Site Philadelphia Pennsylvania
United States 1268.17.01011 Boehringer Ingelheim Investigational Site Raleigh North Carolina
United States 1268.17.01010 Boehringer Ingelheim Investigational Site Saint Louis Missouri
United States 1268.17.01037 Boehringer Ingelheim Investigational Site Saint Louis Missouri
United States 1268.17.01035 Boehringer Ingelheim Investigational Site San Antonio Texas
United States 1268.17.01024 Boehringer Ingelheim Investigational Site San Jose California
United States 1268.17.01025 Boehringer Ingelheim Investigational Site South Bend Indiana
United States 1268.17.01049 Boehringer Ingelheim Investigational Site Spartanburg South Carolina
United States 1268.17.01003 Boehringer Ingelheim Investigational Site Stockton California
United States 1268.17.01047 Boehringer Ingelheim Investigational Site Tacoma Washington
United States 1268.17.01043 Boehringer Ingelheim Investigational Site Tucson Arizona
United States 1268.17.01033 Boehringer Ingelheim Investigational Site Wheat Ridge Colorado

Sponsors (1)

Lead Sponsor Collaborator
Boehringer Ingelheim

Countries where clinical trial is conducted

United States,  Australia,  Canada,  Colombia,  Korea, Republic of,  Mexico,  New Zealand,  Peru,  Philippines,  Taiwan, 

Outcome

Type Measure Description Time frame Safety issue
Primary Forced Expiratory Volume in One Second (FEV1) % Predicted Trough Change From Baseline (Mean Observed in the 2 Weeks Prior to Treatment) After Six Weeks of Treatment Forced expiratory volume in one second (FEV1) % predicted trough change from baseline (mean observed in the 2 weeks prior to treatment) after 6 weeks of treatment, where trough FEV1 % predicted was defined as the mean of the FEV1 % predicted trough values at 25 minutes and 10 minutes prior to dosing on clinic visit.
MMRM in the statistical test comments is mixed effects model with repeated measures.
Measurements at baseline (mean observed in the 2 weeks prior to treatment) and at week 6 of treatment.
Secondary Asthma Control Questionnaire (ACQ) Mean Score Change From Baseline After Six Weeks of Treatment Asthma Control Questionnaire (ACQ) mean score change from baseline (mean ACQ score obtained at Week 0) after six weeks of treatment.
The Asthma Control Questionnaire (ACQ) is a patient-reported outcome questionnaire containing 7 items. The items are equally weighted and the ACQ score is the mean of the 7 items and therefore between 0 (well controlled) and 6 (extremely poorly controlled) These questions based on recall of the previous 7 days comprise breathlessness, nocturnal waking, symptoms on waking, activity limitation, wheeze, frequency of short-acting beta-adrenergic (SABA) use, and categorized pre-bronchodilator FEV1% predicted.
Measurements at baseline (mean ACQ score obtained at Week 0) and at week 6 of treatment.
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