A Study for Disease Profiling of Asthma and Chronic Obstructive Pulmonary Disease
Status: | Completed |
---|---|
Conditions: | Asthma, Chronic Obstructive Pulmonary Disease, Pulmonary, Pulmonary |
Therapuetic Areas: | Pulmonary / Respiratory Diseases |
Healthy: | No |
Age Range: | 18 - 70 |
Updated: | 12/21/2016 |
Start Date: | July 2010 |
End Date: | July 2014 |
A Multicenter Longitudinal Study for Disease Profiling of Asthma and Chronic Obstructive Pulmonary Disease
The purpose of this study is to characterize the clinical, physiologic, and molecular
profiles of healthy participants, participants with mild, moderate, and severe asthma; and
participants with moderate to severe Chronic Obstructive Pulmonary Disease (COPD).
profiles of healthy participants, participants with mild, moderate, and severe asthma; and
participants with moderate to severe Chronic Obstructive Pulmonary Disease (COPD).
This is a multi-center, longitudinal (participants are followed over long period of time
with continuous or repeated observations of health outcomes) exploratory study (biomarkers,
clinical and physiological parameters for participants with asthma and COPD are observed for
the first time). This study will be conducted in 2 parts. Part 1 will include healthy
participants and participants with mild, moderate, and severe asthma. Part 2 will include
healthy nonsmokers, healthy asymptomatic smokers, and participants with moderate and or
severe COPD. Study participants will undergo medical tests that will include pulmonary
function testing, assessment of airway reactivity, bronchoscopy procedure, blood samples for
routine laboratory tests, biomarkers and DNA evaluation (for some study participants),
induced sputum collection, and exhaled nitric oxide collection. Safety evaluations will
includes assessment of adverse events, clinical laboratory tests, 12-lead electrocardiogram,
vital signs, and physical examinations.
with continuous or repeated observations of health outcomes) exploratory study (biomarkers,
clinical and physiological parameters for participants with asthma and COPD are observed for
the first time). This study will be conducted in 2 parts. Part 1 will include healthy
participants and participants with mild, moderate, and severe asthma. Part 2 will include
healthy nonsmokers, healthy asymptomatic smokers, and participants with moderate and or
severe COPD. Study participants will undergo medical tests that will include pulmonary
function testing, assessment of airway reactivity, bronchoscopy procedure, blood samples for
routine laboratory tests, biomarkers and DNA evaluation (for some study participants),
induced sputum collection, and exhaled nitric oxide collection. Safety evaluations will
includes assessment of adverse events, clinical laboratory tests, 12-lead electrocardiogram,
vital signs, and physical examinations.
Inclusion Criteria:
- Age: for Part 1, healthy: 18 and 55 years; for Part 1, asthma: 18 and 70 years; for
Part 2, nonsmokers: 40 and 65 years; for Part 2, smokers: 40 and 65 years; for Part
2, chronic obstructive pulmonary disease (COPD): 40 and 65 years
- Having mild, moderate, or severe asthma (for Part 1, asthma)
- Clinically stable asthma and have been on their current asthma controller therapy for
at least 6 weeks prior to screening (for Part 1, asthma)
- No history of chronic respiratory disease including asthma (for Part 2, nonsmokers)
- Be a nonsmoker for 1 year or more at initial screening visit and have 10 packs or
less per year history of smoking (for all Part 1 and Pat 2, nonsmokers)
- Be a current smoker with a current history of at least 20 pack years (for Part 2,
smokers)
- Stable COPD in the 3 months prior to screening (for Part 2, COPD)
- Treating with Beta-adrenergic receptor agonist, anticholinergic bronchodilators,
inhaled corticosteroid at stable doses for at least 4 weeks prior to screening (for
Part 2, COPD)
Exclusion Criteria:
- History of sleep apnea requiring medical intervention and positive urine pregnancy
screening result (for all Part 1 and Part 2)
- Positive urine screen for nicotine; positive serology test for human immunodeficiency
virus (HIV) antibodies, hepatitis B surface antigen, or hepatitis C virus antibody at
screening (for all Part 1 and Part 2)
- Allergic bronchopulmonary aspergillosis, allergic bronchopulmonary mycosis, or
occupational asthma (for Part 1, asthma)
- Requires long term oxygen therapy on a daily basis for chronic hypoxemia at screening
visit except when used for exercise only (for Part 2, COPD)
- Pneumonia, COPD exacerbation that required systemic steroids, upper or lower
respiratory tract infection, lung cancer surgery, lung volume reduction, or a lung
transplant (for Part 2, COPD)
We found this trial at
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