The symptoms associated with COPD include overproduction of mucus and inflammation in the
lungs. Overproduction of mucus results in impaired lung function and it encourages
bacterial growth and associated COPD exacerbations. Therefore, a treatment that inhibits
mucus overproduction or blocks inflammation could benefit COPD patients. The drug under
evaluation in this study, BIO-11006 Inhalation Solution, is a new drug that may inhibit
overproduction of mucus and may have important anti-inflammatory properties.
Study Type: Intervention
| Condition |
Intervention |
Phase |
COPD
Chronic Obstructive Pulmonary Disease
|
Array: Array
Array: Array
Array: Array
Array: Array
Array: Array
|
Phase 2
|
Study Design:Allocation: Randomized, Control: Placebo Control, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Treatment
Official Title: A Phase 2a, Double Blind, Placebo Controlled, Multicenter, Dose Escalation Study to Evaluate the Safety and Efficacy of BIO 11006 Inhalation Solution in Subjects With Chronic Obstructive Pulmonary Disease
Further Study Details:
Expected Total Enrollment:
Study Dates:June 2008 -
COPD encompasses a number of chronic lung disorders that obstruct the airways and may be
accompanied by airway hyperactivity. The most common form of COPD is a combination of
chronic bronchitis and emphysema. Many of the signs and symptoms associated with chronic
bronchitis are a result of airway mucus hypersecretion induced by chronic inflammation of
the airways. Clinically, mucus hypersecretion results in impaired gas exchange and
compromised mucociliary clearance, encouraging bacterial colonization and associated
exacerbations. A treatment that inhibits mucus hypersecretion or blocks inflammation could
benefit COPD patients with chronic bronchitis. The drug under evaluation in this study,
BIO 11006, is a new therapeutic agent that may inhibit mucus secretion and may have
important anti inflammatory properties. In this study, BIO-11006 will be administered to
COPD patients with chronic bronchitis, and the effects lung function will be assessed.
Ages Eligible for Study- Min: 45 Years Max: N/A
Gender: Both
Criteria
Inclusion Criteria:
Clinically stable male or female outpatients, 45 years of age or older
Active COPD with chronic bronchitis indicated by: (1) FEV1 = 40% to 70%, (2)
FEV1/FVC ≤70%, (3)Chronic productive cough for 3 months in each of 2 successive
years, and (4) Sputum (phlegm) production at least several days a week over the past
4 weeks
Current or previous smoker with a 20-pack year history
Exclusion Criteria:
Treatment with oral prednisone during the 6 weeks before enrollment
Changed inhaled corticosteroid dose or long acting bronchodilator dose during the 6
weeks before enrollment
Treatment with oxygen (with the exception of night time oxygen) during the 6 weeks
before enrollment
Current asthma as determined by the investigator
Change in smoking status during the previous 6 months
Please refer to this study by ClinicalTrials.gov identifier: NCT00648245
Pulmonary Associates - Glendale, Arizona 85306
Greater Los Angeles Healthcare System - Los Angeles, California 91343
Bay Pines VA Heatlhcare System - Bay Pines, Florida 33744
Florida Pulmonary Research Institute, LLC - Winter Park, Florida 32789
Southeastern Lung Care - Decatur, Georgia 30033
University of Louisville - Louisville, Kentucky 40202
VA Sierra Nevada Health Care System - Reno, Nevada 89502
Duke University Medical Center - Durham, North Carolina 27704
North Carolina Clinical Research - Raleigh, North Carolina 27607
Southeastern Research Center, LLC - Winston Salem, North Carolina 27103
Spartanburg Medical Research - Spartanburg, South Carolina 29303
Baylor College of Medicine - Houston, Texas 77030
Michael E. DeBakey VAMC - Houston, Texas 77030
Diagnostics Research Group - San Antonio, Texas 78229
Record Last Reviewed:August 2010
Last Updated:August 19, 2010
Record First Recieved:March 28, 2008
ClinicalTrials.gov Identifier:NCT00648245
Health Authority: United States Food and Drug Administration
Information obtained from ClinicalTrials.gov on September 02, 2010