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Completed Phase 2 Interventional

Effectiveness and Safety of BIO-11006 Inhalation Solution to Treat the Overproduction of Mucus and Inflammation in COPD

ClinicalTrials.gov ID: NCT00648245

Public ClinicalTrials.gov record NCT00648245. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 7, 2026, 4:50 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

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

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

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 identification

NCT ID
NCT00648245
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
BioMarck Pharmaceuticals, Ltd.
Industry
Enrollment
172 participants

Conditions and interventions

Eligibility (public fields only)

Age range
45 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
May 31, 2008
Primary completion
Jun 30, 2010
Completion
Jun 30, 2010
Last update posted
Feb 9, 2011

2008 – 2010

United States locations

U.S. sites
14
U.S. states
9
U.S. cities
13
Facility City State ZIP Site status
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

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00648245, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Feb 9, 2011 · Synced Sep 7, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00648245 live on ClinicalTrials.gov.

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