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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00423137
Other study ID # 1219.5
Secondary ID 2006-001975-40
Status Completed
Phase Phase 2
First received
Last updated
Start date January 17, 2007
Est. completion date July 9, 2008

Study information

Verified date October 2021
Source Boehringer Ingelheim
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Study of BIBW 2948 BS in Patients with COPD and Chronic Bronchitis


Recruitment information / eligibility

Status Completed
Enrollment 48
Est. completion date July 9, 2008
Est. primary completion date July 9, 2008
Accepts healthy volunteers No
Gender All
Age group 40 Years to 70 Years
Eligibility Inclusion Criteria: - COPD smokers - ages between 40 and 70 Exclusion Criteria: - Significant other diseases - abnormal hematology - abnormal liver function - psychiatric disorders - pulmonary obstruction - asthma, allergic rhinitis - dependance on oxygen - patients with history of myocardial infarction - patients with history of cancer - women of child bearing potential - antiplatelet or anticoagulation therapy

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
BIBW 2948 BS
Capsule
Placebo
Capsule

Locations

Country Name City State
Germany 1219.5.06 Boehringer Ingelheim Investigational Site Freiburg/Breisgau
Germany 1219.5.05 Boehringer Ingelheim Investigational Site Hannover
United States 1219.5.03 Boehringer Ingelheim Investigational Site Birmingham Alabama
United States 1219.5.02 Boehringer Ingelheim Investigational Site Denver Colorado
United States 1219.5.04 Boehringer Ingelheim Investigational Site Philadelphia Pennsylvania
United States 1219.5.01 Boehringer Ingelheim Investigational Site San Francisco California

Sponsors (1)

Lead Sponsor Collaborator
Boehringer Ingelheim

Countries where clinical trial is conducted

United States,  Germany, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change From Baseline in Volume of Mucin Per Surface Area of Basal Lamina Change from baseline in volume of mucin per surface area of basal lamina. Volume of mucin per surface area of basal lamina (vs mu,bala) was determined by stereologic quantification of Periodic Acid Schiff's (AB/PAS) reagent staining in endobronchial biopsies at visit 2 (baseline) and at the end of the 4-week period of randomized treatment (visit 5). At baseline (visit 2) and at visit 5.
Secondary Change From Baseline of Volume of Mucin Per Volume of Epithelium (Vv mu, ep) in Endobronchial Biopsies Change from baseline of volume of mucin per volume of epithelium (Vv mu, ep) in endobronchial biopsies. The volume of mucin per volume of epithelium (Vv mu, ep), as measured by stereological quantification of AB/PAS staining in endobronchial biopsies was performed at baseline (visit 2) and at the end of the 4-week period of randomised treatment (visit 5). At baseline (visit 2) and at visit 5.
Secondary Change From Baseline in Bronchoalveolar Lavage (BAL) Cell Differential (in %) Change from baseline in bronchoalveolar lavage (BAL) cell differential (in %). Differential cell counts were performed on bronchoalveolar lavage samples obtained during visit 2 (baseline) and at the end of the 4-week period of randomised treatment (visit 5). At baseline (visit 2) and at visit 5.
Secondary Change From Baseline in Bronchoalveolar Lavage (BAL) Cell Count Change from baseline in bronchoalveolar lavage (BAL) cell count. Total cell counts were performed on bronchoalveolar lavage (BAL) samples obtained during visit 2 (baseline) and at the end of the 4-week period of randomised treatment. At baseline (visit 2) and at visit 5.
Secondary Change From Baseline in Log MUC2 Mucin Gene Expression (RNA) Obtained in Epithelial Brushings Change from baseline in log MUC2 Mucin gene expression (RNA) obtained in epithelial brushings. Gene expression levels of the gel-forming mucins (MUC2) were quantified using two-step real time polymerase chain reaction (PCR) from RNA extracted from the cells obtained from the epithelial brushings during the endobronchial biopsy at visit 2 (baseline) and at the end of the 4-week period of randomised treatment (visit 5). At baseline (visit 2) and at visit 5.
Secondary Change From Baseline in Log Mucin Gene (MUC5AC) Expression Level Obtained in Epithelial Brushings Change from baseline in log mucin gene (MUC5AC) expression level obtained in epithelial brushings. Gene expression levels of the gel-forming mucins (MUC5AC) were quantified using two-step real time polymerase chain reaction (PCR) from RNA extracted from the cells obtained from the epithelial brushings during the endobronchial biopsy at visit 2 (baseline) and at the end of the 4-week period of randomised treatment (visit 5). At baseline (visit 2) and at visit 5.
Secondary Change From Baseline in Log Mucin Gene (MUC5B) Expression Level Obtained in Epithelial Brushings Change from baseline in log mucin gene (MUC5B) expression level obtained in epithelial brushings.
Gene expression levels of the gel-forming mucins (MUC5B) were quantified using two-step real time polymerase chain reaction (PCR) from RNA extracted from the cells obtained from the epithelial brushings during the endobronchial biopsy at visit 2 (baseline) and at the end of the 4-week period of randomised treatment (visit 5).
At baseline (visit 2) and at visit 5.
Secondary Change From Baseline in Log Mucin Gene (MUC8) Expression Level Obtained in Epithelial Brushings Change from baseline in log mucin gene (MUC8) expression level obtained in epithelial brushings. Gene expression levels of the gel-forming mucins (MUC8) were quantified using two-step real time polymerase chain reaction (PCR) from RNA extracted from the cells obtained from the epithelial brushings during the endobronchial biopsy at visit 2 (baseline) and at the end of the 4-week period of randomised treatment (visit 5). At baseline (visit 2) and at visit 5.
Secondary Change From Baseline in Epidermal Growth Factor Receptor (EGRF) Internalization Assay in Epithelial Brushings - Cells With Bright Spots With Marker Change in percentage of cells with bright spots with marker. The degree of EGFR internalization (and hence activation) was measured using antibody or ligand labeling techniques in epithelial brushing samples obtained during the endobronchial biopsy at visit 2 (baseline) and at the end of the 4-week period of randomised treatment (visit 5). Measurements visit 2 are used to standardize measurements at visit 5, and the standardized visit 5 value is calculated in percent (%) control as (visit5/visit2*100). At baseline (visit 2) and at visit 5.
Secondary Change From Baseline in Epidermal Growth Factor Receptor (EGRF) Internalization Assay in Epithelial Brushings - EGRF Spots at Nucleus Change in number of EGRF spots at nucleus. The degree of EGFR internalization (and hence activation) was measured using antibody or ligand labeling techniques in epithelial brushing samples obtained during the endobronchial biopsy at visit 2 (baseline) and at the end of the 4-week period of randomised treatment (visit 5). Measurements visit 2 are used to standardize measurements at visit 5, and the standardized visit 5 value is calculated in percent (%) control as (visit5/visit2*100). At baseline (visit 2) and at visit 5.
Secondary Change From Baseline in Epidermal Growth Factor Receptor (EGFR) Internalization Assay in Epithelial Brushings - EGRF Spots With Marker Change in number of EGRF spots with marker per cell. The degree of EGFR internalization (and hence activation) was measured using antibody or ligand labeling techniques in epithelial brushing samples obtained during the endobronchial biopsy at visit 2 (baseline) and at the end of the 4-week period of randomised treatment (visit 5). Measurements visit 2 are used to standardize measurements at visit 5, and the standardized visit 5 value is calculated in percent (%) control as (visit5/visit2*100). At baseline (visit 2) and at visit 5.
Secondary Change From Baseline in Epidermal Growth Factor Receptor (EGFR) Internalization Assay in Epithelial Brushings - Total Area Bright Spots With Marker Change in total area bright spots with marker. The degree of EGFR internalization (and hence activation) was measured using antibody or ligand labeling techniques in epithelial brushing samples obtained during the endobronchial biopsy at visit 2 (baseline) and at the end of the 4-week period of randomised treatment (visit 5). Measurements visit 2 are used to standardize measurements at visit 5, and the standardized visit 5 value is calculated in percent (%) control as (visit5/visit2*100). At baseline (visit 2) and at visit 5.
Secondary Change From Baseline in Epidermal Growth Factor Receptor (EGFR) Internalization Assay in Epithelial Brushings - EGFR Spots Change in number of EGFR spots per cell. The degree of EGFR internalization (and hence activation) was measured using antibody or ligand labeling techniques in epithelial brushing samples obtained during the endobronchial biopsy at visit 2 (baseline) and at the end of the 4-week period of randomised treatment (visit 5). Measurements visit 2 are used to standardize measurements at visit 5, and the standardized visit 5 value is calculated in % control as (visit5/visit2*100). At baseline (visit 2) and at visit 5.
Secondary Change From Baseline in Epidermal Growth Factor Receptor (EGFR) Internalization Assay in Epithelial Brushings - EGFR Spots at Nucleus With Marker Change in number of EGFR spots at nucleus per cell with marker. The degree of EGFR internalization (and hence activation) was measured using antibody or ligand labeling techniques in epithelial brushing samples obtained during the endobronchial biopsy at visit 2 (baseline) and at the end of the 4-week period of randomised treatment (visit 5). Measurements visit 2 are used to standardize measurements at visit 5, and the standardized visit 5 value is calculated in % control as (visit5/visit2*100). At baseline (visit 2) and at visit 5.
Secondary Change From Baseline in Number of Goblet Cells Per Surface Area of Basel Lamina Change from baseline in number of goblet cells per surface area of basel lamina, using endobronchial biopsies, taken at visit 2 (baseline) and at the end of the 4-week period of randomised treatment (visit 5). At baseline (visit 2) and at visit 5.
Secondary Change From Baseline in Number of Goblet Cells Per Volume of Epithelium Change from baseline in number of goblet cells per volume of epithelium, using endobronchial biopsies, taken at visit 2 (baseline) and at the end of the 4-week period of randomised treatment (visit 5). At baseline (visit 2) and visit 5.
Secondary Change From Baseline in Goblet Cell Volume Change from baseline in goblet cell volume, using endobronchial biopsies, taken at visit 2 (baseline) and at the end of the 4-week period of randomised treatment (visit 5). At baseline (visit 2) and visit 5.
Secondary Change From Baseline of Interleukin-8 (IL-8) Levels in Bronchoalveolar Lavage Change from baseline of Interleukin-8 (IL-8) levels in bronchoalveolar lavage. IL-8 levels, were measured by enzyme linked immunosorbent assay in bronchoalveolar lavage samples at visit 2 (baseline) and at the end of the 4-week period of treatment (visit 5). At baseline (visit 2) and at visit 5.
Secondary Change From Baseline in Myeloperoxidase (MPO) Levels in Bronchoalveolar Lavage Change from baseline in Myeloperoxidase (MPO) levels in bronchoalveolar lavage. Myeloperoxidase (MPO) activity levels were measured by enzyme linked immunosorbent or radioimmunoassay assay in bronchoalveolar lavage samples at visit 2 (baseline) and at the end of the 4-week period of randomised treatment (visit 5). At baseline (visit 2) and at visit 5.
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