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Trial details imported from ClinicalTrials.gov
For full trial details, please see the original record at
https://clinicaltrials.gov/ct2/show/NCT00642148
Registration number
NCT00642148
Ethics application status
Date submitted
17/03/2008
Date registered
24/03/2008
Date last updated
18/08/2017
Titles & IDs
Public title
A 12 Week Study To Assess Efficacy And Safety Of GW856553 In Subjects With Chronic Obstructive Pulmonary Disease (COPD)
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Scientific title
A 12-week, Randomised, Double-blind, Placebo-controlled Study to Assess the Anti-inflammatory Activity, Efficacy and Safety of GW856553 in Subjects With Chronic Obstructive Pulmonary Disease (COPD)
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Secondary ID [1]
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MKI102428
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Universal Trial Number (UTN)
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Trial acronym
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
Pulmonary Disease, Chronic Obstructive
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Condition category
Condition code
Respiratory
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Chronic obstructive pulmonary disease
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
Treatment: Drugs - GW856553
Treatment: Drugs - Placebo
Treatment: Drugs - Seretide
Active Comparator: Seretide -
Placebo Comparator: Placebo - Placebo tablet
Experimental: GW856553 -
Treatment: Drugs: GW856553
Active tablet
Treatment: Drugs: Placebo
Placebo tablet and inhaler
Treatment: Drugs: Seretide
Active comparator inhaler
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Intervention code [1]
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Treatment: Drugs
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Comparator / control treatment
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Control group
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Outcomes
Primary outcome [1]
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Change from Baseline in percentage of neutrophils in induced sputum at Week 12
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Assessment method [1]
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Induced sputum samples were collected at Baseline (Week 0), Week 4 and at Week 12 to evaluate the effects of 12 weeks of treatment with GW856553 7.5 mg twice daily. Baseline was defined at Week 0. Change from Baseline in neutrophil count was calculated as the Week 12 value minus the Baseline value (percentage of neutrophil of total cells in induced sputum at Week 12 minus the Baseline value). Data for adjusted mean was presented for least square mean.
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Timepoint [1]
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Baseline (Week 0) and Week 12
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Secondary outcome [1]
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Change from Baseline in Plethysmography measures at Week 12
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Assessment method [1]
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Plethysmography was performed to assess inspiratory capacity (IC), residual volume (RV), thoracic gas volume (TGV) at Functional Residual Capacity, Total Lung Capacity (TLC) and Slow Vital Capacity (SVC) at baseline and up to Week 12. Baseline was defined at Week 0. Change from Baseline in Plethysmography was calculated as the Week 12 value minus the Baseline value. Data for adjusted mean was presented for least square mean.
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Timepoint [1]
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Baseline (Week 0) and Week 12
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Secondary outcome [2]
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Change from Baseline in pulmonary function assessed by forced vital capacity (FVC), forced expiratory volume in 1 second (FEV1) at Week 12
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Assessment method [2]
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Pre and post bronchodilator FVC and FEV1 values were calculated to assess the pulmonary function. FVC was defined as the total amount of air exhaled during the lung function test and FEV1 was defined as the amount of air which was forcibly exhaled from the lungs in the first second of a forced exhalation. Baseline was defined at Week 0. Change from Baseline in pulmonary function was calculated as the Week 12 value minus the Baseline value. Data for adjusted mean was presented for least square mean.
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Timepoint [2]
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Baseline (Week 0) and Week 12
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Secondary outcome [3]
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Change from Baseline in pulmonary function assessed by FEV1/FVC at Week 12
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Assessment method [3]
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Pre and post bronchodilator FEV1/FVC ratio was measured at baseline and up to Week 12. Baseline was defined at Week 0. Change from Baseline in FEV1/FVC ratio was calculated as the Week 12 value minus the Baseline value.
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Timepoint [3]
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Baseline (Week 0) and Week 12
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Secondary outcome [4]
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Change from Baseline in pulmonary function assessed by impulse oscillometry [Peripheral airway resistance (R5 - R15)] at Week 12
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Assessment method [4]
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Pulmonary function was assessed by impulse oscillometry for pre and post bronchodilator peripheral airway resistance (R5 - R15) at Baseline and up to Week 12. Baseline was defined at Week 0. Change from Baseline in pulmonary function was calculated as the Week 12 value minus the Baseline value. Data for adjusted mean was presented for least square mean.
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Timepoint [4]
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Baseline (Week 0) and Week 12
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Secondary outcome [5]
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Change from Baseline in pulmonary function assessed by impulse oscillometry: Total resistance (R5) and large airway resistance (R25) of the lung at Week 12
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Assessment method [5]
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Pulmonary function was assessed by impulse oscillometry for pre and post bronchodilator Total resistance (R5) and large airway resistance (R25) at Baseline and up to Week 12. Baseline was defined at Week 0. Change from Baseline in pulmonary function was calculated as the Week 12 value minus the Baseline value.
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Timepoint [5]
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Baseline (Week 0) and Week 12
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Secondary outcome [6]
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Change from Baseline in pulmonary function assessed by impulse oscillometry: Resonant frequency (RF) and X5 as indicators of the reactive capacitance properties of the lung at Week 12
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Assessment method [6]
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Pulmonary function was assessed by impulse oscillometry for pre and post bronchodilator RF and X5 as indicators of the reactive capacitance properties of the lung at Baseline and up to Week 12. Baseline was defined at Week 0. Change from Baseline in pulmonary function was calculated as the Week 12 value minus the Baseline value.
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Timepoint [6]
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Baseline (Week 0) and Week 12
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Secondary outcome [7]
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Ratio of pulmonary function assessed by impulse oscillometry at Week 12 to Baseline: low-frequency reactance area (AX) as indicator of the reactive capacitance properties of the lung
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Assessment method [7]
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Pulmonary function was assessed by impulse oscillometry for pre and post bronchodilator AX as indicator of the reactive capacitance properties of the lung at Baseline and up to Week 12.
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Timepoint [7]
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Baseline (Week 0) and Week 12
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Secondary outcome [8]
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Ratio of plasma fibrinogen assessment at Week 12 to Baseline
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Assessment method [8]
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Blood samples for measurement of fibrinogen was collected at Baseline and up to Week 12. Data for Week 12 plasma fibrinogen assessment was reported.
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Timepoint [8]
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Baseline (Week 0) and Week 12
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Secondary outcome [9]
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Ratio of biomarker assessment: Serum Surfactant Protein D (SP-D) and Clara cell protein 16 (CCP-16) at Week 12 to Baseline
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Assessment method [9]
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Blood samples for assessment of systemic biomarkers i.e. SP-D and CCP-16 were collected at Baseline and Up to Week 12. Ratio of geometric means at Week 12 to Baseline has been presented.
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Timepoint [9]
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Baseline (Week 0) and Week 12
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Secondary outcome [10]
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Ratio of High Sensitivity C-reactive Protein (hsCRP) at Week 12 to Baseline
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Assessment method [10]
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Blood samples for assessment of systemic biomarker i.e. hsCRP were collected at Baseline and Up to Week 12. Ratio of geometric means at Week 12 to Baseline has been presented.
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Timepoint [10]
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Baseline (Week 0) and Week 12
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Secondary outcome [11]
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Ratio of biomarker assessment: Interleukin 6 (IL-6), Interleukin 8 (IL-8) Matrix Metallopeptidase 9 (MMP-9) and PARC (Pulmonary and activation-regulated chemokine) at Week 12 to Baseline
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Assessment method [11]
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Blood samples for assessment of systemic biomarkers i.e. IL-6, IL-8, MMP-9 and PARC were collected at Baseline and Up to Week 12. Adjusted ratio to Baseline value at Week 12 has been presented.
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Timepoint [11]
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Baseline (Week 0) and Week 12
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Secondary outcome [12]
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Ratio of biomarker sorbitol-Induced phosphorylated heat shock protein (pHSP-27) in whole blood pre-dose and 2 h post-dose assessment at Week 12 to Baseline
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Assessment method [12]
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Levels of ex vivo pHSP27 in whole blood pre-dose and 2 hours post-dose at selected centres was assessed over 12 Weeks of treatment. Adjusted ratio to Baseline value at Week 12 has been presented.
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Timepoint [12]
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Baseline (Week 0) and Week 12
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Secondary outcome [13]
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Ratio of biomarker LPS-Induced TNFa Release (pre and post dose) assessment at Week 12 to Baseline
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Assessment method [13]
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Levels of ex vivo LPS induced TNF-a in whole blood pre-dose and 2 hours post-dose at selected centres was assessed over 12 Weeks of treatment. Adjusted ratio to Baseline value at Week 12 has been presented.
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Timepoint [13]
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Baseline (Week 0) and Week 12
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Secondary outcome [14]
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Ratio of total leukocyte count in induced sputum assessments at Week 12 to Baseline
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Assessment method [14]
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Induced sputum samples for assessment of total cell count were collected at Baseline (Week 0), Week 4 and at Week 12 to evaluate the effects of 12 weeks of treatment with GW856553 7.5 mg twice daily. Adjusted ratio to Baseline value at Week 12 has been presented.
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Timepoint [14]
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Baseline (Week 0) and Week 12
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Secondary outcome [15]
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Change from Baseline in sputum assessment for macrophages as a percentage of total cells at Week 12
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Assessment method [15]
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Percentage of total cells for macrophages was assessed in induced sputum at Baseline and up to Week 12. Baseline was defined at Week 0. Change from Baseline in Percentage of total cells for macrophages was calculated as the Week 12 value minus the Baseline value. Data for adjusted mean was presented for least square mean.
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Timepoint [15]
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Baseline (Week 0) and Week 12
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Secondary outcome [16]
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Change from Baseline in sputum assessment for lymphocytes and eosinophils as a percentage of total cells at Week 12
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Assessment method [16]
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Percentage of total cells for lymphocyte and eosinophil was assessed in induced sputum at Baseline and up to Week 12. Baseline was defined at Week 0. Change from Baseline in Percentage of total cells for macrophages was calculated as the Week 12 value minus the Baseline value.
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Timepoint [16]
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Baseline (Week 0) and Week 12
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Secondary outcome [17]
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Change from Baseline in sputum assessment for lymphocytes and eosinophils as absolute inflammatory cell numbers at Week 12
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Assessment method [17]
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Absolute inflammatory cell numbers for lymphocyte and eosinophil was assessed in induced sputum at Baseline and up to Week 12. Baseline was defined at Week 0. Change from Baseline in Absolute inflammatory cell numbers for lymphocyte and eosinophil was calculated as the Week 12 value minus the Baseline value.
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Timepoint [17]
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Baseline (Week 0) and Week 12
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Secondary outcome [18]
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Ratio of sputum assessment for Neutrophils and macrophages as absolute inflammatory cell numbers at Week 12 to Baseline
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Assessment method [18]
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Absolute inflammatory cell numbers for neutrophils and macrophages was assessed in induced sputum at Baseline and up to Week 12. Adjusted ratio to Baseline value at Week 12 has been presented.
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Timepoint [18]
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Baseline (Week 0) and Week 12
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Secondary outcome [19]
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Ratio of sputum weight and volume at Week 12 to Baseline
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Assessment method [19]
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Induced sputum weight and volume was assessed up to Week 12. For participants who were not able to produce an induced sputum sample after induction (and for these participants only), missing values were imputed with half lowest weight. Adjusted ratio to Baseline value at Week 12 has been presented.
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Timepoint [19]
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Baseline (Week 0) and Week 12
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Secondary outcome [20]
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Ratio of concentration of inflammatory biomarkers (ng/ml)-myeloperoxidase (MPO) at Week 12 to Baseline
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Assessment method [20]
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Sputum samples were analyzed to determine the concentration of inflammatory biomarker i.e MPO up to Week 12. Adjusted ratio to Baseline value at Week 12 has been presented.
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Timepoint [20]
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Baseline (Week 0) and Week 12
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Secondary outcome [21]
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Ratio of concentration of inflammatory biomarkers (ug/ml)- total protein at Week 12 to Baseline
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Assessment method [21]
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Sputum samples were analyzed to determine the concentration of inflammatory biomarker i.e total protein up to Week 12. Adjusted ratio to Baseline value at Week 12 has been presented.
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Timepoint [21]
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Baseline (Week 0) and Week 12
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Eligibility
Key inclusion criteria
Subjects eligible for enrolment in the study must meet all of the following criteria:
- Male adults or female adults of non-childbearing potential who are between 40 and 75
years of age (inclusive). Note: a female is eligible to enter and participate in the
study if she is of non-childbearing potential (i.e. physiologically incapable of
becoming pregnant). This includes any female who is post-menopausal. For the purposes
of this study, post menopausal is defined as being amenorrhoeic for greater than 1
year with an appropriate clinical profile, e.g. age appropriate, history of vasomotor
symptoms. Postmenopausal status may be confirmed by serum FSH and oestradiol
concentrations at screening if deemed necessary by the PI. Surgical sterility will be
defined as females who have had a hysterectomy and/or bilateral oophorectomy or tubal
ligation.
- Chronic obstructive pulmonary disease diagnosis: an established clinical history of
COPD in accordance with the following description by the American Thoracic
Society/European Respiratory Society [American Thoracic Society / European Respiratory
Society, 2004] Chronic obstructive pulmonary disease is a preventable and treatable
disease characterised by airflow limitation that is not fully reversible. The airflow
limitation is usually progressive and is associated with an abnormal inflammatory
response of the lungs to noxious particles or gases, primarily caused by cigarette
smoking. Although COPD affects the lungs, it also produces significant systemic
consequences.
- Subjects with a cigarette smoking history of =10 pack years (1 pack year = 20
cigarettes smoked per day for 1 year or the equivalent). Both current and former
smokers are eligible to be enrolled. A former smoker is defined as a subject who has
not smoked for =6 months at Visit 1.
- Subjects with a post-bronchodilator FEV1 to FVC ratio (FEV1:FVC) < 0.7 at Visit 1.
Subjects will be assessed 30 (± 5) minutes after receiving salbutamol 400 µg.
- Subjects with a post-bronchodilator FEV1 = 50% and < 80% of predicted normal for
height, age and sex at Visit 1. Subjects will be assessed 30 (± 5) minutes after
receiving salbutamol 400 µg.
- Subjects capable of providing signed written informed consent to participate.
- Subjects must have a QTc <450 msec on baseline ECG or triplicate ECG averaged over a
brief recording interval. For subjects with baseline bundle branch block the QTc will
be <480msec on baseline ECG or triplicate ECG averaged over a brief recording
interval.
- A subject will be eligible for randomisation at the end of the run-in period only if
the following additional criterion applies: Subjects with no evidence of an ongoing
acute infection or sinus symptoms Specific information regarding warnings,
precautions, contraindications, AEs, and other pertinent information on the
investigational product that may impact subject eligibility is provided in the
Investigator Brochure/Investigator Brochure supplement(s), product label, and other
pertinent documents.
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Minimum age
40
Years
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Maximum age
No limit
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Sex
Both males and females
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Can healthy volunteers participate?
No
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Key exclusion criteria
A subject will not be eligible for inclusion in this study if any of the following criteria
apply:
- Women who are pre-menopausal and of child-bearing potential, or pregnant.
- Subjects with a primary diagnosis of asthma or a-1 antitrypsin deficiency.
- Subjects who have required hospitalisation or treatment with oral corticosteroids
and/or antibiotic therapy for acute worsening of COPD or lower respiratory tract
infection in the 6 weeks prior to Visit 1
- Subjects with active tuberculosis or being treated for active tuberculosis,
sarcoidosis or clinically overt bronchiectasis.
- Subjects with a history of any type of malignancy with the exception of successfully
treated squamous cell cancer of the skin.
- Subjects with rheumatoid arthritis, connective tissue disorders and other conditions
known to be associated with chronic inflammation (e.g. inflammatory bowel disease).
- Subjects with chronic infections such as gingivitis, periodontitis, prostatitis,
gastritis, and urinary tract infections.
- Subjects with any acute infection, sinus symptoms, or significant trauma (burns,
fractures).
- Subjects with clinically significant renal disease, diabetes mellitus/metabolic
syndrome, hypertension or any other clinically significant cardiovascular,
neurological, endocrine, or haematological abnormalities that are uncontrolled on
permitted therapy (see Section 6.6.1).
- Subjects with clinically significant gastrointestinal or hepatic abnormalities.
- Subjects with hypoxaemia. (All subjects must have an O2 saturation of = 88% on room
air).
- History of Gilbert's syndrome. Subjects with a total bilirubin concentration above the
upper limit of normal at Visit 1 will be excluded.
- Liver function tests (bilirubin, ALT, or AST) above upper limit of normal at Visit 1.
The subject has a positive Hepatitis B surface antigen or Hepatitis C antibody result
within 3 months of the start of the study.The subject has a history of HIV or other
immunosuppressive disease.
- Subjects who have undergone recent surgery including lung volume reduction surgery or
have conditions that prevent them from performing spirometry.
- Subjects with a history (or suspected history) of alcohol misuse or any other
substance abuse.
- The subject has a three month prior history of regular alcohol consumption exceeding
an average weekly intake of > 21 units (or an average daily intake of greater than 3
units) for males, or an average weekly intake of > 14 units (or an average daily
intake of greater than 2 units) for females. 1 unit is equivalent to a half-pint
(284mL) of beer/lager; 25mL measure of spirits or 125mL of wine; or a positive alcohol
breath test at the screening visit
- Subjects who will commence or who are likely to commence statin therapy
(3-hydroxy-3-methylglutaryl coenzyme A reductase inhibitors) or treatment with
intranasal or topical corticosteroids, acetylsalicyclic acid, non-steroidal
anti-inflammatory drugs, gemfibrozil, clopidogrel, abciximab, peroxidase
proliferator-activated receptor ? agonists (e.g, rosiglitazone), fibrates, or niacin
from Visit 1 until study completion. (Subjects who are receiving these medications at
a stable dose at Visit 1 may be entered in the study.)
- Subjects who require treatment with any of the following from the Visit 1 until study
completion:
- Inhaled corticosteroids
- Inhaled cromolyn sodium or nedocromil
- Xanthines (theophylline preparations)
- Leukotriene modifiers
- Tiotropium
- Long-acting inhaled ß2-agonists (salmeterol, formoterol)
- Oral ß2-agonists
- Macrolide antibiotics for more than five days
- Subjects who have received treatment with oral, intravenous or intra-articular
corticosteroids within 6 weeks of Visit 1 or thereafter.
- Subjects with any known hypersensitivity to salbutamol or ipratropium bromide.
- Subjects who are participating or plan to participate in the active phase of a
pulmonary rehabilitation programme during the study. Maintenance rehabilitation is
permitted.
- Subjects who have received an investigational drug within 30 days or within five drug
half-lives of the investigational drug (whichever is longer).
- Subjects with any clinically relevant abnormality detected by the assessments at Visit
1
- An unwillingness of male subjects to abstain from sexual intercourse with pregnant or
lactating women; or unwillingness of the male subject to use a condom/spermicide in
addition to having their female partner use another form of contraception such as an
intra-uterine devices, diaphragm with spermicide, oral contraceptives, injectable
progesterone, subdermal implants or a tubal ligation if the woman could become
pregnant from the time of the first dose of investigational product for the duration
of the study (i.e., through the follow-up phase).
- Subjects who have had a close household contact treated for active tuberculosis within
the past 12 months, or who in the judgement of the investigator are at high risk for
developing active tuberculosis, shall be excluded from the study.
- A subject will not be eligible for randomisation at the end of the run-in period if
either of the following criteria applies:
- Subjects who have experienced an exacerbation during the run-in period requiring
treatment with oral corticosteroids and/or antibiotics and/or hospitalisation.
- Subjects who are unable to produce an induced sputum sample.
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Study design
Purpose of the study
Treatment
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Allocation to intervention
Randomised controlled trial
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Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
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Masking / blinding
Blinded (masking used)
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Who is / are masked / blinded?
The people receiving the treatment/s
The people administering the treatment/s
The people assessing the outcomes
The people analysing the results/data
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Intervention assignment
Parallel
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Other design features
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Phase
Phase 2
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Type of endpoint/s
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Statistical methods / analysis
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Recruitment
Recruitment status
Completed
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Data analysis
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Reason for early stopping/withdrawal
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Other reasons
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Date of first participant enrolment
Anticipated
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Actual
14/02/2008
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Date of last participant enrolment
Anticipated
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Actual
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Date of last data collection
Anticipated
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Actual
27/07/2009
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Sample size
Target
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Accrual to date
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Final
306
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Recruitment in Australia
Recruitment state(s)
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Recruitment outside Australia
Country [1]
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Estonia
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Tallinn
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Estonia
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Tartu
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Finland
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Helsinki
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Germany
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Bayern
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Germany
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Rheinland-Pfalz
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Germany
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Sachsen-Anhalt
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Germany
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Schleswig-Holstein
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Germany
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Berlin
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Korea, Republic of
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Seoul
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Latvia
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Riga
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Lithuania
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Klaipeda
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Netherlands
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Breda
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Netherlands
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Heerlen
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Netherlands
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Veldhoven
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New Zealand
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Auckland
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New Zealand
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Wellington
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Russian Federation
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Barnaul
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Russian Federation
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Moscow
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Russian Federation
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Saint-Petersburg
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Russian Federation
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St. Petersburg
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Slovenia
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Kamnik
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Slovenia
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Ljubljana
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South Africa
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Gauteng
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South Africa
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Amanzimtoti
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South Africa
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Mowbray
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United Kingdom
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Oxfordshire
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United Kingdom
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Cottingham, East Yorkshire
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United Kingdom
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London
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Funding & Sponsors
Primary sponsor type
Commercial sector/Industry
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Name
GlaxoSmithKline
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Address
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Ethics approval
Ethics application status
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Summary
Brief summary
Phase IIa, randomised, double-blind, double-dummy, parallel group, multi-centre study in
subjects diagnosed with moderate chronic obstructive pulmonary disease (COPD). The primary
objective is to evaluate the effects of 12-weeks of treatment with GW856553 7.5 mg twice
daily (BID) compared with placebo on the percentage of sputum neutrophils at 12 weeks. Twelve
weeks of treatment with SERETIDE 50/500 BID will be compared with placebo for effect on
sputum neutrophils as a positive control arm in the study
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Trial website
https://clinicaltrials.gov/ct2/show/NCT00642148
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Trial related presentations / publications
Lomas DA, Lipson DA, Miller BE, Willits L, Keene O, Barnacle H, Barnes NC, Tal-Singer R; Losmapimod Study Investigators. An oral inhibitor of p38 MAP kinase reduces plasma fibrinogen in patients with chronic obstructive pulmonary disease. J Clin Pharmacol. 2012 Mar;52(3):416-24. doi: 10.1177/0091270010397050. Epub 2011 Nov 16.
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Public notes
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Contacts
Principal investigator
Name
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GSK Clinical Trials
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Address
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GlaxoSmithKline
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Phone
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Fax
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Email
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Contact person for public queries
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Contact person for scientific queries
Summary Results
For IPD and results data, please see
https://clinicaltrials.gov/ct2/show/NCT00642148
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