Study to Assess the Effect of the NEXThaler® Device (DPI - Dry Powder Inhaler) on the Central and Peripheral Airway Dimensions in Asthmatic Patients

Asthma Clinical Trial

Official title:

OPEN-LABEL, PROSPECTIVE EXPLORATORY STUDY TO ASSESS THE EFFECTS OF FORMOTEROL AND BECLOMETASONE DIPROPIONATE COMBINATION THERAPY USING A DPI DEVICE ON CENTRAL AND PERIPHERAL AIRWAY DIMENSIONS IN ASTHMATIC PATIENTS.

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01650441
• Other study ID #: PML_DOC_1102
• Secondary ID: 2011-003249-16
• Status: Completed
• Phase: Phase 2
• First received: June 29, 2012
• Last updated: May 27, 2015
• Start date: April 2012
• Est. completion date: June 2013

Study information

• Verified date: May 2015
• Source: University Hospital, Antwerp
• Contact: n/a
• Is FDA regulated: No
• Health authority: Belgium: Federal Agency for Medicinal Products and Health Products
• Study type: Interventional

Clinical Trial Summary

The objective of this study is to evaluate the effect of the combination of formoterol and beclometasone dipropionate in a dry powder inhaler (NEXThaler®) on central and peripheral airway dimensions in asthmatic patients. Therefore Computational Fluid Dynamics (CFD) will be used. Further more, the effect of this combination therapy on lung function (spirometry, resistance and diffusion), the Asthma Control Test (ACT™) and the Asthma Control Questionnaire (ACQ) will be assessed and the safety will be evaluated.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 31
• Est. completion date: June 2013
• Est. primary completion date: June 2013
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

1. Patients with moderate asthma as defined by the current GINA guidelines. Patients can belong to 2 categories:

Group 1 (n=15 to 20, at least 4 current smokers): Patients not well controlled (partially controlled or uncontrolled according to the GINA guidelines) when using medium daily dose of ICS or medium dose ICS + long acting inhaled 2-agonists (LABA) (for definition please refer to the addendum in section 15) given for at least 6 weeks as large-particle formulation (non extra-fine).

Group 2 (n=15 to 20, at least 4 current smokers ): Patients well controlled (according to GINA guidelines) when using medium daily dose of ICS + LABA (for definition please refer to the addendum in section 15) given for at least 6 weeks as large-particle formulation (non extra-fine).

2. Male or female patients aged =18 years

3. Patients with a documented diagnosis of asthma according to the GINA guidelines

4. Patients with a co-operative attitude and ability to be trained to correctly use the Foster NEXThaler DPI

5. Written informed consent obtained

Exclusion Criteria:

1. Patients treated with extra-fine ICS either alone or with LABA

2. Pregnant or lactating females or females at risk of pregnancy at screening and not willing to use an appropriate contraception method during the study period

3. Inability to carry out pulmonary function testing

4. History of near fatal asthma

5. Hospitalization due to asthma or symptomatic infection of the airways in the previous 8 weeks

6. Patients with an uncontrolled disease or any condition that might, in the judgement of the investigator, place the patient at undue risk or potentially compromise the results or interpretation of the study

7. Cancer

8. Current alcohol or drug abuse

9. Allergy, sensitivity or intolerance to study drugs and/or study drug formulation ingredients

10. Patients unlikely to comply with the protocol or unable to understand the nature, scope and possible consequences of the study

11. Patients who received any investigational new drug within the last 4 weeks prior to the screening visit

12. Patients treated with any non-permitted concomitant medication

Study Design

Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

• Asthma

Intervention

Drug:
• Beclomethasone dipropionate 100 µg + formoterol fumarate 6 µg
In this trial, patients will take two inhalations of the beclometasone dipropionate 100 µg and formoterol fumarate 6 µg combination therapy (Foster®) using a Dry Powder Inhaler (NEXThaler®) device in the morning and two inhalations in the evening, for a total of 4 inhalations a day (total daily dose: BDP 400 µg / FF 24 µg).

Radiation:
• CT thorax
CT scan of the thorax will be performed at 2 time points: baseline and after 6 months of treatment. The CT scan will be performed with low dose radiation using the multi-slice CT scan. Scanning will be performed at Functional Residual Capacity and Total Lung Capacity (2 times 8 sec). The lung volumes will be controlled using adapted spirometry during the CT procedure. The radiation dose will be reduced by reduction of the tube current and voltage. These settings depend on the patients' weight (1mAs/kg). In addition to this there will be an increase in noise factor to further reduce the radiation dose.

Locations

Country	Name	City	State
Belgium	University Hospital of Antwerp	Edegem (Antwerp)	Antwerp

Sponsors (2)

Lead Sponsor	Collaborator
University Hospital, Antwerp	Chiesi Farmaceutici S.p.A.

Country where clinical trial is conducted

Belgium, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Computational Fluid Dynamics (CFD)	The parameters that will be obtained with the CFD based imaging and used as primary outcome parameters are: Total airway resistance for the segmented airways iRtot; Peripheral airway resistance(from 4th bifurcation on) for the segmented airways iRperph; Total airway volume for the segmented airways (iVtot); Peripheral airway volume (from the 4th bifurcation on) for the segmented airways (iVperiph); Relative compliance for each lobe (iClobe-rel); Density of the lung parenchyma given per predefined lung zone (Ldens)	CFD will be performed based on the images of 2 CT thorax scans in a dose reduction protocol (1 CT Thorax taken at baseline and 1 CT Thorax taken after 6 months of treatment with the NEXThaler® device).	No
Secondary	Lung function tests	The parameters that will be obtained with the described lung function tests are: Dynamic lung volumes: FEV1, FVC, PEF, MEF75, MEF50, MEF25; Static lung volumes: VC, IVC, FRC, TLC; Airway resistances: Raw, SGaw	Lung function tests will be performed at screening (visit 1), after 2 week run-in period both pre and post dose (visit 2), after 3 months treatment (visit 5), after 6 months treatment both pre and post dose (visit 8).	No
Secondary	Asthma Control	Asthma Control will be monitored during the study using 2 different questionnaires: the Asthma Control Test (ACT™) and the Asthma Control Questionnaire (ACQ, both the 6-items and the 7-items test will be used.)	Asthma control will be monitored at screening (visit 1), after 2 week run-in period (visit 2), after 3 months treatment (visit 5), after 6 months treatment (visit 8).	No
Secondary	Safety	During the study the patient will be told to record each day taken medication and any possible comments on the daily diary cards, starting from visit 1. Further more, the patient will be contacted at least once a month (either by phone or a visit in the hospital.)	The safety of the NEXThaler® device will be monitored for the duration of the study, an expected average of 24 weeks.	Yes