Health Condition 1: null- Asthma Bronchiale
Conditions
Interventions
Intervention1: FLUTIFORM TM Inhaler: Dosage:2 puffs unit strength-125/5 microgram, dosing frequency:q12h
Mode of administration:Inhaled
Duration:12 weeks
Control Intervention1: Symbicort® Turbohaler:
Sponsors
Mundipharma Research Limited UK
Kendle India Pvt Ltd
Eligibility
Inclusion criteria
Inclusion criteria: 1. Male or female subjects at least 12 years old. 2. Female subjects less than one year post-menopausal must have a negative urine pregnancy test recorded at the screening visit prior to the first dose of study medication, be non-lactating, and willing to use adequate and highly effective methods of contraception throughout the study. A highly effective method of birth control is defined as those which result in a low failure rate (i.e., less than 1% per year) when used consistently and correctly such as sterilisation, implants, injectables, combined oral contraceptives, some IUDs (Intrauterine Device, hormonal), sexual abstinence or vasectomised partner. 3. Known history of moderate to severe persistent, reversible asthma for ≥ 6 months prior to the Screening Visit characterised by: Treatment with an inhaled corticosteroid (ICS) at a dose of 250 , 1000 μg fluticasone or equivalent OR Treatment wth ICS at a dose of 200-500 μg fluticasone or equivalent in combination with a Long Acting β2-Agonist (LABA). 4. Demonstrated a FEV1 of ≥ 50% to ≤ 80% for predicted normal values (Quanjer et al., 1993 (adults), and 1995 (adolescents)) during the Screening Period (Visit 1 or Visit 2) following appropriate withholding of asthma medications (if applicable). - No β2-agonist use on day of testing - No use of inhaled combination asthma therapy on day of testing. - Inhaled corticosteroids are allowed on day of testing. 5. Documented reversibility of ≥ 15% in FEV1 at visit 1 or visit 2. 6. Demonstrated satisfactory technique in the use of the study medications i.e. pMDI and Dry Powder Inhaler (DPI) devices. 7. Willing and able to enter information in the electronic diary and attend all study visits. 8. Willing and able to substitute study medication for their pre study prescribed asthma medication for the duration of the study. 9. Written informed consent obtained. 10. Subject has used rescue medication for at least 3 days and had at least one night with sleep disturbance (i.e., sleep disturbance score of ≥ 1) during the last 7 days of the run in period, OR subject has used rescue medication for at least 3 days and had at least 3 days with asthma symptoms (i.e., a symptom score of ≥ 1) during the last 7 days of the run-in period.
Exclusion criteria
Exclusion criteria: 1. Near fatal or life-threatening (including intubation) asthma within the past year. 2. Hospitalisation or an emergency visit for asthma within the 4 weeks before the Screening Visit. 3. Known history of systemic (injectable or oral) corticosteroid medication use within 1 month of the Screening Visit. 4. Known history of omalizumab use within the past 6 months. 5. Current evidence or known history of any clinically significant disease or abnormality including uncontrolled coronary artery disease, congestive heart failure, myocardial infarction, or cardiac dysrhythmia. Clinically significant‟ is defined as any disease that, in the opinion of the Investigator, would put the subject at risk through study participation, or which would affect the outcome of the study. 6. In the investigator‟s opinion a clinically significant upper or lower respiratory infection within 4 weeks prior to the Screening Visit. 7. Significant, non-reversible, active pulmonary disease (e.g., chronic obstructive pulmonary disease (COPD), cystic fibrosis, bronchiectasis, tuberculosis). 8. Known Human Immunodeficiency Virus (HIV)-positive status. 9. Subject has a smoking history equivalent to 10 pack years (i.e., at least 1 pack of 20 cigarettes/day for 10 years or 10 packs/day for 1 year, etc.). 10. Current smoking history within 12 months prior to the Screening Visit. 11. Current evidence or known history of alcohol and/or substance abuse within 12 months prior to the Screening Visit. 12. Subject has taken -blocking agents, tricyclic antidepressants, monoamine oxidase inhibitors, astemizole (Hismanal), quinidine type antiarrhythmics, or potent CYP 3A4 inhibitors such as ketoconazole within the past week. 13. Current use of medications other than those allowed in the protocol that will have an effect on bronchospasm and/or pulmonary function. 14. Current evidence or known history of hypersensitivity or idiosyncratic reaction to test medications or components. 15. Subject has received an investigational drug within 30 days of the Screening Visit (12 weeks if an oral or injectable steroid). 16. Subject is currently participating in a clinical study.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary endpoint is the change in pre-morning dose FEV1 values from baseline to the end of the 12 week treatment period.Timepoint: at week 12 from baseline to end otf treatment | — |
Secondary
| Measure | Time frame |
|---|---|
| 1. asthma quality of life questionnaire (AQLQ(S) â?¥12 years) 2. subjectâ??s assessment of study medication 3. amount of rescue medication use 4. asthma symptom scores 5. sleep disturbance due to asthma 6. discontinuations due to lack of efficacy 7. asthma excacerbations requiring oral/parenteral steroid use or medical intervention 8. compliance with study medication use 9. Post Dose FEV1 10.PEFR, and other lung function parameters.Timepoint: at 12 week and from baseline to end end of the treatment | — |
Countries
Bulgaria, Hungary, India, Poland, Romania
Contacts
Public ContactDrMamta Singh
Kendle India Pvt Ltd
Outcome results
None listed