Comparison of Flutiform, Fluticasone and Seretide in Treatment of Moderate to Severe Asthma in Paediatric Patients

• Status: Completed
• Trial end date: 2013-11-01
• Target enrollment: 0
• Participant gender: All

Summary

This is a comparator study to assess safety and efficacy of Flutiform compared with Fluticasone pMDI and Seretide pMDI in paediatric asthma patients with moderate to severe persistent, reversible asthma.

• Phase: Phase 3
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: Mundipharma Research Limited
• Treatments: Fluticasone; Fluticasone Propionate, Salmeterol Xinafoate Drug Combination; Fluticasone-Salmeterol Drug Combination

Criteria

Inclusion Criteria

1. Male and Female subjects 5 to <12 years old.

2. Known history of moderate to severe persistent reversible asthma1 for ≥ 6 months prior to the screening visit.

3. Demonstrated FEV1 of ≥ 60% to ≤ 90% for predicted normal values (Polgar 1971) during the screening period following appropriate withholding of asthma medications (if applicable):

• No LABA use within 12 hours and/or no SABA use within 6 hours of the PFT

• No use of inhaled ICS-LABA asthma therapy within 12 hours of the PFT

• Inhaled corticosteroids are allowed on the day of screening

4. Documented reversibility of ≥ 15% in FEV1 in the screening period

5. Current use of an inhaled corticosteroid for asthma at a stable dose for at least 4 weeks prior to the screening visit

6. Inadequate asthma control on an ICS alone at a dose of ≤ 500 µg fluticasone equivalents/day, OR controlled asthma on an ICS-LABA combination at a ICS dose of ≤ 200 µg fluticasone equivalents/day

7. Demonstrated satisfactory technique in the use of the pMDI and spacer device

8. Can perform spirometry adequately

9. Willing and able to enter information in the electronic diary with the help of a parent or guardian, if necessary and attend all study visits

10. Willing and able to substitute pre-study prescribed inhaled asthma medication for the entire duration of the study

11. If a female subject is post menarche a urine pregnancy test may be undertaken at the discretion of the investigator and the subjects' parent(s) /legal representative. This test must be negative.

12. Written informed consent and assent obtained as per national law

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 past 6 months

3. History of systemic (injectable or oral) corticosteroid medication within 1 month of the screening visit

4. Current or prior non-response or partial response only to an ICS-LABA combination1

5. Evidence of a clinically unstable disease, as determined by medical history, clinical laboratory tests, and physical examination that, in the Investigator's opinion, preclude entry into the study. "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. cystic fibrosis, bronchiecstasis, tuberculosis)

8. Known Human Immunodeficiency Virus (HIV)-positive status

9. Current smoking history within 12 months prior to the screening visit

10. Current evidence of alcohol or substance abuse within 12 months prior to the screening visit

11. Subjects who have taken β- blocking agents, tricyclic antidepressants, monoamine oxidase inhibitors, astemizole (Hismanal), quinidine type antiarrythmics, or potent CYP 3A4 inhibitors such as ketoconazole within 1 week prior to the screening visit

12. Current use of medications, other than those allowed in the protocol, that in the investigator's opinion will have an effect on bronchospasm and/or pulmonary function

13. Current evidence of hypersensitivity or idiosyncratic reaction to test medications or components

14. Receipt of an Investigational medicinal product within 30 days of the screening visit

15. Current participation in a clinical study