A Guideline Approach to Therapy Step-down Utilising Flutiform Change and Step-down

The aim of this study is to compare two licensed asthma inhalers and to then evaluate the safety of reducing treatment when patient's asthma is in control. The inhalers used in this study are the Seretide® 250 Evohaler®, which is widely used in UK, and a recently licensed inhaler called Flutiform®. National guidelines recommend that asthma medication should be increased when patients are experiencing worsening of their asthma, and reduced when asthma is in control. However, it is likely that in daily clinical practice some patients are over-treated. It is therefore necessary to conduct more studies which demonstrate that reducing treatment dosage can be done safely.

This study has two phases. In the first phase the investigators aim to recruit 224 patients through approximately 40 clinics in the UK and Ireland. One third of these patients will be selected in random to use the high dosage Seretide® 250 Evohaler® and two thirds will use high dose Flutiform® 250 inhaler for 12 weeks. At the end of phase 1 the investigators will compare how well asthma was controlled between the two groups.

After phase 1 those patients who used Flutiform and did not have any problems with their asthma can participate in phase 2. In phase 2 half of the patients will stay on high dosage Flutiform 250 and half will be switched to the medium dosage Flutiform 125 inhaler. At the end of phase 2 the investigators will compare asthma control between the two groups.

This study will be conducted by Research in Real Life Ltd (Cambridge, UK) with partial funding from Napp Pharmaceuticals Ltd. The estimated total duration of the study is 18 months and each patient will spend a maximum of 6 months in the study.

Study Overview

• Status: Completed
• Conditions: Asthma
• Intervention / Treatment: Drug: Fluticasone 250/salmeterol 25; Drug: Fluticasone 250/formoterol 10; Drug: Fluticasone 125/formoterol 5

• Study Type: Interventional
• Enrollment (Actual): 225
• Phase: Phase 4

Contacts and Locations

Study Locations

• United Kingdom
  • Cambridge, United Kingdom, CB24 3BA
    • Research in Real Life Ltd

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 14 years to 71 years (Adult, Older Adult)
• Accepts Healthy Volunteers: No
• Genders Eligible for Study: All

Description

Inclusion Criteria:

• Able and willing to provide written informed consent and to comply with the study protocol.
• Current diagnosis of asthma (as evidenced by appropriate diagnostic code)
• Received Seretide® 250 Evohaler® 2 puffs twice daily for the last 6 months
• No asthma exacerbation* in last 3 months
• ≤2 exacerbations* in last 12 months
• No errors in device use after training (during baseline visit)

• Women of childbearing potential (not surgically sterile or 2 years postmenopausal) must use a medically accepted method of contraception and must agree to continue use of this method for the duration of the study and for 30 days after discontinuation of study drug. Acceptable methods of contraception include intrauterine device (IUD) known to have a failure rate of less than 1% per year, steroidal contraceptive (oral, implanted, transdermal, or injected), barrier method with spermicide, abstinence, and partner vasectomy.

  • Exacerbation defined as acute course of oral steroids, emergency room attendance and/or hospitalisation for asthma

Exclusion Criteria:

• Other chronic respiratory disease than asthma (e.g. Chronic Obstructive Pulmonary Disease (COPD))
• Uncontrolled asthma (GINA criteria)
• The patient has used a clinical trial investigational drug within the last year before the screening visit
• Hypersensitivity to Flutiform®, its component Formoterol or its excipients
• Pregnant subjects

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Treatment
• Allocation: Randomized
• Interventional Model: Parallel Assignment
• Masking: None (Open Label)

Number of Arms

3

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Active Comparator: Seretide 250; Seretide® Evohaler® 25 microgram /50 microgram per metered dose pressurised inhalation, suspension. 25 micrograms of salmeterol (as salmeterol xinafoate) and 250 micrograms of fluticasone propionate. This is equivalent to a delivered dose (ex actuator) of 21 micrograms of salmeterol and 220 micrograms of fluticasone propionate. 2 puffs twice daily for 12 weeks Phase 1.	Drug: Fluticasone 250/salmeterol 25; Other Names: Seretide 250 Evohaler
Active Comparator: Flutiform 250; flutiform® 250 microgram/10 microgram per actuation pressurised inhalation, suspensions. 250 micrograms of fluticasone propionate and 10 micrograms of formoterol fumarate dihydrate. This is equivalent to a delivered dose (ex-actuator) of approximately 230 microgram of fluticasone propionate/9.0 microgram of formoterol fumarate dihydrate. 2 puffs twice daily for 12 weeks in Phase 1 and 12 weeks in Phase 2.	Drug: Fluticasone 250/formoterol 10; Other Names: Flutiform 250
Active Comparator: Flutiform 125; flutiform 125 microgram/5 microgram per actuation pressurised inhalation, suspensions. 125 micrograms of fluticasone propionate and 5 micrograms of formoterol fumarate dihydrate. This is equivalent to a delivered dose (ex-actuator) of approximately 115 microgram of fluticasone propionate/4.5 microgram of formoterol fumarate dihydrate. 2 puffs twice daily for 12 weeks in Phase 2.	Drug: Fluticasone 125/formoterol 5; Other Names: Flutiform 125

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Asthma Control Questionnaire score (ACQ7)	At week 12 in Phase 1 and Phase 2	12 weeks

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Lung function (FEV1 and FVC)	At week 12 in Phase 1 and Phase 2 and at week 4 interim visit in Phase 2	4 or 12 weeks
Lung inflammation measured as level of Fractional Exhaled Nitric Oxide (FeNO)	Phase 2 only (interim visit at week 4 and final visit at week 12)	4 or 12 weeks
Asthma control defined by Global Initiative of Asthma (GINA) guidelines at week 12 adjusting for baseline	At week 12 in Phase 1 and Phase 2 and at week 4 interim visit in Phase 2	4 or 12 weeks
Visual Analog Scale (VAS) Score at week 12 adjusting for baseline	At week 12 in Phase 1 and Phase 2 and at week 4 interim visit in Phase 2	4 or 12 weeks
Quality of life measured with Mini Asthma Quality of Life questionnaire at week 12 adjusting for baseline	At week 12 in Phase 1 and Phase 2 and at week 4 interim visit in Phase 2	4 or 12 weeks
Proportion of patients with asthma control	Phase 1 and Phase 2; Asthma control defined as No exacerbations, No change in therapy, and GINA asthma control achieved	12 weeks
Number of adverse events	Phase 1 and Phase 2	12 weeks
Blood eosinophil count		Phase 2 baseline
Asthma Control Questionnaire score (ACQ7) at week 4 in Phase 2		4 weeks (Phase 2 interim visit)

Collaborators and Investigators

• Sponsor: Research in Real-Life Ltd
• Collaborators: Napp Pharmaceuticals Limited

Study record dates

Study Major Dates

• Study Start: July 1, 2014
• Primary Completion (Actual): February 1, 2016
• Study Completion (Actual): March 1, 2016

Study Registration Dates

• First Submitted: November 15, 2014
• First Submitted That Met QC Criteria: March 9, 2015
• First Posted (Estimate): March 17, 2015

Study Record Updates

• Last Update Posted (Estimate): June 21, 2016
• Last Update Submitted That Met QC Criteria: June 20, 2016
• Last Verified: June 1, 2016

More Information

Terms related to this study

• Additional Relevant MeSH Terms: Physiological Effects of Drugs; Adrenergic Agents; Neurotransmitter Agents; Molecular Mechanisms of Pharmacological Action; Autonomic Agents; Peripheral Nervous System Agents; Anti-Inflammatory Agents; Adrenergic Agonists; Dermatologic Agents; Bronchodilator Agents; Anti-Asthmatic Agents; Respiratory System Agents; Anti-Allergic Agents; Adrenergic beta-2 Receptor Agonists; Adrenergic beta-Agonists; Fluticasone; Xhance; Salmeterol Xinafoate; Formoterol Fumarate
• Other Study ID Numbers: OR00213; 2013-005365-39 (EudraCT Number)

Plan for Individual participant data (IPD)

• Plan to Share Individual Participant Data (IPD)?: No
• IPD Plan Description: Individual participant data will not be publically released as this was not covered by patient consent. Patients have consented for anonymised data to be used for future medical research by Research in Real-Life.