Evaluating the Efficacy and Safety of Fluticasone Furoate in the Treatment of Asthma in Adults and Adolescents

This study has been completed.
Sponsor:
Information provided by (Responsible Party):
GlaxoSmithKline
ClinicalTrials.gov Identifier:
NCT01431950
First received: August 25, 2011
Last updated: September 25, 2013
Last verified: September 2013

August 25, 2011
September 25, 2013
September 2011
October 2012   (final data collection date for primary outcome measure)
Change from baseline in evening clinic visit (pre-bronchodilator and pre-dose) FEV1 [ Time Frame: up to 24 weeks ] [ Designated as safety issue: No ]
Change from baseline in evening clinic visit FEV1 at the end of the 24 week treatment period
Same as current
Complete list of historical versions of study NCT01431950 on ClinicalTrials.gov Archive Site
  • Change in the percentage of rescue free 24 hour periods [ Time Frame: up to 24 weeks ] [ Designated as safety issue: No ]
    Change from baseline in the percentage of 24 hour periods with no rescue use during the 24 week treatment period
  • Change from baseline in daily trough (pre-dose and pre-rescue bronchodilator) PM PEF [ Time Frame: Averaged over the 24 week treatment period ] [ Designated as safety issue: No ]
  • Change from baseline in daily AM PEF [ Time Frame: Averaged over the 24 week treatment period ] [ Designated as safety issue: No ]
  • Change from baseline in percentage of symptom free 24 hour periods [ Time Frame: up to 24 weeks ] [ Designated as safety issue: No ]
    Change from baseline in the percentage of symptom-free 24 hour periods during the 24 week treatment period
Same as current
Not Provided
Not Provided
 
Evaluating the Efficacy and Safety of Fluticasone Furoate in the Treatment of Asthma in Adults and Adolescents
A Randomised, Double-blind, Multi-centre Study to Evaluate the Efficacy and Safety of Inhaled Fluticasone Furoate in the Treatment of Persistent Asthma in Adults and Adolescents Currently Receiving Mid to High Strength Inhaled Corticosteroids.

A randomised, double-blind, multi-centre study to evaluate the efficacy and safety of two doses of inhaled fluticasone furoate in the treatment of persistent asthma in adults and adolescents currently receiving mid to high strength inhaled corticosteroids.

This will be a multi-centre, randomised, double-blind, parallel-group study. Subjects meeting all the inclusion criteria and none of the exclusion criteria during Visit 1 (screening visit) will enter a four week Run-In period during which they will remain on their baseline ICS medication. In addition, all subjects will be provided with albuterol/salbutamol for relief of asthma symptoms. Subjects failing screening will not be eligible for re-screening. During the Run-In and double-blind treatment periods subjects will maintain an electronic daily diary to record morning and evening Peak Expiratory Flow (PEF), asthma symptom score and rescue albuterol/salbutamol use. Subjects will receive a contact (Phone Contact 1/optional office visit (1b)) during Run-In to reinforce compliance with Run-In medication and diary monitoring. Those subjects who meet the eligibility criteria at the end of the Run-In period will be stratified in an approximately 1:1 ratio according to their baseline FEV1 as a percentage of predicted normal - one stratum for those with FEV1 percent predicted ≥40% to ≤65% and one for those with FEV1 percent predicted >65% to ≤90%. Once stratified, subjects will be randomised to one of the following treatments and enter into a 24 week double-blind treatment period:1) Fluticasone furoate 100mcg once daily in the evening or 2) Fluticasone furoate 200mcg once daily in the evening.

Subjects will then attend 6 on-treatment visits at Visits 3, 4, 5, 6, 7 and 8 (Weeks 2, 4, 8, 12, 18 and 24 respectively). All visits including Visit 1 must be conducted in the evening between 5 PM and 11 PM. Subjects will receive treatment for 24 weeks. Twenty four hour urinary cortisol assessments will be collected at the end of Run-In (Visit 2) and at end of treatment (Visit 8) visits. A follow-up contact will be performed 1-week after completing study medication (Visit 9). Subjects will participate in the study for up to a maximum of 29 weeks (including screening, treatment and follow-up contact). In addition, partially used NDPIs will be collected in a subset of subjects. For subjects who have consented for pharmacogenetics, a blood sample will also be taken for pharmacogenetic analysis.

Interventional
Phase 3
Allocation: Randomized
Endpoint Classification: Safety/Efficacy Study
Intervention Model: Parallel Assignment
Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor)
Primary Purpose: Treatment
Asthma
Drug: GW685698
Inhaled corticosteroid
  • Experimental: FF 100mcg once daily
    Inhaled corticosteroid (ICS)
    Intervention: Drug: GW685698
  • Experimental: FF 200mcg once daily
    Inhaled corticosteroid
    Intervention: Drug: GW685698
Svedsater H, Dale P, Garrill K, Walker R, Woepse MW. Qualitative assessment of attributes and ease of use of the ELLIPTA™ dry powder inhaler for delivery of maintenance therapy for asthma and COPD. BMC Pulm Med. 2013 Dec 7;13:72. doi: 10.1186/1471-2466-13-72.

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
238
October 2012
October 2012   (final data collection date for primary outcome measure)

Inclusion Criteria:

  • Signed informed consent
  • Outpatient at least 12 years of age with diagnosis of asthma at least 12 weeks prior to first visit
  • Both genders; females of child bearing potential must be willing to use appropriate contraception
  • Pre-bronchodilator FEV1 of 40-90% predicted
  • Reversibility FEV1 of at least 12% and 200mLs
  • Current asthma therapy that includes inhaled corticosteroid for at least 4 weeks prior to first visit

Exclusion Criteria:

  • History of life threatening asthma
  • Respiratory infection or candidiasis
  • Asthma exacerbation requiring OCS within last 4 weeks or overnight hospital stay within the last 3 months
  • Concurrent respiratory disease or other disease that would confound study participation of affect subject safety
  • Allergies to study drugs, study drug excipients, medications related to study drugs
  • Taking another investigational medication or medication prohibited for use during the study
  • Previous treatment with FF or FF/VI in a phase II or III study
  • Night shift workers
  • Children in care
Both
12 Years and older
No
Contact information is only displayed when the study is recruiting subjects
United States,   Argentina,   Chile,   France,   Mexico,   Russian Federation
 
NCT01431950
114496
No
GlaxoSmithKline
GlaxoSmithKline
Not Provided
Study Director: GSK Clinical Trials GlaxoSmithKline
GlaxoSmithKline
September 2013

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP