AsthmaPhase 3NCT03248128
Safety and Efficacy Study of Fluticasone Furoate/Vilanterol (FF/VI) Fixed Dose Combination (FDC) Compared to FF Alone in Subjects With Asthma
A Phase 3 study testing FF/VI via ELLIPTA DPI and FF via ELLIPTA DPI in people with Asthma, run by GlaxoSmithKline at 183 sites in 16 countries.
Trial summary
The goal of asthma treatment is to achieve and maintain asthma control and to reduce the future risk of exacerbations. Inhaled corticosteroids (ICS) are considered as the most effective anti- inflammatory treatment for all severities of persistent asthma. Read more about this study
- Who is it for?
- Ages 5 to 17 years
- Conditions the study is for
- Asthma
- What is being tested?
- FF/VI via ELLIPTA DPI and FF via ELLIPTA DPI
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 906 participants
- Where
- 183 sitesin 16 countries
- Study dates
- 20 Oct 2017to 21 Mar 2022
- Phase
- Phase 3
- Are there results?
- Yes, posted in the registrySummary in the doctors' view
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 5 to 17 years
- All sexes
- No healthy volunteers
- Child
Who may be able to join
- For all subjects: Between 5 and 17 years of age inclusive, at the time of signing the informed consent.
- A history of symptoms consistent with a diagnosis of asthma for at least 6 months.
- Pre-bronchodilator FEV1 >50 percent to <=90 percent predicted normal. A minimum of 2 efforts that are considered acceptable (not necessarily repeatable) are required to be eligible.
- Lung function reversibility defined as an increase of >=12 percent in FEV1 within 10 to 40 minutes following 2 to 4 inhalations of salbutamol inhalation aerosol (or 1 nebulized treatment with albuterol/salbutamol solution). Use of a spacer is permitted.
- Uncontrolled asthma, with a childhood asthma control test (cACT)/ACT score <=19.
- Receiving stable asthma therapy (SABA inhaler plus ICS [total daily dose <=FP 250 micrograms (mcg) or equivalent]) for at least 4 weeks prior to Visit 1 (i.e. screening).
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- Able to replace their current SABA treatment with salbutamol aerosol inhaler at Visit 1 for use as needed for the duration of the study. Salbutamol metered dose inhaler (MDI) will be administered with or without a spacer, to be used as determined by the investigator. The use or non-use of the spacer should be consistent for an individual subject throughout the study.
- Male or female subjects will be included. Females of reproductive potential must agree to follow 1 of the options listed (which include abstinence) in the Modified List of Highly Effective Methods for Avoiding Pregnancy in Females of Reproductive Potential (FRP) from 30 days prior to the first dose of study medication and until at least five terminal half-lives or until any continuing pharmacologic effect has ended, whichever is longer after the last dose of study medication and completion of the follow-up call. The investigator is responsible for ensuring that subjects understand how to properly use these methods of contraception.
- Written informed consent from at least 1 parent/care giver (legal guardian) and accompanying informed assent from the subject (where the subject is able to provide assent) prior to admission to the study. If applicable, subject must be able and willing to give assent to take part in the study according to the local requirement. The study investigator is accountable for determining a child's capacity to assent to participation in a research study, taking into consideration any standards set by the responsible independent ethics committee (IEC); subject and their legal guardian(s) understand that the study requires them to be treated on an outpatient basis; subject and their legal guardian(s) understand that they must comply with study medication and study assessments including recording of PEF and rescue SABA use, attending scheduled study visits, and being accessible by a telephone call.
- For subjects eligible for randomization; asthma control: uncontrolled asthma, with a cACT/ACT score <=19.
- A technically acceptable pre-bronchodilator FEV1 >50 percent to <=90 percent predicted normal at Visit 2. A minimum of 2 efforts that are considered acceptable and repeatable following the over read are required to be eligible.
- Symptoms and rescue use: demonstrated and reported in a daily diary symptoms of asthma (a score of >=1 on the day-time or night-time asthma symptom scores) and/or daily albuterol/salbutamol on at least 3 of the last 7 consecutive days of the run-in period (not including the date of randomization).
- Compliance with run-in medication: compliance is defined as use of run-in medication on at least 4 of the last 7 consecutive days of the run-in period (not including the date of randomization) recorded in the electronic subject diary.
- Compliance with completion of the daily diary reporting: defined as completion of all questions on 4 out of the last 7 days during the run-in period (not including the date of randomization).
Who cannot join
- For all subjects: History of life threatening asthma defined as an asthma episode that required intubation and/or was associated with hypercapnea, respiratory arrest or hypoxic seizures.
- Any asthma exacerbation requiring the use of oral steroids within 6 weeks of Visit 1, systemic or depot corticosteroids within 12 weeks of Visit 1, or ER attendance within 3 months of Visit 1 or hospitalization within 6 months of Visit 1.
- A culture documented or suspected bacterial or viral infection of the upper or lower respiratory tract, sinus or middle ear that has not resolved within 4 weeks of Visit 1 and which led to a change in asthma management or, in the opinion of the investigator, is expected to affect the subject's asthma status or the subject's ability to participate in the study.
- Clinical visual evidence of oropharyngeal candidiasis.
- Fasting blood glucose at screening >100 milligrams/deciliter (mg/dL) (5.6 moles per liter [mol/L]).
- Obesity (Body Mass Index [BMI] above the 97th centile based on the centers for disease control and prevention [CDC] charts).
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- Any significant abnormality or medical condition identified at the screening medical assessment (including serious psychological disorder) that in the investigator's opinion, preclude entry into the study due to risk to the subject or that may interfere with the conduct and/or outcome of the study.
- QTc >450 milliseconds (msec) or QTc >480 msec in subjects with bundle branch block or any other clinically significant abnormality in the screening 12-lead ECG.
- Use of any prohibited medications.
- Present use of any tobacco products.
- Drug allergies: any adverse reaction including immediate or delayed hypersensitivity to any beta 2-agonists, sympathomimetic drug or any intranasal, inhaled, or systemic corticosteroid therapy. Known or suspected sensitivity to the constituents of the ELLIPTA Inhaler (i.e. lactose or magnesium stearate).
- Milk Protein Allergy: history of severe milk protein allergy.
- Participated in a clinical trial and has received an investigational product within the following time period prior to the first dosing day in the current study: 30 days, five half-lives or twice the duration of the biological effect of the study treatment (whichever is longer).
- Exposure to more than 4 investigational medicinal products within 12 months prior to the first dosing day.
- An affiliation with the investigator site: the parents/guardians or child is an immediate family member of the participating investigator, sub-investigator, study coordinator, or employee of the participating investigator.
- The parent or guardian has a history of psychiatric disease, intellectual deficiency, substance abuse or other condition (example, inability to read, comprehend or write) which may affect: validity of consent to participate in the study; adequate supervision of the subject during the study; compliance of subject with study medication and study procedures (example, completion of daily diary, attending scheduled clinic visits); subject safety and well-being.
- Children in care: children who are wards of the government or state are not eligible for participation in this study.
- For subjects eligible for randomization; Changes in asthma medication that occur after screening.
- Occurrence of a culture-documented or suspected bacterial or viral infection of the upper or lower respiratory tract, sinus or middle ear during the run-in period that led to a change in asthma management or, in the opinion of the investigator, is expected to affect the subject's asthma status or the subject's ability to participate in the study.
- Evidence of an exacerbation, defined as a: deterioration of asthma requiring the use of oral corticosteroids for at least 3 days, or a depot corticosteroid injection, or an in-patient hospitalization due to asthma that required systemic corticosteroids between screening and randomization.
- Clinical visual evidence of oropharyngeal candidiasis at the randomization Visit.
- Unable to use the ELLIPTA inhaler correctly.
Trial locations and contacts
183 sites in 16 countries.
183 sites in 16 countries
United States49 sites
GSK Investigational Site
Asheville, North Carolina, 28801
GSK Investigational Site
Aventura, Florida, 33180
GSK Investigational Site
Baltimore, Maryland, 21236
GSK Investigational Site
Charlotte, North Carolina, 28277
GSK Investigational Site
Colorado Springs, Colorado, 80907
GSK Investigational Site
Dallas, Texas, 75231-4307
GSK Investigational Site
Denver, Colorado, 80206
GSK Investigational Site
Denver, Colorado, 80230
GSK Investigational Site
Evanston, Illinois, 60201
GSK Investigational Site
Evansville, Indiana, 47715
GSK Investigational Site
Gainesville, Georgia, 30501
GSK Investigational Site
Great Neck, New York, 11021
GSK Investigational Site
Greenville, South Carolina, 29607
GSK Investigational Site
Grove City, Ohio, 43123
GSK Investigational Site
Hoover, Alabama, 35244
GSK Investigational Site
Houston, Texas, 77055
GSK Investigational Site
Huntington Beach, California, 92648
GSK Investigational Site
Lewisville, Texas, 75067
GSK Investigational Site
Little Rock, Arkansas, 72205
GSK Investigational Site
Medford, Oregon, 97504
GSK Investigational Site
Miami, Florida, 33134
GSK Investigational Site
Miami, Florida, 33135
GSK Investigational Site
Miami, Florida, 33142
GSK Investigational Site
Miami, Florida, 33173
GSK Investigational Site
Miami, Florida, 33186
GSK Investigational Site
Miami Lakes, Florida, 33014
GSK Investigational Site
Murray, Utah, 84107
GSK Investigational Site
New Hartford, New York, 13413
GSK Investigational Site
Oak Park, Illinois, 60301
GSK Investigational Site
Ocala, Florida, 34470
GSK Investigational Site
Oklahoma City, Oklahoma, 73120
GSK Investigational Site
Orangeburg, South Carolina, 29118-2040
GSK Investigational Site
Orlando, Florida, 32806
GSK Investigational Site
Orlando, Florida, 32827
GSK Investigational Site
Owensboro, Kentucky, 42301
GSK Investigational Site
Piscataway, New Jersey, 08854
GSK Investigational Site
Raleigh, North Carolina, 27607
GSK Investigational Site
Riverside, California, 92506
GSK Investigational Site
San Antonio, Texas, 78207
GSK Investigational Site
San Antonio, Texas, 78215
GSK Investigational Site
San Antonio, Texas, 78249
GSK Investigational Site
Savannah, Georgia, 31406
GSK Investigational Site
Spartanburg, South Carolina, 29303
GSK Investigational Site
Summerville, South Carolina, 29485
GSK Investigational Site
Verona, New Jersey, 07044
GSK Investigational Site
Waco, Texas, 76712
GSK Investigational Site
Wexford, Pennsylvania, 15090
GSK Investigational Site
White Marsh, Maryland, 21162
GSK Investigational Site
Ypsilanti, Michigan, 48197
Russia29 sites
GSK Investigational Site
Krasnodar, 350012
GSK Investigational Site
Moscow, 1154461
GSK Investigational Site
Moscow, 119333
GSK Investigational Site
Moscow, 119435
GSK Investigational Site
Moscow, 119991
GSK Investigational Site
Moscow, 127473
GSK Investigational Site
Moscow, 129110
GSK Investigational Site
Omsk, 644050
GSK Investigational Site
Penza, 440067
GSK Investigational Site
Perm, 614066
GSK Investigational Site
Saint Petersburg, 191036
GSK Investigational Site
Saint Petersburg, 192148
GSK Investigational Site
Saint Petersburg, 192212
GSK Investigational Site
Saint Petersburg, 193312
GSK Investigational Site
Saint Petersburg, 194100
GSK Investigational Site
Saint Petersburg, 194223
GSK Investigational Site
Saint Petersburg, 194291
GSK Investigational Site
Saint Petersburg, 196191
GSK Investigational Site
Saint Petersburg, 196240
GSK Investigational Site
Saint Petersburg, 196657
GSK Investigational Site
Samara, 443031
GSK Investigational Site
Saransk, 430000
GSK Investigational Site
Saratov, 410012
GSK Investigational Site
St'Petersburg, 191144
GSK Investigational Site
Tomsk, 634 050
GSK Investigational Site
Ufa, 450008
GSK Investigational Site
Volgograd, 400131
GSK Investigational Site
Voronezh, 394036
GSK Investigational Site
Yaroslavl, 150003
Poland17 sites
GSK Investigational Site
Bialystok, 15-430
GSK Investigational Site
Bialystok, 15879
GSK Investigational Site
Bydgoszcz, 85-796
GSK Investigational Site
Częstochowa, 42-200
GSK Investigational Site
Katowice, 40-040
GSK Investigational Site
Krakow, 31-011
GSK Investigational Site
Lodz, 90-153
GSK Investigational Site
Lodz, 90-329
GSK Investigational Site
Ostrów Wielkopolski, 63-400
GSK Investigational Site
Ostrowiec Świętokrzyski, 27-400
GSK Investigational Site
Poznan, 60-693
GSK Investigational Site
Skierniewice, 96-100
GSK Investigational Site
Strzelce Opolskie, 47-100
GSK Investigational Site
Tarnów, 33-100
GSK Investigational Site
Warsaw, ?01-192
GSK Investigational Site
Wroclaw, 50-088
GSK Investigational Site
Zawadzkie, 47-120
Argentina16 sites
GSK Investigational Site
Berazategui, Buenos Aires, 1837
GSK Investigational Site
Buenos Aires, C1121ABE
GSK Investigational Site
Buenos Aires, C1425FVH
GSK Investigational Site
Buenos Aires, C1426ABP
GSK Investigational Site
CABA, Buenos Aires, C1028AAP
GSK Investigational Site
CABA, Buenos Aires, C1425BEN
GSK Investigational Site
Ciudad Autonoma de Buenos Aires, Buenos Aires, C1122AAK
GSK Investigational Site
Florida, Buenos Aires, 1602
GSK Investigational Site
La Plata, Buenos Aires, 1900
GSK Investigational Site
Lanus, Buenos Aires, B1824KAJ
GSK Investigational Site
Lobos, Buenos Aires, 7240
GSK Investigational Site
Mar del Plata, Buenos Aires, 7600
GSK Investigational Site
Mendoza, M5500CCG
GSK Investigational Site
Nueve de Julio, Buenos Aires, B6500BWQ
GSK Investigational Site
Rosario, S2000BRH
GSK Investigational Site
Santa Fe, 3000
Japan16 sites
GSK Investigational Site
Chiba, 260-0001
GSK Investigational Site
Fukui, 918-8205
GSK Investigational Site
Fukuoka, 811-1394
GSK Investigational Site
Fukuoka, 813-0017
GSK Investigational Site
Hiroshima, 721-8511
GSK Investigational Site
Hokkaido, 040-8585
GSK Investigational Site
Hokkaido, 040-8611
GSK Investigational Site
Hyōgo, 653-0836
GSK Investigational Site
Kanagawa, 223-0059
GSK Investigational Site
Osaka, 583-8588
GSK Investigational Site
Tokyo, 104-0031
GSK Investigational Site
Tokyo, 154-0017
GSK Investigational Site
Tokyo, 157-0066
GSK Investigational Site
Tokyo, 158-0097
GSK Investigational Site
Tokyo, 171-0014
GSK Investigational Site
Tokyo, 176-0012
South Africa15 sites
GSK Investigational Site
Bellville, 7530
GSK Investigational Site
Bloemfontein, 9301
GSK Investigational Site
Boksburg, Gauteng, 1459
GSK Investigational Site
Cape Town, 7700
GSK Investigational Site
Durban, 4001
GSK Investigational Site
eMkhomazi, 4170
GSK Investigational Site
Johannesburg, Gauteng, 1818
GSK Investigational Site
Middelburg, Mpumalanga, 1055
GSK Investigational Site
Panorama, Western Province, 7500
GSK Investigational Site
Pretoria, Gauteng, 0083
GSK Investigational Site
Pretoria, Gauteng, 0184
GSK Investigational Site
Pretoria, 0181
GSK Investigational Site
Somerset West, 7130
GSK Investigational Site
Soweto, 1818
GSK Investigational Site
Vosloorus Ext 2, 1475
Italy8 sites
GSK Investigational Site
Ancona, The Marches, 60123
GSK Investigational Site
Bergamo, Lombardy, 24127
GSK Investigational Site
Milan, Lombardy, 20122
GSK Investigational Site
Milan, Lombardy, 20154
GSK Investigational Site
Palermo, Sicily, 9000
GSK Investigational Site
Parma, Emilia-Romagna, 43126
GSK Investigational Site
Perugia, Umbria, 06156
GSK Investigational Site
Rome, Lazio, 00165
Mexico6 sites
GSK Investigational Site
Guadalajara, Jalisco, 44100
GSK Investigational Site
Guadalajara, Jalisco, 44670
GSK Investigational Site
Monterrey, Nuevo León, 64000
GSK Investigational Site
Monterrey, Nuevo León, 64710
GSK Investigational Site
Villahermosa, Tabasco, 86035
GSK Investigational Site
Zapopan, Jalisco, 45070
Romania6 sites
GSK Investigational Site
Brasov, 500091
GSK Investigational Site
Brasov, 500283
GSK Investigational Site
Bucharest, 020395
GSK Investigational Site
Bucharest, 030961
GSK Investigational Site
Bucharest, 051543
GSK Investigational Site
Târgu Mureş, 540136
Bulgaria4 sites
GSK Investigational Site
Rousse, 7002
GSK Investigational Site
Sofia, 1510
GSK Investigational Site
Sofia, 1784
GSK Investigational Site
Stara Zagora, 5400
Germany4 sites
GSK Investigational Site
Geesthacht, Schleswig-Holstein, 21502
GSK Investigational Site
Heidelberg, Baden-Wurttemberg, 69126
GSK Investigational Site
Mannheim, Baden-Wurttemberg, 68161
GSK Investigational Site
Rosenheim, Bavaria, 83026
Spain4 sites
GSK Investigational Site
Badalona, 08916
GSK Investigational Site
Barcelona, 08003
GSK Investigational Site
Barcelona, 08035
GSK Investigational Site
Madrid, 28041
Canada3 sites
GSK Investigational Site
Brampton, Ontario, L6T 0G1
GSK Investigational Site
Québec, G1V 4W2
GSK Investigational Site
Windsor, Ontario, N8X2G1
Hungary3 sites
GSK Investigational Site
Budapest, 1083
GSK Investigational Site
Budapest, 1089
GSK Investigational Site
Szeged, H-6720
China2 sites
GSK Investigational Site
Panzhihua, Sichuan, 617023
GSK Investigational Site
Taiyuan, 030013
About this study
Official title: A Randomised, Double-blind, Parallel Group, Multicentre, Stratified, Study Evaluating the Efficacy and Safety of Once Daily Fluticasone Furoate/Vilanterol Inhalation Powder Compared to Once Daily Fluticasone Furoate Inhalation Powder in the Treatment of Asthma in Participants Aged 5 to 17 Years Old (Inclusive) Currently Uncontrolled on Inhaled Corticosteroids
The goal of asthma treatment is to achieve and maintain asthma control and to reduce the future risk of exacerbations. Inhaled corticosteroids (ICS) are considered as the most effective anti- inflammatory treatment for all severities of persistent asthma. For children >=5 years of age and adolescents whose asthma is uncontrolled, low-dose ICS plus adjunctive therapy with long-acting beta agonist (LABA) is considered as effective. Thus, this study is designed to evaluate the efficacy and safety of FF (ICS component)/VI (LABA component) compared to FF alone for the treatment of asthma, in subjects aged 5 to 17 years old currently uncontrolled on ICS. The study will be conducted over a total duration of approximately 29 weeks: 4 week run-in period, 24-week double-blind treatment period and 1-week follow-up period. Subjects will be randomized to receive FDC of FF/VI or FF administered via ELLIPTA® dry powder inhaler (DPI). The dose of both FF/VI and FF alone will be selected based on the age of subjects. Subjects will receive a short acting beta 2 agonist (SABA) (albuterol /salbutamol) as a rescue medication throughout the study. A total of 870 subjects will be randomized in the study. Of this, 652 subjects will be aged 5 to 11 years (cohort A), and 218 will be aged 12 to 17 years inclusive (cohort B). ELLIPTA is a registered trademark of GlaxoSmithKline (GSK) group of companies.
- Conditions
- Asthma
- Being tested
- FF/VI via ELLIPTA DPI, FF via ELLIPTA DPI
- Keywords
- Fluticasone furoate, Efficacy, Vilanterol, Asthma, Safety, GW642444, GW685698
- Medical subject headings
- Asthma
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
FF/VI via ELLIPTA DPIDrug
ELLIPTA DPI inhaler will contain two individual blister strips; the first strip will contain FF(50 or 100 mcg) and second strip will contain VI (25 mcg).
FF via ELLIPTA DPIDrug
ELLIPTA DPI inhaler will contain a single blister strip of FF (50 or 100 mcg).
| Study group | Role | What they receive |
|---|---|---|
| Subjects receiving FF/VI in cohort A | Experimental | Subjects will be randomized in 1:1 ratio to receive a FDC of FF/VI with a dose of 50/25 mcg administered once daily in the morning via ELLIPTA DPI. Receives: Drug: FF/VI via ELLIPTA DPI |
| Subjects receiving FF in cohort A | Active comparator | Subjects will be randomized in 1:1 ratio to receive FF with a dose of 50 mcg administered once daily in the morning via ELLIPTA DPI. Receives: Drug: FF via ELLIPTA DPI |
| Subjects receiving FF/VI in cohort B | Experimental | Subjects will be randomized in 1:1 ratio to receive a FDC of FF/VI with a dose of 100/25 mcg administered once daily in the morning via ELLIPTA DPI. Receives: Drug: FF/VI via ELLIPTA DPI |
| Subjects receiving FF in cohort B | Active comparator | Subjects will be randomized in 1:1 ratio to receive FF with a dose of 100 mcg administered once daily in the morning via ELLIPTA DPI. Receives: Drug: FF via ELLIPTA DPI |
What is being measured
The primary outcome is the main question the study is designed to answer.
Absolute Weighted Mean of Forced Expiratory Volume in 1 Second (FEV1) (0-4 Hours) at Week 12 in 5-17 Year Old Population
Pulmonary function was measured by FEV1, defined as the maximal amount of air that can be forcefully exhaled in one second using a standardized calibrated spirometer. Weighted mean FEV1 was derived using the post-dose assessments (after 30 minutes and 1, 2, 3, 4 hours) with their actual times and using the pre-dose assessment as the 0 hour measurement.
Measured: Week 12
Change From Baseline in Mean Pre-dose Morning Peak Expiratory Flow (AM PEF) in 5-11 Year Old Population
PEF was defined as the maximum speed of expiration of a participant. PEF was measured using a hand-held electronic peak flow meter each morning prior to the dose of study medication and any rescue albuterol/salbutamol inhalation aerosol use. The best of three measurements were recorded in the electronic patient diary. The mean morning PEF was calculated for each participant as an averaged mean over weeks 1-12 of the treatment period. Baseline was defined as the average of measurements with a non-missing value from Day -6 to Day 1 of pre-dose.
Measured: Baseline and Week 1-12
Secondary outcomes (18)
Change From Baseline in Mean Pre-dose AM PEF Period in 5-17 Year Old Population
PEF was defined as the maximum speed of expiration of a participant. PEF was measured using a hand-held electronic peak flow meter each morning prior to the dose of study medication and any rescue albuterol/salbutamol inhalation aerosol use. The best of three measurements were recorded in the daily diary. The mean morning PEF was calculated for each participant as an averaged mean over weeks 1-12 of the treatment period. Baseline was defined as the average of measurements with a non-missing value from Day -6 to Day 1 of pre-dose.
Measured: Baseline and Week 1-12
Absolute Weighted Mean of FEV1 (0-4 Hours) at Week 12 in 5-11 Year Old Population
Pulmonary function was measured by FEV1, defined as the maximal amount of air that can be forcefully exhaled in one second using a standardized calibrated spirometer. Weighted mean FEV1 was derived using the post-dose assessments (after 30 minutes and 1, 2, 3, 4 hours) with their actual times and using the pre-dose assessment as the 0 hour measurement.
Measured: Week 12
Change From Baseline in the Percentage of Rescue-free 24-hour Periods Over Weeks 1-12 of the Treatment Period in 5-17 Year Old Population
The number of inhalations of rescue albuterol/salbutamol aerosol used during the day and night were recorded in a daily electronic diary. Percentages of rescue-free 24-hour periods was calculated based on the number of 24-hour periods on which a participant recorded no use of albuterol/salbutamol divided by the length of the time period being assessed (with non-missing values of rescue medication recorded, respectively). A 24-hour period in which the response of participants to both the morning and evening assessments indicated no use of rescue medication was considered as rescue free. Baseline was calculated from the evening (Day -7 to Day -1) and morning (Day -6 to Day 1) measurements. Change from Baseline was calculated as the averaged value during the 12-week treatment period minus the Baseline value.
Measured: Baseline and Week 1-12
Change From Baseline in the Percentage of Symptom-free 24-hour Periods Over Weeks 1-12 of the Treatment Period in 5-17 Year Old Population
The symptom-free days were recorded in a daily electronic diary every day in the morning and evening before taking any rescue or study medication and before the PEF measurement. Percentages of symptom-free 24-hour periods was calculated based on the number of 24-hour periods on which a participant recorded no symptoms divided by the length of the time period being assessed (with non-missing values of rescue medication recorded, respectively). A 24-hour period in which the response of participants to both the morning and evening assessments indicated no symptoms was considered as symptom free. Baseline was calculated from evening (Day -7 to Day -1) and morning (Day -6 to Day 1) measurements. Change from Baseline was calculated as the averaged value during the 12-week treatment period minus the Baseline value.
Measured: Baseline and Week 1-12
Change From Baseline in Morning (AM) FEV1 at Week 12 in 5-17 Year Old Population
Pulmonary function was measured by FEV1, defined as the maximal amount of air that can be forcefully exhaled in one second. Morning FEV1 was measured using the pre-dose serial spirometry assessment at the Week 12. Baseline was defined as the pre-dose assessment with a non missing value on Visit 2 (Day -5).
Measured: Baseline and Week 12
Change From Baseline in Asthma Control Questionnaire (ACQ-5) Score at Week 24 in 5-17 Year Old Population
Asthma control as measured by improvements in ACQ-5, a five-item questionnaire with response options for each question rated from 0 to 6 scale. A score of 0 indicates well controlled asthma and a score of 6 indicates extremely poorly controlled asthma. Individual questions (concerning nocturnal awakening, waking in the morning, activity limitation, shortness of breath and wheeze) are equally weighted and the ACQ-5 score is calculated as the mean of these 5 item responses. A lower mean score indicates greater asthma control and higher mean score indicates lesser asthma control. Baseline was defined as the pre-dose assessment with a non-missing value on Visit 3 (Day 1).
Measured: Baseline and Week 24
Change From Baseline in the Percentage of Rescue-free 24-hour Periods Over Weeks 1-12 of the Treatment Period in 5-11 Year Old Population
The number of inhalations of rescue albuterol/salbutamol aerosol used during the day and night were recorded in a daily electronic diary. Percentages of rescue-free 24-hour periods was calculated based on the number of 24-hour periods on which a participant recorded no use of albuterol/salbutamol divided by the length of the time period being assessed (with non-missing values of rescue medication recorded, respectively). A 24-hour period in which the response of participants to both the morning and evening assessments indicated no use of rescue medication was considered as rescue free. Baseline was calculated from the evening (Day -7 to Day -1) and morning (Day -6 to Day 1) measurements. Change from Baseline was calculated as the averaged value during the 12-week treatment period minus the Baseline value.
Measured: Baseline and Week 1-12
Change From Baseline in the Percentage of Symptom-free 24-hour Periods Over Weeks 1-12 of the Treatment Period in 5-11 Year Old Population
The symptom-free days were recorded in a daily electronic diary every day in the morning and evening before taking any rescue or study medication and before the PEF measurement. Percentages of symptom-free 24-hour periods was calculated based on the number of 24-hour periods on which a participant recorded no symptoms divided by the length of the time period being assessed (with non-missing values of rescue medication recorded, respectively). A 24-hour period in which the response of participants to both the morning and evening assessments indicated no symptoms was considered as symptom free. Baseline was calculated from evening (Day -7 to Day -1) and morning (Day -6 to Day 1) measurements. Change from Baseline was calculated as the averaged value during the 12-week treatment period minus the Baseline value.
Measured: Baseline and Week 1-12
Change From Baseline in Morning (AM) FEV1 at Week 12 in 5-11 Year Old Population
Pulmonary function was measured by FEV1, defined as the maximal amount of air that can be forcefully exhaled in one second. Morning FEV1 was measured using the pre-dose serial spirometry assessment at the Week 12. Baseline was defined as the pre-dose assessment with a non-missing value on Visit 2 (Day -5).
Measured: Baseline and Week 12
Change From Baseline ACQ-5 Score at Week 24 in 5-11 Year Old Population
Asthma control as measured by improvements in ACQ-5, a five-item questionnaire with response options for each question rated from 0 to 6 scale. A score of 0 indicates well controlled asthma and a score of 6 indicates extremely poorly controlled asthma. Individual questions (concerning nocturnal awakening, waking in the morning, activity limitation, shortness of breath and wheeze) are equally weighted and the ACQ-5 score is calculated as the mean of these 5 item responses. A lower mean score indicates greater asthma control and higher mean score indicates lesser asthma control. Baseline was defined as the pre-dose assessment with a non-missing value on Visit 3 (Day 1).
Measured: Baseline and Week 24
Number of Participants With Adverse Events (AEs) and Serious Adverse Events (SAEs) in 5-17 Year Old Population
An AE is any untoward medical occurrence in a participant, temporally associated with the use of a medicinal product, whether or not considered related to the medicinal product. An AE can therefore be any unfavorable and unintended sign (including an abnormal laboratory finding), symptom, or disease (new or exacerbated) temporally associated with the use of a medicinal product. SAE is defined as any untoward medical occurrence that, at any dose: results in death; is life-threatening; requires inpatient hospitalization or prolongation of existing hospitalization; results in persistent disability/incapacity; is a congenital anomaly/birth defect and important medical events may jeopardize the participant or may require medical or surgical intervention/SOC to prevent one of the other outcomes mentioned before.
Measured: Up to week 25
Number of Participants With Abnormal Electrocardiogram (ECG) Findings in 5-17 Year Old Population
A single 12-lead ECG was obtained using an ECG machine that automatically calculates the heartrate and measures PR, QRS, QT, and QT interval corrected (QTc).
Measured: Week 24
Change From Baseline in Fasting Glucose in 5-17 Year Old Population
Blood samples were collected for evaluation of fasting blood glucose pre and post-treatment. Baseline was defined as Visit 1 (Screening).
Measured: Baseline and Week 24
Number of Participants With Any Incidence of Asthma Exacerbation Over the 24-week Treatment Period in 5-17 Year Old Population
Asthma exacerbation was defined as deterioration of asthma requiring the use of systemic corticosteroids (tablets, suspension or injection) for at least three days or a single depot corticosteroid injection or an in-patient hospitalization or emergency department visit due to asthma that required systemic corticosteroids.
Measured: Up to week 24
Number of Participants With AEs and SAEs in 5-11 Year Old Population
An AE is any untoward medical occurrence in a participant, temporally associated with the use of a medicinal product, whether or not considered related to the medicinal product. An AE can therefore be any unfavorable and unintended sign (including an abnormal laboratory finding), symptom, or disease (new or exacerbated) temporally associated with the use of a medicinal product. SAE is defined as any untoward medical occurrence that, at any dose: results in death; is life-threatening; requires inpatient hospitalization or prolongation of existing hospitalization; results in persistent disability/incapacity; is a congenital anomaly/birth defect and important medical events may jeopardize the participant or may require medical or surgical intervention/Standard of care (SOC) to prevent one of the other outcomes mentioned before.
Measured: Up to week 25
Number of Participants With Abnormal ECG Findings in 5-11 Year Old Population
A single 12-lead ECG was obtained using an ECG machine that automatically calculates the heartrate and measures PR, QRS, QT, and QTc.
Measured: Week 24
Change From Baseline in Fasting Glucose in 5-11 Year Old Population
Blood samples were collected for evaluation of fasting blood glucose pre and post-treatment. Baseline was defined as Visit 1 (Screening).
Measured: Baseline and Week 24
Number of Participants With Any Incidence of Asthma Exacerbation Over the 24-week Treatment Period in 5-11 Year Old Population
Asthma exacerbation was defined as deterioration of asthma requiring the use of systemic corticosteroids (tablets, suspension or injection) for at least three days or a single depot corticosteroid injection or an in-patient hospitalization or emergency department visit due to asthma that required systemic corticosteroids.
Measured: Up to week 24
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted14 Aug 2017
- Study start20 Oct 2017
- Primary completion21 Mar 2022
- Study completion21 Mar 2022
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Posted resultsParticipant flow, outcome measures and adverse events reported by the sponsor.
- Publications (1)Papers the sponsor has linked to this study.
- Other trials for AsthmaStudies of the same condition, open and under way.
- More trials run by GlaxoSmithKlineThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase 3
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Model description
- Subjects will be randomized to receive FDC of FF/VI inhalation powder compared to FF inhalation powder, once daily in cohort A and cohort B.
- Masking
- Double blind
- Who is masked
- Participant, Investigator
- Enrolment
- 906 participants (actual)
Sponsor and investigators
- Lead sponsor
- GlaxoSmithKline
- Sponsor type
- Industry (pharma, biotech, devices)
- Responsible party
- Sponsor
- Investigators
- GSK Clinical Trials, Study director, GlaxoSmithKline
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT03248128
- Sponsor's protocol ID
- 107116
- Other IDs
- 2016-004086-87, 2016
- Status last verified
- Jun 2025
- First submitted
- 9 Aug 2017
- Last updated
- 22 Jun 2025
- Results posted
- Yes, on ClinicalTrials.gov
- Data monitoring committee
- No
- FDA-regulated drug
- Yes
- FDA-regulated device
- No
- Individual data sharing
- Yes: GSK will assess requests from qualified researchers for anonymized individual patient-level data (IPD) and related study documents. Data sharing is subject to certain criteria, conditions, and exceptions. For further information, refer to https://www.gsk-studyregister.com/About\_GSK\_Patient\_Level\_Data\_Sharing\_Final\_13July2023.pdf
Publications
Bareille P, Forth R, Imber V, Bondarenko I, Michaud A, Majorek-Olechowska B. Once-daily fluticasone furoate/vilanterol vs once-daily fluticasone furoate in patients with asthma aged 5 to 17 years. Ann Allergy Asthma Immunol. 2024 Nov;133(5):537-544.e4. doi: 10.1016/j.anai.2024.06.024. Epub 2024 Jun 25.
PubMed 38936466
Study at a glance
From the registry record, last updated by the sponsor on 22 Jun 2025. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- A Randomised, Double-blind, Parallel Group, Multicentre, Stratified, Study Evaluating the Efficacy and Safety of Once Daily Fluticasone Furoate/Vilanterol Inhalation Powder Compared to Once Daily Fluticasone Furoate Inhalation Powder in the Treatment of Asthma in Participants Aged 5 to 17 Years Old (Inclusive) Currently Uncontrolled on Inhaled Corticosteroids
- ClinicalTrials.gov ID
- NCT03248128
- Acronym / sponsor ID
- 107116
- Conditions
- Asthma
- Keywords
- Fluticasone furoate, Efficacy, Vilanterol, Asthma, Safety, GW642444, GW685698
- Phase
- Phase 3
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 906 participants (actual)
- Lead sponsor
- GlaxoSmithKlineIndustry (pharma, biotech, devices)
- Study start
- 20 Oct 2017 (actual)
- Primary completion
- 21 Mar 2022 (actual)
- Study completion
- 21 Mar 2022 (actual)
- First posted
- 14 Aug 2017 (actual)
- Results
- Posted 12 Oct 2022
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
The goal of asthma treatment is to achieve and maintain asthma control and to reduce the future risk of exacerbations. Inhaled corticosteroids (ICS) are considered as the most effective anti- inflammatory treatment for all severities of persistent asthma. For children >=5 years of age and adolescents whose asthma is uncontrolled, low-dose ICS plus adjunctive therapy with long-acting beta agonist (LABA) is considered as effective. Thus, this study is designed to evaluate the efficacy and safety of FF (ICS component)/VI (LABA component) compared to FF alone for the treatment of asthma, in subjects aged 5 to 17 years old currently uncontrolled on ICS. The study will be conducted over a total duration of approximately 29 weeks: 4 week run-in period, 24-week double-blind treatment period and 1-week follow-up period. Subjects will be randomized to receive FDC of FF/VI or FF administered via ELLIPTA® dry powder inhaler (DPI). The dose of both FF/VI and FF alone will be selected based on the age of subjects. Subjects will receive a short acting beta 2 agonist (SABA) (albuterol /salbutamol) as a rescue medication throughout the study. A total of 870 subjects will be randomized in the study. Of this, 652 subjects will be aged 5 to 11 years (cohort A), and 218 will be aged 12 to 17 years inclusive (cohort B). ELLIPTA is a registered trademark of GlaxoSmithKline (GSK) group of companies.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Double blind (participant, investigator)
- Number of arms
- 4
- Model description
- Subjects will be randomized to receive FDC of FF/VI inhalation powder compared to FF inhalation powder, once daily in cohort A and cohort B.
| Arm | Type | Receives |
|---|---|---|
| Subjects receiving FF/VI in cohort A | Experimental | Drug: FF/VI via ELLIPTA DPISubjects will be randomized in 1:1 ratio to receive a FDC of FF/VI with a dose of 50/25 mcg administered once daily in the morning via ELLIPTA DPI. |
| Subjects receiving FF in cohort A | Active comparator | Drug: FF via ELLIPTA DPISubjects will be randomized in 1:1 ratio to receive FF with a dose of 50 mcg administered once daily in the morning via ELLIPTA DPI. |
| Subjects receiving FF/VI in cohort B | Experimental | Drug: FF/VI via ELLIPTA DPISubjects will be randomized in 1:1 ratio to receive a FDC of FF/VI with a dose of 100/25 mcg administered once daily in the morning via ELLIPTA DPI. |
| Subjects receiving FF in cohort B | Active comparator | Drug: FF via ELLIPTA DPISubjects will be randomized in 1:1 ratio to receive FF with a dose of 100 mcg administered once daily in the morning via ELLIPTA DPI. |
Who may qualify
- Ages
- 5 to 17 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Child
Key inclusion criteria (14 listed)
- For all subjects: Between 5 and 17 years of age inclusive, at the time of signing the informed consent.
- A history of symptoms consistent with a diagnosis of asthma for at least 6 months.
- Pre-bronchodilator FEV1 >50 percent to <=90 percent predicted normal. A minimum of 2 efforts that are considered acceptable (not necessarily repeatable) are required to be eligible.
- Lung function reversibility defined as an increase of >=12 percent in FEV1 within 10 to 40 minutes following 2 to 4 inhalations of salbutamol inhalation aerosol (or 1 nebulized treatment with albuterol/salbutamol solution). Use of a spacer is permitted.
- Uncontrolled asthma, with a childhood asthma control test (cACT)/ACT score <=19.
Key exclusion criteria (22 listed)
- For all subjects: History of life threatening asthma defined as an asthma episode that required intubation and/or was associated with hypercapnea, respiratory arrest or hypoxic seizures.
- Any asthma exacerbation requiring the use of oral steroids within 6 weeks of Visit 1, systemic or depot corticosteroids within 12 weeks of Visit 1, or ER attendance within 3 months of Visit 1 or hospitalization within 6 months of Visit 1.
- A culture documented or suspected bacterial or viral infection of the upper or lower respiratory tract, sinus or middle ear that has not resolved within 4 weeks of Visit 1 and which led to a change in asthma management or, in the opinion of the investigator, is expected to affect the subject's asthma status or the subject's ability to participate in the study.
- Clinical visual evidence of oropharyngeal candidiasis.
- Fasting blood glucose at screening >100 milligrams/deciliter (mg/dL) (5.6 moles per liter [mol/L]).
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| FF/VI via ELLIPTA DPIELLIPTA DPI inhaler will contain two individual blister strips; the first strip will contain FF(50 or 100 mcg) and second strip will contain VI (25 mcg). | Drug | Subjects receiving FF/VI in cohort A, Subjects receiving FF/VI in cohort B |
| FF via ELLIPTA DPIELLIPTA DPI inhaler will contain a single blister strip of FF (50 or 100 mcg). | Drug | Subjects receiving FF in cohort A, Subjects receiving FF in cohort B |
Primary outcome
Absolute Weighted Mean of Forced Expiratory Volume in 1 Second (FEV1) (0-4 Hours) at Week 12 in 5-17 Year Old Population
Time frame: Week 12
Pulmonary function was measured by FEV1, defined as the maximal amount of air that can be forcefully exhaled in one second using a standardized calibrated spirometer. Weighted mean FEV1 was derived using the post-dose assessments (after 30 minutes and 1, 2, 3, 4 hours) with their actual times and using the pre-dose assessment as the 0 hour measurement.
Change From Baseline in Mean Pre-dose Morning Peak Expiratory Flow (AM PEF) in 5-11 Year Old Population
Time frame: Baseline and Week 1-12
PEF was defined as the maximum speed of expiration of a participant. PEF was measured using a hand-held electronic peak flow meter each morning prior to the dose of study medication and any rescue albuterol/salbutamol inhalation aerosol use. The best of three measurements were recorded in the electronic patient diary. The mean morning PEF was calculated for each participant as an averaged mean over weeks 1-12 of the treatment period. Baseline was defined as the average of measurements with a non-missing value from Day -6 to Day 1 of pre-dose.
18 secondary outcomes
Change From Baseline in Mean Pre-dose AM PEF Period in 5-17 Year Old Population
Time frame: Baseline and Week 1-12
Absolute Weighted Mean of FEV1 (0-4 Hours) at Week 12 in 5-11 Year Old Population
Time frame: Week 12
Change From Baseline in the Percentage of Rescue-free 24-hour Periods Over Weeks 1-12 of the Treatment Period in 5-17 Year Old Population
Time frame: Baseline and Week 1-12
Change From Baseline in the Percentage of Symptom-free 24-hour Periods Over Weeks 1-12 of the Treatment Period in 5-17 Year Old Population
Time frame: Baseline and Week 1-12
Change From Baseline in Morning (AM) FEV1 at Week 12 in 5-17 Year Old Population
Time frame: Baseline and Week 12
Change From Baseline in Asthma Control Questionnaire (ACQ-5) Score at Week 24 in 5-17 Year Old Population
Time frame: Baseline and Week 24
Change From Baseline in the Percentage of Rescue-free 24-hour Periods Over Weeks 1-12 of the Treatment Period in 5-11 Year Old Population
Time frame: Baseline and Week 1-12
Change From Baseline in the Percentage of Symptom-free 24-hour Periods Over Weeks 1-12 of the Treatment Period in 5-11 Year Old Population
Time frame: Baseline and Week 1-12
Change From Baseline in Morning (AM) FEV1 at Week 12 in 5-11 Year Old Population
Time frame: Baseline and Week 12
Change From Baseline ACQ-5 Score at Week 24 in 5-11 Year Old Population
Time frame: Baseline and Week 24
Number of Participants With Adverse Events (AEs) and Serious Adverse Events (SAEs) in 5-17 Year Old Population
Time frame: Up to week 25
Number of Participants With Abnormal Electrocardiogram (ECG) Findings in 5-17 Year Old Population
Time frame: Week 24
Change From Baseline in Fasting Glucose in 5-17 Year Old Population
Time frame: Baseline and Week 24
Number of Participants With Any Incidence of Asthma Exacerbation Over the 24-week Treatment Period in 5-17 Year Old Population
Time frame: Up to week 24
Number of Participants With AEs and SAEs in 5-11 Year Old Population
Time frame: Up to week 25
Number of Participants With Abnormal ECG Findings in 5-11 Year Old Population
Time frame: Week 24
Change From Baseline in Fasting Glucose in 5-11 Year Old Population
Time frame: Baseline and Week 24
Number of Participants With Any Incidence of Asthma Exacerbation Over the 24-week Treatment Period in 5-11 Year Old Population
Time frame: Up to week 24
Results and safety
Loading the posted results from ClinicalTrials.gov…
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 22 Jun 2025.
- Posted resultsParticipant flow, baseline, all outcome measures and adverse events.
- Background: PubMed 38936466Bareille P, Forth R, Imber V, Bondarenko I, Michaud A, Majorek-Olechowska B. Once-daily fluticasone furoate/vilanterol vs once-daily fluticasone furoate in patients with asthma aged 5 to 17 years. Ann Allergy Asthma Immunol. 2024 Nov;133(5):537-544.e4. doi: 10.1016/j.anai.2024.06.024. Epub 2024 Jun 25.
- Individual participant dataSharing planned: Yes. GSK will assess requests from qualified researchers for anonymized individual patient-level data (IPD) and related study documents. Data sharing is subject to certain criteria, conditions, and exceptions. For further information, refer to https://www.gsk-studyregister.com/About_GSK_Patient_Level_Data_Sharing_Final_13July2023.pdf
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
GSK Clinical Trials study director
GlaxoSmithKline
183 sites in 16 countries: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A Phase 3 study testing FF/VI via ELLIPTA DPI and FF via ELLIPTA DPI in people with Asthma, run by GlaxoSmithKline at 183 sites in 16 countries.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 14 inclusion and 22 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 22 Jun 2025. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 183 sites in United States, Russia, Poland, Argentina, Japan and 11 more countries. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
What does this phase mean?
Phase 3 studies compare the treatment with the current standard treatment or a placebo in a large group, to confirm how well it works and watch for side effects.
Not every study follows the same path, and some studies (observational studies, device studies) have no phase.
Are results available for this study?
Yes. Results are posted in the registry (first posted 12 Oct 2022). A summary is in the For doctors view, and the full results are on ClinicalTrials.gov.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Absolute Weighted Mean of Forced Expiratory Volume in 1 Second (FEV1) (0-4 Hours) at Week 12 in 5-17 Year Old Population (time frame: Week 12). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT03248128, which also lists 1 linked publication.
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 22 Jun 2025.