Phase 3 Asthma Trial, Recruiting
Who may be able to join
AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI
Who might be able to join this trial:
- People who are between 12 and 17 years old (inclusive) at the time of signing the consent forms.
- People who were diagnosed with asthma at least 1 year before the first study visit.
- People who have been using a daily combination inhaler (containing both a steroid and a long-acting bronchodilator) for at least 12 weeks before the first study visit, with no changes to their asthma medications in the 6 weeks before that visit, and a stable steroid dose within a specific range (confirm with trial site for exact dosing details).
- People who, in the year before the second study visit, had a documented medical contact for sudden worsening asthma symptoms, or had a documented temporary change in their asthma treatment as part of an agreed asthma action plan.
- People whose asthma is not well controlled despite using their combination inhaler, as measured by a standard asthma control questionnaire score of 1.5 or higher at the second study visit.
- People whose lung function test results fall within a specific range and show a meaningful improvement after using a reliever inhaler (confirm with trial site for exact values).
Who may not be able to join:
- People who have had a chest X-ray confirmed case of pneumonia in the 6 weeks before the second study visit.
- People who have had a serious asthma flare-up requiring a change in their regular asthma medication or the use of steroid tablets or injections for 3 or more days in the 6 weeks before the second study visit (though some exceptions may apply at the doctor's discretion — confirm with trial site).
- People who have a history of life-threatening asthma.
- People who currently have an active lung disease or lung abnormality other than asthma, such as active tuberculosis or significant bronchiectasis.
- People who have smoked or used any inhaled recreational products — including cigarettes, e-cigarettes, vaping devices, cigars, or pipe tobacco — at any point in the 12 months before the second study visit.
Important: Always verify eligibility with the trial site directly before applying.
Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.
Contact this trial
Principal Investigator: GSK Clinical Trials, GlaxoSmithKline
Phone: 877-379-3718
Australian sites
877-379-3718
877-379-3718
877-379-3718
Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
Where this trial is recruiting
3 site(s) in Australia. Confirm current status and contact details directly with the trial site.
Primary endpoints
Change from baseline in trough forced expiratory volume in 1 second (FEV1) (Liters) at Week 24
Can't join this trial?
Data last synced from ClinicalTrials.gov: 23 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.