Primary objective: \- Describe the characteristics of enrolled severe asthma patients Secondary objectives: * Assess the control of asthma under dupilumab (Dupixent®) treatment until 1 year * Assess the clinical objectives of the asthma care * Assess comorbidities associated with Type 2 inflammation * Assess safety during the year of treatment
Age range
12 Years – 17 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
Medical history (including history of asthma)
Timeframe: At the start of treatment with Dupixent® (day 1)
Previous treatments for asthma
Timeframe: At the start of treatment with Dupixent® (day 1)
Demographic characteristics
Timeframe: At the start of treatment with Dupixent® (day 1)
Disease characteristics
Timeframe: At the start of treatment with Dupixent® (day 1)
Concomitant medication
Timeframe: At the start of treatment with Dupixent® (day 1)