At a glance
- What the study gets you
- Access to the study treatment being tested
- Type of study
- Interventional (receives a drug or procedure)
- Time in hospital
- In-person visits at study sites — visit count not specified by the sponsor
- Drug or intervention
- Dupilumab (drug), Placebo (drug)
- How long the study runs
- Study runs about 59 months (dates as stated)
- About the drug or intervention
- Dupilumab — drug: Pharmaceutical form: Injection solution Route of administration: Subcutaneous · Placebo — drug: Pharmaceutical form: Injection solution Route of administration: Subcutaneous
- Patient visit burden
- Not specified by the sponsor
- Type of study
- Testing a treatment
- Ages
- 2 Years to 5 Years
- Who
- All
- Number of participants
- 90
- Started
- 2024-01-03
- Last checked
- 2026-08
Plain English Summary
What is this study?
- • Testing a new treatment for wheezing
- • Phase3 - 90 participants
- • This is a parallel, Phase 3, 2-arm study to evaluate the efficacy and long-term safety of dupilumab treatment in children 2 to \<6 years of age with uncontrolled asthma and/or recurrent severe asthmatic wheeze
Who can take part?
- • Ages 2 Years to 5 Years
- • Diagnosed with wheezing
Where?
- • Birmingham - Investigational Site Number : 8260003
- • Leicester - Investigational Site Number : 8260002
- • London - Investigational Site Number : 8260001
- • Bradford - Investigational Site Number : 8260004
This is a simplified summary. Always discuss with your doctor before making any decisions.
About This Trial
This is a parallel, Phase 3, 2-arm study to evaluate the efficacy and long-term safety of dupilumab treatment in children 2 to \<6 years of age with uncontrolled asthma and/or recurrent severe asthmatic wheeze. The study will be conducted in 2 parts. Part A will be a 52-week, randomized, double-blind, placebo-controlled study to assess the safety and efficacy of dupilumab in children aged 2 to \<6 years old with uncontrolled asthma and/or recurrent severe asthmatic wheeze. At the end of Part A, all eligible participants will be offered participation in Part B, an optional open-label extension phase. Study details include: Part A: The study duration of part A will be up to 68 weeks consisting of a 4-week Screening, a 52week treatment period, and a 12-week post-treatment follow-up period. For participants who will chose to participate in Part B, the study duration will be up to 120 weeks (additional 52-week treatment period). Part B: For participants who will choose to participate in Part B, the study duration will be up to 120 weeks (Part A \[4-week Screening and a 52-week treatment period\] plus additional 52-week treatment period and a 12-week post-treatment follow-up period).
More detail
The duration per participant is up to 120 Weeks.
How this trial compares with your answers
Answer 2 more questions to improve match
What we know so far
Still need:
- • Tell us your age for better matching
- • Tell us your sex for better matching
Preliminary match based on your answers. Full eligibility requires on-site assessment including medical history, physical exam, and lab tests. This does not guarantee enrolment.
Eligibility at a Glance
Key info
- Age: 2 Years - 5 Years
- Who can join: All genders
Biomarkers mentioned
What the study is looking for
- ✓Participant must be 2 to \<6 years of age
- ✓At least one additional major criterion from the modified asthma predictive index:
- ✓Physician diagnosed Atopic Dermatitis,
- ✓Allergic sensitization to at least 1 aeroallergen (with a positive serum IgE defined as a value ≥0.35 kU/L).
- ✓OR 2 minor criteria:
Who cannot take part
- ✗Participants are excluded from the study if any of the following criteria apply:
- ✗Severe asthma with the need for chronic oral/systemic corticosteroid use (\>1 month continuous) at the time of...
- ✗History of a systemic hypersensitivity reaction or anaphylaxis to biologic therapy, including any excipient.
- ✗History of prematurity (\<34 weeks gestation).
- ✗History of life-threatening asthma (eg, requiring intubation).
See the full criteria
Where Is This Study? (4 UK sites)
Investigational Site Number : 8260003
Birmingham B4 6NH, United Kingdom
Investigational Site Number : 8260002
Leicester LE1 5WW, United Kingdom
Investigational Site Number : 8260001
London SE5 9RL, United Kingdom
Investigational Site Number : 8260004
Bradford BD9 6RJ, United Kingdom
