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ENROLLING BY INVITATIONPhase3

Efficacy and Safety of Subcutaneous Dupilumab in Participants With Asthma/Asthmatic Wheeze Aged 2 to <6 Years (LIBERTY ASTHMA TREKIDS)

Sponsor: Sanofi

NCT ID: NCT06191315

View on ClinicalTrials.gov ↗

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.

WheezingAsthma

How this trial compares with your answers

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What we know so far

Condition· Matched your search
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Still need:

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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

with a positive

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
Inclusion Criteria: * Participant must be 2 to \<6 years of age * Diagnosis of asthma or recurrent severe asthmatic wheeze that is not controlled with chronic ICS for at least 3 months with stable use of at least low dose ICS for ≥1 month prior to Screening Visit 1 with evidence of uncontrolled asthma and/or recurrent severe asthmatic wheeze. * At least one additional major criterion from the modified asthma predictive index: 1. Physician diagnosed Atopic Dermatitis, 2. Allergic sensitization to at least 1 aeroallergen (with a positive serum IgE defined as a value ≥0.35 kU/L). OR 2 minor criteria: 3. Wheezing unrelated to colds, 4. Peripheral blood eosinophilia ≥4%, 5. Allergic sensitization to milk, eggs, or peanuts (defined by serum specific IgE \>0.35 kU/L. * Parent(s)/caregiver(s)/legal guardian(s) willing and able to comply with clinic visits and study-related procedures. * Parent(s)/caregiver(s)/legal guardian(s) able to understand the study requirements. * Participants/parent(s)/caregiver(s)/legal guardian(s), as appropriate, must be able to understand and complete study-related questionnaires * Body weight at screening and randomization \>5 kg and \<30 kg. * Parents or caregivers or legal guardian capable of giving signed informed consent. Exclusion Criteria: 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 screening enrollment. * History of a systemic hypersensitivity reaction or anaphylaxis to biologic therapy, including any excipient. * History of prematurity (\<34 weeks gestation). * Any other chronic lung disease that would impair lung function (eg, cystic fibrosis, bronchopulmonary dysplasia) or chronic lung disease of prematurity or need for oxygen for more than 5 days in the neonatal period. * History of life-threatening asthma (eg, requiring intubation). The above information is not intended to contain all considerations relevant to a patient's potential participation in a clinical trial.

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

Data sourced from ClinicalTrials.gov · Last verified: 2026-08