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Study details
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A Trial to Evaluate the Efficacy and Safety of Tralokinumab in Combination With Topical Corticosteroids in Children and Infants With Moderate-to-severe Atopic Dermatitis

LEO Pharma
NCT IDNCT06311682ClinicalTrials.gov data as of Apr 2026
Phase

Phase 3

Target enrollment

195

Study length

about 3.9 years

Ages

0.5–11

Locations

15 sites in AL, AR, CA +7

About this study

Researchers are testing whether a treatment with tralokinumab (given by injection) combined with topical corticosteroids is safe and effective for children and infants with moderate-to-severe atopic dermatitis. The trial will last up to 4 years, involving visits every few weeks initially, followed by less frequent visits. It compares tralokinumab + TCS to placebo + TCS for children with moderate-to-severe AD and evaluates tralokinumab + TCS for infants with moderate-to-severe AD.

Based on ClinicalTrials.gov records.

What participants do

  • 1.Take Placebo + TCS
  • 2.Take Tralokinumab + TCS
PhasePhase 3
DrugTralokinumab

Participation effort

Estimated from trial records. Details can vary by site.

Time + visits
Low9%
Logistics
Moderate50%

Logistics difficulty varies by site location and availability.

Trial highlights

Treatment details

Auto-extracted from trial records to preview treatments and outcomes.

Drug classes

tralokinumab

Endpoints

Secondary: Change in Child Worst Itch NRS (weekly average) for subjects aged 6 to <12 years at screening., Number of treatment-emergent adverse events (AEs) per subject aged 2 to <12 years at screening., Number of treatment-emergent adverse events (AEs) per subject aged 6 month to <2 years at screening., Reduction in Child Worst Itch numeric rating score (NRS) (weekly average) ≥4 for subjects aged 6 to <12 years at screening., Reduction of ≥4 in Child Worst Itch NRS (weekly average) for subjects aged 6 to <12 years at screening or Scratch ObsRO (weekly average) for subjects aged 2 to <6 years at screening.

Body systems

Dermatology