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Dupilumab Efficacy in Children with Atopic Dermatitis with Different Phenotypes and Endotypes: A Case Series
Ana B Rossi1, Adriana M Mello2, Joseph Zahn3
1Sanofi, 450 Water Street, Cambridge, MA, 02141, USA. ana.rossi@sanofi.com.
Insights
Dupilumab significantly improved moderate-to-severe atopic dermatitis (AD) in young children. The treatment reduced skin symptoms, itch, and improved quality of life, with biomarker reductions observed.
Area of Science:
- Dermatology
- Pediatric Medicine
- Immunology
Background:
- Atopic dermatitis (AD) is a common skin condition affecting infants and children globally.
- Dupilumab has demonstrated efficacy in improving AD signs, symptoms, and quality of life in pediatric patients with moderate-to-severe disease.
Purpose of the Study:
- To present photographic cases of dupilumab treatment in pediatric patients with atopic dermatitis.
- To illustrate treatment outcomes across diverse phenotypes and endotypes in young children with moderate-to-severe AD.
Main Methods:
- A phase 3, randomized, double-blind, placebo-controlled trial (LIBERTY AD PRESCHOOL) was conducted.
- Patients aged 6 months to 5 years with moderate-to-severe AD received dupilumab or placebo subcutaneously every 4 weeks for 16 weeks, with concomitant topical corticosteroids.
- Photographic cases, clinical outcome measures, and biomarker data were analyzed before and after treatment.
Main Results:
- Dupilumab treatment led to visible improvements in AD signs like lichenification, erythema, and dryness.
- Clinically meaningful improvements were observed in AD severity, itch, sleep, symptoms, and quality of life.
- Substantial reductions in AD-related biomarkers were associated with clinical improvements.
Conclusions:
- Dupilumab effectively improved signs, symptoms, and quality of life in young children with moderate-to-severe AD.
- The treatment also led to a reduction in AD-related serum biomarkers across various patient phenotypes and endotypes.
Introduction:
Atopic dermatitis (AD) is a prevalent disease in infants and young children worldwide. Dupilumab has been shown to rapidly and significantly improve AD signs, symptoms, and quality of life in pediatric patients with moderate-to-severe AD.
Methods:
In LIBERTY AD PRESCHOOL, a randomized, double-blind, placebo-controlled, phase 3 clinical trial, patients aged 6 months to 5 years with moderate-to-severe AD received subcutaneous dupilumab or matched placebo every 4 weeks for 16 weeks. All patients received concomitant low-potency topical corticosteroids. Here, we present 12 photographic cases of patients with different phenotypes and endotypes in the dupilumab group, representative of the study population, before and after treatment. Each case is presented with clinical outcome measures of AD severity and quality of life, as well as relevant biomarkers, with percent improvement from baseline.
Results:
Treatment with dupilumab led to visible improvements in signs of lichenification, erythema, excoriations, skin dryness, and oozing/crusting. Clinically meaningful improvements in the measured outcomes were observed in most of the patients, including AD extent and severity, clinical lesions, itch, sleep loss, frequency of symptoms, and quality of life. These improvements were associated with substantial reductions in AD-related biomarkers.
Conclusion:
Treatment with dupilumab improved signs, symptoms, and quality of life, and reduced AD-related serum biomarkers in young children with moderate-to-severe AD with different phenotypes and endotypes.
Trial Registration:
The trial was registered with ClinicalTrials.gov with ID number NCT03346434 on November 17, 2017. Video abstract available for this article. Video abstract (MP4 1,02,609 KB).
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