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Comparison of Efficacy and Mechanism Exploration of Dupilumab and Upadacitinib in Moderate-to-Severe Atopic Dermatitis with Facial and Scalp Lesions

Comparison of Efficacy and Mechanism Exploration of Dupilumab and Upadacitinib in Moderate-to-Severe Atopic Dermatitis with Facial and Scalp Lesions

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500107737
Enrollment
Unknown
Registered
2025-08-18
Start date
2025-08-18
Completion date
Unknown
Last updated
2025-08-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Atopic Dermatitis

Interventions

Dupixent :Dupixent (dupilumab) (Sanofi/, France) for adults: an initial dose of 600 mg, followed by 300 mg every two weeks via subcutaneous injection
for children weighing between 15 kg and 30 kg, a single 300 mg injection every four weeks after the initial dose.
Upadacitinib:The therapeutic dose should be adjusted based on the patient’s condition and treatment response. The starting dose is 15 mg once daily, which can be increased to 30 mg once daily if neces

Sponsors

The Fourth Affiliated Hospital of Soochow University (Suzhou Dushuhu Hospital)
Lead Sponsor

Eligibility

Sex/Gender
All
Age
12 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1 Age >= 12 years, body weight >= 40 kg, gender not limited; 2 Meets the diagnostic criteria for moderate-to-severe atopic dermatitis according to the Williams scoring standard; 3 Capable of understanding and voluntarily signing a written informed consent form, able to complete treatment and follow-up as required.

Exclusion criteria

Exclusion criteria: 1 Pregnant or breastfeeding; 2 Received systemic treatment (including phototherapy, systemic corticosteroids, immunosuppressants, 3 etc.) within 6 months before the first treatment; 3 Systemic diseases, such as malignant tumors, severe infections, immunodeficiency disorders, impaired liver or kidney function, diabetes, lupus, etc.; 4 Neurological or psychiatric disorders. 5 During the study, patients were informed not to use any other treatment methods specifically for atopic dermatitis.

Design outcomes

Primary

MeasureTime frame
EASI;SCORAD;DLQI;SAS;SAS;Skin moisture test;Sebum test;TEWL;Allergen testing;IgE;Epidermal RNA Metabolomics;Epidermal Lipidomics;

Secondary

MeasureTime frame
Likert satisfactions;

Countries

China

Contacts

Public Contactmin li

The Fourth Affiliated Hospital of Soochow University

lm@suda.edu.cn+86 189 3614 0383

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026