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Exploriation of Serum Type II Inflammatory Pathway-Related Biomarkers in Patients with Bullous Pemphigoid Treated with Dupilumab

Exploriation of Serum Type II Inflammatory Pathway-Related Biomarkers in Patients with Bullous Pemphigoid Treated with Dupilumab

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400085072
Enrollment
Unknown
Registered
2024-05-30
Start date
2024-06-01
Completion date
Unknown
Last updated
2024-06-03

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

Conditions

bullous pemphigoid

Interventions

Dupi-retrospective:We will retrospectively recruit patients with bullous pemphigoid who received dupilumab treatment and their serum sample information at the outpatient department of Peking Universit
Dupi-prospective:A prospective study will include patients receiving dupilumab treatment and their serum sample information at the outpatient department of Peking University First Hospital from June 2

Sponsors

Peking university first hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 90 Years

Inclusion criteria

Inclusion criteria: Inclusion Criteria for Patients: 1. Age between 18 and 80 years. 2. Meets the following diagnostic criteria for bullous pemphigoid: a. Clinical manifestations: Symmetrical blisters and bullae formation on normal skin or edematous erythema, which may be accompanied by itching and urticarial-like rashes. b. Histopathology: Subepidermal blister formation with infiltration of eosinophils or neutrophils. c. Immunological indicators: Positive anti-BP180 and/or BP230 antibodies detected in serum by enzyme-linked immunosorbent assay (ELISA); or linear IgG/C3 deposition along the epidermal basement membrane zone observed by direct immunofluorescence (DIF). 3. Voluntary participation in this study with the provision of signed informed consent.

Exclusion criteria

Exclusion criteria: Exclusion Criteria: 1. Previous use of biological agents such as rituximab, omalizumab, or other similar biologics. 2. Usage of systemic glucocorticoids for a duration of =3 months; or received oral systemic steroids, immunosuppressants, biologics, intravenous immunoglobulin (IVIG) therapy, or plasmapheresis within the past month; or application of topical glucocorticoid treatment for =6 months. 3. Long-term use of DPP-4 inhibitors for diabetes management or PD-1 checkpoint inhibitors, with an inability to discontinue these medications. 4. Patients with severe active infections. 5. Concurrent diagnosis of psoriasis, linear IgA bullous dermatosis, pemphigoid gestationis, mucous membrane pemphigoid, dermatitis herpetiformis, or lupus erythematosus.

Design outcomes

Primary

MeasureTime frame
anti-BP180 IgG Antibody;29 inflammatory cytokine/chemokine biomarkers;

Countries

China

Contacts

Public ContactMingyue Wang

Department of Dermatology, Peking University First Hospital

MingyueWPKUFH@163.com+86 10 8357 3075

Outcome results

None listed

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