Join us at Health Research Day — June 6th at Canton Waterfront Park, Baltimore!   Learn More →
← Back to all trials
Recruiting NCT05649579

Efficacy and Safety of Dupilumab in Patients With Bullous Pemphigoid

Conditions: Bullous Pemphigoid

Sex: All
Ages: 18 Years – N/A
Enrollment: 146
Sponsor: Peking University First Hospital

Location: China

Summary

This study was designed to be a retrospective, multicentre, observational study to evaluate the efficacy and safety of dupilumab in the treatment of bullous pemphigoid and to find predictors of efficacy.

Eligibility Criteria

Inclusion Criteria:Adult bullous pemphigoid patients treated with dupilumab between January 1, 2021, and July 31, 2022, at six leading dermatology departments in the Chinese Collaborative Network for Autoimmune Bullous Diseases.The diagnosis of BP requires clinical manifestations and immunological or pathological evidences.Dupilumab treatment should continue for at least 4 weeks and possibly longer.Exclusion Criteria:Drug-induced BP, γ-1 pemphigoidPatients with less than 4 weeks of follow-upPatients were given any other biologicals within 6 months before the first dupilumab administration

Interested in this study? View the official listing for contact and enrollment details.

View on ClinicalTrials.gov

Source: ClinicalTrials.gov (NCT05649579). StuddyBuddy aggregates publicly available trial information.