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Secukinumab Treatment for Moderate to Severe Hidradenitis Suppurativa
Sponsor: Peking Union Medical College
Summary
This single-center, prospective, observational study aimed to evaluate the efficacy and safety of Secukinumab in treating moderate-to-severe hidradenitis suppurativa (HS). The study was conducted from June 1, 2025, to June 1, 2026, and all participants were treated at the Department of Dermatology, Peking Union Medical College Hospital. The study was approved by the Clinical and Research Ethics Committee of the Chinese Academy of Medical Sciences, Peking Union Medical College Hospital (Ethics Approval No. I-24PJ1844). All procedures involving human participants adhered to the Declaration of Helsinki. Written informed consent form was signed and obtained from the participant.
Official title: Real-World Evaluation of Secukinumab in Moderate-to-Severe Hidradenitis Suppurativa
Key Details
Gender
All
Age Range
18 Years - Any
Study Type
OBSERVATIONAL
Enrollment
50
Start Date
2025-06-01
Completion Date
2026-06-01
Last Updated
2025-08-07
Healthy Volunteers
Not specified
Conditions
Interventions
Secukinumab
secukinumab 300 mg weekly for five weeks, followed by 300 mg monthly subcutaneous injection
Locations (1)
No. 1 Shuai Fu Yuan, Dongcheng District, Beijing
Beijing, Beijing Municipality, China