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RECRUITING
NCT07109765

Secukinumab Treatment for Moderate to Severe Hidradenitis Suppurativa

Sponsor: Peking Union Medical College

View on ClinicalTrials.gov

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

Interventions

DRUG

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