Secukinumab Treatment for Moderate to Severe Hidradenitis Suppurativa

NCT ID: NCT07109765

Last Updated: 2025-08-07

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

RECRUITING

Total Enrollment

50 participants

Study Classification

OBSERVATIONAL

Study Start Date

2025-06-01

Study Completion Date

2026-06-01

Brief Summary

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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.

Detailed Description

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Conditions

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Hidradenitis Suppurativa (HS)

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Interventions

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Secukinumab

secukinumab 300 mg weekly for five weeks, followed by 300 mg monthly subcutaneous injection

Intervention Type DRUG

Eligibility Criteria

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Inclusion Criteria

* age ≥18 years
* diagnosis of moderate-to-severe HS with Hurley stage II or III
* Disease duration of ≥6 months, presence of at least one draining tunnel or two inflammatory nodules
* inadequate response to prior treatments, such as antibiotics, isotretinoin, or TNF inhibitors

Exclusion Criteria

* active infections (e.g., viral hepatitis, active tuberculosis)
* use of other biologics or systemic immunosuppressants within the past three months
* severe organ dysfunction (e.g., hepatic or renal failure)
* any other conditions that might affect study results
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Peking Union Medical College

OTHER

Sponsor Role lead

Responsible Party

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Xiao Ma

Resident physician of dermatology

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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No. 1 Shuai Fu Yuan, Dongcheng District, Beijing

Beijing, Beijing Municipality, China

Site Status RECRUITING

Countries

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China

Facility Contacts

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Xiao Ma

Role: primary

86-18511599355

Provided Documents

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Document Type: Study Protocol

View Document

Other Identifiers

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No. I-24PJ1844

Identifier Type: -

Identifier Source: org_study_id

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