Secukinumab Treatment for Moderate to Severe Hidradenitis Suppurativa
NCT ID: NCT07109765
Last Updated: 2025-08-07
Study Results
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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RECRUITING
50 participants
OBSERVATIONAL
2025-06-01
2026-06-01
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Interventions
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Secukinumab
secukinumab 300 mg weekly for five weeks, followed by 300 mg monthly subcutaneous injection
Eligibility Criteria
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Inclusion Criteria
* 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
* 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
18 Years
ALL
No
Sponsors
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Peking Union Medical College
OTHER
Responsible Party
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Xiao Ma
Resident physician of dermatology
Locations
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No. 1 Shuai Fu Yuan, Dongcheng District, Beijing
Beijing, Beijing Municipality, China
Countries
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Facility Contacts
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Provided Documents
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Document Type: Study Protocol
Other Identifiers
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No. I-24PJ1844
Identifier Type: -
Identifier Source: org_study_id
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