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Prospective real-world study: Evaluation of the clinical efficacy and safety of secukinumab or spesolimab in the treatment of hidradenitis suppurativa

A real-world study on the efficacy and safety of biological agents in the treatment of Hidradenitis suppurativa

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600120670
Enrollment
Unknown
Registered
2026-03-18
Start date
2025-10-30
Completion date
Unknown
Last updated
2026-03-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

hidradenitis suppurativa

Interventions

Secukinumab treatment group:None
Pesolimab treatment group:None

Sponsors

Peking Union Medical College Hospital, Chinese Academy of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
12 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Age: 12 to 70 years old; 2. Clinically or pathologically diagnosed as hidradenitis suppurativa; 3. Voluntarily participate in this study and sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Patients who have received IL-12/23 or IL-23 inhibitors within 6 months before enrollment, any TNF inhibitor or IL-17A inhibitor within 3 months, physical therapy or systemic treatment (systemic antibiotics, retinoids, glucocorticoids, immunosuppressants, etc.) within 4 weeks, or topical medications (topical antibiotics, retinoids, etc.) within 2 weeks; 2. Patients with unclear primary disease diagnosis; 3. Patients with contraindications to the use of IL-17A or IL-36R inhibitors; 4. Patients with other active skin diseases that may affect disease assessment; 5. Pregnant women, lactating women, and those with plans to conceive within 1 year; 6. Patients with severe, uncontrolled systemic diseases, autoimmune diseases, malignant tumors, or infectious disease histories.

Design outcomes

Primary

MeasureTime frame
International Hidradenitis Suppurativa Severity Score System (IHS4);Hidradenitis Suppurativa Clinical Response 50 (HiSCR50);

Secondary

MeasureTime frame
Numeric Rating Scale;DLQI, Dermatology Life Quality Index;

Countries

China

Contacts

Public ContactChao Wu

Peking Union Medical College Hospital, Chinese Academy of Medical Sciences

wuchao198978@163.com+86 135 2124 5077

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Apr 3, 2026