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Effectiveness, safety and tolerance of guselkumab for the treatment of psoriasis in mainland China

Effectiveness, safety and tolerance of guselkumab for the treatment of psoriasis in mainland China

Status
Recruiting
Phases
Phase 4
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2000041398
Enrollment
Unknown
Registered
2020-12-25
Start date
2020-04-01
Completion date
Unknown
Last updated
2021-03-08

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

Conditions

psoriasis

Interventions

singel arm:Guselkumab

Sponsors

Dermatology Hosipital of Southern Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1) Aged >= 18 years; 2) Patients with Psoriasis Area Severity Index score (PASI) >= 10; 3) Patients with PASI < 10, who presented with involovement of sensitive areas such as the face, scalp, genital areas or nails. 4) Wash-out period of at least 4 weeks from systemic or UV treatment. 5) Patients were treated with standard dose of guselkumab (100 mg administered by subcutaneous injection at Week 0 and Week 4, followed by a maintenance dose every 8 weeks).

Exclusion criteria

Exclusion criteria: 1) Patients suffer with active infectious diseases, such as active tuberculosis, etc. 2) Patients suffer serious chronic systemic diseases. 3) Women who are pregnant or breastfeeding. 4) Inoculated live virus or live bacteria vaccine within 2 weeks.

Design outcomes

Primary

MeasureTime frame
Psoriasis Area Severity Index;Nail Psoriasis Severity Index;Physician's Global Assessment;

Secondary

MeasureTime frame
Dermatology Life Quality Index;Skindex-16;Frequency of related immune cells;Related immunocytokine;

Countries

China

Contacts

Public ContactYongfeng Chen

Dermatology Hosipital of Southern Medical University

gdcyf@163.com+86 13802920269

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 10, 2026