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A Comprehensive Multicenter Clinical Evaluation of Xeligekimab in the Treatment of Moderate-to-Severe Psoriasis

A Comprehensive Multicenter Clinical Evaluation of Xeligekimab in the Treatment of Moderate-to-Severe Psoriasis

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500112656
Enrollment
Unknown
Registered
2025-11-18
Start date
2025-12-01
Completion date
Unknown
Last updated
2025-11-24

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

Conditions

Moderate-to-Severe Psoriasis

Interventions

Xeligekimab group:None

Sponsors

Chongqing Hospital of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Age >= 18 years, male or female; 2.Diagnosed with moderate to severe plaque psoriasis 3.Considered by the investigator to be a candidate for initial treatment with Xeligekimab 4.Voluntary participation and signed informed consent form.

Exclusion criteria

Exclusion criteria: 1.Drug-induced psoriasis at screening or baseline (e.g., psoriasis onset or exacerbation due to beta-blockers, calcium channel blockers, lithium, etc.); 2.Presence of other inflammatory diseases, including but not limited to inflammatory bowel disease, which in the investigator’s judgment may affect efficacy or safety assessments; 3.Patients with currently treated or untreated malignant tumors; 4.History of severe hypersensitivity to the active ingredient or any excipient of Setokimab injection; 5.Active infection of clinical significance; 6.Pregnant or lactating women; 7.History of severe psychiatric disorder or family history thereof; 8.Patients with other contraindications as per the prescribing information; 9.Any other condition considered by the investigator to make the patient unsuitable for participation.

Design outcomes

Primary

MeasureTime frame
PASI 90 response;

Secondary

MeasureTime frame
PASI 90 response;DLQI 0/1 response;PGA(0/1)response;Median time to achieve PASI 75 response in patients;PASI75 response;PASI 100 response;Median time to achieve PASI 90 response in patients;Median time to achieve PASI 100 response in patients;

Countries

China

Contacts

Public ContactDiao Qingchun/Wang Qin

Chongqing Hospital of Traditional Chinese Medicine

wangyuyi188@126.com+86 139 8373 5555

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026