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Efficacy and Safety of Xeligekimab in Patients with Mild-to-Moderate Psoriasis: A Prospective, Multicenter, Single-Arm Clinical Study

Efficacy and Safety of Xeligekimab in Patients with Mild-to-Moderate Psoriasis: A Prospective, Multicenter, Single-Arm Clinical Study

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600123675
Enrollment
Unknown
Registered
2026-04-28
Start date
2026-04-28
Completion date
Unknown
Last updated
2026-05-04

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

Conditions

Mild to Moderate Psoriasis

Interventions

Sponsors

Shandong Provincial Hospital for Skin Diseases & Shandong Provincial Institute of Dermatology and Venerology, Shandong First Medical University & Shandong Academy of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1.Age >= 18 years old; 2.During screening, the clinical diagnosis is mild or moderate psoriasis; including but not limited to guttate psoriasis and plaque psoriasis. Note: For the diagnosis of mild to moderate psoriasis, it is recommended to meet the following conditions simultaneously: at baseline, mild: BSA < 3%, PASI < 3, DLQI < 6; moderate: BSA 3% to <10%, PASI 3 to <10, DLQI 6 to <10. 3.Patients who are assessed by a clinician to be suitable for treatment with Xeligekimab Injection and are planning to receive Xeligekimab Injection treatment for the first time; 4.Those who voluntarily sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1.Drug-induced psoriasis (such as new-onset psoriasis or worsening of psoriasis caused by ß-blockers, calcium channel blockers, or lithium); 2.Allergic to the active ingredient of XeligekimabInjection or any excipients; 3.Patients with other contraindications listed in the package insert; 4.Patients who are currently participating in other clinical studies; 5.Women of childbearing potential (defined as all women with the physiological conditions necessary for pregnancy) and men who are unwilling or unable to use effective contraception during pregnancy, during the study, and within 20 weeks after the last administration of the study drug; 6.Researchers consider any other circumstances that might hinder participants from following and completing the study protocol.

Design outcomes

Primary

MeasureTime frame
12 weeks PASI 90 response rate;

Secondary

MeasureTime frame
4, 8, 12, 24 weeks PASI 90 response rate;4, 8, 12, 24 weeks DLQI 0/1 response rate;4, 8, 12, 24 weeks PGA0/1 response rate;4, 8, 12, 24 weeks PASI 75, PASI 100 response rate;

Countries

China

Contacts

Public ContactHong Liu

Shandong Provincial Hospital for Skin Diseases & Shandong Provincial Institute of Dermatology and Venerology, Shandong First Medical University & Shandong Academy of Medical Sciences

hongyue2519@hotmail.com+86 531 87298870

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: May 7, 2026