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Real-world study of treatment with Xeligekimab in patients with moderate to severe plaque psoriasis in Xinjiang region

Evaluation of the efficacy and safety of Xeligekimab in the treatment of moderate to severe plaque psoriasis patients in Xinjiang region: a multicenter, prospective real-world study

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600124090
Enrollment
Unknown
Registered
2026-05-07
Start date
2026-05-07
Completion date
Unknown
Last updated
2026-05-11

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

Conditions

Diagnosed with chronic moderate to severe plaque psoriasis (psoriasis-involved body surface area (BSA) >= 3% and Psoriasis Area and Severity Index (PASI) score >= 3 at screening baseline)

Interventions

Sponsors

People‘s Hospital of Xinjiang Uygur Autonomous Region
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 100 Years

Inclusion criteria

Inclusion criteria: 1.Age >=18 years; 2.Diagnosed with chronic moderate to severe plaque psoriasis (with psoriasis affected area (BSA) >=3% and psoriasis area and severity index (PASI) score >=3 at screening baseline); 3.From the screening period until 6 months after the last drug administration, the subjects had no plans to give birth or donate sperm or eggs, and voluntarily adopted highly effective physical contraception measures; 4.Patients who are assessed by clinicians as suitable for treatment withXeligekimab and are intended to receive Xeligekimab for the first time; 5.Those who voluntarily participate and sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1.During screening, patients with guttate, pustular, erythrodermic, or drug-induced psoriasis were excluded; 2.Allergic to the active ingredient or any adjuvant of CIMZIA; 3.Suffering from active tumors; 4.Women who are pregnant or breastfeeding; 5.The researchers evaluated other situations that were not suitable for inclusion in this study.

Design outcomes

Primary

MeasureTime frame
The proportion of subjects who achieve PASI 90 at week 12;

Secondary

MeasureTime frame
The proportion of patients who achieved a PASI score of 90 at weeks 4, 24, 36 and 52;The proportion of patients who achieved a PASI 75 and a PGA score of 0 or 1 at weeks 4, 12, 24, 36 and 52;The proportion of patients achieving a PGA 0 and PASI 100 response at weeks 4, 12, 24, 36 and 52;Changes in the Psoriasis Area and Severity Index (PASI) score and body surface area (BSA) relative to baseline at weeks 4, 12, 24, 36 and 52;

Countries

China

Contacts

Public ContactKang Xiaojing

People‘s Hospital of Xinjiang Uygur Autonomous Region

drkangxj666@163.com+86 991 856 3678

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: May 16, 2026