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Evaluation of Short-term Efficacy, Safety and Related Factors of IL-12/23, IL-17 and IL-23 Inhibitors in the Treatment of Moderate-to-Severe Plaque Psoriasis in Real-World Settings

Evaluation of Short-term Efficacy, Safety and Related Factors of IL-12/23, IL-17 and IL-23 Inhibitors in the Treatment of Moderate-to-Severe Plaque Psoriasis in Real-World Settings

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500113970
Enrollment
Unknown
Registered
2025-12-04
Start date
2025-12-30
Completion date
Unknown
Last updated
2025-12-08

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

Conditions

Psoriasis

Interventions

IL-23 Inhibitor Group:NA
IL-17Inhibitor Group:NA
IL-12/23 Inhibitor Group:NA

Sponsors

Zhongshan People’s Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Patients aged 18 years or older, regardless of gender. 2. Patients who meet the diagnostic criteria: diagnosed with moderate-to-severe plaque psoriasis by physicians in our department based on clinical manifestations and pathological examination, with a baseline Body Surface Area (BSA) of >= 3, Psoriasis Area and Severity Index (PASI) of >= 3, and Dermatology Life Quality Index (DLQI) of >= 6. 3. Patients who voluntarily receive long-term biologic therapy and cooperate with follow-up visits and regular re-examinations.

Exclusion criteria

Exclusion criteria: 1. Presence of severe infections. 2. Allergy to biological agents. 3. Patients with active tuberculosis infection or active hepatitis B virus infection that is untreated. 4. Patients with malignant tumors, autoimmune diseases, or severe systemic diseases (such as cardiovascular, renal, hepatic, or pulmonary diseases) that are either untreated or poorly controlled. 5. History of substance abuse or psychiatric disorders. 6. Women who are pregnant, lactating, or patients with short-term plans for childbearing. 7. Significant abnormalities in laboratory test indicators. 8. Patients who, due to other circumstances, are deemed unsuitable to participate in this study by the researchers.

Design outcomes

Primary

MeasureTime frame
Dermatology Life Quality Index;Standard Lesion Body Surface Area;Psoriasis Area and Severity Index;

Countries

China

Contacts

Public ContactLi Chen

Zhongshan People’s Hospital

knoberlee@163.com+86 18686883773

Outcome results

None listed

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