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Efficacy and Predictive Factors of Vunakizumab in the Treatment of Moderate-to-Severe Plaque Psoriasis

Efficacy and Predictive Factors of Vunakizumab in the Treatment of Moderate-to-Severe Plaque Psoriasis: A Multicenter, Prospective, Multi-Omics Dedicated Disease Cohort Study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600123062
Enrollment
Unknown
Registered
2026-04-21
Start date
2025-03-04
Completion date
Unknown
Last updated
2026-04-27

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

Conditions

Plaque Psoriasis

Interventions

The group treated with nivolumab:None

Sponsors

Shanghai Skin Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1.Willing to participate in this study and sign the informed consent form; 2.Male or female aged =18 years; 3.Diagnosed with moderate-to-severe plaque psoriasis with a disease duration of =3 months, according to the 2023 Chinese Guidelines for the Diagnosis and Treatment of Psoriasis.

Exclusion criteria

Exclusion criteria: 1.Patients who do not meet the recommendations for switching biologics as outlined in the 2024 Chinese Guidelines for the Treatment of Psoriasis with Biologics and Small Molecule Drugs. 2.Presence of psoriasis forms other than chronic plaque type at screening or baseline (e.g., pustular, erythrodermic, or guttate psoriasis). 3.Drug-induced psoriasis. 4.Presence of other skin conditions that may interfere with psoriasis assessment, such as skin infections, as judged by the investigator. 5.History of inflammatory bowel disease or other ongoing active autoimmune diseases. 6.History of unstable malignancy within the past 5 years. 7.Severe cardiovascular, cerebrovascular, endocrine, or other systemic diseases considered by the investigator to be unsuitable for study participation. 8.Untreated or uncontrolled active infection. 9.Poor compliance or any other condition deemed by the investigator as inappropriate for trial participation.

Design outcomes

Primary

MeasureTime frame
PASI 100 response rate at week 24 of treatment;

Secondary

MeasureTime frame
Psoriasis Area and Severity Index(PASI) 75/90;Psoriasis Area and Severity Index(PASI) =3;Psoriasis Area and Severity Index(PASI) =1;Investigator’s Global Assessment (PGA) 0/1;Relapse rate;

Countries

China

Contacts

Public ContactYuling Shi

Shanghai Skin Hospital

shiyuling1973@126.com+86 138 1621 3884

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: May 1, 2026