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Exploring biomarkers for the efficacy and safety of IL-17 inhibitors in the treatment of moderate to severe psoriasis vulgarisof adults

Exploring biomarkers for the efficacy and safety of IL-17 inhibitors in the treatment of moderate to severe psoriasis vulgarisof adults

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400091735
Enrollment
Unknown
Registered
2024-11-01
Start date
2024-11-01
Completion date
Unknown
Last updated
2024-11-04

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

Conditions

psoriasis

Interventions

Group Secukinumab:Secukinumab
Group Ixekizumab:Ixekizumab

Sponsors

General Hospital of Ningxia Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: ? Patients aged from 18 to 75 years old, both male and female; ?Moderate to severe plaque psoriasis was defined as involving 10% or more of the total surface area at baseline, a physician's global assessment PGA score of 3 or more (on a scale of 0 to 5, 0 indicating no psoriatic lesions and 5 indicating severe psoriasis), and a psoriatic Area and severity score (PASI) of 3 or more (on a scale of 0 to 72, 5 indicating severe psoriasis). The higher the score, the more severe the condition). In addition, patients who have previously received systemic therapy (including biologics) or phototherapy are also eligible; ? Volunteer to participate in this experiment and sign the informed consent.

Exclusion criteria

Exclusion criteria: 1) Severe infection; 2) Allergic to biologics or a history of multiple drug allergies; 3) Patients with active TB infection or untreated latent TB infection indicated by T-spot and chest radiography; 4) Have hepatitis B virus infection or hepatitis B surface antigen positive and have obvious liver function damage; 5) Have a malignant tumor; 6) Recent use of immunosuppressants; 7) A history of substance abuse or mental illness; 8) Patients with severe heart failure; 9) Patients with immune deficiency; 10) Women who are pregnant, breastfeeding, or have a family planning patient in the short term

Design outcomes

Primary

MeasureTime frame
biomarker;

Secondary

MeasureTime frame
treatment effect;Adverse reactions;

Countries

China

Contacts

Public ContactYu Nan

General Hospital of Ningxia Medical University

13895095009@163.com+86 138 9509 5009

Outcome results

None listed

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