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A study on the combination of Benvimod and IL-17A inhibitors in the treatment of moderate to severe psoriasis

A study on the combination of Benvimod and IL-17A inhibitors in the treatment of moderate to severe psoriasis

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300071836
Enrollment
Unknown
Registered
2023-05-26
Start date
2023-05-29
Completion date
Unknown
Last updated
2023-06-12

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

Conditions

Moderate to severe psoriasis

Interventions

Experimental group:Biologics combined with Benvermod cream
control group:Using IL-17A inhibitors alone

Sponsors

Shanghai Dermatology Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: (1) Patients with moderate to severe psoriasis who still have residual skin lesions (BSA = 10%) after 4 weeks of treatment with IL-17A inhibitors alone; (2) Women who are not pregnant and do not plan to conceive during the study period; (3) Fully understand the research content, voluntarily participate in the study, and have signed an informed consent form.

Exclusion criteria

Exclusion criteria: (1) Women during pregnancy or breastfeeding, or men/women preparing for pregnancy; (2) those who are known to be allergic to the active ingredient or excipients of the investigational drug; (3) Patients may not be able to complete the study for other reasons, or researchers may not consider it appropriate to participate in the study.

Design outcomes

Primary

MeasureTime frame
Area and severity of psoriasis in patients;PGA response rate (PGA0/1);

Secondary

MeasureTime frame
dermatology life quality index;

Countries

China

Contacts

Public ContactDing Yangfeng

Shanghai Dermatology Hospital

dingyangfeng@aliyun.com+86 180 1733 6363

Outcome results

None listed

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