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A Multicenter Study on the Impact of Long-Term and Proactive Intermittent Maintenance Treatment with Benvitimod on Psoriasis Recurrence

A Multicenter Study on the Impact of Long-Term and Proactive Intermittent Maintenance Treatment with Benvitimod on Psoriasis Recurrence

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500098254
Enrollment
Unknown
Registered
2025-03-05
Start date
2025-03-20
Completion date
Unknown
Last updated
2025-03-10

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

Conditions

Psoriasis

Interventions

Screening Period:Apply 1% Benvitimod cream topically to the lesions twice daily (morning and evening) for 12 consecutive weeks
Proactive Maintenance Treatment Group:Apply 1% Benvitimod cream twice weekly for 12 weeks
Drug Withdrawal Group:Apply the vehicle cream twice weekly for 12 weeks

Sponsors

Peking University Third Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Age 18~65 years old; 2. Have typical clinical signs and symptoms, diagnosed with psoriasis (psoriasis with or without palmoplantar area) by 2 or more senior dermatologists for at least 6 months, and involve 10% of the total area =2, the target lesion must be representative of the subject's disease state; 4. Psoriasis patients who are using systemic therapy (including but not limited to cyclosporine, methotrexate, acitretin, apremiste, adalimumab, secukinumab, ixekizumab, guselkumab, upadatinib, etc.) and/or phototherapy have residual skin lesions, and the skin lesions are stable and do not resolve after regular use of systemic therapy and/or phototherapy for nearly 3 months, and systemic therapy and/or phototherapy can continue to be used regularly during the 24-week follow-up period; 5. No external glucocorticoids, calcipotriol, tretinoin and other physical therapy in the past 2 weeks.

Exclusion criteria

Exclusion criteria: 1. Pregnant or breastfeeding women. 2. Patients with severe cardiovascular, pulmonary, renal, or psychiatric diseases. 3. Any other conditions deemed unsuitable for inclusion by the investigators.

Design outcomes

Primary

MeasureTime frame
Physician Global Assessment;

Secondary

MeasureTime frame
Psoriasis area and severity index;Body Surface Area;

Countries

China

Contacts

Public ContactWang Wenhui

Peking University Third Hospital

wwh0608@126.com+86 188 0139 2031

Outcome results

None listed

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