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A Pharmacoeconomic Study Comparing Long-Acting Biologics with Short-Acting Biologics for the Treatment of Moderate-to-Severe Plaque Psoriasis

A Pharmacoeconomic Study Comparing Long-Acting Biologics with Short-Acting Biologics for the Treatment of Moderate-to-Severe Plaque Psoriasis

Status
Active, not recruiting
Phases
Phase 4
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600129460
Enrollment
Unknown
Registered
2026-08-05
Start date
2026-09-15
Completion date
Unknown
Last updated
2026-08-10

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

Short-acting biological therapy group:None
Long-acting biological agent treatment group:None

Sponsors

The First Affiliated Hospital of Guangxi Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Age >= 18 years, any gender, and a confirmed diagnosis of moderate-to-severe plaque psoriasis; 2. Have received treatment with usulumab injection or secukinumab injection, or have switched from another biologic agent; 3. Voluntarily sign a written informed consent form and be able to comply with the requirements of the study protocol.

Exclusion criteria

Exclusion criteria: 1. Presence of an active infection (e.g., active tuberculosis, HBV/HCV/HIV infection); 2. History of malignant tumors (excluding basal cell carcinoma or squamous cell carcinoma of the skin, provided that the condition has been cured for >=5 years); 3. People who are allergic to biologics and their excipients; 4. Those who have received a live vaccine within the past 3 months or plan to receive one; 5. Researchers determined that the participant was not eligible for this study.

Design outcomes

Primary

MeasureTime frame
Incremental Cost-Utility Ratio (ICUR);

Secondary

MeasureTime frame
Quality-Adjusted Life Year (QALY);The proportion of cases where the DLQI score improved by >=50% compared to the baseline value;Incidence of serious adverse events (SAE);Changes in the number of outpatient visits, hospitalizations, and drug retention rates;26/5000 Per capita annual direct medical costs (including drug expenses, examination fees, hospitalization fees, and outpatient fees);Continuous remission rate;The response rate of PASI75 and the changes from the baseline;Frequency of recurrence;

Countries

China

Contacts

Public ContactHongliang Zhang

The First Affiliated Hospital of Guangxi Medical University

277749097@qq.com+86 771 5356154

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Aug 25, 2026