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Real-World Study on the Efficacy and Safety Assessment of Ultra-Low-Dose Rituximab in the Treatment of Pemphigus

Ultra-Low Dose Rituximab for Pemphigus: Efficacy and Safety Analysis

Status
Recruiting
Phases
Phase 4
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500106964
Enrollment
Unknown
Registered
2025-08-01
Start date
2025-03-17
Completion date
Unknown
Last updated
2025-08-18

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

Conditions

The autoimmune blistering disease

Interventions

Observation group:None

Sponsors

The First Medical Center of Chinese PLA General Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Those who have a clear diagnosis of pemphigus and are treated with rituximab combined with systemic glucocorticoids in our department. 2. Voluntarily sign the informed consent form; 3. Subjects who are able to comply with the study protocols and visit plan.

Exclusion criteria

Exclusion criteria: 1. Patients who have had or are receiving rituxib treatment due to lupus, nephritis, lymphoma and other diseases. 2. Patients with incomplete clinical data. 3. Patients who have previously used rituximab for pemphigus disease in other hospitals. 4. At the same time, there are other patients such as dermatitis herpetiformis that affect the evaluation of pemphigus condition. 5. Patients who use systemic or topical glucocorticoids and other immunosuppressants due to other diseases.

Design outcomes

Primary

MeasureTime frame
Pemphigusdiseaseareaindex,PDAI;Complete remission, CRmin;

Secondary

MeasureTime frame
Measurement of peripheral blood B lymphocyte percentage and absolute count;Autoantibodies against Dsg1 and Dsg3;

Countries

China

Contacts

Public ContactChengxin Li

The First Medical Center of Chinese PLA General Hospital

lichengxinderm@163.com+86 185 0196 9456

Outcome results

None listed

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