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Telitacicept in the Treatment of Bullous Pemphigoid

A Real word Study on the Efficacy and Safety of Telitacicept in the Treatment of Adult Patients with Bullous Pemphigoid

Status
Recruiting
Phases
Phase 4
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500106895
Enrollment
Unknown
Registered
2025-07-31
Start date
2025-03-26
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

Bullous pemphigoid

Interventions

Telitacicept in the Treatment of Adult Patients with Bullous Pemphigoid:NA

Sponsors

Hospital for Skin Diseases, Shandong First Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Patients meeting diagnostic criteria for bullous pemphigoid (a: clinical manifestations of flaccid vesicles, erosions on skin and mucous membranes, negative Nikolsky's sign; b: histopathological examination indicating subepidermal vesicles; c: direct immunofluorescence demonstrating IgG and/or C3 deposition in a reticular pattern at the basement membrane zone). 2. Adult patients aged 18-80 years. 3. Moderate-to-severe bullous pemphigoid (as measured by BPDAI score: mild =50 points); 4. First-time receipt of telitacicept treatment; 5. Provided written informed consent. 6. Able to adhere to the treatment schedule and follow-up protocol.

Exclusion criteria

Exclusion criteria: 1.Patients younger than 18 years or older than 80 years, those with contraindications including severe cardiovascular diseases, severe hepatic or renal impairment, severe active infections, history of severe infusion reactions, severe hypersensitivity to related drugs, history of malignancy, pregnant or breastfeeding women, individuals who recently received or plan to receive vaccinations, and patients previously treated with biologics such as telitacicept will be excluded from the study.

Design outcomes

Primary

MeasureTime frame
complete remission off therapy;The proportion and time to achieve pathogenic antibodies converting to negative.;

Secondary

MeasureTime frame
Cumulative glucocorticoid dose (prednisone equivalent);Relapse rates;

Countries

China

Contacts

Public ContactHong Liu

Hospital for Skin Diseases, Shandong First Medical University

hongyue2519@hotmail.com+86 531 87298870

Outcome results

None listed

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