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The Efficacy of Telitacicept in the Treatment of Persistent Hypocomplementemia in Patients with Lupus Nephritis

The Efficacy of Telitacicept in the Treatment of Persistent Hypocomplementemia in Patients with Lupus Nephritis

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600116745
Enrollment
Unknown
Registered
2026-01-14
Start date
2026-01-15
Completion date
Unknown
Last updated
2026-01-27

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

Conditions

Lupus Nephritis

Interventions

Standard treatment group:None
Lupus nephritis (LN) patients treated with telitacicept:None

Sponsors

Affiliated Hospital of Guangdong Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1.Patients aged between 18 and 65 years who meet the diagnostic criteria for LN and present with persistent hypocomplementemia; 2.Patients receiving either standard lupus therapy or Telitacicept combined with standard therapy (glucocorticoids and/or antimalarials and/or immunosuppressants including cyclophosphamide, mycophenolate mofetil, tacrolimus, cyclosporine, etc.).

Exclusion criteria

Exclusion criteria: 1. Patients with a history of treatment with any biological agents other than Telitacicept; 2. Patients with severe organic lesions in important organs such as the liver, spleen, or lungs; 3. Patients with primary hematopoietic system diseases; 4. Patients with rheumatoid arthritis, viral hepatitis, or other immune system diseases; 5. Female patients who are breastfeeding or pregnant; 6. Patients with missing clinical data.

Design outcomes

Primary

MeasureTime frame
Serum complement C3 and C4 levels;

Secondary

MeasureTime frame
Covering multiple disease-related indicators: including the degree of reduction in SLEDAI score, reduction in urinary protein quantification, improvement in renal function indicators (such as serum creatinine and estimated glomerular filtration rate), and incidence of adverse events.;

Countries

China

Contacts

Public ContactYao Cuiwei

Affiliated Hospital of Guangdong Medical University

yaocuiwei826@163.com+86 10 2369576

Outcome results

None listed

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