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Efficacy and safety of telitacicept in the treatment of primary IgA nephropathy: a prospective cohort study

Efficacy and safety of telitacicept in the treatment of primary IgA nephropathy: a prospective cohort study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400083991
Enrollment
Unknown
Registered
2024-05-08
Start date
2024-05-13
Completion date
Unknown
Last updated
2024-05-13

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

Conditions

IgA nephropathy

Interventions

Sponsors

The Second Hospital of Shanxi Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Willing to sign an informed consent form for medication and follow-up; 2. Patients diagnosed with IgA nephropathy through renal biopsy; 3. Ages older than 18 years; 4. eGFR > 15 ml/min per 1.73m^2 (using the CKD-EPI formula); 5. Urinary protein = 0.75 g/24h; 6. Patients who, in the clinician's judgment, require initiation of immunosuppressive therapy after receiving adequate supportive care.

Exclusion criteria

Exclusion criteria: 1. IgA vasculitis, and IgA nephropathy with clear secondary causes; 2. Patients with IgA nephropathy requiring high-dose hormone shock therapy in clinical judgment, including, but not limited to, patients with other types of glomerular disease such as crescentic nephritis (pathologic diagnosis present in >50% of cases); 3. Patients in whom other types of glomerular disease cannot be definitively ruled out, such as membranous nephropathy with IgA deposits or minimal change disease with IgA deposits, etc; 4. Patients with severe underlying diseases; 5. Received other biologic agents within 24 weeks prior to enrollment; 6. Subjects deemed unsuitable by the researcher.

Design outcomes

Primary

MeasureTime frame
Changes in proteinuria;

Secondary

MeasureTime frame
Changes in glomerular filtration rate (GFR);Changes in urinary albumin-to-creatinine ratio (ACR) ;

Countries

China

Contacts

Public ContactBingjuan Yan

The Second Hospital of Shanxi Medical University

564381781@qq.com+86 151 3510 7375

Outcome results

None listed

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