drugset / Trial / NCT04291781
A Study of RC18 Administered Subcutaneously to Subjects With Primary IgA(Immunoglobulin A) Nephropathy
RandomizedParallel-groupQuadruple-blindTreatment
Summary
To evaluate the safety and efficacy of Tai Ai(Recombinant Human B Lymphocyte Stimulator Receptor-Antibody Fusion Protein for Injection) in the treatment of IgA nephropathy.
Timeline
- Start
- 2020-04-13
- Primary completion
- 2021-05-20
- Completion
- 2021-05-20
Publications
- Pei J, Xu X, Huang R, Sun X, Zhang J, Chen X, Yao L, Zhang H, Shao L, Li Y. Efficacy and safety of low- to medium-dose telitacicept in adults with high-risk progressive IgA nephropathy: a retrospective real-world study. BMC Nephrol. 2025 Dec 17;27(1):92. doi: 10.1186/s12882-025-04708-w.
- Tunnicliffe DJ, Reid S, Craig JC, Samuels JA, Molony DA, Strippoli GF. Non-immunosuppressive treatment for IgA nephropathy. Cochrane Database Syst Rev. 2024 Feb 1;2(2):CD003962. doi: 10.1002/14651858.CD003962.pub3.
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Telitacicept | Protein / enzyme biologic | 160 mg | Subcutaneous |
| Subject | Telitacicept | Protein / enzyme biologic | 240 mg | Subcutaneous |