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Efficacy and safety of Telitacicept in the treatment of recurrent IgA nephropathy after transplantation

Efficacy and safety of Telitacicept in the treatment of recurrent IgA nephropathy after transplantation

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400084654
Enrollment
Unknown
Registered
2024-05-22
Start date
2024-06-01
Completion date
Unknown
Last updated
2024-05-27

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

Conditions

recurrent IgA nephropathy after transplantation

Interventions

Experimental grou:Conventional treatment+Taetaxel
Control group:Conventional treatment

Sponsors

Tongji Hospital Affiliated to Tongji Medical College of Huazhong University of Science and Technology
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1: Adult recipients aged =18 and =65 years old 2: graft biopsy considered recurrence of IgA nephropathy 3: Have received ACEi/ARB standard treatment for at least 12 weeks, and received the maximum tolerated dose 4 weeks before enrollment 4: 24-hour urine protein quantification = 0.75g and =3g 5: time span between 24-hour urine protein quantification = 0.3g and the enrollment is less than 1 year 6: eGFR =35ml/min/1.73m^2

Exclusion criteria

Exclusion criteria: 1: PRA or DSA positive recipients; 2: recipients whose transplanted kidney biopsy shows rejection; 3: Other known causes of proteinuria; 4: ABO-incompatible kidney transplant recipients 5: Multiple organ transplant recipients; 6: Glycated hemoglobin>6.5%; 7: Those who took Tripterygium wilfordii preparations within 1 month before enrollment; 8: Patients with malignant tumor or patients who have been diagnosed with malignant tumor within the past 5 years but have been cured, except treated basal cell carcinoma of the skin, effectively resected squamous cell carcinoma of the skin, colon polyps, or cervical cancer in situ; 9: Pregnant women, lactating women, and men or women who plan to have children during the trial; 10: Those allergic to human biological products; 11: Subjects deemed unsuitable by the researcher;

Design outcomes

Primary

MeasureTime frame
24-hour urinary protein quantification;

Secondary

MeasureTime frame
blood protein levels;eGFR;Serum IgA level;Abnormal glycosylation IgA;Serum IgM level;Serum IgG level;

Countries

China

Contacts

Public ContactGang Chen

Institute of Organ Transplantation, Affiliated Tongji Hospital, Tongji Medical College, Huazhong University

gchen@tjh.tjmu.edu.cn+86 130 0618 7015

Outcome results

None listed

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