drugset / Trial / NCT06677801

Immune Cell Subsets in SLE Patients Treated with Telitacicept

NCT06677801

NaSingle-groupOpen-labelDiagnostic

Summary

This study is a single-center cohort study. Patients with SLE who met the inclusion criteria were treated with tetanercept 160 mg once a week for a total of 24 weeks, and the clinical and laboratory indicators were collected before treatment, at the 4th week, at the 12th week, and at the 24th week, and blood samples were collected for the detection of immune cell subsets.

Timeline

Start
2024-10-11
Primary completion
2026-10-31
Completion
2027-10-31

Drugs

EvaluationDrugModalityDoseRoute
Comparator Telitacicept Protein / enzyme biologic 160 mg