drugset / Trial / NCT07643038

Treatment Strategy for Patients With RA-ILD

NCT07643038

Phase 4 Not yet recruiting 204 enrolled Chinese SLE Treatment And Research Group
RandomizedParallel-groupOpen-labelTreatment

Summary

This is a 52-week, multicenter, prospective, open-label, randomized controlled clinical study, comparing the efficacy and safety of tocilizumab, telitacicept, and csDMARD methotrexate in patients with RA-ILD.

Timeline

Start
2026-07-01
Primary completion
2029-07-31
Completion
2029-07-31

Drugs

EvaluationDrugModalityDoseRoute
Comparator Methotrexate Small molecule 15 mg Oral
Subject Telitacicept Protein / enzyme biologic 160 mg Subcutaneous
Subject Tocilizumab Monoclonal antibody 8 mg/kg Intravenous