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, rituximab, and csDMARD methotrexate in patients with RA-ILD.

Timeline

Start
2026-09-20
Primary completion
2029-07-31
Completion
2029-07-31

Drugs

EvaluationDrugModalityDoseRoute
Comparator Methotrexate Small molecule 15 mg Oral
Subject Rituximab Monoclonal antibody 500 mg Intravenous
Subject Tocilizumab Monoclonal antibody 8 mg/kg Intravenous