drugset / Trial / NCT06549231

Evaluation of Efficacy and Safety of Rituximab and Mycophenolate Mofetil Combination in Patients With Interstitial Lung Disease Related to Systemic Sclerosis

NCT06549231

Phase 3 Recruiting 102 enrolled University Hospital, Tours
RandomizedParallel-groupTriple-blindTreatment

Summary

The goal of this clinical trial is to evaluate the efficacy on lung function after 24 weeks of rituximab + MMF combination comparatively to placebo + MMF combination in patients with SSc-ILD severe at the initial assessment or at high risk of progression.

Timeline

Start
2025-01-08
Primary completion
2028-07-08
Completion
2029-01-08

Drugs

EvaluationDrugModalityDoseRoute
Subject Rituximab Monoclonal antibody 500 mg Intravenous