drugset / Trial / NCT07013838

The Efficacy and Safety of Deucravacitinib in Takayasu's Arteritis

NCT07013838

Phase 4 Not yet recruiting 50 enrolled Chinese SLE Treatment And Research Group
RandomizedParallel-groupOpen-labelTreatment

Summary

This is a 24-week, single-center, randomized, open-label trial conducted by Peking Union Medical College Hospital. The aim of this study is to assess the efficacy and safety of deucravacitinib in adult patients with relapsing TAK in comparison to patients treated with TNF inhibitor (TNFi), the most well-recognized therapeutic choice of non-glucocorticoid immunosuppressive for patients with relapsed or refractory TAK.

Timeline

Start
2025-06-15
Primary completion
2027-12-31
Completion
2028-03-31

Drugs

EvaluationDrugModalityDoseRoute
Comparator Adalimumab Monoclonal antibody 40 mg Subcutaneous
Subject CRAVACITINIB Small molecule 6 mg Oral

Indications