drugset / Trial / NCT06498089

A Randomized, Controlled, Open-label, Multicenter Clinical Trial Comparing the Efficacy and Safety of a Precision Treatment Regimen Based on Clinical-molecular Phenotypes with a Conventional Treatment Regimen in the Treatment of Patients with Active Takayasu's Arteritis

NCT06498089

Phase 4 Recruiting 124 enrolled Shanghai Zhongshan Hospital
RandomizedParallel-groupSingle-blindTreatment

Summary

This study aimed to compare the efficacy and safety of a precision treatment regimen based on clinical-molecular phenotypes with a conventional treatment regimen in the treatment of patients with active Takayasu's arteritis based on a randomized, controlled, open-label, multicenter study.

Timeline

Start
2024-06-28
Primary completion
2026-06-30
Completion
2027-06-30

Drugs

EvaluationDrugModalityDoseRoute
Subject Adalimumab Monoclonal antibody 40 mg
Subject Methotrexate Small molecule 15 mg
Subject Tocilizumab Monoclonal antibody 8 mg/kg Intravenous
Subject Tofacitinib Small molecule 11 mg
Background Prednisone Other / unclassified 0.6 mg/kg

Indications