Efficacy and Safety for Telitacicept in the Remission Maintenance Treatment of ANCA-associated Vasculitis (TTCAZAREM)
Condition(s) studied
Investigational drug(s) / intervention(s)
Azathioprine: All patients included into this study will be treated with Azathioprine tablets 100mg QD for 12 months.
Telitacicept: Patient will be treated with Telitacicept (Taiai the commercial name) 160 mg every week subcutaneously for 12 months
Study summary
This study is a prospective, open-labelled, randomized, controlled, single-center clinical trial. The aim of this study is to compare the remission rate of patients treated with Telitacicept combined with azathioprine and azathioprine alone in remission-maintenance treatment of AAV.
Eligibility
Primary outcome measure(s)
- The time of first relapse during 12 months follow-up of two groups — from inclusion to the end of the study, 12 months in total
The time from baseline to first relapse(re-appearance of disease with a BVAS \>0) of patients during 12 months follow-up of two groups
Trial sites (1)
| Facility | City | Region | Status |
|---|---|---|---|
| Peking Union Medical College Hospital | Beijing | Beijing Municipality | Recruiting |
More Chinese SLE Treatment And Research Group trials in China
Other trials for the same condition
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT05965284 on ClinicalTrials.gov ↗ ← All trials in China