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Study identifier: NCT07491913 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Biologic Treatment Withdrawal in Takayasu Arteritis Patients in Sustained Remission

Condition: Takayasu Arteritis  ·  Sponsor: Marmara University

PhaseNA
Planned participants40
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

Takayasu arteritis is a chronic large-vessel vasculitis affecting the aorta and its major branches. Biologic therapies such as tumor necrosis factor inhibitors and tocilizumab are commonly used in patients with refractory or relapsing disease. However, there is limited evidence regarding the optimal duration of biologic therapy and the safety of treatment discontinuation in patients who achieve sustained remission. This prospective study aims to evaluate the outcomes of planned biologic treatment withdrawal in patients with Takayasu arteritis who have been in long-standing clinical and radiologic remission and have received biologic therapy for at least three years. Eligible patients will undergo a predefined 3-month dose tapering protocol. Patients who remain relapse-free during this period will discontinue biologic therapy and will be followed for 12 months. The primary objective of the study is to determine the proportion of patients who maintain remission after biologic treatment withdrawal. Secondary objectives include evaluating the rate and timing of disease relapse during the tapering phase and the post-withdrawal follow-up period.

This description comes directly from the study's public registry record.

Talk to the study team

Fatma Alibaz-Oner, MD  ·  05326368554  ·  falibaz@gmail.com

Always discuss trial participation with your own doctor first.

Locations (1)

Marmara University Pendik Training and Research HospitalIstanbul, Turkey (Türkiye)Recruiting

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Source record: clinicaltrials.gov/study/NCT07491913