Efficacy and Tolerance of Tocilizumab In Takayasu Arteritis
- Sponsor
- Assistance Publique - Hôpitaux de Paris
- Study ID
- NCT02101333
- Phase
- PHASE3
- Status
- Completed
Conditions
- TAKAYASU ARTERITIS
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - 77 Years
- Healthy Volunteers
- Not accepted
Interventions
- Tocilizumab — DRUGintravenous injection 8 mg/kg, monthly during 6 months
Study Details
First-line tocilizumab treatment during 6 months could permit rapid steroid-tapering and induction of remission in Takayasu arteritis (TA).
Key Dates
- Start date
- Jun 10, 2014
- Status verified
- Jul 2020
- Primary completion
- Dec 10, 2018
- Completion
- Feb 1, 2019
Study Design
- Enrollment
- 18 participants (actual)
- Allocation
- NA
- Intervention model
- SINGLE_GROUP
- Primary purpose
- TREATMENT
Arms
- Experimental: TOCILIZUMAB MONTHLY DURING 6intravenous injection, 8 mg/kg, monthly during 6 months
Primary Outcome Measure
number of good responders without prednisone after 6-months tocilizumab treatment [ Time Frame: 6 months ]
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