Ankylosing Spondylitis Clinical Trial
Official title:
A Multicenter Uncontrolled Extension Study Evaluating the Long Term Safety and Efficacy of SAR153191 in Patients With Ankylosing Spondylitis (AS)
Primary Objective:
- To assess the long term safety of Sarilumab (SAR153191/REGN88) in patients with
ankylosing spondylitis (AS)
Secondary Objective:
- To assess the long term efficacy of Sarilumab (SAR153191/REGN88) in patients with AS
The maximum study duration per participant was to be 267 weeks (approximatively 5 years)
broken down as follows:
- screening up to a maximum of 1 week;
- treatment up to a maximum of 260 weeks;
- follow-up of 6 weeks after treatment discontinuation.
;
Endpoint Classification: Safety Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment
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