Clinical study to examine the clinical efficacy and the NSAID-sparing effect of Secukinumab in patients with ankylosing spondylitis

Update Il y a 4 ans
Reference: EUCTR2015-004575-74

Woman and Man

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Extract

To demonstrate that the efficacy of Secukinumab 150 mg s.c. (Secukinumab from week 0 with NSAID tapering allowed from week 4; “delayed tapering”) at Week 12 is superior to placebo based on the proportion of patients achieving an ASAS20 response.


Inclusion criteria

  • Ankylosing spondylitis

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