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

Mise à jour : Il y a 4 ans
Référence : EUCTR2015-004575-74

Femme et Homme

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Extrait

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.


Critère d'inclusion

  • Ankylosing spondylitis

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