Last updated on January 2019

Study of Efficacy and Safety of Secukinumab in Patients With Non-radiographic Axial Spondyloarthritis

Brief description of study

To demonstrate the clinical efficacy, safety and tolerability of secukinumab compared to placebo in patients with nr-axSpA at Week 16 as well as Week 52 and long term efficacy and safety up to Week 104 followed by an optional 16-week randomized dose escalation treatment period and a continuous treatment period for up to Week 208

Clinical Study Identifier: NCT02696031

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Novartis Pharmaceuticals

Novartis Investigative Site
Harlow, United Kingdom

Recruitment Status: Closed

Brief Description Eligibility Contact Research Team

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