drugset / Trial / NCT01863732

Extension in AS: Sustainability of Benefits, Safety and Tolerability

NCT01863732

Phase 3 Completed 274 enrolled Novartis Pharmaceuticals
RandomizedParallel-groupQuadruple-blindTreatment

Summary

This 3-year extension study aims at making available the treatment with secukinumab in prefilled syringes (PFS) to patients with ankylosing spondylitis who took part in phase III study CAIN457F2305, defined as "core study", as well as to generate additional data on the sustainability of clinical benefits, safety and tolerability during long-term administration of secukinumab.

Timeline

Start
2013-11-06
Primary completion
2018-03-16
Completion
2018-03-16

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Secukinumab Monoclonal antibody 75 mg Subcutaneous
Subject Secukinumab Monoclonal antibody 150 mg Subcutaneous