drugset / Trial / NCT02409667

Plaque Psoriasis Efficacy and Safety With Secukinumab

NCT02409667

Phase 3 Completed 16487 enrolled Novartis Pharmaceuticals
RandomizedParallel-groupDouble-blindTreatment

Summary

To demonstrate in the patient pool of PASI 90 responders at Week 24 that secukinumab 300 mg s.c. when administered at a longer dosing interval is non-inferior to secukinumab 300 mg s.c. every 4 weeks treatment with respect to maintaining a PASI 90 response rate at Week 52.

Timeline

Start
2015-05-07
Primary completion
2017-03-14
Completion
2017-05-08

Drugs

EvaluationDrugModalityDoseRoute
Subject Secukinumab Monoclonal antibody 300 mg Subcutaneous

Indications