drugset / Trial / NCT02474069

Secukinumab Dosage Optimisation in Partial Responders With Moderate to Severe Plaque-type Psoriasis

NCT02474069

Phase 3 Completed 772 enrolled Novartis Pharmaceuticals
RandomizedParallel-groupDouble-blindTreatment

Summary

This study is designed to support the optimal use of secukinumab by providing data to refine guidance on dosing flexibility in patients with psoriasis. The purpose of the study is to explore the effects of dosage interval shorteng to achieve PASI 90 at week 32 for patients who had less than almost clear skin at week 16.

Timeline

Start
2015-02-08
Primary completion
2016-09-15
Completion
2016-09-15

Drugs

EvaluationDrugModalityDoseRoute
Comparator Secukinumab Monoclonal antibody 300 mg

Indications