drugset / Trial / NCT03713619

This Was a Study of Efficacy and Safety of Two Secukinumab Dose Regimens in Subjects With Moderate to Severe Hidradenitis Suppurativa (HS).

NCT03713619

Phase 3 Completed 544 enrolled Novartis Pharmaceuticals
RandomizedParallel-groupTriple-blindTreatment

Summary

The purpose of this study was to demonstrate superiority of secukinumab at Week 16, based on Hidradenitis Suppurativa Clinical Response (HiSCR) rates versus placebo, along with the maintenance of efficacy of secukinumab at Week 52 in subjects with moderate to severe HS. Moreover, this study also assessed the safety and tolerability of secukinumab.

Timeline

Start
2019-01-31
Primary completion
2021-10-01
Completion
2022-07-26

Publications

Drugs

EvaluationDrugModalityDoseRoute
Comparator Secukinumab Monoclonal antibody 300 mg Subcutaneous