drugset / Trial / NCT02798211

Study to Evaluate the Safety and Efficacy of Secukinumab 300 mg and 150 mg in Adult Patients With Active Psoriatic Arthritis (PsA) After 16 Weeks of Treatment Compared to Placebo

NCT02798211

Phase 4 Completed 258 enrolled Novartis Pharmaceuticals
RandomizedParallel-groupDouble-blindTreatment

Summary

To demonstrate that the efficacy of secukinumab 300 mg at Week 16 was superior to placebo in adult patients with active PsA based on the proportion of patients achieving an American College of Rheumatology 20 (ACR20) response.

Timeline

Start
2016-06-27
Primary completion
2018-12-05
Completion
2018-12-05

Drugs

EvaluationDrugModalityDoseRoute
Comparator Secukinumab Monoclonal antibody 150 mg Subcutaneous
Comparator Secukinumab Monoclonal antibody 300 mg Subcutaneous

Indications