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
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Comparator | Secukinumab | Monoclonal antibody | 150 mg | Subcutaneous |
| Comparator | Secukinumab | Monoclonal antibody | 300 mg | Subcutaneous |