An Efficacy and Safety Study of Ustekinumab in Participants With Active Nonradiographic Axial Spondyloarthritis
Stopped This study was stopped because ustekinumab did not achieve key endpoints in a related study. The safety profile was consistent with past ustekinumab studies.
Conditions
- Nonradiographic Axial Spondylitis, Ankylosing
Interventions
- DRUG: Group 1: Placebo
- DRUG: Group 2: Ustekinumab 45 mg
- DRUG: Group 3: Ustekinumab 90 mg
Sponsor
Janssen Research & Development, LLC