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A Study Evaluating the Safety and Efficacy of Upadacitinib in Adults With Active Ankylosing Spondylitis (SELECT-AXIS 1)
The purpose of this study is to evaluate the safety and efficacy of upadacitinib in participants with active ankylosing spondylitis (AS) who have had an inadequate response to at least 2 non-steroidal anti-inflammatory drugs (NSAIDs) or intolerance to or a contraindication for NSAIDs, and who are naïve to biologic disease-modifying anti-rheumatic drugs (bDMARD).
Details
| Lead sponsor | AbbVie |
|---|---|
| Phase | PHASE2 |
| Status | COMPLETED |
| Enrolment | 187 |
| Start date | Tue Oct 24 2017 00:00:00 GMT+0000 (Coordinated Universal Time) |
| Completion | Thu Feb 17 2022 00:00:00 GMT+0000 (Coordinated Universal Time) |
Conditions
- Ankylosing Spondylitis (AS)
Interventions
- Upadacitinib
- Placebo
Countries
Italy, Finland, Japan, Poland, South Korea, Croatia, Denmark, New Zealand, Netherlands, Belgium, Sweden, Portugal, United States, France, Hungary, Canada, Spain, United Kingdom, Germany, Australia, Czechia