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A Study Evaluating the Safety and Efficacy of Upadacitinib in Adults With Active Ankylosing Spondylitis (SELECT-AXIS 1)

NCT03178487 PHASE2 COMPLETED Results posted

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 sponsorAbbVie
PhasePHASE2
StatusCOMPLETED
Enrolment187
Start dateTue Oct 24 2017 00:00:00 GMT+0000 (Coordinated Universal Time)
CompletionThu Feb 17 2022 00:00:00 GMT+0000 (Coordinated Universal Time)

Conditions

Interventions

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