The objective of this study was to evaluate the efficacy and safety of adalimumab 40 mg administered every other week (eow) subcutaneously (SC) compared to placebo for 12 weeks followed by open label (OL) safety and efficacy assessments in participants with non-ankylosing spondylitis (AS), non-psoriatic arthritis (PsA) active peripheral spondyloarthritis (SpA) who have had an inadequate response to \>= 2 non-steroidal anti-inflammatory drugs (NSAIDs), or are intolerant to, or have a contraindication for, NSAIDs.
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Percentage of Responders According to the Composite Peripheral SpA Response Criteria (PSpARC 40) at Week 12
Timeframe: Week 12
Number of Participants With Adverse Events
Timeframe: Baseline (day of first study drug administration) through Week 156 plus 70 days