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Multicenter, Double-blind, Randomized, Placebo-controlled, Parallel Group Study to Evaluate the Efficacy, Safety and Pharmacokinetics of Apremilast in Children From 5 to Less Than 18 Years of Age With Active Juvenile Psoriatic Arthritis (PEAPOD)","PEAPOD","Inclusion Criteria:\n\n* Male or Female participants 5 to \\\u003C 18 years of age at the time of randomization.\n* Participant must have a confirmed diagnosis of juvenile psoriatic arthritis (JPsA) according to the International League of Associations for Rheumatology (ILAR) Edmonton Revision (Petty, 2001) classification criteria of at least 6 months duration:\n\n  * Arthritis and psoriasis, OR\n  * Arthritis with at least 2 of the following:\n  * Dactylitis\n  * Nail pitting or onycholysis\n  * Psoriasis in a first-degree relative\n* Active disease: at least 3 active joints.\n* Inadequate response (at least 2 months) or intolerance to ≥ 1 disease-modifying anti-rheumatic drugs (DMARD), (which may include methotrexate \\[MTX\\] or biologic agents).\n\nExclusion Criteria:\n\n* Exclusions per ILAR Edmonton Revision (Edmonton, 2001) criteria for JPsA include:\n\n  * Arthritis in an HLA-B27-positive male with arthritis onset after 6 years of age\n  * Ankylosing spondylitis, sacroiliitis with inflammatory bowel disease, Reiter's syndrome, acute anterior uveitis, or a history of one of these disorders in a first-degree relative\n  * History of IgM rheumatoid factor on at least 2 occasions at least 3 months apart\n  * Presence of systemic juvenile idiopathic arthritis (JIA).\n* Rheumatic autoimmune disease other than psoriatic arthritis (PsA), including, but not limited to: systemic lupus erythematosus, mixed connective tissue disease, scleroderma, polymyositis, or fibromyalgia.\n* Prior history of or current inflammatory joint disease other than PsA (eg, gout, reactive arthritis, rheumatoid arthritis, ankylosing spondylitis, Lyme disease).","ALL","5 Years","17 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