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Apremilast Pediatric Study in Children With Active Juvenile Psoriatic Arthritis
Apremilast Pediatric Study in Children With Active Juvenile Psoriatic Arthritis
RecruitingPhase 3
Sponsor: Amgen
Conditions: Active Juvenile Psoriatic Arthritis
Interventions: Apremilast, Placebo
Countries: Austria, Belgium, France, Germany, Greece, Italy, Lithuania, Netherlands
The study will aim to estimate the efficacy of apremilast compared with placebo in the treatment of juvenile psoriatic arthritis (JPsA) in pediatric participants 5 to less than 18 years of age.
Eligibility overview
Sex: ALL
Age: 5 Years to 17 Years
Healthy volunteers: No
Study type: INTERVENTIONAL
Eligibility criteria
Inclusion Criteria: * Male or Female participants 5 to \< 18 years of age at the time of randomization. * 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: * Arthritis and psoriasis, OR * Arthritis with at least 2 of the following: * Dactylitis * Nail pitting or onycholysis * Psoriasis in a first-degree relative * Active disease: at least 3 active joints. * Inadequate response (at least 2 months) or intolerance to ≥ 1 disease-modifying anti-rheumatic drugs (DMARD), (which may include methotrexate \[MTX\] or biologic agents). Exclusion Criteria: * Exclusions per ILAR Edmonton Revision (Edmonton, 2001) criteria for JPsA include: * Arthritis in an HLA-B27-positive male with arthritis onset after 6 years of age * 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 * History of IgM rheumatoid factor on at least 2 occasions at least 3 months apart * Presence of systemic juvenile idiopathic arthritis (JIA). * Rheumatic autoimmune disease other than psoriatic arthritis (PsA), including, but not limited to: systemic lupus erythematosus, mixed connective tissue disease, scleroderma, polymyositis, or fibromyalgia. * Prior history of or current inflammatory joint disease other than PsA (eg, gout, reactive arthritis, rheumatoid arthritis, ankylosing spondylitis, Lyme disease).
Locations (45)
- Bregenz, Austria
- Ghent, Belgium
- Liège, Belgium
- Merksem, Belgium
- Bron, France
- Lille, France
- Berlin, Germany
- Dresden, Germany
- Hamburg, Germany
- Sankt Augustin, Germany
- Athens, Greece
- Athens, Greece
- Thessaloniki, Greece
- Chieti, Italy
- Genova, Italy
- Milan, Italy
- Roma, Italy
- Vilnius, Lithuania
- Utrecht, Netherlands
- Krakow, Poland
- Lodz, Poland
- Warsaw, Poland
- Lisbon, Portugal
- Lisbon, Portugal
- Ponte de Lima, Portugal
- Porto, Portugal
- Vila Nova de Gaia, Portugal
- Cluj-Napoca, Romania
- Timișoara, Romania
- Panorama, Western Cape, South Africa
- + 15 more on CT.gov