Psoriatic Arthritis Clinical Trial
Official title:
A Phase 4, Multicenter, Single-Arm, Open-Label Study to Evaluate the Impact of Apremilast (CC-10004) on MRI Outcomes in Subjects With Active Psoriatic Arthritis
This study is designed to assess the efficacy of apremilast, either in monotherapy or with stable methotrexate, on imaging outcomes in adults with active psoriatic arthritis with less than 5 years of disease duration (since diagnosis), and who are naïve to biologic therapies.
This study consists of 3 phases: - Screening Phase - up to 4 weeks - Single-arm, Open-label Treatment Phase - Weeks 0 to 48 - Participants will receive apremilast 30 mg BID (after a 5-day titration period) for the entire duration of this phase. - MRI of the most affected hand and whole body MRI (WB-MRI) will be performed at weeks 0, 24, and 48. - The hand with the greater inflammatory burden of swollen joints and/or dactylitis will be considered as the most affected hand. If both hands are equally affected, the dominant hand will be designated as the index hand. - Observational Follow-up Phase - 4 Weeks - All participants who complete the study or discontinue early will participate in the 4-week Post-Treatment Observational Follow-up Phase. ;
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