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Phase 3 study to evaluate safety and effectiveness of oral Apremilast (CC-10004) in patients with Psoriatic Arthritis who have not been previously treated with disease-modifiying antirheumatic drugs

Update Il y a 4 ans
Reference: EUCTR2010-020324-22

Woman and Man

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Extract

The primary objective of the study is to evaluate the clinical efficacy of 2 doses of apremilast (20 mg or 30 mg orally BID) compared with placebo, on the signs and symptoms of psoriatic arthritis (PsA) after 16 weeks' administration

Inclusion criteria

  • Psoriatic arthritis, an inflammatory arthritis that occurs in 6 to 39% of patients with psoriasis

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