Phase 3 study to evaluate safety and effectiveness of oral Apremilast (CC-10004) in patients with Psoriatic Arthritis and a psoriasis lesion

Update Il y a 4 ans
Reference: EUCTR2010-019941-24

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, depending on the method of ascertainment, occurs in 6 to 39% of patients with psoriasis