A Phase 3, Multicenter, Randomized, Double-blind, Placebo-controlled, Parallel-group, Efficacy and Safety Study of Two Doses of Apremilast (CC-10004) in Subjects with Active Psoriatic Arthritis

Mise à jour : Il y a 4 ans
Référence : EUCTR2010-018385-23

Femme et Homme

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Extrait

To evaluate the clinical efficacy of 2 doses of apremilast (20 mg or 30 mg orally twice per day [BID]), compared with placebo, on the signs and symptoms of psoriatic arthritis (PsA) after 24 weeks’ administration


Critère d'inclusion

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