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Celgene Corporation improvements on Phase II research evaluating apremilast in psoriatic arthritis patients Celgene Company announced that updated results of a phase II, multi-middle, randomized, double-blind, placebo-controlled, three-arm study of apremilast in adult individuals with psoriatic arthritis were presented today in the American College of Rheumatology 2009 annual conference in Philadelphia, PA. CC-10004-PSA-001 sought to determine the efficacy and safety of apremilast in 204 sufferers at two different dosing regimens – 20mg two times per time or 40mg once per day in comparison to placebo after 12 weeks, with 126 sufferers participating in an expansion of the study for yet another 12 weeks is propranolol an otc drug .

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