Ontology highlight
ABSTRACT: Background
The efficacy and safety of apremilast were assessed in patients with psoriatic arthritis (PsA) in three phase III clinical trials with similar designs (PALACE 1, 2, and 3).Methods
Following a 24-week, randomized (1:1:1 to apremilast 30 mg twice daily, 20 mg twice daily, or placebo), double-blind phase and a 28-week blinded active treatment phase, patients could receive apremilast in open-label extension studies for an additional 4 years. Eligible adult patients had active PsA for ≥ 6 months and three or more swollen joints and three or more tender joints despite prior treatment with disease-modifying anti-rheumatic drugs.Results
A total of 1493 randomized patients received one or more doses of study medication (placebo: n = 496; apremilast 30 mg twice dai
SUBMITTER: Kavanaugh A
PROVIDER: S-EPMC6509758 | biostudies-literature | 2019 May
REPOSITORIES: biostudies-literature