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14,15 In brief, both were phase III multicenter trials, double-blind and placebo-controlled to 16 weeks, assessing the efficacy and safety of bimekizumab in patients with active PsA who were bDMARD-nave or TNFi-IR

such compositions are prepared either as liquid solutions or suspensions, however solid forms such as tablets, pills, powders and the like are also contemplated

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A conditional logistic regression was performed using the middle 25%-75% category as reference, adjusting for age, education level, traditional risk factors, and migraine with aura