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Budget Impact of Adding Vedolizumab to a Health Plan Formulary as Another First-Line Biologic Option for Ulcerative Colitis and Crohns Disease

机译:将维多珠单抗作为溃疡性结肠炎和克罗恩氏病的另一种第一线生物选择加入健康计划的预算影响

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摘要

BackgroundVedolizumab is a biologic drug approved by the US Food and Drug Administration (FDA) for the treatment of adults with moderately to severely active Crohn's disease (CD) or ulcerative colitis (UC) who have had inadequate response to, lost response to, or were intolerant of immunomodulators or tumor necrosis factor (TNF) blocker therapy, or who had an inadequate response with, were intolerant to, or demonstrated dependence on corticosteroid therapy. The biologics approved by the FDA for CD and/or UC include adalimumab, infliximab, golimumab, certolizumab, and ustekinumab.
机译:背景Vedolizumab是一种经美国食品和药物管理局(FDA)批准用于治疗中度至重度活动性克罗恩氏病(CD)或溃疡性结肠炎(UC)的成年人,这些患者对反应不足,反应迟钝或无反应的成年人对免疫调节剂或肿瘤坏死因子(TNF)阻滞剂治疗不耐受,或对皮质类固醇治疗反应不足,不耐受或证明依赖皮质类固醇治疗。 FDA批准的CD和/或UC生物制剂包括阿达木单抗,英夫利昔单抗,戈利木单抗,西妥珠单抗和乌斯替单抗。

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