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首页> 外文期刊>The Lancet >Efficacy and safety of biosimilar CT-P13 compared with originator infliximab in patients with active Crohn's disease: an international, randomised, double-blind, phase 3 non-inferiority study
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Efficacy and safety of biosimilar CT-P13 compared with originator infliximab in patients with active Crohn's disease: an international, randomised, double-blind, phase 3 non-inferiority study

机译:生物仿制性CT-P13的疗效和安全性与患有活跃的Crohn疾病患者的发起者英夫利昔单抗:国际,随机,双盲,第3期非劣级研究

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摘要

Background The infliximab biosimilar CT-P13 was approved for use in Crohn's disease after clinical comparison with originator infliximab in ankylosing spondylitis and rheumatoid arthritis; however, concerns about such indication extrapolation have been expressed. This study investigated whether CT-P13 is non-inferior to infliximab in patients with Crohn's disease who were naive to biological therapy.
机译:背景技术incriximab BioSimilar CT-P13在临床比较后批准用于Crohn疾病,临床比较脊柱型脊柱炎和类风湿性关节炎的发芽; 然而,已经表达了对这种指示外推的担忧。 本研究调查了CT-P13是否对克罗恩病的患者对英夫利昔单抗非逊色于生物治疗。

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