Certolizumab pegol: a polyethylene glycolated Fab' fragment of humanized anti-tumor necrosis factor alpha monoclonal antibody for the treatment of Crohn's disease.

Danial E Baker
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Abstract

Certolizumab pegol offers an alternative to the other biologic response modifiers for the treatment of Crohn's disease. Results from phase II dose-ranging studies were mixed because a number of the studies had high placebo response rates and a large number of patients with low C-reactive protein (CRP) levels. Phase III clinical trials have demonstrated induction of clinical responses and maintenance of remission for patients independent of whether baseline CRP levels were normal or elevated. Although concomitant immune suppressants reduced the immunogenicity, there were no differences in clinical response at 6 to 12 months for patients receiving immunosuppressives compared with those not receiving concomitant medications. There is also evidence that patients treated earlier in the course of disease may have improved responses and that patients who have lost response to infliximab will respond to certolizumab pegol.

Certolizumab pegol:用于治疗克罗恩病的人源抗肿瘤坏死因子α单克隆抗体的聚乙烯糖化Fab'片段。
Certolizumab pegol为治疗克罗恩病提供了一种替代其他生物反应调节剂的方法。II期剂量范围研究的结果好坏参半,因为许多研究的安慰剂反应率很高,而且大量患者的c反应蛋白(CRP)水平较低。III期临床试验已经证明,无论基线CRP水平是正常还是升高,患者都能诱导临床反应并维持缓解。虽然同时使用免疫抑制剂降低了免疫原性,但与未同时使用药物的患者相比,接受免疫抑制剂的患者在6至12个月的临床反应没有差异。也有证据表明,在病程早期接受治疗的患者可能有改善的反应,对英夫利昔单抗失去反应的患者将对certolizumab pegol有反应。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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