首页> 美国卫生研究院文献>Dermatology and Therapy >Biosimilar Drugs for Psoriasis: Principles Present and Near Future
【2h】

Biosimilar Drugs for Psoriasis: Principles Present and Near Future

机译:银屑病生物仿制药:原则现在和不久的将来

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Psoriasis is a chronic, inflammatory, lifelong disease with a high prevalence (afflicting approximately 1–5% of the population worldwide) and is associated with significant morbidity. The introduction of biologic therapies has improved the management of this disease. Multiple biologic medicines that block cytokine signaling, including tumor necrosis factor (TNF) antagonists (adalimumab, etanercept, and infliximab) and inhibitors of interleukin (IL)-17 (brodalumab, ixekizumab, and secukinumab), IL-23 (guselkumab), or IL-12/23 (ustekinumab), are approved for the treatment of psoriasis. Despite the clinical benefits associated with use of biologics in psoriasis, many patients are not treated with biologic therapy, and access to treatment may be limited for various reasons, such as high treatment costs. Patents for many biologics have expired or will soon expire, and biosimilar versions of these agents are available or in development. A biosimilar is a biological product that is highly similar to an approved biologic (i.e., originator or reference) product, and has no clinically meaningful differences in safety, purity, or potency when compared with the reference product. Biosimilars may offer less expensive treatment options for patients with psoriasis; they also may increase access to and address problems with underutilization of biologic therapy. Biosimilar development and approval follows a well-regulated process in many countries, with guidelines developed by the European Medicines Agency, US Food and Drug Administration, and World Health Organization. Currently, several anti-TNF biosimilars are available for use in patients with psoriasis, and other monoclonal antibodies are in development. This review provides dermatologists and those who treat and/or manage psoriasis with a working knowledge of the scientific principles of biosimilar development and approval. It also examines real-world experience with biosimilars available for or used in dermatology that will enable physicians to make informed treatment decisions for their patients with psoriasis.>Funding: Pfizer Inc.
机译:牛皮癣是一种慢性,炎症性,终生性疾病,患病率很高(折磨全世界约1–5%的人口),并且与明显的发病率相关。生物疗法的引入改善了该疾病的管理。多种可阻止细胞因子信号传导的生物药物,包括肿瘤坏死因子(TNF)拮抗剂(阿达木单抗,依那西普和英夫利昔单抗)和白介素(IL)-17抑制剂(溴达鲁单抗,依克珠单抗和苏金单抗),IL-23(guselkumab)或IL-12 / 23(ustekinumab)被批准用于治疗牛皮癣。尽管在牛皮癣中使用生物制剂具有临床益处,但许多患者仍未接受生物疗法治疗,并且由于各种原因(例如高昂的治疗费用)可能无法获得治疗。许多生物制剂的专利已经过期或即将到期,并且这些制剂的生物仿制药已经上市或正在开发中。生物仿制药是一种生物产品,与经批准的生物仿制药(即原始产品或参考产品)高度相似,并且与参考产品相比,在安全性,纯度或效力方面没有临床上有意义的差异。生物仿制药可能为牛皮癣患者提供较便宜的治疗选择;它们还可能增加获得和解决生物疗法利用不足的问题的机会。生物仿制药的开发和批准遵循许多国家的严格监管程序,并由欧洲药品管理局,美国食品药品监督管理局和世界卫生组织制定了指南。当前,几种抗TNF生物仿制药可用于牛皮癣患者,并且其他单克隆抗体正在开发中。这篇综述为皮肤科医生和那些治疗和/或管理牛皮癣的人提供了有关生物仿制药开发和批准的科学原理的工作知识。它还研究了皮肤病学可用的或在皮肤病学中使用的生物仿制药的现实经验,这些经验将使医生能够为牛皮癣患者做出明智的治疗决策。>资金:辉瑞公司。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号