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Bringing new therapy options to the hemophilia community

机译:为血友病社区带来新的治疗选择

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摘要

In patients with hemophilia A, outcomes have improved dramatically over the last few decades due to several advances in care, including the availability of factor VIII (FVIII) concentrates. Current research has focused on enhancing the properties of FVIII concentrates and other coagulation factor products using recombinant DNA technology. However, there are several challenges to the development of new products for hemophilia patients, including the relative rarity of the disease, rapidly evolving standards of care, and the varying requirements of regulatory authorities around the world. In the development of two innovative coagulation factor products (recombinant single-chain factor VIII [rVIII-SingleChain] and a recombinant fusion protein linking coagulation factor VIIa with albumin [rVIIa-FP]), these issues have been addressed through novel clinical trial designs, including an ongoing three-part study evaluating the safety, efficacy, and pharmacokinetics of rVIII-SingleChain in patients with severe hemophilia A, and a randomized, placebo-controlled, dose-escalation study of rVIIa-FP in healthy volunteers. The design of these trials is intended to answer as many important clinical questions as possible while limiting the burden on hemophilia patients. ? 2013 Elsevier Ltd.
机译:在A型血友病患者中,由于护理方面的一些进步,包括可获得的VIII因子(FVIII)浓缩物,在过去的几十年中,结局有了显着改善。当前的研究集中在使用重组DNA技术提高FVIII浓缩物和其他凝血因子产品的性能上。但是,为血友病患者开发新产品面临一些挑战,包括疾病的相对稀有性,护理标准的迅速发展以及全球监管机构的不同要求。在开发两种创新性凝血因子产品(重组单链因子VIII [rVIII-SingleChain]和将凝血因子VIIa与白蛋白[rVIIa-FP]连接的重组融合蛋白)时,这些问题已通过新颖的临床试验设计得以解决,包括一项正在进行的三部分研究,该研究评估rVIII-SingleChain在重度A型血友病患者中的安全性,疗效和药代动力学,以及一项针对健康志愿者的rVIIa-FP随机,安慰剂对照,剂量递增研究。这些试验的设计旨在回答尽可能多的重要临床问题,同时限制血友病患者的负担。 ? 2013爱思唯尔有限公司

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