首页> 外国专利> MEDIUM MOLECULAR WEIGHT HEPARIN FOR TREATMENT AND SECONDARY PREVENTION OF ISCHEMIC STROKE

MEDIUM MOLECULAR WEIGHT HEPARIN FOR TREATMENT AND SECONDARY PREVENTION OF ISCHEMIC STROKE

机译:中分子量肝素用于缺血性卒中的治疗和二次预防

摘要

It is the thorough consistency between the pathophysiological pattern of ischemic stroke and the haemostaseological characteristics of LD Heparin 10,5 Kd that confer specificity to the pertinent patent claim.In particular it is specific role of Tissue factor (TF) and its complex with Factor Vila respectively trigging off cerebral thrombogenesis that condition the rationale of LD Heparin in ischemic stroke. It is the TF/F Vila - complex that makes up the adequate substrate for LD Heparin which is rather resistant to the classical antithrombin-mediated influence but primarily responsive to Tissue Factor Pathway Inhibitor (TFPI). Its extraordinary release on LD Heparin in which LMWH (Enoxaparin) is exceeded threefold constitutes the rationale of striking out on the new indication of stroke.The TFPI-dependent impact is safeguarded by the controlled curtailment of anti-factor Xa activity as permissive for the inhibition of TF/F VIIa, the ratios of activities between TFPI and anti-factor Xa as expressed in the AUC's of both heparins differing threefold either.;It is not only that disease-centered antithrombotic effect but also the way how the risk of bleeding is tackled in general in which LD Heparin contrasts with all others in its class: Owing to the "double truncation" of the molecular spectrum i.e. through the curtailment of its low and very long molecular species major sources of bleeding are excluded.The inventory of auxiliary properties in particular the adequate pharmacokinetics, the trimmed peak blood levels, the lack of plasmatic accumulation in age-dependent decline of renal function and renal insufficiency, the availability of valid and sensitive monitoring (APTT), and last but not least the prompt and complete reversibility of the anticoagulatory effect as contrasted to LMWH substantiates the indication-specific profile.On the whole the multipronged refinements of LD Heparin are aiming at a heightened benefit-risk-ratio ("therapeutic window") which takes specific shape in cerebral thrombosis.The patent claim associated reads: LD Heparin 10,5 Kd (10-11Kd) for the treatment and secondary prevention of ischemic stroke.
机译:缺血性中风的病理生理模式与LD肝素10,5 Kd的血液流变学特征之间的彻底一致性赋予了相关专利权利要求特异性。特别是组织因子(TF)及其与因子VIIa的复合物分别触发脑血栓形成的特定作用决定了缺血性卒中中LD肝素的基本原理。正是TF / F Vila-复合物构成了LD肝素的适当底物,该底物对经典的抗凝血酶介导的影响具有相当的抵抗力,但主要对组织因子途径抑制剂(TFPI)产生反应。它在LD肝素中的非凡释放量(其中LMWH(依诺肝素)超过三倍)构成了中风新适应症的基本原理。TFPI依赖的影响可通过控制性削减抗因子Xa活性来保证,以抑制TF / F VIIa,两种肝素的AUC中表达的TFPI和抗因子Xa之间的活性比值相差三倍LD肝素不仅与以疾病为中心的抗血栓形成作用有关,而且还与如何解决出血风险的方法形成了鲜明对比:LD肝素与同类中的所有其他药物形成对比:由于分子谱的“双重截断”,即通过排除了减少其低分子和非常长的分子物种出血的主要来源。辅助特性的清单,尤其是足够的药代动力学,降低的峰值血药浓度,年龄依赖性肾功能下降和肾功能不全所致血浆缺乏积累,有效而敏感的监测(APTT)的可用性,以及最后但并非最不重要的与LMWH相比,抗凝作用的迅速和完全可逆性证实了适应症的特异性。总体上,LD肝素的多管齐下精炼旨在提高脑血栓形成中特定形状的获益风险比(“治疗窗口”)。相关专利权利要求为:LD肝素10,5 Kd(10-11Kd),用于治疗和继发预防缺血性中风。

著录项

  • 公开/公告号EP3581189A1

    专利类型

  • 公开/公告日2019-12-18

    原文格式PDF

  • 申请/专利权人 FYTAGORAS B.V.;

    申请/专利号EP20180177815

  • 发明设计人 WELZEL DIETER;

    申请日2018-06-14

  • 分类号A61K31/727;A61P9/10;A61P7/02;

  • 国家 EP

  • 入库时间 2022-08-21 11:39:19

相似文献

  • 专利
  • 外文文献
  • 中文文献
获取专利

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