DOSAGE REGIMEN FOR THERAPEUTIC METHOD
    1.
    发明公开
    DOSAGE REGIMEN FOR THERAPEUTIC METHOD 审中-公开
    用于治疗方法的剂量方案

    公开(公告)号:EP2968458A1

    公开(公告)日:2016-01-20

    申请号:EP14763641.9

    申请日:2014-03-14

    IPC分类号: A61K38/17 A61K38/16 A61P35/00

    摘要: Disclosed herein is the use of an active agent comprising a peptide derived from atrial natriuretic peptide (ANP) prohormone or a mimetic thereof in the manufacture of a medicament for treating a disease in a subject. The medicament is administered subcutaneously in a multimodal dosage regime comprising at least an initial dosage stage and at least one maintenance dosage stage. The initial dosage stage comprises infusing the active agent at an initial dosage rate for an initial period to achieve a target steady state blood plasma concentration of the active agent or metabolite thereof. The maintenance dosage stage(s) comprise(s) adjusting the dosage rate to a maintenance dosage rate for a maintenance period to substantially maintain said target steady state blood plasma concentration of the active agent or metabolite thereof.

    摘要翻译: 本文公开了包含源自心房利钠肽(ANP)激素原或其模拟物的肽的活性剂在制备用于治疗受试者中的疾病的药物中的用途。 皮下以包含至少初始剂量阶段和至少一个维持剂量阶段的多模式剂量方案施用药物。 初始剂量阶段包括以初始剂量率将活性剂注入初始阶段以实现活性剂或其代谢物的目标稳态血浆浓度。 维持剂量阶段包括将维持剂量率调整为维持剂量率维持一段时间以基本上维持活性剂或其代谢物的所述目标稳态血浆浓度。

    METHOD OF PRODUCING A RECOMBINANT PEPTIDE
    3.
    发明公开
    METHOD OF PRODUCING A RECOMBINANT PEPTIDE 有权
    生产重组肽的方法

    公开(公告)号:EP2839010A4

    公开(公告)日:2015-12-09

    申请号:EP13765199

    申请日:2013-03-19

    摘要: Methods of producing a recombinant peptide, such as vessel dilator peptide (VSDL), are disclosed, including a particular method involving expressing a fusion polypeptide comprising concatemeric repeats of the peptide wherein the peptide is flanked by peptide cleavage sites, and cleaving the fusion polypeptide at the peptide cleavage sites with a cleaving agent(s) so as to release the peptide from the fusion polypeptide. Expression constructs and host cells for producing the fusion polypeptide and purification methods for the recombinant peptide are also disclosed.

    摘要翻译: 公开了生产重组肽如血管扩张肽(VSDL)的方法,包括涉及表达融合多肽的特定方法,所述融合多肽包含所述肽的连续重复序列,其中所述肽侧翼为肽切割位点,并将所述融合多肽切割 具有切割剂的肽切割位点,以便从融合多肽释放肽。 还公开了用于产生融合多肽的表达构建体和宿主细胞以及重组肽的纯化方法。

    THERAPEUTIC METHOD FOR TREATING CONGESTIVE HEART FAILURE
    6.
    发明公开
    THERAPEUTIC METHOD FOR TREATING CONGESTIVE HEART FAILURE 有权
    VSDL ZUR BEHANDLUNG VON AKUTER DEKOMPENSIERTER HERZINSUFFIZIENZ

    公开(公告)号:EP2678025A1

    公开(公告)日:2014-01-01

    申请号:EP11815913.6

    申请日:2011-08-11

    CPC分类号: A61K38/1709 A61K38/2242

    摘要: The present invention relates to a method of treating congestive heart failure (CHF) in a subject comprising administering a peptide derived from atrial natriuretic peptide (ANP) prohormone (eg vessel dilator; VSDL) or a mimetic thereof. In a particular application, the invention provides a method of treating the particular indication known as acute decompensated congestive heart failure (ADCHF). Devices for intravenous or subcutaneous infusion for use in the method of the invention are also disclosed.

    摘要翻译: 本发明涉及一种治疗受试者的充血性心力衰竭(CHF)的方法,包括给予源自心房利尿钠肽(ANP)激素原(例如血管扩张剂; VSDL)或其模拟物的肽。 在特定应用中,本发明提供了治疗被称为急性失代偿性充血性心力衰竭(ADCHF)的特定指征的方法。 还公开了用于本发明方法的用于静脉内或皮下输注的装置。

    DOSAGE REGIMEN FOR THERAPEUTIC METHOD
    9.
    发明公开
    DOSAGE REGIMEN FOR THERAPEUTIC METHOD 审中-公开
    给药时间表对于治疗程序

    公开(公告)号:EP2968458A4

    公开(公告)日:2016-08-24

    申请号:EP14763641

    申请日:2014-03-14

    IPC分类号: A61K38/17 A61K38/16 A61P35/00

    摘要: Disclosed herein is the use of an active agent comprising a peptide derived from atrial natriuretic peptide (ANP) prohormone or a mimetic thereof in the manufacture of a medicament for treating a disease in a subject. The medicament is administered subcutaneously in a multimodal dosage regime comprising at least an initial dosage stage and at least one maintenance dosage stage. The initial dosage stage comprises infusing the active agent at an initial dosage rate for an initial period to achieve a target steady state blood plasma concentration of the active agent or metabolite thereof. The maintenance dosage stage(s) comprise(s) adjusting the dosage rate to a maintenance dosage rate for a maintenance period to substantially maintain said target steady state blood plasma concentration of the active agent or metabolite thereof.