Methods for treating bleeding disorders using sulfated polysaccharides
    2.
    发明授权
    Methods for treating bleeding disorders using sulfated polysaccharides 有权
    使用硫酸化多糖治疗出血性疾病的方法

    公开(公告)号:US08771973B2

    公开(公告)日:2014-07-08

    申请号:US13111746

    申请日:2011-05-19

    Inventor: Kirk W. Johnson

    Abstract: Methods for treating bleeding disorders using non-anticoagulant sulfated polysaccharides (NASPs) as procoagulants are disclosed. NASPs can be administered as single agents, or in combination with one another, or, with other medications (such as factors VII, VIII and IX) to promote hemostasis. In particular, the use of NASPs in treatment of bleeding disorders, including congenital coagulation disorders, acquired coagulation disorders, and trauma induced hemorrhagic conditions is described.

    Abstract translation: 公开了使用非抗凝血硫酸多糖(NASP)作为促凝剂治疗出血性疾病的方法。 NASP可作为单一药物或彼此组合施用,或与其它药物(如因子VII,VIII和IX)一起施用以促进止血。 特别地,描述了使用NASP治疗出血性疾病,包括先天性凝血障碍,获得性凝血障碍和创伤诱导的出血性病症。

    Methods for Treating Bleeding Disorders Using Sulfated Polysaccharides
    4.
    发明申请
    Methods for Treating Bleeding Disorders Using Sulfated Polysaccharides 有权
    使用硫酸化多糖治疗出血障碍的方法

    公开(公告)号:US20110237512A1

    公开(公告)日:2011-09-29

    申请号:US12893798

    申请日:2010-09-29

    Inventor: Kirk W. Johnson

    Abstract: Methods for treating bleeding disorders using non-anticoagulant sulfated polysaccharides (NASPs) as procoagulants are disclosed. NASPs can be administered as single agents, or in combination with one another, or with other medications (such as factors VII, VIII and IX) to promote hemostasis. In particular, the use of NASPs in treatment of bleeding disorders, including congenital coagulation disorders, acquired coagulation disorders, and trauma induced hemorrhagic conditions is described.

    Abstract translation: 公开了使用非抗凝血硫酸多糖(NASP)作为促凝剂治疗出血性疾病的方法。 NASP可以作为单一药剂或彼此组合施用,或与其它药物(例如因子VII,VIII和IX)一起施用以促进止血。 特别地,描述了使用NASP治疗出血性疾病,包括先天性凝血障碍,获得性凝血障碍和创伤诱导的出血性病症。

    NOVEL ALBUMIN-FREE FACTOR VIII FORMULATIONS
    6.
    发明申请
    NOVEL ALBUMIN-FREE FACTOR VIII FORMULATIONS 有权
    新型无氨基因因子VIII配方

    公开(公告)号:US20080176791A1

    公开(公告)日:2008-07-24

    申请号:US11764770

    申请日:2007-06-18

    Abstract: A Factor VIII composition formulated without albumin, comprising the following formulation excipients in addition to Factor VIII: 4% to 10% of a bulking agent selected from the group consisting of mannitol, glycine and alanine; 1% to 4% of a stabilizing agent selected from the group consisting of sucrose, trehalose, raffinose, and arginine; 1 mM to 5 mM calcium salt; 100 mM to 300 mM NaCl; and a buffering agent for maintaining a pH of approximately between 6 and 8. Alternatively, the formulation can comprise 2% to 6% hydroxyethyl starch; 1% to 4% of a stabilizing agent selected from the group consisting of sucrose, trehalose, raffinose, and arginine; 1 mM to 5 mM calcium salt; 100 mM to 300 mM NaCl; and a buffering agent for maintaining a pH of approximately between 6 and 8. In a further embodiment, the formulation can comprise: 300 mM to 500 mM NaCl; 1% to 4% of a stabilizing agent selected from the group consisting of sucrose, trehalose, raffinose, and arginine; 1 mM to 5 mM calcium salt; and a buffering agent.

    Abstract translation: 不含白蛋白的因子VIII组合物,除了因子VIII外还包含以下制剂赋形剂:4%至10%的选自甘露醇,甘氨酸和丙氨酸的填充剂; 1%至4%的选自蔗糖,海藻糖,棉子糖和精氨酸的稳定剂; 1mM至5mM钙盐; 100mM至300mM NaCl; 以及用于保持约6至8的pH的缓冲剂。或者,制剂可以包含2%至6%的羟乙基淀粉; 1%至4%的选自蔗糖,海藻糖,棉子糖和精氨酸的稳定剂; 1mM至5mM钙盐; 100mM至300mM NaCl; 以及用于保持约6至8的pH的缓冲剂。在另一个实施方案中,制剂可以包含:300mM至500mM NaCl; 1%至4%的选自蔗糖,海藻糖,棉子糖和精氨酸的稳定剂; 1mM至5mM钙盐; 和缓冲剂。

    Albumin-free factor VIII formulations
    7.
    发明授权
    Albumin-free factor VIII formulations 有权
    无白蛋白因子VIII配方

    公开(公告)号:US07247707B2

    公开(公告)日:2007-07-24

    申请号:US11434634

    申请日:2006-05-15

    Abstract: A Factor VIII composition formulated without albumin, comprising the following formulation excipients in addition to Factor VIII: 4% to 10% of a bulking agent selected from the group consisting of mannitol, glycine and alanine; 1% to 4% of a stabilizing agent selected from the group consisting of sucrose, trehalose, raffinose, and arginine; 1 mM to 5 mM calcium salt; 100 mM to 300 mM NaCl; and a buffering agent for maintaining a pH of approximately between 6 and 8. Alternatively, the formulation can comprise 2% to 6% hydroxyethyl starch; 1% to 4% of a stabilizing agent selected from the group consisting of sucrose, trehalose, raffinose, and arginine; 1 mM to 5 mM calcium salt; 100 mM to 300 mM NaCl; and a buffering agent for maintaining a pH of approximately between 6 and 8. In a further embodiment, the formulation can comprise: 300 mM to 500 mM NaCl; 1% to 4% of a stabilizing agent selected from the group consisting of sucrose, trehalose, raffinose, and arginine; 1 mM to 5 mM calcium salt; and a buffering agent.

    Abstract translation: 不含白蛋白的因子VIII组合物,除了因子VIII外还包含以下制剂赋形剂:4%至10%的选自甘露醇,甘氨酸和丙氨酸的填充剂; 1%至4%的选自蔗糖,海藻糖,棉子糖和精氨酸的稳定剂; 1mM至5mM钙盐; 100mM至300mM NaCl; 以及用于保持约6至8的pH的缓冲剂。或者,制剂可以包含2%至6%的羟乙基淀粉; 1%至4%的选自蔗糖,海藻糖,棉子糖和精氨酸的稳定剂; 1mM至5mM钙盐; 100mM至300mM NaCl; 以及用于保持约6至8的pH的缓冲剂。在另一个实施方案中,制剂可以包含:300mM至500mM NaCl; 1%至4%的选自蔗糖,海藻糖,棉子糖和精氨酸的稳定剂; 1mM至5mM钙盐; 和缓冲剂。

Patent Agency Ranking