ERGONOMIC FOOTWEAR AND INSOLE, AND METHOD OF SELECTING SAME
    1.
    发明申请
    ERGONOMIC FOOTWEAR AND INSOLE, AND METHOD OF SELECTING SAME 审中-公开
    ERGONOMIC FOOTWEAR AND INSOLE,AND METHOD OF SELECTING SAME

    公开(公告)号:WO2006088902A2

    公开(公告)日:2006-08-24

    申请号:PCT/US2006/005235

    申请日:2006-02-14

    Abstract: The present invention provides individual solutions to workplace fatigue and stress by determining the specific support needed for each individual. Specifically, the present invention defines and utilizes an ergonomic interaction factor to enable selection of a proper fitting shoe. Such selection occurs in one embodiment by dividing a person's weight by the contact area of the bottom of their feet.

    Abstract translation: 本发明通过确定每个人所需的具体支持,为工作场所的疲劳和压力提供单独的解决方案。 具体地说,本发明定义并利用符合人机工程学的相互作用因子,以使得能够选择合适的配合鞋。 在一个实施例中,通过将人的重量除以其脚底部的接触面积来进行这种选择。

    STAIR CLIMBING WHEELCHAIR
    2.
    发明申请
    STAIR CLIMBING WHEELCHAIR 审中-公开
    平静的轮椅

    公开(公告)号:WO1996019374A1

    公开(公告)日:1996-06-27

    申请号:PCT/US1995016743

    申请日:1995-12-19

    Abstract: In order to provide safe and effective surface climbing vehicles, the vehicle includes a base (56) for supporting a platform (57) to be maintained in a generally horizontal orientation. The mechanism (98) automatically raises and lowers the platform as the vehicle is descending or climbing the surface, respectively, in order to maintain the platform in the generally horizontal orientation. With this arrangement, the vehicle further includes a pair of endless belts (1) normally to be maintained in driving engagement with the surface in a manner to conform to the surface during climbing and descending.

    Abstract translation: 为了提供安全有效的表面爬坡车辆,车辆包括用于支撑平台(57)的基座(56),以保持大致水平的方向。 机构(98)分别在车辆下降或爬升时自动升高和降低平台,以便将平台保持在大致水平的方向。 通过这种布置,车辆还包括一对环形皮带(1),通常在爬升和下降过程中保持与表面的驱动接合。

    STABLE PH OPTIMIZED FORMULATION OF A MODIFIED ANTIBODY
    4.
    发明申请
    STABLE PH OPTIMIZED FORMULATION OF A MODIFIED ANTIBODY 审中-公开
    稳定的PH优化配制的改良抗体

    公开(公告)号:WO2004019861A2

    公开(公告)日:2004-03-11

    申请号:PCT/US2003/024414

    申请日:2003-08-05

    IPC: A61K

    CPC classification number: C07K16/241 A61K39/39591 C07K2317/24

    Abstract: The present invention is directed to stable formulations of modified antibodies, each comprising an antibody fragment in an aqueous solution covalently attached to at least one nonproteinaceous polymer, such as @>lC(ethyleneglycol), through 0 succinimide moiety. CDP870 is an example of one such modified antibody. The formulations of the present invention include 0 buffer that maintains the solution at 0 pH of 3.5 to about 6, wherein all components of the modified antibody, including 0 succinimide ring of the succinimide moiety, are stable.

    Abstract translation: 本发明涉及修饰抗体的稳定制剂,其各自包含在共价连接至至少一种非蛋白性聚合物如@> 1C(乙二醇)至0琥珀酰亚胺部分的水溶液中的抗体片段。 CDP870是一种这样的修饰抗体的实例。 本发明的制剂包括将溶液保持在pH为3.5至约6的溶液的0缓冲液,其中修饰的抗体包括琥珀酰亚胺部分的琥珀酰亚胺环的所有组分都是稳定的。

    FORMULATIONS OF MODIFIED ANTIBODIES AND METHODS OF MAKING THE SAME
    5.
    发明申请
    FORMULATIONS OF MODIFIED ANTIBODIES AND METHODS OF MAKING THE SAME 审中-公开
    修饰的抗体的制备方法和制备方法

    公开(公告)号:WO2004019860A2

    公开(公告)日:2004-03-11

    申请号:PCT/US2003/024413

    申请日:2003-08-05

    IPC: A61K

    CPC classification number: C07K16/1289 A61K47/60 C07K2317/55

    Abstract: The present invention is directed to novel formulations of modified antibodies and to methods of producing the same. The modified antibodies formulated according to the present invention each comprise an antibody fragment covalently attached to at least one nonproteinaceous polymer, such as poly(ethyleneglycol). CDP870 is an example of one such modified antibody, a therapeutic modified antibody. One method disclosed herein involves the removal from a solution of the modified antibody of molecules capable of adversely affecting the stability or solubility of the modified antibody after lyophilization (e.g., by dialysis or diafiltration), followed by lyophilization of the modified antibody. Another method involves concentration of a modified antibody solution by equilibrium dialysis. The methods of the present invention can be used to produce formulations suitable for use in subcutaneous and parenteral injection, including high concentration formulations.

    Abstract translation: 本发明涉及修饰抗体的新制剂及其制备方法。 根据本发明配制的修饰的抗体各自包含与至少一种非蛋白质聚合物如聚(乙二醇)共价连接的抗体片段。 CDP870是一种这样的修饰抗体(治疗性修饰的抗体)的实例。 本文公开的一种方法包括从修饰的抗体的溶液中除去能够不利地影响修饰的抗体在冻干(例如通过透析或渗滤)之后的稳定性或溶解度,然后冻干修饰的抗体的分子。 另一种方法涉及通过平衡透析浓缩修饰的抗体溶液。 本发明的方法可用于制备适用于皮下和肠胃外注射的制剂,包括高浓度制剂。

    ERGONOMIC FOOTWEAR AND INSOLE, AND METHOD OF SELECTING SAME
    7.
    发明申请
    ERGONOMIC FOOTWEAR AND INSOLE, AND METHOD OF SELECTING SAME 审中-公开
    ERGONOMIC FOOTWEAR AND INSOLE,AND METHOD OF SELECTING SAME

    公开(公告)号:WO2006088902A3

    公开(公告)日:2009-04-30

    申请号:PCT/US2006005235

    申请日:2006-02-14

    Inventor: JOHNSON PAUL R

    Abstract: The present invention provides individual solutions to workplace fatigue and stress by determining the specific support needed for each individual. Specifically, the present invention defines and utilizes an ergonomic interaction factor to enable selection of a proper fitting shoe. Such selection occurs in one embodiment by dividing a person's weight by the contact area of the bottom of their feet.

    Abstract translation: 本发明通过确定每个人所需的具体支持,为工作场所的疲劳和压力提供单独的解决方案。 具体地说,本发明定义并利用符合人机工程学的相互作用因子,以使得能够选择合适的配合鞋。 在一个实施例中,通过将人的重量除以其脚底部的接触面积来进行这种选择。

    STABLE PH OPTIMIZED FORMULATION OF A MODIFIED ANTIBODY
    9.
    发明申请
    STABLE PH OPTIMIZED FORMULATION OF A MODIFIED ANTIBODY 审中-公开
    一种改良抗体的稳定pH优化配方

    公开(公告)号:WO2004019861A3

    公开(公告)日:2004-07-22

    申请号:PCT/US0324414

    申请日:2003-08-05

    CPC classification number: C07K16/241 A61K39/39591 C07K2317/24

    Abstract: The present invention is directed to stable formulations of modified antibodies, each comprising an antibody fragment in an aqueous solution covalently attached to at least one nonproteinaceous polymer, such as @>lC(ethyleneglycol), through 0 succinimide moiety. CDP870 is an example of one such modified antibody. The formulations of the present invention include 0 buffer that maintains the solution at 0 pH of 3.5 to about 6, wherein all components of the modified antibody, including 0 succinimide ring of the succinimide moiety, are stable.

    Abstract translation: 本发明涉及经修饰的抗体的稳定制剂,其各自包含水溶液中的抗体片段,所述抗体片段通过0琥珀酰亚胺部分与至少一种非蛋白质聚合物(例如≥1C(乙二醇))共价连接。 CDP870是这种修饰抗体的一个例子。 本发明的制剂包括使溶液维持在3.5至约6的pH值的缓冲液,其中修饰的抗体的所有组分(包括琥珀酰亚胺部分的0琥珀酰亚胺环)都是稳定的。

    FORMULATIONS OF MODIFIED ANTIBODIES AND METHODS OF MAKING THE SAME
    10.
    发明申请
    FORMULATIONS OF MODIFIED ANTIBODIES AND METHODS OF MAKING THE SAME 审中-公开
    改良抗体的制剂及其制备方法

    公开(公告)号:WO2004019860A3

    公开(公告)日:2004-07-22

    申请号:PCT/US0324413

    申请日:2003-08-05

    CPC classification number: C07K16/1289 A61K47/60 C07K2317/55

    Abstract: The present invention is directed to novel formulations of modified antibodies and to methods of producing the same. The modified antibodies formulated according to the present invention each comprise an antibody fragment covalently attached to at least one nonproteinaceous polymer, such as poly(ethyleneglycol). CDP870 is an example of one such modified antibody, a therapeutic modified antibody. One method disclosed herein involves the removal from a solution of the modified antibody of molecules capable of adversely affecting the stability or solubility of the modified antibody after lyophilization (e.g., by dialysis or diafiltration), followed by lyophilization of the modified antibody. Another method involves concentration of a modified antibody solution by equilibrium dialysis. The methods of the present invention can be used to produce formulations suitable for use in subcutaneous and parenteral injection, including high concentration formulations.

    Abstract translation: 本发明涉及修饰抗体的新型制剂及其制备方法。 根据本发明配制的经修饰的抗体各自包含与至少一种非蛋白质聚合物如聚(乙二醇)共价连接的抗体片段。 CDP870是一种这样的修饰抗体,治疗性修饰抗体的实例。 本文公开的一种方法涉及从冻干(例如通过透析或渗滤)后可以不利地影响修饰抗体的稳定性或溶解度的分子的修饰抗体的溶液中除去,然后冻干该修饰的抗体。 另一种方法包括通过平衡透析浓缩修饰的抗体溶液。 本发明的方法可用于制备适用于皮下和肠胃外注射的制剂,包括高浓度制剂。

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