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公开(公告)号:US20110076273A1
公开(公告)日:2011-03-31
申请号:US12879486
申请日:2010-09-10
IPC分类号: A61K39/395 , A61P35/00
CPC分类号: C07K16/2887 , A61K9/0019 , A61K9/19 , A61K38/47 , A61K39/3955 , A61K45/06 , A61K47/10 , A61K47/183 , A61K47/20 , A61K47/22 , A61K47/26 , A61K47/42 , A61K2039/505 , C07K16/3061 , C07K2317/21 , C07K2317/24 , C07K2317/734 , C07K2317/94
摘要: The present invention relates to a highly concentrated, stable pharmaceutical formulation of a pharmaceutically active anti-CD20 antibody, such as e.g. Rituximab, Ocrelizumab, or HuMab , or a mixture of such antibody molecules for subcutaneous injection. In particular, the present invention relates to formulations comprising, in addition to a suitable amount of the anti-CD20 antibody, an effective amount of at least one hyaluronidase enzyme as a combined formulation or for use in form of a co-formulation. The said formulations comprise additionally at least one buffering agent, such as e.g. a histidine buffer, a stabilizer or a mixture of two or more stabilizers (e.g. a saccharide, such as e.g. α,α-trehalose dihydrate or sucrose, and optionally methionine as a second stabilizer), a nonionic surfactant and an effective amount of at least one hyaluronidase enzyme. Methods for preparing such formulations and their uses thereof are also provided.
摘要翻译: 本发明涉及药物活性抗CD20抗体的高浓度,稳定的药物制剂,例如, 利妥昔单抗,奥昔布单抗或HuMab
,或用于皮下注射的这种抗体分子的混合物。 特别地,本发明涉及除了合适量的抗CD20抗体外,还包含有效量的至少一种作为组合制剂的透明质酸酶或用于共同制剂形式的制剂。 所述制剂还包含至少一种缓冲剂,例如, 组氨酸缓冲液,稳定剂或两种或更多种稳定剂的混合物(例如糖,例如α,α-海藻糖二水合物或蔗糖,以及任选的甲硫氨酸作为第二稳定剂),非离子表面活性剂和有效量的至少 一种透明质酸酶。 还提供了制备这些制剂的方法及其用途。 -
公开(公告)号:US09345661B2
公开(公告)日:2016-05-24
申请号:US12804703
申请日:2010-07-27
IPC分类号: C07K16/00 , A61K9/00 , A61K9/19 , A61K39/395 , A61K47/18 , A61K47/26 , A61K47/42 , C07K16/32
CPC分类号: A61K39/39558 , A61K9/0019 , A61K9/08 , A61K9/19 , A61K38/47 , A61K39/39591 , A61K45/06 , A61K47/18 , A61K47/183 , A61K47/26 , A61K47/42 , C07K16/32 , C12Y302/01035
摘要: The present invention relates to a highly concentrated, stable pharmaceutical formulation of a pharmaceutically active anti-HER2 antibody, such as e.g. Trastuzumab (HERCEPTIN™), Pertuzumab or T-DM1, or a mixture of such antibody molecules for subcutaneous injection. In particular, the present invention relates to formulations comprising, in addition to a suitable amount of the anti-HER2 antibody, an effective amount of at least one hyaluronidase enzyme as a combined formulation or for use in form of a co-formulation. The formulations comprise additionally at least one buffering agent, such as e.g. a histidine buffer, a stabilizer or a mixture of two or more stabilizers (e.g. a saccharide, such as e.g. α,α-trehalose dihydrate or sucrose, and optionally methionine as a second stabilizer), a nonionic surfactant and an effective amount of at least one hyaluronidase enzyme. Methods for preparing such formulations and their uses thereof are also provided.
摘要翻译: 本发明涉及药物活性抗HER2抗体的高浓度,稳定的药物制剂,例如, 曲妥珠单抗(HERCEPTIN TM),Pertuzumab或T-DM1,或用于皮下注射的这种抗体分子的混合物。 特别地,本发明涉及包含除合适量的抗HER2抗体之外的有效量的至少一种透明质酸酶作为组合制剂或用于共同制剂形式的制剂。 制剂还包含至少一种缓冲剂,例如, 组氨酸缓冲液,稳定剂或两种或更多种稳定剂的混合物(例如糖,例如α,α-海藻糖二水合物或蔗糖,以及任选的甲硫氨酸作为第二稳定剂),非离子表面活性剂和有效量的至少 一种透明质酸酶。 还提供了制备这些制剂的方法及其用途。
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公开(公告)号:US20110044977A1
公开(公告)日:2011-02-24
申请号:US12804703
申请日:2010-07-27
IPC分类号: A61K39/395 , A61P35/00
CPC分类号: A61K39/39558 , A61K9/0019 , A61K9/08 , A61K9/19 , A61K38/47 , A61K39/39591 , A61K45/06 , A61K47/18 , A61K47/183 , A61K47/26 , A61K47/42 , C07K16/32 , C12Y302/01035
摘要: The present invention relates to a highly concentrated, stable pharmaceutical formulation of a pharmaceutically active anti-HER2 antibody, such as e.g. Trastuzumab (HERCEPTIN™), Pertuzumab or T-DM1, or a mixture of such antibody molecules for subcutaneous injection. In particular, the present invention relates to formulations comprising, in addition to a suitable amount of the anti-HER2 antibody, an effective amount of at least one hyaluronidase enzyme as a combined formulation or for use in form of a co-formulation. The formulations comprise additionally at least one buffering agent, such as e.g. a histidine buffer, a stabilizer or a mixture of two or more stabilizers (e.g. a saccharide, such as e.g. α,α-trehalose dihydrate or sucrose, and optionally methionine as a second stabilizer), a nonionic surfactant and an effective amount of at least one hyaluronidase enzyme. Methods for preparing such formulations and their uses thereof are also provided.
摘要翻译: 本发明涉及药物活性抗HER2抗体的高浓度,稳定的药物制剂,例如, 曲妥珠单抗(HERCEPTIN TM),Pertuzumab或T-DM1,或用于皮下注射的这种抗体分子的混合物。 特别地,本发明涉及包含除合适量的抗HER2抗体之外的有效量的至少一种透明质酸酶作为组合制剂或用于共同制剂形式的制剂。 制剂还包含至少一种缓冲剂,例如, 组氨酸缓冲液,稳定剂或两种或更多种稳定剂的混合物(例如糖,例如α,α-海藻糖二水合物或蔗糖,以及任选的甲硫氨酸作为第二稳定剂),非离子表面活性剂和有效量的至少 一种透明质酸酶。 还提供了制备这些制剂的方法及其用途。
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公开(公告)号:US20090162352A1
公开(公告)日:2009-06-25
申请号:US12333341
申请日:2008-12-12
IPC分类号: A61K39/395
CPC分类号: C07K16/2887 , A61K9/0019 , A61K9/08 , A61K9/19 , A61K39/3955 , A61K39/39591 , A61K47/12 , A61K47/183 , A61K47/22 , A61K47/26 , A61K47/34 , A61K2039/505 , C07K2317/24 , C07K2317/94
摘要: The present invention relates to a pharmaceutical formulation comprising an anti-CD20 antibody. The formulation may additionally comprise a buffer, a surfactant and/or an isotonicity agent.
摘要翻译: 本发明涉及包含抗CD20抗体的药物制剂。 制剂可另外包含缓冲剂,表面活性剂和/或等渗剂。
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公开(公告)号:US20100098712A1
公开(公告)日:2010-04-22
申请号:US12454598
申请日:2009-05-20
IPC分类号: A61K39/395 , A61P37/08
CPC分类号: A61K9/08 , A61K9/0019 , A61K47/183 , A61K47/26 , A61K2039/505 , C07K16/2875 , C07K2317/21 , C07K2317/71
摘要: Pharmaceutical formulations of an antibody against OX40L and processes for making the same.
摘要翻译: 针对OX40L抗体的药物制剂及其制备方法。
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公开(公告)号:US20110158987A1
公开(公告)日:2011-06-30
申请号:US12977509
申请日:2010-12-23
IPC分类号: A61K39/395 , A61P35/00
CPC分类号: A61K9/0019 , A61K39/39591 , A61K47/183 , A61K47/26 , C07K16/2863
摘要: This invention relates to a pharmaceutical formulation of an antibody against Epidermal Growth Factor Receptor (EGFR), a process for the preparation and uses of the formulation.
摘要翻译: 本发明涉及针对表皮生长因子受体(EGFR)的抗体的药物制剂,该制剂的制备和用途的方法。
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公开(公告)号:US10685129B2
公开(公告)日:2020-06-16
申请号:US15689794
申请日:2017-08-29
申请人: Michael Adler , Klaus-Peter Hofmann
发明人: Michael Adler , Klaus-Peter Hofmann
摘要: A data processing system is provided with a data verification system that is configured to perform a validation check upon receipt of a request from a field device to transfer data to the data processing system. The data verification system is also configured to verify a permission of the field device to exchange data and to validate the data integrity. A data landing zone is provided for temporary storage of the data in the event that a validation check fails, so that data errors may be corrected.
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公开(公告)号:US20180060594A1
公开(公告)日:2018-03-01
申请号:US15689794
申请日:2017-08-29
申请人: Michael Adler , Klaus-Peter Hofmann
发明人: Michael Adler , Klaus-Peter Hofmann
摘要: A data processing system is provided with a data verification system that is configured to perform a validation check upon receipt of a request from a field device to transfer data to the data processing system. The data verification system is also configured to verify a permission of the field device to exchange data and to validate the data integrity. A data landing zone is provided for temporary storage of the data in the event that a validation check fails, so that data errors may be corrected.
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公开(公告)号:US09021878B2
公开(公告)日:2015-05-05
申请号:US13642602
申请日:2011-04-04
CPC分类号: G01F23/266 , A61B5/208 , A61B2562/0271 , G01F1/007 , G01F1/684
摘要: The present invention is flow rate meters which are able to accurately measure the volumetric rate of flow of a liquid through a conduit without requiring foreknowledge of the physicochemical characteristics of the liquid, e.g., for the purpose of calibration of the thermal mass flow rate. One application of the flow meters of the invention is to incorporate them in a system for measuring the flow rate of urine excreted by a catheterized patient. The invention also provides methods for using the flow rate meters.
摘要翻译: 本发明是流量计,其能够精确地测量通过管道的液体的体积流速,而不需要预先知道液体的物理化学特性,例如用于校准热质量流量的目的。 本发明的流量计的一个应用是将它们并入用于测量由导管的患者排泄的尿液的流量的系统中。 本发明还提供了使用流量计的方法。
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10.
公开(公告)号:US08840351B2
公开(公告)日:2014-09-23
申请号:US12728355
申请日:2010-03-22
申请人: Michael Adler , Frank Sommerer , Andreas Steinert
发明人: Michael Adler , Frank Sommerer , Andreas Steinert
CPC分类号: B42C19/08 , B42C1/12 , B42C9/0037 , Y10S412/901 , Y10S412/902
摘要: A book binding machine includes a collating machine, a perfect binder and a transfer device disposed between the collating machine and the perfect binder. The collating machine and the perfect binder are actuated by a common control device. In each case, one transport segment is assigned to a respective book block clamp by the control device. The control device also has a program which, if a defective or missing book block clamp is detected, actuates the collating machine in such a way that no book block is collated for that book block clamp. A method for operating a book binding machine is also provided.
摘要翻译: 书籍装订机包括整理机,完美的装订器和设置在整理机和完美的装订器之间的传送装置。 整理机和完美的装订器由公共控制装置致动。 在每种情况下,通过控制装置将一个传送段分配给相应的书本夹具。 控制装置还具有程序,如果检测到有缺陷或缺失的书夹夹具,则使得对照机器以对于该书夹夹不整理书本块的方式启动。 还提供了一种操作装订机的方法。
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