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公开(公告)号:US09592197B2
公开(公告)日:2017-03-14
申请号:US11012267
申请日:2004-12-16
申请人: Viswanathan Srinivasan , Juan Carlos Menendez , Venkatesh Balasubramanian , Somphet Peter Suphasawud , Ralph Brown , David Brown
发明人: Viswanathan Srinivasan , Juan Carlos Menendez , Venkatesh Balasubramanian , Somphet Peter Suphasawud , Ralph Brown , David Brown
IPC分类号: A61K9/20 , A61K9/10 , A61K9/24 , A61K31/485 , A61K45/06
CPC分类号: A61K9/10 , A61K9/209 , A61K31/485 , A61K45/06 , A61K2300/00
摘要: A pharmaceutical dosage form which comprises diphenhydramine and/or a pharmaceutically acceptable salt thereof and at least one second drug. The dosage form provides a plasma concentration within the therapeutic range of the at least one second drug over a period which is coextensive with a substantial part of the period over which the dosage form provides a plasma concentration within the therapeutic range of diphenhydramine or salt thereof. This Abstract is neither intended to define the invention disclosed in this specification nor intended to limit the scope of the invention in any way.
摘要翻译: 包含苯海拉明和/或其药学上可接受的盐和至少一种第二种药物的药物剂型。 所述剂型在与所述剂型在苯海拉明或其盐的治疗范围内提供血药浓度的相当长的一段时间内共同延长的时期内提供至少一种第二药物的治疗范围内的血浆浓度。 本摘要既不旨在限定本说明书中公开的发明,也不旨在以任何方式限制本发明的范围。
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公开(公告)号:US09492541B2
公开(公告)日:2016-11-15
申请号:US10939351
申请日:2004-09-14
申请人: Viswanathan Srinivasan , Ralph Brown , David Brown , Juan Carlos Menendez , Venkatesh Balasubramanian , Somphet Peter Suphasawud
发明人: Viswanathan Srinivasan , Ralph Brown , David Brown , Juan Carlos Menendez , Venkatesh Balasubramanian , Somphet Peter Suphasawud
IPC分类号: A61K9/20 , A61K31/137 , A61K45/06 , A61K9/24 , A61K31/485
CPC分类号: A61K45/06 , A61K9/209 , A61K31/137 , A61K31/485 , A61K2300/00
摘要: A pharmaceutical dosage form which comprises phenylepherine or a pharmaceutically acceptable salt thereof and a second drug. The dosage form provides a plasma concentration within the therapeutic range of the second drug over a period which is coextensive with at least about 70% of the period over which the dosage form provides a plasma concentration within the therapeutic range of phenylepherine. This abstract is neither intended to define the invention disclosed in this specification nor intended to limit the scope of the invention in any way.
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公开(公告)号:US20050232987A1
公开(公告)日:2005-10-20
申请号:US10798884
申请日:2004-03-12
申请人: Viswanathan Srinivasan , Ralph Brown , David Brown , Himanshu Patel , Juan Menendez , Venkatesh Balasubramanian
发明人: Viswanathan Srinivasan , Ralph Brown , David Brown , Himanshu Patel , Juan Menendez , Venkatesh Balasubramanian
IPC分类号: A61K9/00 , A61K9/20 , A61K9/24 , A61K31/137 , A61K31/485
CPC分类号: A61K9/2077 , A61K9/209 , A61K31/137 , A61K31/485 , A61K2300/00
摘要: A pharmaceutical dosage form which comprises a first drug which comprises at least one morphine derivative with antitussive activity and at least one second drug. The dosage form provides a plasma concentration within the therapeutic range of the at least one second drug over a period which is coextensive with at least about 70% of the period over which the dosage form provides a plasma concentration within the therapeutic range of the first drug. This abstract is neither intended to define the invention disclosed in this specification nor intended to limit the scope of the invention in any way.
摘要翻译: 一种药物剂型,其包含含有至少一种具有镇咳活性的吗啡衍生物和至少一种第二药物的第一药物。 所述剂型在所述至少一种第二药物的治疗范围内提供血浆浓度,所述时间段与至少约70%的所述时间段共同延长的时间段内,所述剂型在该时间段内提供在第一药物的治疗范围内的血浆浓度 。 该摘要既不旨在限定本说明书中公开的发明,也不旨在以任何方式限制本发明的范围。
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公开(公告)号:US20060134207A1
公开(公告)日:2006-06-22
申请号:US11012267
申请日:2004-12-16
申请人: Viswanathan Srinivasan , Juan Menendez , Venkatesh Balasubramanian , Somphet Suphasawud , Ralph Brown , David Brown
发明人: Viswanathan Srinivasan , Juan Menendez , Venkatesh Balasubramanian , Somphet Suphasawud , Ralph Brown , David Brown
IPC分类号: A61K31/485 , A61K9/22
CPC分类号: A61K9/10 , A61K9/209 , A61K31/485 , A61K45/06 , A61K2300/00
摘要: A pharmaceutical dosage form which comprises diphenhydramine and/or a pharmaceutically acceptable salt thereof and at least one second drug. The dosage form provides a plasma concentration within the therapeutic range of the at least one second drug over a period which is coextensive with a substantial part of the period over which the dosage form provides a plasma concentration within the therapeutic range of diphenhydramine or salt thereof. This Abstract is neither intended to define the invention disclosed in this specification nor intended to limit the scope of the invention in any way.
摘要翻译: 包含苯海拉明和/或其药学上可接受的盐和至少一种第二种药物的药物剂型。 所述剂型在与所述剂型在苯海拉明或其盐的治疗范围内提供血药浓度的相当长的一段时间内共同延长的时期内提供至少一种第二药物的治疗范围内的血浆浓度。 本摘要既不旨在限定本说明书中公开的发明,也不旨在以任何方式限制本发明的范围。
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公开(公告)号:US20060029664A1
公开(公告)日:2006-02-09
申请号:US10910806
申请日:2004-08-04
申请人: Viswanathan Srinivasan , Ralph Brown , David Brown , Juan Menendez , Venkatesh Balasubramanian , Somphet Suphasawud
发明人: Viswanathan Srinivasan , Ralph Brown , David Brown , Juan Menendez , Venkatesh Balasubramanian , Somphet Suphasawud
IPC分类号: A61K9/20
CPC分类号: A61K9/209 , A61K9/0095
摘要: A pharmaceutical dosage form which comprises carbetapentane and/or a pharmaceutically acceptable salt thereof and an additional drug. The dosage form provides a plasma concentration within the therapeutic range of the additional drug over a period which is coextensive with at least about 70% of the period over which the dosage form provides a plasma concentration within the therapeutic range of carbetapentane. This abstract is neither intended to define the invention disclosed in this specification nor intended to limit the scope of the invention in any way.
摘要翻译: 包含碳代戊烷和/或其药学上可接受的盐和另外的药物的药物剂型。 所述剂型在额外药物的治疗范围内提供血浆浓度,所述时间段与至少约70%的剂型共同延长的时间段内,所述剂型在该时间段内提供血浆浓度在碳卡巴坦的治疗范围内。 该摘要既不旨在限定本说明书中公开的发明,也不旨在以任何方式限制本发明的范围。
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公开(公告)号:US20070003622A1
公开(公告)日:2007-01-04
申请号:US11102726
申请日:2005-04-11
申请人: Viswanathan Srinivasan , Juan Menendez , Venkatesh Balasubramanian , Somphet Suphasawud , Ralph Brown , David Brown
发明人: Viswanathan Srinivasan , Juan Menendez , Venkatesh Balasubramanian , Somphet Suphasawud , Ralph Brown , David Brown
IPC分类号: A61K9/24
CPC分类号: A61K9/10 , A61K9/209 , A61K31/485 , A61K45/06 , A61K2300/00
摘要: A pharmaceutical dosage form which comprises diphenhydramine and/or a pharmaceutically acceptable salt thereof. The dosage form is capable of providing a diphenhydramine plasma concentration within a therapeutic range for at least about 24 hours per single dose. This Abstract is neither intended to define the invention disclosed in this specification nor intended to limit the scope of the invention in any way.
摘要翻译: 包含苯海拉明和/或其药学上可接受的盐的药物剂型。 该剂型能够将治疗范围内的苯海拉姆血浆浓度提供至少约24小时/单次剂量。 本摘要既不旨在限定本说明书中公开的发明,也不旨在以任何方式限制本发明的范围。
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公开(公告)号:US20050266032A1
公开(公告)日:2005-12-01
申请号:US11115321
申请日:2005-04-27
申请人: Viswanathan Srinivasan , Ralph Brown , David Brown , Himanshu Patel , Juan Menendez , Venkatesh Balasubramanian , Somphet Suphasawud
发明人: Viswanathan Srinivasan , Ralph Brown , David Brown , Himanshu Patel , Juan Menendez , Venkatesh Balasubramanian , Somphet Suphasawud
IPC分类号: A61K31/137 , A61K31/485
CPC分类号: A61K45/06 , A61K31/137 , A61K31/485 , A61K2300/00
摘要: A pharmaceutical dosage form comprising a first drug and a second drug, both of which are selected from decongestants, antitussives, expectorants, analgesics and antihistamines. The dosage form provides a plasma concentration within a therapeutic range of the second drug over a period which is coextensive with at least about 70% of a period over which the dosage form provides a plasma concentration within a therapeutic range of the first drug. This Abstract is neither intended to define the invention disclosed in this specification nor intended to limit the scope of the invention in any way.
摘要翻译: 一种包含第一药物和第二药物的药物剂型,它们都选自减充血剂,镇咳药,祛痰剂,止痛剂和抗组胺剂。 剂型提供在第二药物的治疗范围内的血浆浓度,其在与第一药物的治疗范围内提供血浆浓度的至少约70%的期间共同延长的时期内。 本摘要既不旨在限定本说明书中公开的发明,也不旨在以任何方式限制本发明的范围。
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公开(公告)号:US20060057205A1
公开(公告)日:2006-03-16
申请号:US10939351
申请日:2004-09-14
申请人: Viswanathan Srinivasan , Raph Brown , David Brown , Juan Menendez , Venkatesh Balasubramanian , Somphet Suphasawud
发明人: Viswanathan Srinivasan , Raph Brown , David Brown , Juan Menendez , Venkatesh Balasubramanian , Somphet Suphasawud
IPC分类号: A61K31/485 , A61K31/137 , A61K9/24
CPC分类号: A61K45/06 , A61K9/209 , A61K31/137 , A61K31/485 , A61K2300/00
摘要: A pharmaceutical dosage form which comprises phenylepherine or a pharmaceutically acceptable salt thereof and a second drug. The dosage form provides a plasma concentration within the therapeutic range of the second drug over a period which is coextensive with at least about 70% of the period over which the dosage form provides a plasma concentration within the therapeutic range of phenylepherine. This abstract is neither intended to define the invention disclosed in this specification nor intended to limit the scope of the invention in any way.
摘要翻译: 一种药物剂型,其包含苯乙醇或其药学上可接受的盐和第二种药物。 该剂型在第二药物的治疗范围内提供血浆浓度,该时间段与至少约70%的期间共同延长,在该时间内,剂型提供在苯乙醇的治疗范围内的血浆浓度。 该摘要既不旨在限定本说明书中公开的发明,也不旨在以任何方式限制本发明的范围。
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公开(公告)号:US20120201887A1
公开(公告)日:2012-08-09
申请号:US13021240
申请日:2011-02-04
申请人: Nils Ahlgren , Mark Nuttall , Jeannie Wong , Venkatesh Balasubramanian , Craig Belongie , Ashfaq Khan , Neil Campbell Muir
发明人: Nils Ahlgren , Mark Nuttall , Jeannie Wong , Venkatesh Balasubramanian , Craig Belongie , Ashfaq Khan , Neil Campbell Muir
IPC分类号: A61K9/24 , A61K31/795 , A61K31/785 , A61K31/787 , A61P11/14 , A61K31/485 , A61K9/30 , A61P11/00 , A61P11/02 , A61K31/09 , A61K9/22
CPC分类号: A61K31/09 , A61K9/20 , A61K9/2027 , A61K9/2054 , A61K9/209 , A61K9/4808 , A61K9/5026 , A61K9/5042 , A61K9/5047 , A61K31/137 , A61K31/485 , A61K45/06 , A61K2300/00
摘要: A pharmaceutical composition in the form of a tablet including a first portion and a second portion, wherein said first portion includes guaifenesin having an immediate release profile and a second drug having a sustained release profile, and wherein the second portion includes guaifenesin having a sustained release profile. The second drug can be in the form of a drug-resin complex. The second drug can be either an anti-tussive or a decongestant. The drug-resin complex includes a drug complexed to an ion exchange resin. The ion exchange resin can be a polystyrene sulfonate resin, polacrilex resin, polacrilin potassium, cholestyramine resin, or a colestyramine resin. The drug-resin complex can be provided with a coating, the coating thickness being selected to obtain the desired release profile. The drug-resin complex can be provided with a coating level of from 5% to 50%. The coating level can be from 10% to 35%.
摘要翻译: 一种片剂形式的药物组合物,包括第一部分和第二部分,其中所述第一部分包括立即释放曲线的愈创甘油醚和具有持续释放曲线的第二药物,其中第二部分包括持久释放的愈创甘油醚 个人资料 第二种药物可以是药物 - 树脂复合物的形式。 第二种药物可以是抗咳嗽或减充血剂。 药物 - 树脂复合物包括与离子交换树脂络合的药物。 离子交换树脂可以是聚苯乙烯磺酸酯树脂,聚乙烯树脂,聚丙烯酸钾,考来烯胺树脂或考来烯胺树脂。 药物 - 树脂复合物可以设置有涂层,选择涂层厚度以获得所需的释放曲线。 药物 - 树脂复合物可以具有5%至50%的包衣水平。 涂层水平可以为10%至35%。
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公开(公告)号:US20080109287A1
公开(公告)日:2008-05-08
申请号:US11973913
申请日:2007-10-10
申请人: Gopinath Ganapathy , Rajesh Iyer , Ravi Krishnamurthy , Muthu Krishnan , Venkatesh Balasubramanian , Ramasubramaniam Lakshminarayan
发明人: Gopinath Ganapathy , Rajesh Iyer , Ravi Krishnamurthy , Muthu Krishnan , Venkatesh Balasubramanian , Ramasubramaniam Lakshminarayan
IPC分类号: G06Q10/00
CPC分类号: G06Q10/10 , G06Q10/06311 , G06Q10/06375 , G06Q10/06393 , G06Q30/0283 , G06Q50/04 , Y02P90/30
摘要: Systems, architectures, and data structures are described which are used to manage distributed design chains, specifically for domains in which data reside in multiple applications and are linked through complex interrelationships. The design chains or design networks integrated by the invention may include multiple companies in multiple sites collaborating to design and develop a new product. The invention is intended to integrate seamlessly and transparently with existing, diverse legacy applications, which include inter-linked data relevant to the design, thereby addressing the needs identified above.
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