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公开(公告)号:EP4335507A2
公开(公告)日:2024-03-13
申请号:EP23199180.3
申请日:2014-03-14
IPC分类号: A61P27/06
摘要: Described herein are compounds and compositions for treating glaucoma and/or reducing intraocular pressure. Compositions may comprise an isoquinoline compound and a prostaglandin or a prostaglandin analog. Compounds described herein include those in which an isoquinoline compound is covalently linked to a prostaglandin or a prostaglandin analog, and those in which an isoquinoline compound and a prostaglandin free acid together form a salt.
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公开(公告)号:EP4218759A3
公开(公告)日:2023-09-06
申请号:EP23156661.3
申请日:2014-03-14
IPC分类号: A61K31/47 , A61K31/557 , A61P27/06
摘要: Described herein are compounds and compositions for treating glaucoma and/or reducing intraocular pressure. Compositions may comprise an isoquinoline compound and a prostaglandin or a prostaglandin analog. Compounds described herein include those in which an isoquinoline compound is covalently linked to a prostaglandin or a prostaglandin analog, and those in which an isoquinoline compound and a prostaglandin free acid together form a salt.
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公开(公告)号:EP4218759A2
公开(公告)日:2023-08-02
申请号:EP23156661.3
申请日:2014-03-14
IPC分类号: A61K31/47 , A61K31/557 , A61P27/06
摘要: Described herein are compounds and compositions for treating glaucoma and/or reducing intraocular pressure. Compositions may comprise an isoquinoline compound and a prostaglandin or a prostaglandin analog. Compounds described herein include those in which an isoquinoline compound is covalently linked to a prostaglandin or a prostaglandin analog, and those in which an isoquinoline compound and a prostaglandin free acid together form a salt.
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公开(公告)号:EP3773580A1
公开(公告)日:2021-02-17
申请号:EP19777599.2
申请日:2019-03-29
IPC分类号: A61K31/47 , C07D217/22
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公开(公告)号:EP3506890A1
公开(公告)日:2019-07-10
申请号:EP17765001.7
申请日:2017-08-30
发明人: LIN, Cheng-Wen , KOPCZYNSKI, Casey , DELONG, Mitchell, A. , STURDIVANT, Jill, M. , KRISHNAMOORTHY, Ramesh
IPC分类号: A61K31/00
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公开(公告)号:EP4335507A3
公开(公告)日:2024-06-05
申请号:EP23199180.3
申请日:2014-03-14
IPC分类号: A61K31/47 , A61K31/557 , A61P27/06
CPC分类号: A61K31/557 , A61K31/5575 , A61K31/559 , A61K31/4725 , A61K31/472 , C07D409/12 , C07D217/22 , A61K47/55 , A61P27/02 , A61P27/06 , A61P43/00 , A61K9/0048 , A61K9/08 , A61K47/10 , A61K47/26 , A61K31/47
摘要: Described herein are compounds and compositions for treating glaucoma and/or reducing intraocular pressure. Compositions may comprise an isoquinoline compound and a prostaglandin or a prostaglandin analog. Compounds described herein include those in which an isoquinoline compound is covalently linked to a prostaglandin or a prostaglandin analog, and those in which an isoquinoline compound and a prostaglandin free acid together form a salt.
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7.
公开(公告)号:EP2571526A1
公开(公告)日:2013-03-27
申请号:EP11784089.2
申请日:2011-05-17
发明人: KOPCZYNSKI, Casey , LIN, Cheng-Wen , SUTAY, Chris
IPC分类号: A61K47/32
CPC分类号: A61K9/0051 , A61F9/0017 , A61K31/00 , A61K31/215 , A61K47/32 , A61K47/36
摘要: Drug delivery devices comprising a non-bioabsorbable polymer structure configured to support a composition comprising an active agent. The devices include a plurality of portions fused together and a recess configured to support the composition. At least one of the portions includes an impermeable polymer and at least one other portion includes a rate-limiting water-permeable polymer. The rate-limiting water-permeable polymer allows for transportation of the active agent to an exterior of the device.
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公开(公告)号:EP3934646A1
公开(公告)日:2022-01-12
申请号:EP20766052.3
申请日:2020-03-05
发明人: DAS, Sanjib, Kumar , LIN, Cheng-Wen
IPC分类号: A61K31/472 , A61K47/34 , A61P27/02
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公开(公告)号:EP2376058A1
公开(公告)日:2011-10-19
申请号:EP09796554.5
申请日:2009-12-18
发明人: KOPCZYNSKI, Casey , LIN, Cheng-Wen , SUTAY, Chris
CPC分类号: A61K9/0051 , A61K31/00
摘要: Drug delivery devices comprising a non-bioabsorbable polymer structure and a composition comprising an active agent have been discovered. The drug delivery devices may be used to treat ocular conditions, among other diseases and conditions. In addition, a method of treating an ocular condition has been discovered comprising implanting a drug delivery device which releases the active agent at a rate of Q = 0.001 x N x C wherein C is the topical effective concentration (in milligram/mL) of the active agent and N=0.01 to 0.5 for prostaglandins in their ester, amide, free acid or salt form, and N=0.5 to 5 for any active agent other than prostaglandins in their ester, amide, free acid or salt form.
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