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公开(公告)号:US09504747B2
公开(公告)日:2016-11-29
申请号:US14200359
申请日:2014-03-07
申请人: Jeremy Lee Baryza , Rohan Eric John Beckwith , Keith Bowman , Crystal Byers , Tanzina Fazal , Gabriel Grant Gamber , Cameron Chuck-munn Lee , Ritesh Bhanudasji Tichkule , Chandra Vargeese , Shuangxi Wang , Laura Ellen West , Thomas Zabawa , Junping Zhao
发明人: Jeremy Lee Baryza , Rohan Eric John Beckwith , Keith Bowman , Crystal Byers , Tanzina Fazal , Gabriel Grant Gamber , Cameron Chuck-munn Lee , Ritesh Bhanudasji Tichkule , Chandra Vargeese , Shuangxi Wang , Laura Ellen West , Thomas Zabawa , Junping Zhao
IPC分类号: A61K47/18 , C07C229/12 , A61K47/22 , A61K9/127 , C07C217/58 , C07C217/60 , C07C217/62 , C07C219/22 , C07C219/28 , C07C235/46 , C07C237/08 , C07D213/79 , C07D317/24 , C07D317/28 , C07D205/04 , C07D295/096 , C07D213/69 , C12N15/113
CPC分类号: A61K47/18 , A61K9/1271 , A61K9/1272 , A61K47/183 , A61K47/22 , C07C217/58 , C07C217/60 , C07C217/62 , C07C219/22 , C07C219/28 , C07C229/12 , C07C235/46 , C07C237/08 , C07D205/04 , C07D213/69 , C07D213/79 , C07D295/096 , C07D317/24 , C07D317/28 , C12N15/1137 , C12N2310/14 , C12N2320/32
摘要: This invention provides for a compound of formula (I): or a pharmaceutically acceptable salt thereof, wherein R1-R4, L and X are defined herein. The compounds of formula (I) and pharmaceutically acceptable salts thereof are cationic lipids useful in the delivery of biologically active agents to cells and tissues.
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公开(公告)号:US10519446B2
公开(公告)日:2019-12-31
申请号:US15025852
申请日:2014-09-30
申请人: Novartis AG , Jeremy Lee Baryza , Marcel Blommers , Cesar Fernandez , Erin Geno , Alvar Gossert , Paulette Greenidge , Dieter Huesken , Juerg Hunziker , Francois Jean-Charles Natt , Anup Patnaik , Andrew Patterson , Jean-Michel Rene Rondeau , Jan Weiler , Meicheng Zhu , Meghan Holdorf
发明人: Jeremy Lee Baryza , Marcel Blommers , Cesar Fernandez , Erin Geno , Alvar Gossert , Paulette Greenidge , Dieter Huesken , Juerg Hunziker , Francois Jean-Charles Natt , Anup Patnaik , Andrew Patterson , Jean-Michel Rene Rondeau , Jan Weiler , Meicheng Zhu , Meghan Holdorf
IPC分类号: C12N15/113
摘要: The disclosure relates to compositions comprising a HBV RNAi agent. In some embodiments, the HBV RNAi agent comprises a sense and an anti-sense strand, each strand being an 18-mer and the strands together forming a blunt-ended duplex, wherein the 3′ end of at least one strand terminates in a phosphate or modified internucleoside linker and further comprises, in 5′ to 3′ order: a spacer; a second phosphate or modified internucleoside linker; and a 3′ end cap. In some embodiments, the 3′ end of both the sense and anti-sense strand further comprise, in 5′ to 3′ order: a spacer; a second phosphate or modified internucleoside linker; and a 3′ end cap. The two strands can have the same or different spacers, phosphates or modified internucleoside linkers, and/or 3′ end caps. The strands can be ribonucleotides, or, optionally, one or more nucleotide can be modified or substituted. Optionally, at least one nucleotide comprises a modified internucleoside linker. Optionally, the RNAi agent can be modified on one or both 5′ end. Optionally, the sense strand can comprise a 5′ end cap which reduces the amount of the RNA interference mediated by this strand. Optionally, the RNAi agent is attached to a ligand. This format can be used to devise RNAi agents to a variety of different targets and sequences. The disclosure also relates to processes for making such compositions, and methods and uses of such compositions, e.g., to mediate RNA interference. The disclosure also pertains to methods of treating, ameliorating and preventing HBV in a patient involving the step of administering to the patient a therapeutic amount of a HBV RNAi agent.
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公开(公告)号:US20170196979A1
公开(公告)日:2017-07-13
申请号:US15277402
申请日:2016-09-27
申请人: Jeremy Lee Baryza , Rohan Eric John Beckwith , Keith Bowman , Crystal Byers , Tanzina Fazal , Gabriel Grant Gamber , Cameron Chuck-munn Lee , Ritesh Bhanudasji Tichkule , Chandra Vargeese , Shuangxi Wang , Laura Ellen West , Thomas Zabawa , Junping Zhao
发明人: Jeremy Lee Baryza , Rohan Eric John Beckwith , Keith Bowman , Crystal Byers , Tanzina Fazal , Gabriel Grant Gamber , Cameron Chuck-munn Lee , Ritesh Bhanudasji Tichkule , Chandra Vargeese , Shuangxi Wang , Laura Ellen West , Thomas Zabawa , Junping Zhao
IPC分类号: A61K47/18 , C12N15/113 , A61K47/22
CPC分类号: A61K47/18 , A61K9/1271 , A61K9/1272 , A61K47/183 , A61K47/22 , C07C217/58 , C07C217/60 , C07C217/62 , C07C219/22 , C07C219/28 , C07C229/12 , C07C235/46 , C07C237/08 , C07D205/04 , C07D213/69 , C07D213/79 , C07D295/096 , C07D317/24 , C07D317/28 , C12N15/1137 , C12N2310/14 , C12N2320/32
摘要: This invention provides for a compound of formula (I): or a pharmaceutically acceptable salt thereof, wherein R1-R4, L and X are defined herein. The compounds of formula (I) and pharmaceutically acceptable salts thereof are cationic lipids useful in the delivery of biologically active agents to cells and tissues.
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公开(公告)号:US20160304863A1
公开(公告)日:2016-10-20
申请号:US15025779
申请日:2014-10-01
申请人: Jeremy Lee BARYZA , Marcel BLOMMERS , Cesar FERNANDEZ , Erin GENO , Alvar GOSSERT , Paulette GREENIDGE , Dieter HUESKEN , Juerg HUNZIKER , Francois Jean-Charles NATT , Anup PATNAIK , Andrew PATTERSON , Jean-Michel Rene RONDEAU , Jan WEILER , Meicheng ZHU
发明人: Jeremy Lee Baryza , Marcel Blommers , Cesar Fernandez , Erin Geno , Alvar Gossert , Paulette Greenidge , Dieter Huesken , Juerg Hunziker , Francois Jean-Charles Natt , Anup Patnaik , Andrew Patterson , Jean-Michel Rene Rondeau , Jan Weiler , Meicheng Zhu
IPC分类号: C12N15/11 , C07C233/01 , C07D217/18 , C07D215/14 , C07D217/16
CPC分类号: C12N15/111 , C07C43/23 , C07C69/40 , C07C233/01 , C07D213/30 , C07D215/12 , C07D215/14 , C07D217/14 , C07D217/16 , C07D217/18 , C07D311/80 , C07D401/04 , C12N2310/14 , C12N2310/344 , C12N2310/351 , C12N2320/51
摘要: The disclosure relates to novel compounds and compositions comprising a RNAi agent comprising a novel compound as a 3′ end cap. The disclosure also relates to processes for making such compositions, and methods and uses of such compositions, e.g., to mediate RNA interference.
摘要翻译: 本公开涉及包含含有作为3'端帽的新化合物的RNAi剂的新化合物和组合物。 本公开还涉及制备这种组合物的方法,以及这种组合物的方法和用途,例如介导RNA干扰。
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公开(公告)号:US20140303232A1
公开(公告)日:2014-10-09
申请号:US14200359
申请日:2014-03-07
申请人: Jeremy Lee BARYZA , Rohan Eric John BECKWITH , Keith BOWMAN , Crystal BYERS , Tanzina FAZAL , Gabriel Grant GAMBER , Cameron Chuck-munn LEE , Ritesh Bhanudasji TICHKULE , Chandra VARGEESE , Shuangxi WANG , Laura Ellen West , Thomas ZABAWA , Junping ZHAO
发明人: Jeremy Lee BARYZA , Rohan Eric John BECKWITH , Keith BOWMAN , Crystal BYERS , Tanzina FAZAL , Gabriel Grant GAMBER , Cameron Chuck-munn LEE , Ritesh Bhanudasji TICHKULE , Chandra VARGEESE , Shuangxi WANG , Laura Ellen West , Thomas ZABAWA , Junping ZHAO
IPC分类号: A61K47/18 , A61K47/12 , A61K47/14 , C12N15/113 , A61K47/22
CPC分类号: A61K47/18 , A61K9/1271 , A61K9/1272 , A61K47/183 , A61K47/22 , C07C217/58 , C07C217/60 , C07C217/62 , C07C219/22 , C07C219/28 , C07C229/12 , C07C235/46 , C07C237/08 , C07D205/04 , C07D213/69 , C07D213/79 , C07D295/096 , C07D317/24 , C07D317/28 , C12N15/1137 , C12N2310/14 , C12N2320/32
摘要: This invention provides for a compound of formula (I): or a pharmaceutically acceptable salt thereof, wherein R1-R4, L and X are defined herein. The compounds of formula (I) and pharmaceutically acceptable salts thereof are cationic lipids useful in the delivery of biologically active agents to cells and tissues.
摘要翻译: 本发明提供式(I)化合物或其药学上可接受的盐,其中R 1 -R 4,L和X如本文所定义。 式(I)化合物及其药学上可接受的盐是可用于将生物活性剂递送至细胞和组织的阳离子脂质。
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公开(公告)号:US20160215288A1
公开(公告)日:2016-07-28
申请号:US15025852
申请日:2014-09-30
申请人: Jeremy Lee Baryza , Marcel Blommers , Cesar Femandez , Erin Geno , Alvar Gossert , Paulette Greenidge , Dieter Huesken , Juerg Hunziker , Francois Jean-Charles Natt , Anup Patnaik , Andrew Patterson , Jean-Michel Rene Rondeau , Jan Weiler , Meicheng zhu , Meghan Holdorf
发明人: Jeremy Lee Baryza , Marcel Blommers , Cesar Femandez , Erin Geno , Alvar Gossert , Paulette Greenidge , Dieter Huesken , Juerg Hunziker , Francois Jean-Charles Natt , Anup Patnaik , Andrew Patterson , Jean-Michel Rene Rondeau , Jan Weiler , Meicheng zhu , Meghan Holdorf
IPC分类号: C12N15/113
CPC分类号: C12N15/1131 , C12N2310/14 , C12N2310/317 , C12N2310/321 , C12N2310/322 , C12N2310/332 , C12N2310/351 , C12N2310/3515 , C12N2320/30 , C12N2310/3521 , C12N2310/3525 , C12N2310/3533
摘要: The disclosure relates to compositions comprising a HBV RNAi agent. In some embodiments, the HBV RNAi agent comprises a sense and an anti-sense strand, each strand being an 18-mer and the strands together forming a blunt-ended duplex, wherein the 3′ end of at least one strand terminates in a phosphate or modified internucleoside linker and further comprises, in 5′ to 3′ order: a spacer; a second phosphate or modified internucleoside linker; and a 3′ end cap. In some embodiments, the 3′ end of both the sense and anti-sense strand further comprise, in 5′ to 3′ order: a spacer; a second phosphate or modified internucleoside linker; and a 3′ end cap. The two strands can have the same or different spacers, phosphates or modified internucleoside linkers, and/or 3′ end caps. The strands can be ribonucleotides, or, optionally, one or more nucleotide can be modified or substituted. Optionally, at least one nucleotide comprises a modified internucleoside linker. Optionally, the RNAi agent can be modified on one or both 5′ end. Optionally, the sense strand can comprise a 5′ end cap which reduces the amount of the RNA interference mediated by this strand. Optionally, the RNAi agent is attached to a ligand. This format can be used to devise RNAi agents to a variety of different targets and sequences. The disclosure also relates to processes for making such compositions, and methods and uses of such compositions, e.g., to mediate RNA interference. The disclosure also pertains to methods of treating, ameliorating and preventing HBV in a patient involving the step of administering to the patient a therapeutic amount of a HBV RNAi agent.
摘要翻译: 本公开涉及包含HBV RNAi剂的组合物。 在一些实施方案中,HBV RNAi剂包含有义链和反义链,每条链是18聚体,并且所述链一起形成平端双链体,其中至少一条链的3'末端终止于磷酸酯 或修饰的核苷间连接体,并且还包含以5'至3'的顺序:间隔物; 第二磷酸酯或修饰的核苷间连接体; 和3'端盖。 在一些实施方案中,有义和反义链两者的3'末端还包含5'至3'的顺序:间隔基; 第二磷酸酯或修饰的核苷间连接体; 和3'端盖。 两条链可以具有相同或不同的间隔物,磷酸酯或修饰的核苷间接头,和/或3'端帽。 链可以是核糖核苷酸,或者任选地,一个或多个核苷酸可以被修饰或取代。 任选地,至少一个核苷酸包含修饰的核苷间连接体。 任选地,RNAi剂可以在一个或两个5'端修饰。 任选地,有义链可以包含5'端帽,其减少由该链介导的RNA干扰的量。 任选地,RNAi试剂连接到配体上。 这种格式可用于将RNAi试剂设计成各种不同的靶标和序列。 本公开还涉及制备这种组合物的方法,以及这种组合物的方法和用途,例如介导RNA干扰。 本公开还涉及在患者中治疗,改善和预防HBV的方法,其涉及向患者施用治疗量的HBV RNAi剂的步骤。
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公开(公告)号:US09988627B2
公开(公告)日:2018-06-05
申请号:US15025826
申请日:2014-10-06
申请人: Jeremy Lee Baryza , Marcel Blommers , William Chutkow , Cesar Fernandez , Erin Geno , Alvar Gossert , Paulette Greenidge , Dieter Huesken , Juerg Hunziker , Francois Jean-Charles Natt , Anup Patnaik , Andrew Patterson , Jean-Michel Rene Rondeau , Jan Weiler , Meicheng Zhu
发明人: Jeremy Lee Baryza , Marcel Blommers , William Chutkow , Cesar Fernandez , Erin Geno , Alvar Gossert , Paulette Greenidge , Dieter Huesken , Juerg Hunziker , Francois Jean-Charles Natt , Anup Patnaik , Andrew Patterson , Jean-Michel Rene Rondeau , Jan Weiler , Meicheng Zhu
IPC分类号: C12N15/113
CPC分类号: C12N15/113 , C12N2310/14 , C12N2310/317 , C12N2310/321 , C12N2310/322 , C12N2310/332 , C12N2310/341 , C12N2310/351 , C12N2310/3515 , C12N2310/3521 , C12N2310/3525 , C12N2310/3533
摘要: The disclosure relates to compositions comprising a RNAi agent having a novel format including a spacer subunit. The disclosure relates to compositions comprising a RNAi agent having a novel format: an 18-mer format with at least one internal spacer. These RNAi agents comprise a first and a second 18-mer strand, wherein the first strand is 18 ribonucleotides or 18 total ribonucleotides and spacer subunit(s), and the second strand is 18 total ribonucleotides and spacer subunit(s), wherein: each spacer subunit consists of: (a) a phosphate or modified internucleoside linker and (b) a spacer; a spacer subunit can be at any position in the strand; the two strands form a duplex with at least one blunt end; and the 3 end of one or both strands terminates in a phosphate or modified internucleoside linker and further comprises, in 5 to 3 order: a second spacer; a second phosphate or modified internucleoside linker, and a 3 end cap. In various embodiments, the RNAi agents comprise a first and a second strand, wherein each strand is a 30-mer or shorter, the first strand comprises ribonucleotides, and the second strand comprises ribonucleotides and one or more spacer subunit(s), wherein: each spacer subunit consists of: (a) a phosphate or modified internucleoside linker and (b) a spacer; a spacer subunit can be at any position in the strand. In some embodiments, the 3 end of both strands further comprise, in 5 to 3 order: a second spacer; a second phosphate or modified internucleoside linker; and a 3 end cap. The two strands can have the same or different spacers, phosphates or modified internucleoside linkers, and/or 3 end caps. The strands can be ribonucleotides, or, optionally, one or more nucleotide can be modified or substituted. Optionally, at least one nucleotide comprises a modified internucleoside linker. Optionally, the first two base-pairing nucleotides on the 3 end of the one or both strand are 2-MOE. Optionally, the RNAi agent can be modified on one or both 5 end. Optionally, the first or second strand is the sense strand, and the sense strand can comprise a 5 end cap which reduces the amount of the RNA interference mediated by this strand. Optionally, the RNAi agent is attached to a ligand. This format can be used to devise RNAi agents to a variety of different targets and sequences. The disclosure also relates to processes for making such compositions, and methods and uses of such compositions, e.g., to mediate RNA interference.
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公开(公告)号:US20160244756A1
公开(公告)日:2016-08-25
申请号:US15025826
申请日:2014-10-06
申请人: Jeremy Lee BARYZA , Marcel BLOMMERS , William CHUTKOW , Cesar FERNANDEZ , Erin GENO , Alvar GOSSERT , Paulette GREENIDGE , Dieter HUESKEN , Juerg HUNZIKER , Francois Jean-Charles NATT , Anup PATNAIK , Andrew PATTERSON , Jean-Michel Rene RONDEAU , Jan WEILER , Meicheng ZHU
发明人: Jeremy Lee Baryza , Marcel Blommers , William Chutkow , Cesar Femandez , Erin Geno , Alvar Gossert , Paulette Greenridge , Dieter Huesken , Juerg Hunziker , Francois Jean-Charles Natt , Anup Patnaik , Andrew Patterson , Jean-Michel Rene Rondeau , Jan Weiler , Meicheng Zhu
IPC分类号: C12N15/113
CPC分类号: C12N15/113 , C12N2310/14 , C12N2310/317 , C12N2310/321 , C12N2310/322 , C12N2310/332 , C12N2310/341 , C12N2310/351 , C12N2310/3515 , C12N2310/3521 , C12N2310/3525 , C12N2310/3533
摘要: The disclosure relates to compositions comprising a RNAi agent having a novel format including a spacer subunit. The disclosure relates to compositions comprising a RNAi agent having a novel format: an 18-mer format with at least one internal spacer. These RNAi agents comprise a first and a second 18-mer strand, wherein the first strand is 18 ribonucleotides or 18 total ribonucleotides and spacer subunit(s), and the second strand is 18 total ribonucleotides and spacer subunit(s), wherein: each spacer subunit consists of: (a) a phosphate or modified internucleoside linker and (b) a spacer; a spacer subunit can be at any position in the strand; the two strands form a duplex with at least one blunt end; and the 3 end of one or both strands terminates in a phosphate or modified internucleoside linker and further comprises, in 5 to 3 order: a second spacer; a second phosphate or modified internucleoside linker, and a 3 end cap. In various embodiments, the RNAi agents comprise a first and a second strand, wherein each strand is a 30-mer or shorter, the first strand comprises ribonucleotides, and the second strand comprises ribonucleotides and one or more spacer subunit(s), wherein: each spacer subunit consists of: (a) a phosphate or modified internucleoside linker and (b) a spacer; a spacer subunit can be at any position in the strand. In some embodiments, the 3 end of both strands further comprise, in 5 to 3 order: a second spacer; a second phosphate or modified internucleoside linker; and a 3 end cap. The two strands can have the same or different spacers, phosphates or modified internucleoside linkers, and/or 3 end caps. The strands can be ribonucleotides, or, optionally, one or more nucleotide can be modified or substituted. Optionally, at least one nucleotide comprises a modified internucleoside linker. Optionally, the first two base-pairing nucleotides on the 3 end of the one or both strand are 2-MOE. Optionally, the RNAi agent can be modified on one or both 5 end. Optionally, the first or second strand is the sense strand, and the sense strand can comprise a 5 end cap which reduces the amount of the RNA interference mediated by this strand. Optionally, the RNAi agent is attached to a ligand. This format can be used to devise RNAi agents to a variety of different targets and sequences. The disclosure also relates to processes for making such compositions, and methods and uses of such compositions, e.g., to mediate RNA interference.
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9.
公开(公告)号:US20160106842A1
公开(公告)日:2016-04-21
申请号:US14779939
申请日:2014-03-06
申请人: Jeremy Lee BARYZA , Rohan Eric John BECKWITH , Keith BOWMAN , Crystal BYERS , Tanzina FAZAL , Gabriel Grant GAMBER , Cameron Chuck-Munn LEE , Ritesh Bhanudasji TICHKULE , Chandra VARGEESE , Shuangxi WANG , Laura WEST , Thomas ZABAWA , Junping ZHAO
发明人: Jeremy Lee Baryza , Rohan Eric John Beckwith , Keith Bowman , Crystal Byers , Tanzina Fazal , Gabriel Grant Gamber , Cameron Chuck-Munn Lee , Ritesh Bhanudasji Tichkule , Chandra Vargeese , Shuangxi Wang , Laura West , Thomas Zabawa , Junping Zhao
IPC分类号: A61K47/18 , C12N15/113 , A61K38/22 , C07D295/096 , C07D205/04 , C07C235/42 , A61K47/22 , C07C229/14 , C07C229/12 , C07D213/79 , C07D213/69 , C07C217/58 , C07D317/28
CPC分类号: A61K47/18 , A61K9/0019 , A61K9/1272 , A61K9/5123 , A61K31/713 , A61K38/2264 , A61K47/22 , A61K48/00 , C07C217/58 , C07C219/06 , C07C229/12 , C07C229/14 , C07C235/42 , C07D205/04 , C07D213/69 , C07D213/79 , C07D295/096 , C07D317/28 , C12N15/113 , C12N2310/14 , C12N2320/32
摘要: This invention provides for a compound of formula (I): or a pharmaceutically acceptable salt thereof, wherein R1-R4, L and X are defined herein. The compounds of formula (I) and pharmaceutically acceptable salts thereof are cationic lipids useful in the delivery of biologically active agents to cells and tissues.
摘要翻译: 本发明提供式(I)化合物或其药学上可接受的盐,其中R 1 -R 4,L和X如本文所定义。 式(I)化合物及其药学上可接受的盐是可用于将生物活性剂递送至细胞和组织的阳离子脂质。
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