JP2016521753A5 - - Google Patents
Download PDFInfo
- Publication number
- JP2016521753A5 JP2016521753A5 JP2016519662A JP2016519662A JP2016521753A5 JP 2016521753 A5 JP2016521753 A5 JP 2016521753A5 JP 2016519662 A JP2016519662 A JP 2016519662A JP 2016519662 A JP2016519662 A JP 2016519662A JP 2016521753 A5 JP2016521753 A5 JP 2016521753A5
- Authority
- JP
- Japan
- Prior art keywords
- disease
- composition
- disorder
- treatment
- therapeutic
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 239000000203 mixture Substances 0.000 claims 38
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims 32
- 108091034117 Oligonucleotide Proteins 0.000 claims 28
- 230000001225 therapeutic effect Effects 0.000 claims 25
- 201000010099 disease Diseases 0.000 claims 15
- 208000035475 disorder Diseases 0.000 claims 15
- 150000007523 nucleic acids Chemical class 0.000 claims 13
- 108020004707 nucleic acids Proteins 0.000 claims 12
- 102000039446 nucleic acids Human genes 0.000 claims 12
- 102000004169 proteins and genes Human genes 0.000 claims 10
- 108090000623 proteins and genes Proteins 0.000 claims 9
- 108020004999 messenger RNA Proteins 0.000 claims 8
- 230000000692 anti-sense effect Effects 0.000 claims 7
- 230000002018 overexpression Effects 0.000 claims 6
- 230000009452 underexpressoin Effects 0.000 claims 6
- 108091005461 Nucleic proteins Proteins 0.000 claims 5
- 239000002679 microRNA Substances 0.000 claims 5
- 239000002773 nucleotide Substances 0.000 claims 5
- 125000003729 nucleotide group Chemical group 0.000 claims 5
- 208000024172 Cardiovascular disease Diseases 0.000 claims 4
- 208000012902 Nervous system disease Diseases 0.000 claims 4
- JLCPHMBAVCMARE-UHFFFAOYSA-N [3-[[3-[[3-[[3-[[3-[[3-[[3-[[3-[[3-[[3-[[3-[[5-(2-amino-6-oxo-1H-purin-9-yl)-3-[[3-[[3-[[3-[[3-[[3-[[5-(2-amino-6-oxo-1H-purin-9-yl)-3-[[5-(2-amino-6-oxo-1H-purin-9-yl)-3-hydroxyoxolan-2-yl]methoxy-hydroxyphosphoryl]oxyoxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(5-methyl-2,4-dioxopyrimidin-1-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(6-aminopurin-9-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(6-aminopurin-9-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(6-aminopurin-9-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(6-aminopurin-9-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxyoxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(5-methyl-2,4-dioxopyrimidin-1-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(4-amino-2-oxopyrimidin-1-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(5-methyl-2,4-dioxopyrimidin-1-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(5-methyl-2,4-dioxopyrimidin-1-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(6-aminopurin-9-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(6-aminopurin-9-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(4-amino-2-oxopyrimidin-1-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(4-amino-2-oxopyrimidin-1-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(4-amino-2-oxopyrimidin-1-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(6-aminopurin-9-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(4-amino-2-oxopyrimidin-1-yl)oxolan-2-yl]methyl [5-(6-aminopurin-9-yl)-2-(hydroxymethyl)oxolan-3-yl] hydrogen phosphate Polymers Cc1cn(C2CC(OP(O)(=O)OCC3OC(CC3OP(O)(=O)OCC3OC(CC3O)n3cnc4c3nc(N)[nH]c4=O)n3cnc4c3nc(N)[nH]c4=O)C(COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3CO)n3cnc4c(N)ncnc34)n3ccc(N)nc3=O)n3cnc4c(N)ncnc34)n3ccc(N)nc3=O)n3ccc(N)nc3=O)n3ccc(N)nc3=O)n3cnc4c(N)ncnc34)n3cnc4c(N)ncnc34)n3cc(C)c(=O)[nH]c3=O)n3cc(C)c(=O)[nH]c3=O)n3ccc(N)nc3=O)n3cc(C)c(=O)[nH]c3=O)n3cnc4c3nc(N)[nH]c4=O)n3cnc4c(N)ncnc34)n3cnc4c(N)ncnc34)n3cnc4c(N)ncnc34)n3cnc4c(N)ncnc34)O2)c(=O)[nH]c1=O JLCPHMBAVCMARE-UHFFFAOYSA-N 0.000 claims 4
- 239000000074 antisense oligonucleotide Substances 0.000 claims 4
- 238000012230 antisense oligonucleotides Methods 0.000 claims 4
- 208000027866 inflammatory disease Diseases 0.000 claims 4
- 208000030159 metabolic disease Diseases 0.000 claims 4
- 125000004573 morpholin-4-yl group Chemical group N1(CCOCC1)* 0.000 claims 4
- 108091032973 (ribonucleotides)n+m Proteins 0.000 claims 3
- 206010048643 Hypereosinophilic syndrome Diseases 0.000 claims 3
- 230000001594 aberrant effect Effects 0.000 claims 3
- 230000002159 abnormal effect Effects 0.000 claims 3
- 230000005284 excitation Effects 0.000 claims 3
- 230000014509 gene expression Effects 0.000 claims 3
- 238000001727 in vivo Methods 0.000 claims 3
- 239000002777 nucleoside Substances 0.000 claims 3
- 150000003833 nucleoside derivatives Chemical class 0.000 claims 3
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 claims 2
- 208000035473 Communicable disease Diseases 0.000 claims 2
- 108020004414 DNA Proteins 0.000 claims 2
- 206010028980 Neoplasm Diseases 0.000 claims 2
- 208000025966 Neurological disease Diseases 0.000 claims 2
- 238000012228 RNA interference-mediated gene silencing Methods 0.000 claims 2
- RYYWUUFWQRZTIU-UHFFFAOYSA-N Thiophosphoric acid Chemical class OP(O)(S)=O RYYWUUFWQRZTIU-UHFFFAOYSA-N 0.000 claims 2
- 201000011510 cancer Diseases 0.000 claims 2
- 230000000295 complement effect Effects 0.000 claims 2
- 208000016097 disease of metabolism Diseases 0.000 claims 2
- NAGJZTKCGNOGPW-UHFFFAOYSA-N dithiophosphoric acid Chemical class OP(O)(S)=S NAGJZTKCGNOGPW-UHFFFAOYSA-N 0.000 claims 2
- 208000030533 eye disease Diseases 0.000 claims 2
- 230000009368 gene silencing by RNA Effects 0.000 claims 2
- 208000026278 immune system disease Diseases 0.000 claims 2
- 208000015181 infectious disease Diseases 0.000 claims 2
- 108091070501 miRNA Proteins 0.000 claims 2
- 125000001147 pentyl group Chemical group C(CCCC)* 0.000 claims 2
- 150000008039 phosphoramides Chemical class 0.000 claims 2
- 230000002062 proliferating effect Effects 0.000 claims 2
- MWWATHDPGQKSAR-UHFFFAOYSA-N propyne Chemical compound CC#C MWWATHDPGQKSAR-UHFFFAOYSA-N 0.000 claims 2
- 208000017520 skin disease Diseases 0.000 claims 2
- 238000012385 systemic delivery Methods 0.000 claims 2
- 108091026898 Leader sequence (mRNA) Proteins 0.000 claims 1
- 108091028043 Nucleic acid sequence Proteins 0.000 claims 1
- 208000030852 Parasitic disease Diseases 0.000 claims 1
- 108091081024 Start codon Proteins 0.000 claims 1
- 108091036066 Three prime untranslated region Proteins 0.000 claims 1
- 208000036142 Viral infection Diseases 0.000 claims 1
- 230000033228 biological regulation Effects 0.000 claims 1
- 230000001939 inductive effect Effects 0.000 claims 1
- 208000032839 leukemia Diseases 0.000 claims 1
- 208000037819 metastatic cancer Diseases 0.000 claims 1
- 208000011575 metastatic malignant neoplasm Diseases 0.000 claims 1
- 238000012986 modification Methods 0.000 claims 1
- 230000004048 modification Effects 0.000 claims 1
- 125000003835 nucleoside group Chemical group 0.000 claims 1
- 230000009385 viral infection Effects 0.000 claims 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201361834383P | 2013-06-12 | 2013-06-12 | |
| US61/834,383 | 2013-06-12 | ||
| PCT/US2014/042202 WO2014201306A1 (en) | 2013-06-12 | 2014-06-12 | Systemic in vivo delivery of oligonucleotides |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2019088413A Division JP2019135259A (ja) | 2013-06-12 | 2019-05-08 | オリゴヌクレオチドの全身性イン−ビボ送達 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2016521753A JP2016521753A (ja) | 2016-07-25 |
| JP2016521753A5 true JP2016521753A5 (https=) | 2021-07-29 |
| JP7011389B2 JP7011389B2 (ja) | 2022-01-26 |
Family
ID=52022784
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2016519662A Active JP7011389B2 (ja) | 2013-06-12 | 2014-06-12 | オリゴヌクレオチドの全身性イン－ビボ送達 |
| JP2019088413A Pending JP2019135259A (ja) | 2013-06-12 | 2019-05-08 | オリゴヌクレオチドの全身性イン−ビボ送達 |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2019088413A Pending JP2019135259A (ja) | 2013-06-12 | 2019-05-08 | オリゴヌクレオチドの全身性イン−ビボ送達 |
Country Status (5)
| Country | Link |
|---|---|
| US (3) | US20160367587A1 (https=) |
| EP (1) | EP3007705A4 (https=) |
| JP (2) | JP7011389B2 (https=) |
| CA (1) | CA2951816A1 (https=) |
| WO (1) | WO2014201306A1 (https=) |
Families Citing this family (22)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20160319278A1 (en) | 2015-04-03 | 2016-11-03 | University Of Massachusetts | Fully stabilized asymmetric sirna |
| WO2017030973A1 (en) | 2015-08-14 | 2017-02-23 | University Of Massachusetts | Bioactive conjugates for oligonucleotide delivery |
| EP3827838B1 (en) | 2015-12-16 | 2023-06-07 | The Walter and Eliza Hall Institute of Medical Research | Inhibition of cytokine-induced sh2 protein in nk cells |
| PH12018501207B1 (en) | 2015-12-21 | 2024-02-23 | Novartis Ag | Compositions and methods for decreasing tau expression |
| US10478503B2 (en) | 2016-01-31 | 2019-11-19 | University Of Massachusetts | Branched oligonucleotides |
| JP7406793B2 (ja) | 2017-06-23 | 2023-12-28 | ユニバーシティー オブ マサチューセッツ | ２テイル自己デリバリー型ｓｉＲＮＡおよび関連方法 |
| EP3806850A2 (en) * | 2018-06-15 | 2021-04-21 | Ideaya Biosciences, Inc. | Methods of inhibiting proliferative cells |
| WO2020033899A1 (en) | 2018-08-10 | 2020-02-13 | University Of Massachusetts | Modified oligonucleotides targeting snps |
| US11279930B2 (en) | 2018-08-23 | 2022-03-22 | University Of Massachusetts | O-methyl rich fully stabilized oligonucleotides |
| CN113614232A (zh) | 2019-01-18 | 2021-11-05 | 马萨诸塞大学 | 动态药代动力学修饰锚 |
| US11820985B2 (en) | 2019-03-26 | 2023-11-21 | University Of Massachusetts | Modified oligonucleotides with increased stability |
| EP3947680A2 (en) * | 2019-04-03 | 2022-02-09 | Bristol-Myers Squibb Company | Angptl2 antisense oligonucleotides and uses thereof |
| KR20220047989A (ko) | 2019-08-09 | 2022-04-19 | 유니버시티 오브 매사추세츠 | Snp를 표적화하는 화학적으로 변형된 올리고뉴클레오타이드 |
| US12365894B2 (en) | 2019-09-16 | 2025-07-22 | University Of Massachusetts | Branched lipid conjugates of siRNA for specific tissue delivery |
| WO2021132648A1 (ja) * | 2019-12-27 | 2021-07-01 | ルクサナバイオテク株式会社 | Ｒｅｃｑｌの発現を阻害するアンチセンスオリゴヌクレオチド及びその用途 |
| CA3167444A1 (en) * | 2020-01-11 | 2021-07-15 | Oncoimmunin, Inc. | Targeted and localized in vivo delivery of oligonucleotides |
| CN115666636A (zh) * | 2020-03-10 | 2023-01-31 | 中佛罗里达大学研究基金会有限公司 | 递送基因表达调节剂用于治疗癌症和病毒感染 |
| JP7837560B2 (ja) | 2020-03-26 | 2026-03-31 | ユニバーシティー オブ マサチューセッツ | 安定性の向上を有する修飾オリゴヌクレオチドの合成 |
| WO2021242883A1 (en) | 2020-05-26 | 2021-12-02 | University Of Massachusetts | Synthetic oligonucleotides having regions of block and cluster modifications |
| US20230065782A1 (en) * | 2021-07-14 | 2023-03-02 | Oncoimmunin, Inc. | Targeted and localized in vivo delivery of oligonucleotides |
| WO2025171411A1 (en) | 2024-02-09 | 2025-08-14 | Herophilus, Inc. | Compositions and methods related to modulating macrophage migration inhibitory factor (mif)-cd74 signaling and related treatments for neuroinflammatory conditions |
| WO2025227100A2 (en) * | 2024-04-26 | 2025-10-30 | Purdue Research Foundation | Targeted delivery of therapeutic agent to retinal pigment epithelium in treatment of ocular diseases |
Family Cites Families (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6893868B2 (en) * | 1997-02-20 | 2005-05-17 | Onco Immunin, Inc. | Homo-doubly labeled compositions for the detection of enzyme activity in biological samples |
| US6133032A (en) * | 1999-09-09 | 2000-10-17 | Isis Pharmaceutical Inc. | Antisense modulation of PI3 kinase p110 beta expression |
| WO2002059137A1 (en) * | 2000-11-03 | 2002-08-01 | Isis Pharmaceuticals, Inc. | Nuclease-based method for detecting and quantitating oligonucleotides |
| CA2459347C (en) * | 2001-09-04 | 2012-10-09 | Exiqon A/S | Locked nucleic acid (lna) compositions and uses thereof |
| AU2003225495B2 (en) * | 2002-04-05 | 2009-01-15 | Roche Innovation Center Copenhagen A/S | Oligomeric compounds for the modulation HIF-1alpha expression |
| GB2406169B (en) * | 2002-06-12 | 2006-11-01 | Ambion Inc | Methods and compositions relating to labeled rna molecules that reduce gene expression |
| US20050142581A1 (en) * | 2003-09-04 | 2005-06-30 | Griffey Richard H. | Microrna as ligands and target molecules |
| US20080199960A1 (en) * | 2004-05-13 | 2008-08-21 | Juliano Rudolph L | Methods for the Delivery of Oligomeric Compounds |
| WO2008134593A1 (en) * | 2007-04-25 | 2008-11-06 | President And Fellows Of Harvard College | Molecular circuits |
| EP2167660A1 (en) * | 2007-06-22 | 2010-03-31 | Keygene N.V. | Targeted nucleotide exchange with improved modified oligonucleotides |
| US20100280098A1 (en) * | 2007-10-05 | 2010-11-04 | Juliano Rudolph L | Receptor targeted oligonucleotides |
| US8911948B2 (en) * | 2008-04-30 | 2014-12-16 | Integrated Dna Technologies, Inc. | RNase H-based assays utilizing modified RNA monomers |
| WO2010071852A2 (en) * | 2008-12-19 | 2010-06-24 | University Of Florida Research Foundation, Inc. | Oligonucleotide micelles |
| WO2011072082A2 (en) * | 2009-12-09 | 2011-06-16 | Nitto Denko Corporation | Modulation of hsp47 expression |
| JP2015502365A (ja) * | 2011-12-12 | 2015-01-22 | オンコイミューニン，インコーポレイティド | オリゴヌクレオチドのイン−ビボ送達 |
-
2014
- 2014-06-12 EP EP14811033.1A patent/EP3007705A4/en not_active Withdrawn
- 2014-06-12 JP JP2016519662A patent/JP7011389B2/ja active Active
- 2014-06-12 CA CA2951816A patent/CA2951816A1/en not_active Abandoned
- 2014-06-12 WO PCT/US2014/042202 patent/WO2014201306A1/en not_active Ceased
- 2014-06-12 US US14/897,872 patent/US20160367587A1/en not_active Abandoned
-
2018
- 2018-10-29 US US16/174,091 patent/US20190183918A1/en not_active Abandoned
-
2019
- 2019-05-08 JP JP2019088413A patent/JP2019135259A/ja active Pending
-
2021
- 2021-05-04 US US17/307,350 patent/US20220033815A1/en not_active Abandoned
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP2016521753A5 (https=) | ||
| JP2015502365A5 (https=) | ||
| JP7837560B2 (ja) | 安定性の向上を有する修飾オリゴヌクレオチドの合成 | |
| US20240141362A1 (en) | Modified oligonucleotides with increased stability | |
| Lennox et al. | Chemical modification and design of anti-miRNA oligonucleotides | |
| Zhang | MicroRNAs: role in cardiovascular biology and disease | |
| US20190276892A1 (en) | Micrornas in neurodegenerative disorders | |
| McDermott et al. | The therapeutic potential of microRNAs: disease modulators and drug targets | |
| US8207325B2 (en) | MicroRNA biomarkers for human breast and lung cancer | |
| US20110152352A1 (en) | Smad proteins control drosha-mediated mirna maturation | |
| US20070299030A1 (en) | MicroRNA biomarkers for human breast and lung cancer | |
| JP2019503394A5 (https=) | ||
| WO2016115490A1 (en) | Compounds and methods for modulation of dux4 | |
| US20160362688A1 (en) | Compositions and methods of using microrna inhibitors | |
| Peng et al. | Cancer and non-coding RNAs | |
| Sundaramoorthi et al. | Knockdown of αIIb by RNA degradation by delivering deoxyoligonucleotides piggybacked with control vivo-morpholinos into zebrafish thrombocytes | |
| EP3647423A1 (en) | HETERO DOUBLE-STRANDED antimiR | |
| JP7530836B2 (ja) | 代謝性疾患の処置において使用するためのマイクロｒｎａインヒビター | |
| JP6934695B2 (ja) | 核酸医薬とその使用 | |
| Zhou et al. | Role of the AKT pathway in microRNA expression of human U251 glioblastoma cells Retraction in/10.3892/ijo. 2023.5597 | |
| WO2015038593A1 (en) | Targeting microrna-26a/b for the treatment of neurodegenerative disease | |
| WO2024228398A1 (ja) | グアニン四重鎖構造を誘導するための核酸剤 | |
| Vinther et al. | MicroRNAs and their antagonists as novel therapeutics | |
| AU2013202292B2 (en) | MicroRNAs that regulate muscle cell proliferation and differentiation | |
| Ling et al. | MicroRNAs as Drugs and Drug Targets in Cancer |