ES2620472T3 - Compuestos antisentido - Google Patents
Compuestos antisentido Download PDFInfo
- Publication number
- ES2620472T3 ES2620472T3 ES11186203.3T ES11186203T ES2620472T3 ES 2620472 T3 ES2620472 T3 ES 2620472T3 ES 11186203 T ES11186203 T ES 11186203T ES 2620472 T3 ES2620472 T3 ES 2620472T3
- Authority
- ES
- Spain
- Prior art keywords
- lna
- moe
- wing
- nucleosides
- certain embodiments
- 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.)
- Active
Links
- 150000001875 compounds Chemical class 0.000 title description 13
- 230000000692 anti-sense effect Effects 0.000 title description 7
- 239000002777 nucleoside Substances 0.000 abstract description 38
- 239000000074 antisense oligonucleotide Substances 0.000 abstract description 15
- 238000012230 antisense oligonucleotides Methods 0.000 abstract description 15
- 108091034117 Oligonucleotide Proteins 0.000 abstract description 8
- -1 bicyclic nucleoside Chemical class 0.000 abstract description 5
- 125000003835 nucleoside group Chemical group 0.000 description 28
- YIMATHOGWXZHFX-WCTZXXKLSA-N (2r,3r,4r,5r)-5-(hydroxymethyl)-3-(2-methoxyethoxy)oxolane-2,4-diol Chemical compound COCCO[C@H]1[C@H](O)O[C@H](CO)[C@H]1O YIMATHOGWXZHFX-WCTZXXKLSA-N 0.000 description 20
- 230000004048 modification Effects 0.000 description 16
- 238000012986 modification Methods 0.000 description 16
- ABEXEQSGABRUHS-UHFFFAOYSA-N 16-methylheptadecyl 16-methylheptadecanoate Chemical compound CC(C)CCCCCCCCCCCCCCCOC(=O)CCCCCCCCCCCCCCC(C)C ABEXEQSGABRUHS-UHFFFAOYSA-N 0.000 description 13
- 241000764238 Isis Species 0.000 description 13
- 238000005417 image-selected in vivo spectroscopy Methods 0.000 description 13
- 238000012739 integrated shape imaging system Methods 0.000 description 13
- 239000002773 nucleotide Substances 0.000 description 12
- 125000003729 nucleotide group Chemical group 0.000 description 12
- 108020004999 messenger RNA Proteins 0.000 description 9
- 108020000948 Antisense Oligonucleotides Proteins 0.000 description 8
- 108090000340 Transaminases Proteins 0.000 description 7
- 102000003929 Transaminases Human genes 0.000 description 7
- 235000000346 sugar Nutrition 0.000 description 7
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 6
- 102000014160 PTEN Phosphohydrolase Human genes 0.000 description 6
- 108010011536 PTEN Phosphohydrolase Proteins 0.000 description 6
- 108010003415 Aspartate Aminotransferases Proteins 0.000 description 5
- 102000004625 Aspartate Aminotransferases Human genes 0.000 description 5
- 210000004185 liver Anatomy 0.000 description 5
- 150000003833 nucleoside derivatives Chemical class 0.000 description 5
- 206010019851 Hepatotoxicity Diseases 0.000 description 4
- 241000699670 Mus sp. Species 0.000 description 4
- 231100000304 hepatotoxicity Toxicity 0.000 description 4
- 230000007686 hepatotoxicity Effects 0.000 description 4
- 108020004707 nucleic acids Proteins 0.000 description 4
- 102000039446 nucleic acids Human genes 0.000 description 4
- 150000007523 nucleic acids Chemical class 0.000 description 4
- 210000002966 serum Anatomy 0.000 description 4
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 229910052757 nitrogen Inorganic materials 0.000 description 3
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 3
- 102000018616 Apolipoproteins B Human genes 0.000 description 2
- 108010027006 Apolipoproteins B Proteins 0.000 description 2
- 101100346155 Caenorhabditis elegans oma-2 gene Proteins 0.000 description 2
- 241001346558 Pseudognaphalium sandwicensium Species 0.000 description 2
- 125000004429 atom Chemical group 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 125000004432 carbon atom Chemical group C* 0.000 description 2
- 230000000116 mitigating effect Effects 0.000 description 2
- 125000004573 morpholin-4-yl group Chemical group N1(CCOCC1)* 0.000 description 2
- 102100036475 Alanine aminotransferase 1 Human genes 0.000 description 1
- 108010082126 Alanine transaminase Proteins 0.000 description 1
- 102100034343 Integrase Human genes 0.000 description 1
- 101710203526 Integrase Proteins 0.000 description 1
- 206010067125 Liver injury Diseases 0.000 description 1
- 101710163270 Nuclease Proteins 0.000 description 1
- 102000006382 Ribonucleases Human genes 0.000 description 1
- 108010083644 Ribonucleases Proteins 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000003776 cleavage reaction Methods 0.000 description 1
- 125000000596 cyclohexenyl group Chemical group C1(=CCCCC1)* 0.000 description 1
- 125000002637 deoxyribonucleotide group Chemical group 0.000 description 1
- 150000002243 furanoses Chemical group 0.000 description 1
- 231100000234 hepatic damage Toxicity 0.000 description 1
- 238000009396 hybridization Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007928 intraperitoneal injection Substances 0.000 description 1
- 230000008818 liver damage Effects 0.000 description 1
- 125000001644 phenoxazinyl group Chemical class C1(=CC=CC=2OC3=CC=CC=C3NC12)* 0.000 description 1
- 102000004196 processed proteins & peptides Human genes 0.000 description 1
- 108090000765 processed proteins & peptides Proteins 0.000 description 1
- 125000002652 ribonucleotide group Chemical group 0.000 description 1
- 230000007017 scission Effects 0.000 description 1
- 150000008163 sugars Chemical class 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/70—Carbohydrates; Sugars; Derivatives thereof
- A61K31/7088—Compounds having three or more nucleosides or nucleotides
- A61K31/712—Nucleic acids or oligonucleotides having modified sugars, i.e. other than ribose or 2'-deoxyribose
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/70—Carbohydrates; Sugars; Derivatives thereof
- A61K31/7088—Compounds having three or more nucleosides or nucleotides
- A61K31/7125—Nucleic acids or oligonucleotides having modified internucleoside linkage, i.e. other than 3'-5' phosphodiesters
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N15/00—Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
- C12N15/09—Recombinant DNA-technology
- C12N15/11—DNA or RNA fragments; Modified forms thereof; Non-coding nucleic acids having a biological activity
- C12N15/111—General methods applicable to biologically active non-coding nucleic acids
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N15/00—Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
- C12N15/09—Recombinant DNA-technology
- C12N15/11—DNA or RNA fragments; Modified forms thereof; Non-coding nucleic acids having a biological activity
- C12N15/113—Non-coding nucleic acids modulating the expression of genes, e.g. antisense oligonucleotides; Antisense DNA or RNA; Triplex- forming oligonucleotides; Catalytic nucleic acids, e.g. ribozymes; Nucleic acids used in co-suppression or gene silencing
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N2310/00—Structure or type of the nucleic acid
- C12N2310/10—Type of nucleic acid
- C12N2310/11—Antisense
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N2310/00—Structure or type of the nucleic acid
- C12N2310/30—Chemical structure
- C12N2310/31—Chemical structure of the backbone
- C12N2310/315—Phosphorothioates
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N2310/00—Structure or type of the nucleic acid
- C12N2310/30—Chemical structure
- C12N2310/32—Chemical structure of the sugar
- C12N2310/321—2'-O-R Modification
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N2310/00—Structure or type of the nucleic acid
- C12N2310/30—Chemical structure
- C12N2310/32—Chemical structure of the sugar
- C12N2310/323—Chemical structure of the sugar modified ring structure
- C12N2310/3231—Chemical structure of the sugar modified ring structure having an additional ring, e.g. LNA, ENA
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N2310/00—Structure or type of the nucleic acid
- C12N2310/30—Chemical structure
- C12N2310/33—Chemical structure of the base
- C12N2310/334—Modified C
- C12N2310/3341—5-Methylcytosine
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N2310/00—Structure or type of the nucleic acid
- C12N2310/30—Chemical structure
- C12N2310/34—Spatial arrangement of the modifications
- C12N2310/341—Gapmers, i.e. of the type ===---===
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N2310/00—Structure or type of the nucleic acid
- C12N2310/30—Chemical structure
- C12N2310/34—Spatial arrangement of the modifications
- C12N2310/346—Spatial arrangement of the modifications having a combination of backbone and sugar modifications
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N2310/00—Structure or type of the nucleic acid
- C12N2310/30—Chemical structure
- C12N2310/35—Nature of the modification
- C12N2310/351—Conjugate
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N2320/00—Applications; Uses
- C12N2320/50—Methods for regulating/modulating their activity
- C12N2320/53—Methods for regulating/modulating their activity reducing unwanted side-effects
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical & Material Sciences (AREA)
- Genetics & Genomics (AREA)
- Biomedical Technology (AREA)
- Molecular Biology (AREA)
- Organic Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Biochemistry (AREA)
- Biotechnology (AREA)
- General Engineering & Computer Science (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Public Health (AREA)
- Plant Pathology (AREA)
- Biophysics (AREA)
- Epidemiology (AREA)
- Physics & Mathematics (AREA)
- Microbiology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- General Chemical & Material Sciences (AREA)
- Saccharide Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Abstract
Un oligonucleótido antisentido gapmer que tiene un hueco desoxi y al menos un engarce internucleosídico modificado, una región ala 5' situada en el extremo 5' del hueco desoxi, y una región ala 3' situada en el extremo 3' del hueco desoxi, en donde al menos uno de los nucleósidos bicíclicos 4' a 2' y el ala 5' tiene al menos un nucleósido 2' modificado no biciclíco.
Description
5
15
25
35
45
55
65
14-4, 4-14-2, 3-14-3, 1-13-6, 6-13-1, 2-13-5, 5-13-2, 3-13-4, 4-13-3, 1-12-7, 7-12-1, 2-12-6, 6-12-2, 3-12-5, 5-12-3, 412-4, 1-11-8, 8-11-1, 2-11-7, 7-11-2, 3-11-6, 6-11-3, 4-11-5, 5-11-4, 1-18-1, 1-17-2, 2-17-1, 1-16-3, 3-16-1, 2-16-2, 115-4, 4-15-1, 2-15-3, 3-15-2, 1-14-5, 2-14-4, 4-14-2, 3-14-3, 1-13-6, 6-13-1, 2-13-5, 5-13-2, 3-13-4, 4-13-3, 1-12-7, 712-1, 2-12-6, 6-12-2, 3-12-5, 5-12-3, 4-12-4, 1-11-8, 8-11-1, 2-11-7, 7-11-2, 3-11-6, 6-11-3, 4-11-5, 5-11-4, 1-19-1, 118-2, 2-18-1, 1-17-3, 3-17-1, 2-17-2, 1-16-4, 4-16-1, 2-16-3, 3-16-2, 1-15-5, 2-15-4, 4-15-2, 3-15-3, 1-14-6, 6-14-1, 214-5, 5-14-2, 3-14-4, 4-14-3, 1-13-7, 7-13-1, 2-13-6, 6-13-2, 3-13-5, 5-13-3, 4-13-4, 1-12-8, 8-12-1, 2-12-7, 7-12-2, 312-6, 6-12-3, 4-12-5, 5-12-4, 2-11-8, 8-11-2, 3-11-7, 7-11-3, 4-11-6, 6-11-4, 5-11-5, 1-20-1, 1-19-2, 2-19-1, 1-18-3, 318-1, 2-18-2, 1-17-4, 4-17-1, 2-17-3, 3-17-2, 1-16-5, 2-16-4, 4-16-2, 3-16-3, 1-15-6, 6-15-1, 2-15-5, 5-15-2, 3-15-4, 415-3, 1-14-7. 7-14-1, 2-14-6, 6-14-2. 3-14-5, 5-14-3, 4-14-4, 1-13-8, 8-13-1, 2-13-7, 7-13-2, 3-13-6, 6-13-3, 4-13-5, 513-4, 2-12-8, 8-12-2, 3-12-7, 7-12-3, 4-12-6, 6-12-4, 5-12-5, 3-11-8, 8-11-3, 4-11-7, 7-11-4, 5-11-6, 6-11-5, 1-21-1, 120-2, 2-20-1, 1-20-3, 3-19-1, 2-19-2, 1-18-4, 4-18-1, 2-18-3, 3-18-2, 1-17-5, 2-17-4, 4-17-2, 3-17-3, 1-16-6, 6-16-1, 216-5, 5-16-2, 3-16-4, 4-16-3, 1-15-7, 7-15-1, 2-15-6, 6-15-2, 3-15-5, 5-15-3, 4-15-4, 1-14-8, 8-14-1, 2-14-7, 7-14-2, 314-6, 6-14-3, 4-14-5, 5-14-4, 2-13-8, 8-13-2, 3-13-7, 7-13-3, 4-13-6, 6-13-4, 5-13-5, 1-12-10, 10-12-1, 2-12-9, 9-12-2, 3-12-8, 8-12-3, 4-12-7, 7-12-4, 5-12-6, 6-12-5, 4-11-8, 8-11-4, 5-11-7, 7-11-5, 6-11-6, 1-22-1, 1-21-2, 2-21-1, 1-21-3, 3-20-1, 2-20-2, 1-19-4, 4-19-1, 2-19-3, 3-19-2, 1-18-5, 2-18-4, 4-18-2, 3-18-3, 1-17-6, 6-17-1, 2-17-5, 5-17-2, 3-17-4, 4-17-3, 1-16-7, 7-16-1, 2-16-6, 6-16-2, 3-16-5, 5-16-3, 4-16-4, 1-15-8, 8-15-1, 2-15-7, 7-15-2, 3-15-6, 6-15-3, 4-15-5, 5-15-4, 2-14-8, 8-14-2, 3-14-7, 7-14-3, 4-14-6, 6-14-4, 5-14-5, 3-13-8, 8-13-3, 4-13-7, 7-13-4, 5-13-6, 6-13-5, 4-12-8, 8-12-4, 5-12-7, 7-12-5, 6-12-6, 5-11-8, 8-11-5, 6-11-7 ó 7-11-6. En una realización particular, los oligonucleótidos antisentido de hueco ensanchado de la presente invención tienen un motivo de ala-hueco-ala 2-16-2, 3-14-3 ó 4-12
4.
Como se usa en el presente documento, la expresión “nucleótido modificado de alta afinidad” se refiere a un nucleótido que tiene al menos una base nitrogenada, engarce internucleosídico o resto de azúcar modificado, de modo que la modificación aumenta la afinidad de un compuesto antisentido que comprende el nucleótido modificado por un ácido nucleico diana. Las modificaciones de alta afinidad incluyen, pero sin limitación, BNA, LNA y 2’-MOE.
Como se usa en el presente documento el término “mimético” se refiere a grupos que sustituyen a un azúcar, una base nitrogenada y/o engarce internucleosídico. En general, se usa un mimético en lugar del azúcar o combinación azúcar-engarce internucleosídico, y la base nitrogenada se mantiene para hibridación con una diana seleccionada. Los ejemplos representativos de un mimético de azúcar incluyen, pero sin limitación, ciclohexenilo o morfolino. Los ejemplos representativos de un mimético para una combinación de azúcar-engarce internucleosídico, incluyen, pero sin limitación, ácidos péptido nucleicos (PNA) y grupos morfolino ligados por engarces aquirales no cargados. En algunos casos se usa un mimético en lugar de la base nitrogenada. Los miméticos de base nitrogenada representativos se conocen bien en la técnica e incluyen, pero sin limitación, análogos de fenoxazina tricíclica y bases universales (Berger y col., Nuc Acid Res. 2000, 28: 2911-14, incorporado en el presente documento por referencia). Se conocen bien por los expertos en la materia procedimientos de síntesis de miméticos de azúcar, nucleósidos y bases nitrogenadas.
Como se usa en el presente documento, la expresión “nucleósido bicíclico” o “BNA” se refiere a un nucleósido en el que la parte de furanosa del nucleósido incluye un enlace que conecta dos átomos en el anillo de furanosa, formando de este modo un sistema de anillo bicíclico. Los BNA incluyen, pero sin limitación, α-L-LNA, β-D-LNA, ENA, Oxiamino BNA (2’-O-N(CH3)-CH2-4’) y Aminooxi BNA (2’-N(CH3)-O-CH2-4’).
Como se usa en el presente documento, la expresión “nucleósido bicíclico 4’ a 2’” se refiere a un BNA en el que el enlace que conecta dos átomos del anillo de furanosa enlaza el átomo de carbono 4’ y átomo de carbono 2’ del anillo de furanosa, formando de este modo un sistema de anillo bicíclico. Las estructuras representativas de BNA incluyen pero sin limitación:
Aminooxi BNA Oxiamino BNA 9
5
15
25
- ala 5’
- ala 3’
- Posición de nucleósido (5’ a 3’)
- Tipo de nucleósido/ modificaciones engarce dentro del ala Posición de nucleósido (5’ a 3’) Tipo de nucleósido/ modificaciones engarce dentro del ala
- 1 2
- MOE BNA P=S 1 2 LNA LNA P=S
- 1
- LNA Ninguno 1 2 ENA DNA P=S
- 1 2
- ENA MOE P=O 1 MOE Ninguno
- 1
- ENA Ninguno 1 2 MOE LNA P=S
- 1 2
- MOE LNA P=S 1 2 MOE LNA P=S
- 1 2
- MOE LNA P=S 1 2 LNA MOE P=O
- 1 2
- 2’-F Oxiamino BNA P=S 1 Oxiamino BNA Ninguno
- 1 2
- ENA ENA P=S 1 2 3 ENA ENA MOE P=S; P=O
- 1 2 3
- LNA MOE LNA P=S: P=S 1 2 3 LNA MOE LNA P=S; P=S
- 1 2
- MOE LNA P=S 1 2 LNA MOE P=S
Ciertas alas asimétricas
En ciertas realizaciones, los compuestos oligoméricos comprenden alas asimétricas. En tales realizaciones,
cada uno de los nucleósidos del ala 3’ comprende la misma modificación (o no modificación) y cada uno de los
nucleósidos del ala 5’ comprende la misma modificación (o no modificación), pero las modificaciones del ala 5’ y el
35 ala 3’ son diferentes entre sí.
Ciertos huecos
En ciertas realizaciones, los compuestos oligoméricos comprenden un hueco entre el ala 5’ y el ala 3’. En ciertas realizaciones el hueco comprende cinco, seis, siete, ocho, nueve, diez, once, doce, trece o catorce nucleósidos. En ciertas realizaciones, los nucleósidos del hueco son desoxirribonucleótidos no modificados. En ciertas realizaciones, los nucleósidos del hueco son ribonucleótidos no modificados. En ciertas realizaciones, las modificaciones del hueco (si las hubiera) dan como resultado un compuesto antisentido que, cuando se une a su ácido nucleico diana, soporta la escisión por una RNasa, incluyendo, pero sin limitación, RNasa H.
45 En ciertas realizaciones, los engarces internucleosídicos en el hueco son engarces internucleosídicos de origen natural. En ciertas realizaciones, los engarces internucleosídicos en el hueco son engarces de origen no natural. En ciertas realizaciones tales, los engarces internucleosídicos en el hueco son más resistentes a una o más nucleasas que los engarces internucleosídicos de origen natural. En ciertas realizaciones tales, los engarces internucleosídicos en el hueco son engarces de fosforotioato (P=S). En ciertas realizaciones, los engarces internucleosídicos en el hueco son todos iguales entre sí. En ciertas realizaciones, los engarces internucleosídicos dentro de hueco no son todos iguales.
En ciertas realizaciones, el hueco comprende al menos 2 nucleósidos. En ciertas realizaciones, el hueco
55 comprende al menos 3 nucleósidos. En ciertas realizaciones, el hueco comprende al menos 4 nucleósidos. En ciertas realizaciones, el hueco comprende al menos 5 nucleósidos. En ciertas realizaciones, el hueco comprende al menos 6 nucleósidos. En ciertas realizaciones, el hueco comprende al menos 7 nucleósidos. En ciertas realizaciones, el hueco comprende al menos 8 nucleósidos. En ciertas realizaciones, el hueco comprende al menos 9 nucleósidos. En ciertas realizaciones, el hueco comprende al menos 10 nucleósidos. En ciertas realizaciones, el hueco comprende al menos 11 nucleósidos. En ciertas realizaciones, el hueco comprende al menos 12 nucleósidos. En ciertas realizaciones, el hueco comprende al menos 13 nucleósidos. En ciertas realizaciones, el hueco comprende al menos 14 nucleósidos. En ciertas realizaciones, el hueco comprende al menos 15 nucleósidos. En ciertas realizaciones, el hueco comprende al menos 16 nucleósidos. En ciertas realizaciones, el hueco comprende al menos 17 nucleósidos. En ciertas realizaciones, el hueco comprende al menos 18 nucleósidos. En ciertas
65 realizaciones, el hueco comprende al menos 19 nucleósidos. En ciertas realizaciones, el hueco comprende al menos
18
5
15
25
35
45
55
65
Los resultados de un estudio tal, usando gapmer 2-10-2 modificados por LNA que tienen diversos números de modificaciones de ala 2’-MOE se resumen en la Tabla 3.
Tabla 3
- Reducción de ARNm Diana y Transaminasas de Hígado después de la Administración de Oligonucleótidos Antisentido Modificados por 2’-MOE y Modificados por LNA
- Nº de ISIS
- ALT AST ARNm de PTEN (% de UTC) Química del Ala
- Solución salina
- 39 68 100,0 N/D
- 394424
- 38 75 89,7 Alas 2’-MOE
- 392056
- 1249 770 32,4 Alas LNA
- 396570
- 51 84 57,8 Alas LNA con un MOE 2’ en la posición 5’ 1
- 396571
- 42 79 63,8 Alas LNA con un MOE 2’ en la posición 5’ 2
- 396574
- 36 67 71,0 2’-MOE en el ala 5’ LNA en el ala 3’
- 396572
- 497 327 48,8 Alas LNA con un 2’-MOE en la posición 3’ 13
- 396573
- 531 316 46,7 Alas LNA con un 2’-MOE en la posición 3’ 14
- 396575
- 473 341 41,8 LNA en el ala 5’ 2’-MOE en el ala 3’
La administración de oligonucleótidos antisentido gapmer 2-10-2 con alas de nucleótidos 2’-MOE (ISIS 394424) tenían niveles de ALT/AST que son adecuados con los niveles descritos en la técnica asociados con otros oligonucleótidos antisentido gapmer 2’MOE. Por el contrario, el oligonucleótido antisentido gapmer con alas modificadas con LNA (ISIS 392056) redujo el ARNm diana (PTEN), pero dio como resultado niveles gravemente elevados de transaminasas de hígado en suero de ratones tratados, lo que indica hepatotoxicidad. Los oligonucleótidos antisentido gapmer que tienen nucleótidos 2’-MOE añadidos a las regiones ala 3’ y 5’ dieron como resultado una mitigación de las transaminasas en suero elevadas causadas por el gapmer de LNA, ISIS 392056. Los gapmer con modificación 2’-MOE de solamente las alas 5’ (uno o ambos nucleótidos) de oligonucleótidos antisentido modificados con LNA (ISIS 396570, ISIS 396571 y ISIS 396574) dieron como resultado concentraciones de transaminasa en suero cercanas a las del oligonucleótido antisentido gapmer 2’MOE (ISIS 394424) después de administración a ratones, lo que indica que la sustitución de nucleósido o nucleósidos LNA específicos con nucleósido o nucleósidos 2’ modificados proporcionó un compuestos con un perfil de hepatotoxicidad mejorado. Estos compuestos también redujeron el ARNm de PTEN diana en relación con el UTC. La modificación 2’-MOE de los nucleótidos del ala 3’ (ISIS 396572, ISIS 396573, ISIS 396575) dio como resultado la mitigación de la elevación de transaminasas causada por el oligonucleótido antisentido gapmer LNA. Juntos, estos datos indican que la modificación 2’-MOE de los nucleótidos de ala pueden mitigar la hepatotoxicidad de gapmer de LNA 2-10-2 a niveles que son proporcionados para otros gapmer 2’-MOE, mientras que mantienen la reducción del ARNm diana.
Ejemplo 4
Compuestos Antisentido Gapmer 2-10-2 Cortos con Conjugados C16 en Nucleótido 5’ Terminal que se Dirigen a ApoB.
Los estudios descritos en el presente documento se realizaron usando dos oligonucleótidos antisentido gapmer 2-10-2 modificados para determinar si la modificación de nucleótidos podría mitigar la hepatotoxicidad asociada con el resto de ácido nucleico bloqueado (LNA). Las secuencias y motivos de compuestos antisentido se muestran en la Tabla 4. Cada compuestos se dirige a secuencias de ApoB publicadas incluyendo Nº de Acceso de Genbank U92437.1 (SEC ID Nº: 7), (sitio 140). Cada compuesto es un gapmer 2-10-2 (shortmer), que es de 14 nucleótidos de longitud que tiene una región “hueco” central que consiste en diez 2’-desoxinucleótidos que están flanqueados por una región “ala” 5’ y una 3’, cada una de 2 nucleótidos de longitud. Como se muestra en la Tabla 4, los nucleótidos ala de los compuestos ASO individuales portan modificaciones de azúcares distintas. Cada
29
Tabla 8
5
15
- Compuestos Antisentido LNA Cortos con Modificaciones MOE
- Nº de ISIS
- Secuencia SEC ID Nº
- 394420
- meCeTeGCTAGCCTCTGGATTeTe 10
- 394425
- meClTlGCTAGCCTCTGGATTlTl 10
- 399700
- meCeTlGCTAGCCTCTGGATTlTl 10
- 399701
- meClTeGCTAGCCTCTGGATTlTl 10
- 399702
- meCeTeGCTAGCCTCTGGATTlTl 10
- 399703
- meC1T1GCTAGCCTCTGGATTeTe 10
- 400521
- C5lU5lGCTAGCCTCTGGATU5lU5l 10
- 400522
- C6lU6lGCTAGCCTCTGGATU6lU6l 10
- 400523
- C6lU6lGCTAGCCTCTGGATU6lU6l 10
- 400524
- C6lU6lGCTAGCCTCTGGATU6lU6l 10
- 400525
- C6lU6lGCTAGCCTCTGGATU6lU6l 10
25 Se proporcionó a ratones macho Balb/c de 6 semanas de edad (Jackson Laboratory. Bar Harbor, ME) una inyección intraperitoneal sencilla de 10 ó 2 µmol/kg de un oligonucleótido antisentido PTEN (ASO) de la Tabla 9. Los ratones se sacrificaron 72 horas después de la inyección de ASO o control (solución salina) y las concentraciones en suero de transaminasas de hígado (alanina aminotransferasa) [ALT] y aspartato aminotransferasa [AST]) se midieron en unidades internacionales (UI)/l como indicadores de daño del hígado, usando procedimientos bien conocidos por los expertos habituales en la materia. Los niveles de ARNm diana (PTEN) en el hígado se determinaron por procedimientos bien conocidos por los expertos habituales en la materia y la reducción del ARNm diana se enumeró como porcentaje de control no tratado (% de UTC). Los resultados se resumen en la Tabla 9.
Tabla 9
35
45
55
65
- Reducción de ARNm Diana y Transaminasas de Hígado Después de la Administración de Oligonucleótidos Antisentido Modificados por LNA y Modificados por 2’-MOE
- Nº de ISIS
- Dosis (µmol/kg) ALT AST ARNm de PTEN (% de UTC) Química de ala
- Solución salina
- 39 66 100 N/D
- 394420
- 2 30 78 79 Alas 2’-MOE
- 10
- 49 91 26
- 394425
- 2 41 78 11 Alas LNA
- 10
- 2453 2240 2
- 399700
- 2 45 148 36 Alas LNA con un 2’-MOE en la pos. 5’ 1
- 10
- 71 245 6
- 399701
- 2 42 140 48 Alas LNA con un 2’-MOE en la pos. 5’ 2
- 10
- 40 109
- 10
- 399702
- 2 36 78 69 2’-MOE en ala 5’ LNA en ala 3’
- 10
- 41 99 19
- 399703
- 2 33 99 17 LNA en ala 5’ 2’-MOE en ala 3’
- 10
- 807 731 2
- 400521
- 2 37 81 21 5l = alas 5’-(S)-Me-BNA
- 10
- 152 182 4
- 2
- 44 113 18
- 10
- 794 696 4
- 2
- 43 153 17
- 10
- 1374 818 4
- 2
- 31 59 23
- 10
- 269 263 4
- 2
- 43 110 21
- 10
- 765 636 3
- *pos. = posición en secuencia de nucleótidos
32
Claims (1)
-
imagen1
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US85289406P | 2006-10-18 | 2006-10-18 | |
US852894P | 2006-10-18 |
Publications (2)
Publication Number | Publication Date |
---|---|
ES2620472T3 true ES2620472T3 (es) | 2017-06-28 |
ES2620472T5 ES2620472T5 (es) | 2020-07-09 |
Family
ID=39052713
Family Applications (3)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ES11186113T Active ES2526295T5 (es) | 2006-10-18 | 2007-10-18 | Compuestos antisentido |
ES07844422T Active ES2377327T5 (es) | 2006-10-18 | 2007-10-18 | Compuestos antisentido |
ES11186203T Active ES2620472T5 (es) | 2006-10-18 | 2007-10-18 | Compuestos antisentido |
Family Applications Before (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ES11186113T Active ES2526295T5 (es) | 2006-10-18 | 2007-10-18 | Compuestos antisentido |
ES07844422T Active ES2377327T5 (es) | 2006-10-18 | 2007-10-18 | Compuestos antisentido |
Country Status (10)
Country | Link |
---|---|
US (4) | US9550988B2 (es) |
EP (5) | EP3916095A1 (es) |
JP (2) | JP5665317B2 (es) |
AT (1) | ATE540118T1 (es) |
AU (3) | AU2007310989B2 (es) |
CA (1) | CA2667055C (es) |
DK (3) | DK2410053T4 (es) |
ES (3) | ES2526295T5 (es) |
HK (1) | HK1166643A1 (es) |
WO (1) | WO2008049085A1 (es) |
Families Citing this family (226)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
ES2386578T3 (es) | 2006-05-05 | 2012-08-23 | Isis Pharmaceuticals, Inc. | Compuestos y procedimientos para modular la expresión de PCSK9 |
JP5665317B2 (ja) * | 2006-10-18 | 2015-02-04 | アイシス ファーマシューティカルズ, インコーポレーテッド | アンチセンス化合物 |
DK2149605T3 (da) * | 2007-03-22 | 2013-09-30 | Santaris Pharma As | Korte RNA antagonist forbindelser til modulering af det ønskede mRNA |
WO2009046426A2 (en) * | 2007-10-04 | 2009-04-09 | Isis Pharmaceuticals, Inc. | Compounds and methods for improving cellular uptake of oligomeric compounds |
WO2009124295A2 (en) * | 2008-04-04 | 2009-10-08 | Isis Pharmaceuticals, Inc. | Oligomeric compounds comprising bicyclic nucleosides and having reduced toxicity |
MX2011004097A (es) | 2008-10-15 | 2011-07-28 | Isis Pharmaceuticals Inc | Modulacion de la expresion del factor 11. |
RU2015151857A (ru) | 2008-12-02 | 2019-01-15 | Уэйв Лайф Сайенсес Джапан, Инк. | Способ синтеза модифицированных по атому фосфора нуклеиновых кислот |
AU2010270714B2 (en) | 2009-07-06 | 2015-08-13 | Wave Life Sciences Ltd. | Novel nucleic acid prodrugs and methods use thereof |
US9006198B2 (en) | 2010-02-08 | 2015-04-14 | Isis Pharmaceuticals, Inc. | Selective reduction of allelic variants |
EP3561060A1 (en) | 2010-02-08 | 2019-10-30 | Ionis Pharmaceuticals, Inc. | Selective reduction of allelic variants |
CN106434648A (zh) * | 2010-07-19 | 2017-02-22 | F·C·贝内特 | 肌强直性营养障碍蛋白激酶(dmpk)表达的调节 |
US8648053B2 (en) | 2010-10-20 | 2014-02-11 | Rosalind Franklin University Of Medicine And Science | Antisense oligonucleotides that target a cryptic splice site in Ush1c as a therapeutic for Usher syndrome |
AU2011325956B2 (en) | 2010-11-12 | 2016-07-14 | The General Hospital Corporation | Polycomb-associated non-coding RNAs |
US9920317B2 (en) | 2010-11-12 | 2018-03-20 | The General Hospital Corporation | Polycomb-associated non-coding RNAs |
CA3077910A1 (en) | 2010-11-17 | 2012-05-24 | Ionis Pharmaceuticals, Inc. | Modulation of alpha synuclein expression |
EP2673361B1 (en) | 2011-02-08 | 2016-04-13 | Ionis Pharmaceuticals, Inc. | Oligomeric compounds comprising bicyclic nucleotides and uses thereof |
WO2012161806A1 (en) * | 2011-02-25 | 2012-11-29 | Isis Pharmaceuticals, Inc. | Modulation of stat3 expression |
LT3505528T (lt) | 2011-04-21 | 2021-04-26 | Glaxo Group Limited | Hepatito b viruso (hbv) raiškos moduliacija |
WO2012151324A1 (en) | 2011-05-02 | 2012-11-08 | Isis Pharmaceuticals, Inc. | Antisense compounds targeting genes associated with usher syndrome |
CN107365339A (zh) | 2011-07-19 | 2017-11-21 | 波涛生命科学有限公司 | 合成官能化核酸的方法 |
US9752142B2 (en) | 2011-08-11 | 2017-09-05 | Ionis Pharmaceuticals, Inc. | Gapped oligomeric compounds comprising 5′-modified deoxyribonucleosides in the gap and uses thereof |
EP2756080B1 (en) | 2011-09-14 | 2019-02-20 | Translate Bio MA, Inc. | Multimeric oligonucleotide compounds |
US9243291B1 (en) * | 2011-12-01 | 2016-01-26 | Isis Pharmaceuticals, Inc. | Methods of predicting toxicity |
WO2013138353A2 (en) * | 2012-03-12 | 2013-09-19 | Shire Human Genetic Therapies, Inc. | Compositions and methods for modulation of atxn3 expression |
EP3336189A1 (en) | 2012-04-20 | 2018-06-20 | Ionis Pharmaceuticals, Inc. | Oligomeric compounds comprising bicyclic nucleotides and uses thereof |
AU2013262649A1 (en) | 2012-05-16 | 2015-01-22 | Rana Therapeutics, Inc. | Compositions and methods for modulating smn gene family expression |
US10837014B2 (en) | 2012-05-16 | 2020-11-17 | Translate Bio Ma, Inc. | Compositions and methods for modulating SMN gene family expression |
WO2013173645A1 (en) | 2012-05-16 | 2013-11-21 | Rana Therapeutics, Inc. | Compositions and methods for modulating utrn expression |
JP2015519057A (ja) * | 2012-05-16 | 2015-07-09 | ラナ セラピューティクス インコーポレイテッド | Pten発現を調節するための組成物及び方法 |
EA201492120A1 (ru) | 2012-05-16 | 2015-10-30 | Рана Терапьютикс, Инк. | Композиции и способы для модулирования экспрессии atp2a2 |
EA201492116A1 (ru) | 2012-05-16 | 2015-05-29 | Рана Терапьютикс, Инк. | Композиции и способы для модулирования экспрессии mecp2 |
AU2013262700A1 (en) | 2012-05-16 | 2015-01-22 | Rana Therapeutics, Inc. | Compositions and methods for modulating hemoglobin gene family expression |
US9574193B2 (en) | 2012-05-17 | 2017-02-21 | Ionis Pharmaceuticals, Inc. | Methods and compositions for modulating apolipoprotein (a) expression |
WO2013173789A2 (en) | 2012-05-17 | 2013-11-21 | Isis Pharmaceuticals, Inc. | Antisense oligonucleotide compositions |
DK2855500T3 (da) | 2012-05-24 | 2020-09-14 | Ionis Pharmaceuticals Inc | Fremgangsmåder og sammensætninger til modulering af apolipoprotein (A)-ekspression |
US9487780B2 (en) | 2012-06-01 | 2016-11-08 | Ionis Pharmaceuticals, Inc. | Antisense compounds targeting genes associated with fibronectin |
US9828602B2 (en) | 2012-06-01 | 2017-11-28 | Ionis Pharmaceuticals, Inc. | Antisense compounds targeting genes associated with fibronectin |
AU2013287630B2 (en) | 2012-07-13 | 2017-05-25 | Shin Nippon Biomedical Laboratories, Ltd. | Chiral nucleic acid adjuvant |
CA2879023C (en) | 2012-07-13 | 2017-03-28 | Wave Life Sciences Japan | Asymmetric auxiliary group |
CN104661664B (zh) | 2012-07-13 | 2020-07-03 | 波涛生命科学有限公司 | 手性控制 |
JP2015529469A (ja) | 2012-09-14 | 2015-10-08 | ラナ セラピューティクス インコーポレイテッド | 多量体オリゴヌクレオチド化合物 |
EP2906699A4 (en) | 2012-10-11 | 2016-06-08 | Ionis Pharmaceuticals Inc | OLIGOMER COMPOUNDS WITH BICYCLIC NUCLEOSIDES AND USES THEREOF |
US20160138014A1 (en) * | 2012-10-12 | 2016-05-19 | Isis Pharmaceuticals, Inc. | Antisense compounds and uses thereof |
JP6574383B2 (ja) * | 2012-12-05 | 2019-09-11 | アルナイラム ファーマシューティカルズ, インコーポレイテッドAlnylam Pharmaceuticals, Inc. | PCSK9iRNA組成物及びその使用方法 |
JP6440170B2 (ja) | 2013-03-01 | 2018-12-19 | 国立大学法人 東京医科歯科大学 | キメラ一本鎖アンチセンスポリヌクレオチドおよび二本鎖アンチセンス剤 |
PL2970974T3 (pl) * | 2013-03-14 | 2018-01-31 | Alnylam Pharmaceuticals Inc | Kompozycje komponentu C5 dopełniacza iRNA i sposoby ich zastosowania |
RU2650510C2 (ru) | 2013-05-01 | 2018-04-16 | Ионис Фармасьютикалз, Инк. | Композиции и способы модулирования экспрессии аполипопротеина c-iii |
TW201536329A (zh) | 2013-08-09 | 2015-10-01 | Isis Pharmaceuticals Inc | 用於調節失養性肌強直蛋白質激酶(dmpk)表現之化合物及方法 |
US11162096B2 (en) | 2013-10-14 | 2021-11-02 | Ionis Pharmaceuticals, Inc | Methods for modulating expression of C9ORF72 antisense transcript |
WO2015084884A2 (en) | 2013-12-02 | 2015-06-11 | Isis Pharmaceuticals, Inc. | Antisense compounds and uses thereof |
JPWO2015108046A1 (ja) | 2014-01-15 | 2017-03-23 | 株式会社新日本科学 | 抗アレルギー作用を有するキラル核酸アジュバンド及び抗アレルギー剤 |
EP3095461A4 (en) | 2014-01-15 | 2017-08-23 | Shin Nippon Biomedical Laboratories, Ltd. | Chiral nucleic acid adjuvant having immunity induction activity, and immunity induction activator |
JPWO2015108048A1 (ja) | 2014-01-15 | 2017-03-23 | 株式会社新日本科学 | 抗腫瘍作用を有するキラル核酸アジュバンド及び抗腫瘍剤 |
KR20230152178A (ko) | 2014-01-16 | 2023-11-02 | 웨이브 라이프 사이언시스 리미티드 | 키랄 디자인 |
RS62526B1 (sr) | 2014-03-19 | 2021-11-30 | Ionis Pharmaceuticals Inc | Kompozicije za modulaciju ekspresije ataksina 2 |
WO2015143245A1 (en) | 2014-03-19 | 2015-09-24 | Isis Pharmaceuticals, Inc. | Methods for modulating ataxin 2 expression |
EP4137573A3 (en) | 2014-04-01 | 2023-05-03 | Biogen MA Inc. | Compositions for modulating sod-1 expression |
CR20200228A (es) | 2014-05-01 | 2020-07-09 | Ionis Pharmaceuticals Inc | COMPOSICIONES Y MÈTODOS PARA MODULAR LA EXPRESIÒN DEL FACTOR B DEL COMPLEMENTO (Divisional 2016-0554) |
WO2015187989A1 (en) | 2014-06-04 | 2015-12-10 | Isis Pharmaceuticals, Inc. | Antisense compounds targeting apolipoprotein e receptor 2 |
GB201410693D0 (en) | 2014-06-16 | 2014-07-30 | Univ Southampton | Splicing modulation |
WO2015200697A1 (en) | 2014-06-25 | 2015-12-30 | The General Hospital Corporation | Targeting human satellite ii (hsatii) |
WO2016040748A1 (en) | 2014-09-12 | 2016-03-17 | Ionis Pharmaceuticals, Inc. | Compositions and methods for detection of smn protein in a subject and treatment of a subject |
WO2016041058A1 (en) | 2014-09-18 | 2016-03-24 | The University Of British Columbia | Allele-specific therapy for huntington disease haplotypes |
JP6867945B2 (ja) | 2014-10-03 | 2021-05-12 | コールド スプリング ハーバー ラボラトリー | 核内遺伝子出力の標的とされた増強 |
WO2016070060A1 (en) | 2014-10-30 | 2016-05-06 | The General Hospital Corporation | Methods for modulating atrx-dependent gene repression |
EP3221329A1 (en) * | 2014-11-19 | 2017-09-27 | Roche Innovation Center Copenhagen A/S | Lna gapmer oligonucleotides comprising chiral phosphorothioate linkages |
DK3234131T3 (da) | 2014-12-16 | 2020-06-29 | Roche Innovation Ct Copenhagen As | Fremgangsmåde til screening af kiral toksicitet |
US10793855B2 (en) | 2015-01-06 | 2020-10-06 | Ionis Pharmaceuticals, Inc. | Compositions for modulating expression of C9ORF72 antisense transcript |
US10538763B2 (en) | 2015-01-16 | 2020-01-21 | Ionis Pharmaceuticals, Inc. | Compounds and methods for modulation of DUX4 |
CN107636159B (zh) | 2015-02-04 | 2022-06-14 | 百时美施贵宝公司 | 选择治疗性分子的方法 |
EP3253875B1 (en) | 2015-02-04 | 2020-01-08 | H. Hoffnabb-La Roche Ag | Tau antisense oligomers and uses thereof |
EP3256592A4 (en) * | 2015-02-13 | 2018-09-12 | Translate Bio Ma, Inc. | Compositions and methods for modulating rna |
EP3256591A4 (en) | 2015-02-13 | 2018-08-08 | Translate Bio Ma, Inc. | Hybrid oligonucleotides and uses thereof |
US11129844B2 (en) | 2015-03-03 | 2021-09-28 | Ionis Pharmaceuticals, Inc. | Compositions and methods for modulating MECP2 expression |
US10900036B2 (en) | 2015-03-17 | 2021-01-26 | The General Hospital Corporation | RNA interactome of polycomb repressive complex 1 (PRC1) |
WO2016167780A1 (en) | 2015-04-16 | 2016-10-20 | Ionis Pharmaceuticals, Inc. | Compositions for modulating expression of c9orf72 antisense transcript |
MA43072A (fr) * | 2015-07-22 | 2018-05-30 | Wave Life Sciences Ltd | Compositions d'oligonucléotides et procédés associés |
US10533175B2 (en) | 2015-09-25 | 2020-01-14 | Ionis Pharmaceuticals, Inc. | Compositions and methods for modulating Ataxin 3 expression |
WO2017060731A1 (en) | 2015-10-09 | 2017-04-13 | University Of Southampton | Modulation of gene expression and screening for deregulated protein expression |
EP3389670A4 (en) | 2015-12-04 | 2020-01-08 | Ionis Pharmaceuticals, Inc. | METHODS OF TREATING BREAST CANCER |
SG11201804443UA (en) | 2015-12-14 | 2018-06-28 | Cold Spring Harbor Laboratory | Antisense oligomers for treatment of autosomal dominant mental retardation-5 and dravet syndrome |
US11096956B2 (en) | 2015-12-14 | 2021-08-24 | Stoke Therapeutics, Inc. | Antisense oligomers and uses thereof |
US10907160B2 (en) | 2016-01-05 | 2021-02-02 | Ionis Pharmaceuticals, Inc. | Methods for reducing LRRK2 expression |
WO2017142054A1 (ja) | 2016-02-17 | 2017-08-24 | 国立大学法人東京工業大学 | 人工ヌクレオシド及び人工ヌクレオチド並びに人工オリゴヌクレオチド |
AU2017234678A1 (en) | 2016-03-16 | 2018-08-16 | Ionis Pharmaceuticals, Inc. | Methods of modulating KEAP1 |
WO2017161168A1 (en) | 2016-03-16 | 2017-09-21 | Ionis Pharmaceuticals, Inc. | Modulation of dyrk1b expression |
MA45270A (fr) | 2016-05-04 | 2017-11-09 | Wave Life Sciences Ltd | Compositions d'oligonucléotides et procédés associés |
MA45496A (fr) | 2016-06-17 | 2019-04-24 | Hoffmann La Roche | Molécules d'acide nucléique pour la réduction de l'arnm de padd5 ou pad7 pour le traitement d'une infection par l'hépatite b |
CA3023514A1 (en) | 2016-06-17 | 2017-12-21 | Ionis Pharmaceuticals, Inc. | Modulation of gys1 expression |
WO2018055577A1 (en) * | 2016-09-23 | 2018-03-29 | Synthena Ag | Mixed tricyclo-dna, 2'-modified rna oligonucleotide compositions and uses thereof |
EP3516061A1 (en) | 2016-09-23 | 2019-07-31 | Synthena AG | Mixed tricyclo-dna, 2'-modified rna oligonucleotide compositions and uses thereof |
US11260134B2 (en) | 2016-09-29 | 2022-03-01 | National University Corporation Tokyo Medical And Dental University | Double-stranded nucleic acid complex having overhang |
US11400161B2 (en) | 2016-10-06 | 2022-08-02 | Ionis Pharmaceuticals, Inc. | Method of conjugating oligomeric compounds |
JOP20190104A1 (ar) | 2016-11-10 | 2019-05-07 | Ionis Pharmaceuticals Inc | مركبات وطرق لتقليل التعبير عن atxn3 |
EP3548005A4 (en) | 2016-11-29 | 2020-06-17 | Puretech Health LLC | EXOSOMES FOR THE ADMINISTRATION OF THERAPEUTIC AGENTS |
US11033570B2 (en) | 2016-12-02 | 2021-06-15 | Cold Spring Harbor Laboratory | Modulation of Lnc05 expression |
BR112019014547A2 (pt) | 2017-02-06 | 2020-02-18 | Nissan Chemical Corporation | Oligonucleotídeo de fita simples |
JP7095893B2 (ja) | 2017-02-21 | 2022-07-05 | 国立大学法人大阪大学 | アンチセンスオリゴ核酸 |
JOP20190215A1 (ar) | 2017-03-24 | 2019-09-19 | Ionis Pharmaceuticals Inc | مُعدّلات التعبير الوراثي عن pcsk9 |
US20200115710A1 (en) | 2017-06-30 | 2020-04-16 | National University Corporation Tokyo Medical And Dental University | HETERO DOUBLE-STRANDED antimiR |
KR20200035301A (ko) * | 2017-08-08 | 2020-04-02 | 웨이브 라이프 사이언시스 리미티드 | 올리고뉴클레오티드 조성물 및 이의 방법 |
AU2018318231A1 (en) | 2017-08-18 | 2020-02-13 | Ionis Pharmaceuticals, Inc. | Modulation of the notch signaling pathway for treatment of respiratory disorders |
LT3673080T (lt) | 2017-08-25 | 2023-12-27 | Stoke Therapeutics, Inc. | Priešprasminiai oligomerai, skirti būklėms ir ligoms gydyti |
WO2019051173A1 (en) | 2017-09-08 | 2019-03-14 | Ionis Pharmaceuticals, Inc. | MODULATORS OF SMAD7 EXPRESSION |
CN111226114A (zh) | 2017-10-13 | 2020-06-02 | 罗氏创新中心哥本哈根有限公司 | 用部分立体限定的寡核苷酸子文库鉴定反义寡核苷酸改进的立体限定硫代磷酸酯寡核苷酸变体的方法 |
TWI816066B (zh) | 2017-10-16 | 2023-09-21 | 瑞士商赫孚孟拉羅股份公司 | 用於降低PAPD5及PAPD7 mRNA以治療B型肝炎感染之核酸分子 |
TWI809004B (zh) | 2017-11-09 | 2023-07-21 | 美商Ionis製藥公司 | 用於降低snca表現之化合物及方法 |
JP2021505175A (ja) | 2017-12-11 | 2021-02-18 | ロシュ イノベーション センター コペンハーゲン エーエス | Fndc3bの発現を調節するためのオリゴヌクレオチド |
WO2019115417A2 (en) | 2017-12-12 | 2019-06-20 | Roche Innovation Center Copenhagen A/S | Oligonucleotides for modulating rb1 expression |
EP3729095A1 (en) | 2017-12-21 | 2020-10-28 | F. Hoffmann-La Roche AG | Companion diagnostic for htra1 rna antagonists |
WO2019126641A2 (en) | 2017-12-21 | 2019-06-27 | Ionis Pharmaceuticals, Inc. | Modulation of frataxin expression |
CN111448316A (zh) | 2017-12-22 | 2020-07-24 | 罗氏创新中心哥本哈根有限公司 | 新的硫代亚磷酰胺 |
CA3085406A1 (en) | 2017-12-22 | 2019-06-27 | Roche Innovation Center Copenhagen A/S | Oligonucleotides comprising a phosphorodithioate internucleoside linkage |
WO2019122282A1 (en) | 2017-12-22 | 2019-06-27 | Roche Innovation Center Copenhagen A/S | Gapmer oligonucleotides comprising a phosphorodithioate internucleoside linkage |
JP2021511022A (ja) | 2018-01-10 | 2021-05-06 | ロシュ イノベーション センター コペンハーゲン エーエス | Pias4発現を調節するためのオリゴヌクレオチド |
EP3737760A1 (en) | 2018-01-12 | 2020-11-18 | Roche Innovation Center Copenhagen A/S | Oligonucleotides for modulating gsk3b expression |
CN111902537A (zh) | 2018-01-15 | 2020-11-06 | Ionis制药公司 | Dnm2表达的调节剂 |
CN111615558A (zh) | 2018-01-17 | 2020-09-01 | 罗氏创新中心哥本哈根有限公司 | 用于调节erc1表达的寡核苷酸 |
JP2021511029A (ja) | 2018-01-18 | 2021-05-06 | ロシュ イノベーション センター コペンハーゲン エーエス | Srebp1を標的とするアンチセンスオリゴヌクレオチド |
WO2019145386A1 (en) | 2018-01-26 | 2019-08-01 | Roche Innovation Center Copenhagen A/S | Oligonucleotides for modulating csnk1d expression |
KR20200108315A (ko) | 2018-02-09 | 2020-09-17 | 제넨테크, 인크. | Tmem106b의 발현을 조절하기 위한 올리고뉴클레오티드 |
JP7317029B2 (ja) | 2018-02-12 | 2023-07-28 | アイオーニス ファーマシューティカルズ, インコーポレーテッド | 修飾化合物及びその使用 |
US11674141B2 (en) | 2018-02-28 | 2023-06-13 | National University Corporation Tokyo Medical And Dental University | Ischemic-lesion-site-specific gene therapy |
WO2019169243A1 (en) | 2018-03-02 | 2019-09-06 | Ionis Pharmaceuticals, Inc. | Compounds and methods for the modulation of amyloid-beta precursor protein |
CN111886011B (zh) | 2018-03-02 | 2024-03-08 | Ionis制药公司 | Irf4表达的调节剂 |
WO2019177061A1 (ja) | 2018-03-14 | 2019-09-19 | 国立大学法人東京医科歯科大学 | 核酸複合体 |
EP3769769A4 (en) | 2018-03-19 | 2022-05-04 | National University Corporation Tokyo Medical and Dental University | NUCLEIC ACID WITH REDUCED TOXICITY |
EP3770256A4 (en) | 2018-03-20 | 2021-12-22 | Tokyo Institute of Technology | ANTISENSE OLIGONUCLEOTIDE WITH REDUCED TOXICITY |
US11661601B2 (en) | 2018-03-22 | 2023-05-30 | Ionis Pharmaceuticals, Inc. | Methods for modulating FMR1 expression |
WO2019182109A1 (ja) | 2018-03-22 | 2019-09-26 | 国立大学法人東京医科歯科大学 | ヘテロ核酸のbbb通過脂質リガンド |
SG11202008660TA (en) | 2018-04-11 | 2020-10-29 | Ionis Pharmaceuticals Inc | Modulators of ezh2 expression |
US20210371860A1 (en) | 2018-05-08 | 2021-12-02 | Roche Innovation Center Copenhagen A/S | Oligonucleotides for modulating myh7 expression |
BR112020021253A2 (pt) | 2018-05-09 | 2021-02-02 | Ionis Pharmaceuticals, Inc. | compostos e métodos para redução da expressão de atxn3 |
MX2020011913A (es) | 2018-05-09 | 2021-01-29 | Ionis Pharmaceuticals Inc | Compuestos y metodos para la reduccion de la expresion de fxi. |
WO2019233921A1 (en) | 2018-06-05 | 2019-12-12 | F. Hoffmann-La Roche Ag | Oligonucleotides for modulating atxn2 expression |
US11833168B2 (en) | 2018-06-14 | 2023-12-05 | Ionis Pharmaceuticals, Inc. | Compounds and methods for increasing STMN2 expression |
TWI833770B (zh) | 2018-06-27 | 2024-03-01 | 美商Ionis製藥公司 | 用於減少 lrrk2 表現之化合物及方法 |
WO2020007700A1 (en) | 2018-07-02 | 2020-01-09 | Roche Innovation Center Copenhagen A/S | Antisense oligonucleotides targeting spi1 |
WO2020007772A1 (en) | 2018-07-02 | 2020-01-09 | Roche Innovation Center Copenhagen A/S | Antisense oligonucleotides targeting gbp-1 |
WO2020007702A1 (en) | 2018-07-02 | 2020-01-09 | Roche Innovation Center Copenhagen A/S | Antisense oligonucleotides targeting bcl2l11 |
PE20210346A1 (es) * | 2018-07-03 | 2021-02-25 | Hoffmann La Roche | Oligonucleotidos para modular la expresion de tau |
WO2020007889A1 (en) | 2018-07-05 | 2020-01-09 | Roche Innovation Center Copenhagen A/S | Antisense oligonucleotides targeting stat1 |
WO2020007826A1 (en) | 2018-07-05 | 2020-01-09 | Roche Innovation Center Copenhagen A/S | Antisense oligonucleotides targeting mbtps1 |
WO2020011653A1 (en) | 2018-07-09 | 2020-01-16 | Roche Innovation Center Copenhagen A/S | Antisense oligonucleotides targeting kynu |
WO2020011743A1 (en) | 2018-07-09 | 2020-01-16 | Roche Innovation Center Copenhagen A/S | Antisense oligonucleotides targeting mafb |
WO2020011745A2 (en) | 2018-07-11 | 2020-01-16 | Roche Innovation Center Copenhagen A/S | Antisense oligonucleotides targeting cers6 |
WO2020011744A2 (en) | 2018-07-11 | 2020-01-16 | Roche Innovation Center Copenhagen A/S | Antisense oligonucleotides targeting cers5 |
WO2020011869A2 (en) | 2018-07-11 | 2020-01-16 | Roche Innovation Center Copenhagen A/S | Antisense oligonucleotides targeting tlr2 |
JP7411632B2 (ja) | 2018-07-25 | 2024-01-11 | アイオーニス ファーマシューティカルズ, インコーポレーテッド | Atxn2発現を低減するための化合物及び方法 |
JP7182308B2 (ja) | 2018-07-27 | 2022-12-02 | 国立大学法人大阪大学 | 老化の抑制、加齢性の疾患もしくは症状の予防、改善、もしくは治療、または寿命の延長のための組成物 |
WO2020025527A1 (en) | 2018-07-31 | 2020-02-06 | Roche Innovation Center Copenhagen A/S | Oligonucleotides comprising a phosphorotrithioate internucleoside linkage |
WO2020025563A1 (en) | 2018-07-31 | 2020-02-06 | Roche Innovation Center Copenhagen A/S | Oligonucleotides comprising a phosphorotrithioate internucleoside linkage |
JP2021533200A (ja) | 2018-08-02 | 2021-12-02 | ダイン セラピューティクス, インコーポレーテッドDyne Therapeutics, Inc. | 顔面・肩甲・上腕筋ジストロフィーを処置するための筋標的化複合体およびそれらの使用 |
US12018087B2 (en) | 2018-08-02 | 2024-06-25 | Dyne Therapeutics, Inc. | Muscle-targeting complexes comprising an anti-transferrin receptor antibody linked to an oligonucleotide and methods of delivering oligonucleotide to a subject |
US11911484B2 (en) | 2018-08-02 | 2024-02-27 | Dyne Therapeutics, Inc. | Muscle targeting complexes and uses thereof for treating myotonic dystrophy |
WO2020038973A1 (en) | 2018-08-23 | 2020-02-27 | Roche Innovation Center Copenhagen A/S | Antisense oligonucleotides targeting sptlc1 |
WO2020038971A1 (en) | 2018-08-23 | 2020-02-27 | Roche Innovation Center Copenhagen A/S | Antisense oligonucleotides targeting vcan |
WO2020038976A1 (en) | 2018-08-23 | 2020-02-27 | Roche Innovation Center Copenhagen A/S | Antisense oligonucleotides targeting usp8 |
EP3620519A1 (en) | 2018-09-04 | 2020-03-11 | F. Hoffmann-La Roche AG | Use of isolated milk extracellular vesicles for delivering oligonucleotides orally |
EP3873920A1 (en) | 2018-11-01 | 2021-09-08 | F. Hoffmann-La Roche AG | Antisense oligonucleotides targeting tia1 |
TW202028222A (zh) | 2018-11-14 | 2020-08-01 | 美商Ionis製藥公司 | Foxp3表現之調節劑 |
EP3880821A4 (en) | 2018-11-15 | 2023-01-25 | Ionis Pharmaceuticals, Inc. | IRF5 EXPRESSION MODULATORS |
EP3898975A2 (en) | 2018-12-21 | 2021-10-27 | Boehringer Ingelheim International GmbH | Antisense oligonucleotides targeting card9 |
CN113365607A (zh) | 2019-01-25 | 2021-09-07 | 豪夫迈·罗氏有限公司 | 用于口服药物递送的脂质囊泡 |
CN113395971A (zh) | 2019-01-31 | 2021-09-14 | Ionis制药公司 | Yap1表达的调节剂 |
EP3927716A1 (en) | 2019-02-20 | 2021-12-29 | Roche Innovation Center Copenhagen A/S | Novel phosphoramidites |
TW202102516A (zh) | 2019-02-20 | 2021-01-16 | 丹麥商羅氏創新中心哥本哈根有限公司 | 膦醯基乙酸酯間隙子寡核苷酸 |
CN113474633A (zh) | 2019-02-26 | 2021-10-01 | 罗氏创新中心哥本哈根有限公司 | 寡核苷酸配制方法 |
WO2020176771A1 (en) | 2019-02-27 | 2020-09-03 | Ionis Pharmaceuticals, Inc. | Modulators of malat1 expression |
WO2020184700A1 (ja) | 2019-03-14 | 2020-09-17 | レナセラピューティクス株式会社 | Ihh発現を調節するための核酸複合体 |
JP2022527105A (ja) | 2019-03-29 | 2022-05-30 | アイオーニス ファーマシューティカルズ, インコーポレーテッド | Ube3a-atsを調節するための化合物及び方法 |
US11286485B2 (en) | 2019-04-04 | 2022-03-29 | Hoffmann-La Roche Inc. | Oligonucleotides for modulating ATXN2 expression |
WO2020209285A1 (ja) | 2019-04-08 | 2020-10-15 | 国立大学法人東京医科歯科大学 | 筋疾患治療用医薬組成物 |
WO2020245233A1 (en) | 2019-06-06 | 2020-12-10 | F. Hoffmann-La Roche Ag | Antisense oligonucleotides targeting atxn3 |
US11786546B2 (en) | 2019-07-26 | 2023-10-17 | Ionis Pharmaceuticals, Inc. | Compounds and methods for modulating GFAP |
JPWO2021054370A1 (es) | 2019-09-18 | 2021-03-25 | ||
EP4043565A4 (en) | 2019-10-11 | 2024-01-24 | National University Corporation Tokyo Medical and Dental University | MODIFIED HETERONUCLEIC ACID |
US20240116977A1 (en) | 2019-10-11 | 2024-04-11 | Sumitomo Chemical Company, Limited | Method for producing nucleic acid oligomers |
EP4067489A4 (en) * | 2019-11-27 | 2024-06-12 | Tokyo Institute of Technology | METHODS FOR REDUCING THE TOXICITY OF ANTISENSE NUCLEIC ACIDS |
MX2022007908A (es) | 2019-12-24 | 2022-07-21 | Hoffmann La Roche | Combinacion farmaceutica de un oligonucleotido terapeutico que actua sobre hbv y un agonista de tlr7 para el tratamiento de hbv. |
EP4081217A1 (en) | 2019-12-24 | 2022-11-02 | F. Hoffmann-La Roche AG | Pharmaceutical combination of antiviral agents targeting hbv and/or an immune modulator for treatment of hbv |
EP4097234A1 (en) | 2020-01-28 | 2022-12-07 | Université de Strasbourg | Antisense oligonucleotide targeting linc00518 for treating melanoma |
DK4097117T3 (da) | 2020-01-29 | 2024-07-22 | Sumitomo Chemical Company Ltd | Fremgangsmåde til fremstilling af nukleinsyreoligomer |
JPWO2021153047A1 (es) | 2020-01-29 | 2021-08-05 | ||
US20230127437A1 (en) | 2020-01-31 | 2023-04-27 | Sanwa Kagaku Kenkyusho Co., Ltd. | Antisense oligonucleotide of atn1 |
BR112022016238A2 (pt) | 2020-02-28 | 2022-10-11 | Ionis Pharmaceuticals Inc | Compostos e métodos para modular smn2 |
US20230159925A1 (en) | 2020-03-04 | 2023-05-25 | Nissan Chemical Corporation | Antisense oligonucleotide of calm2 |
WO2021178374A2 (en) * | 2020-03-05 | 2021-09-10 | Synerk Inc. | Compounds and methods for reducing apoe expression |
US20230174981A1 (en) | 2020-03-16 | 2023-06-08 | National University Corporation Tokyo Medical And Dental University | Heteronucleic acid containing morpholino nucleic acid |
EP4130018A4 (en) | 2020-03-27 | 2024-04-17 | Sumitomo Chemical Company, Limited | PROCESS FOR THE PRODUCTION OF NUCLEIC ACID OLIGOMERS |
MX2022013707A (es) | 2020-05-01 | 2022-12-07 | Ionis Pharmaceuticals Inc | Compuestos y metodos para modular atxn1. |
MX2022014151A (es) | 2020-05-11 | 2022-11-30 | Stoke Therapeutics Inc | Oligomeros antisentido de opa1 para tratamiento de afecciones y enfermedades. |
EP4172338A2 (en) | 2020-06-29 | 2023-05-03 | Ionis Pharmaceuticals, Inc. | Compounds and methods for modulating plp1 |
EP4180442A1 (en) | 2020-07-09 | 2023-05-17 | Sumitomo Chemical Company, Limited | Method for producing nucleic acid oligomer |
KR20230074205A (ko) | 2020-09-24 | 2023-05-26 | 스미또모 가가꾸 가부시끼가이샤 | 핵산 올리고머의 제조 방법 |
KR20230108728A (ko) | 2020-11-18 | 2023-07-18 | 아이오니스 파마수티컬즈, 인코포레이티드 | 앤지오텐시노겐 발현을 조절하기 위한 화합물 및 방법 |
WO2022117747A2 (en) | 2020-12-03 | 2022-06-09 | F. Hoffmann-La Roche Ag | Antisense oligonucleotides targeting atxn3 |
US20220177883A1 (en) | 2020-12-03 | 2022-06-09 | Hoffmann-La Roche Inc. | Antisense Oligonucleotides Targeting ATXN3 |
TW202242111A (zh) | 2020-12-18 | 2022-11-01 | 美商Ionis製藥公司 | 用於調節因子xii之化合物及方法 |
WO2022162015A1 (en) | 2021-01-26 | 2022-08-04 | Universite Brest Bretagne Occidentale | Novel stim1 splicing variants and uses thereof |
WO2022241408A1 (en) | 2021-05-10 | 2022-11-17 | Entrada Therapeutics, Inc. | Compositions and methods for modulating tissue distribution of intracellular therapeutics |
CA3219942A1 (en) * | 2021-05-10 | 2022-11-17 | Q-State Biosciences, Inc. | Compositions targeting sodium channel 1.6 |
US20240240183A1 (en) | 2021-05-25 | 2024-07-18 | National University Corporation Tokyo Medical And Dental University | Heteronucleic acid containing scpBNA or AmNA |
BR112023024384A2 (pt) | 2021-05-31 | 2024-02-15 | Rena Therapeutics Inc | Complexo de ácido nucleico ligado ao ligante |
AU2022293556A1 (en) | 2021-06-18 | 2024-01-18 | Ionis Pharmaceuticals, Inc. | Compounds and methods for reducing ifnar1 expression |
MX2023015509A (es) | 2021-06-23 | 2024-01-22 | Entrada Therapeutics Inc | Compuestos antisentido y metodos para dirigirse a repeticiones cug. |
US11638761B2 (en) | 2021-07-09 | 2023-05-02 | Dyne Therapeutics, Inc. | Muscle targeting complexes and uses thereof for treating Facioscapulohumeral muscular dystrophy |
US11633498B2 (en) | 2021-07-09 | 2023-04-25 | Dyne Therapeutics, Inc. | Muscle targeting complexes and uses thereof for treating myotonic dystrophy |
EP4389891A1 (en) | 2021-08-19 | 2024-06-26 | National University Corporation Tokyo Medical and Dental University | Modified heteronucleic acid containing morpholino nucleic acid |
WO2023026994A1 (ja) | 2021-08-21 | 2023-03-02 | 武田薬品工業株式会社 | ヒトトランスフェリンレセプター結合ペプチド-薬物コンジュゲート |
EP4396352A2 (en) | 2021-09-01 | 2024-07-10 | Ionis Pharmaceuticals, Inc. | Compounds and methods for reducing dmpk expression |
JPWO2023042876A1 (es) | 2021-09-15 | 2023-03-23 | ||
WO2023054350A1 (ja) | 2021-09-28 | 2023-04-06 | 住友化学株式会社 | 精製ジクロロ酢酸の製造方法 |
WO2023080159A1 (ja) | 2021-11-02 | 2023-05-11 | レナセラピューティクス株式会社 | リガンド結合核酸複合体 |
CN118318042A (zh) | 2021-11-03 | 2024-07-09 | 豪夫迈·罗氏有限公司 | 用于调节载脂蛋白e4表达的寡核苷酸 |
CN118284695A (zh) | 2021-11-11 | 2024-07-02 | 豪夫迈·罗氏有限公司 | 用于治疗hbv的药物组合 |
WO2023117738A1 (en) | 2021-12-20 | 2023-06-29 | F. Hoffmann-La Roche Ag | Threose nucleic acid antisense oligonucleotides and methods thereof |
WO2023141507A1 (en) | 2022-01-20 | 2023-07-27 | Genentech, Inc. | Antisense oligonucleotides for modulating tmem106b expression |
WO2023178144A2 (en) | 2022-03-16 | 2023-09-21 | Empirico Inc. | Galnac compositions for improving sirna bioavailability |
US11931421B2 (en) | 2022-04-15 | 2024-03-19 | Dyne Therapeutics, Inc. | Muscle targeting complexes and formulations for treating myotonic dystrophy |
WO2024026474A1 (en) | 2022-07-29 | 2024-02-01 | Regeneron Pharmaceuticals, Inc. | Compositions and methods for transferrin receptor (tfr)-mediated delivery to the brain and muscle |
WO2024050261A1 (en) | 2022-08-29 | 2024-03-07 | University Of Rochester | Antisense oligonucleotide-based anti-fibrotic therapeutics |
EP4332221A1 (en) | 2022-08-29 | 2024-03-06 | Roche Innovation Center Copenhagen A/S | Threose nucleic acid antisense oligonucleotides and methods thereof |
WO2024073386A1 (en) * | 2022-09-29 | 2024-04-04 | Celanese Eva Performance Polymers Llc | Implantable medical device for the delivery of a nucleic acid |
WO2024098002A1 (en) | 2022-11-04 | 2024-05-10 | Regeneron Pharmaceuticals, Inc. | Calcium voltage-gated channel auxiliary subunit gamma 1 (cacng1) binding proteins and cacng1-mediated delivery to skeletal muscle |
WO2024107765A2 (en) | 2022-11-14 | 2024-05-23 | Regeneron Pharmaceuticals, Inc. | Compositions and methods for fibroblast growth factor receptor 3-mediated delivery to astrocytes |
Family Cites Families (82)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5118800A (en) | 1983-12-20 | 1992-06-02 | California Institute Of Technology | Oligonucleotides possessing a primary amino group in the terminal nucleotide |
FR2567892B1 (fr) | 1984-07-19 | 1989-02-17 | Centre Nat Rech Scient | Nouveaux oligonucleotides, leur procede de preparation et leurs applications comme mediateurs dans le developpement des effets des interferons |
US5591722A (en) | 1989-09-15 | 1997-01-07 | Southern Research Institute | 2'-deoxy-4'-thioribonucleosides and their antiviral activity |
DK0497875T3 (da) | 1989-10-24 | 2000-07-03 | Gilead Sciences Inc | 2'-modificerede oligonukleotider |
US5670633A (en) | 1990-01-11 | 1997-09-23 | Isis Pharmaceuticals, Inc. | Sugar modified oligonucleotides that detect and modulate gene expression |
US5646265A (en) | 1990-01-11 | 1997-07-08 | Isis Pharmceuticals, Inc. | Process for the preparation of 2'-O-alkyl purine phosphoramidites |
GB9009980D0 (en) | 1990-05-03 | 1990-06-27 | Amersham Int Plc | Phosphoramidite derivatives,their preparation and the use thereof in the incorporation of reporter groups on synthetic oligonucleotides |
DE69032425T2 (de) | 1990-05-11 | 1998-11-26 | Microprobe Corp., Bothell, Wash. | Teststreifen zum Eintauchen für Nukleinsäure-Hybridisierungsassays und Verfahren zur kovalenten Immobilisierung von Oligonucleotiden |
US6582908B2 (en) | 1990-12-06 | 2003-06-24 | Affymetrix, Inc. | Oligonucleotides |
EP0538194B1 (de) * | 1991-10-17 | 1997-06-04 | Novartis AG | Bicyclische Nukleoside, Oligonukleotide, Verfahren zu deren Herstellung und Zwischenprodukte |
US5359044A (en) | 1991-12-13 | 1994-10-25 | Isis Pharmaceuticals | Cyclobutyl oligonucleotide surrogates |
US20010044145A1 (en) * | 1991-12-24 | 2001-11-22 | Monia Brett P. | Methods of using mammalian RNase H and compositions thereof |
FR2687679B1 (fr) | 1992-02-05 | 1994-10-28 | Centre Nat Rech Scient | Oligothionucleotides. |
FR2692265B1 (fr) | 1992-05-25 | 1996-11-08 | Centre Nat Rech Scient | Composes biologiquement actifs de type phosphotriesters. |
EP0577558A2 (de) | 1992-07-01 | 1994-01-05 | Ciba-Geigy Ag | Carbocyclische Nukleoside mit bicyclischen Ringen, Oligonukleotide daraus, Verfahren zu deren Herstellung, deren Verwendung und Zwischenproduckte |
JPH08504559A (ja) | 1992-12-14 | 1996-05-14 | ハネウエル・インコーポレーテッド | 個別に制御される冗長巻線を有するモータシステム |
MX9306994A (es) | 1992-12-15 | 1994-06-30 | Ericsson Telefon Ab L M | Sistema de control de flujo para interruptores de paquete. |
US5446786A (en) * | 1993-03-03 | 1995-08-29 | Northern Telecom Limited | Two-wire telecommunications line detection arrangements |
EP0691968B1 (en) * | 1993-03-30 | 1997-07-16 | Sanofi | Acyclic nucleoside analogs and oligonucleotide sequences containing them |
DE4311944A1 (de) | 1993-04-10 | 1994-10-13 | Degussa | Umhüllte Natriumpercarbonatpartikel, Verfahren zu deren Herstellung und sie enthaltende Wasch-, Reinigungs- und Bleichmittelzusammensetzungen |
FR2705099B1 (fr) | 1993-05-12 | 1995-08-04 | Centre Nat Rech Scient | Oligonucléotides phosphorothioates triesters et procédé de préparation. |
US5801154A (en) | 1993-10-18 | 1998-09-01 | Isis Pharmaceuticals, Inc. | Antisense oligonucleotide modulation of multidrug resistance-associated protein |
US5446137B1 (en) | 1993-12-09 | 1998-10-06 | Behringwerke Ag | Oligonucleotides containing 4'-substituted nucleotides |
US5519134A (en) | 1994-01-11 | 1996-05-21 | Isis Pharmaceuticals, Inc. | Pyrrolidine-containing monomers and oligomers |
US5627053A (en) | 1994-03-29 | 1997-05-06 | Ribozyme Pharmaceuticals, Inc. | 2'deoxy-2'-alkylnucleotide containing nucleic acid |
US5597909A (en) | 1994-08-25 | 1997-01-28 | Chiron Corporation | Polynucleotide reagents containing modified deoxyribose moieties, and associated methods of synthesis and use |
US5792747A (en) | 1995-01-24 | 1998-08-11 | The Administrators Of The Tulane Educational Fund | Highly potent agonists of growth hormone releasing hormone |
US6770748B2 (en) | 1997-03-07 | 2004-08-03 | Takeshi Imanishi | Bicyclonucleoside and oligonucleotide analogue |
JP3756313B2 (ja) | 1997-03-07 | 2006-03-15 | 武 今西 | 新規ビシクロヌクレオシド及びオリゴヌクレオチド類縁体 |
US6794499B2 (en) | 1997-09-12 | 2004-09-21 | Exiqon A/S | Oligonucleotide analogues |
EP2253639A1 (en) | 1997-09-12 | 2010-11-24 | Exiqon A/S | Bi- and tri-cyclic nucleoside, nucleotide and oligonucleoide analogues |
US20030228597A1 (en) | 1998-04-13 | 2003-12-11 | Cowsert Lex M. | Identification of genetic targets for modulation by oligonucleotides and generation of oligonucleotides for gene modulation |
US6043352A (en) | 1998-08-07 | 2000-03-28 | Isis Pharmaceuticals, Inc. | 2'-O-Dimethylaminoethyloxyethyl-modified oligonucleotides |
ID30093A (id) | 1999-02-12 | 2001-11-01 | Sankyo Co | Analog-analog nukleosida dan oligonukleotida baru |
US7084125B2 (en) | 1999-03-18 | 2006-08-01 | Exiqon A/S | Xylo-LNA analogues |
US7098192B2 (en) * | 1999-04-08 | 2006-08-29 | Isis Pharmaceuticals, Inc. | Antisense oligonucleotide modulation of STAT3 expression |
EP1178999B1 (en) | 1999-05-04 | 2007-03-14 | Santaris Pharma A/S | L-ribo-lna analogues |
US6525191B1 (en) | 1999-05-11 | 2003-02-25 | Kanda S. Ramasamy | Conformationally constrained L-nucleosides |
US20040002153A1 (en) | 1999-07-21 | 2004-01-01 | Monia Brett P. | Modulation of PTEN expression via oligomeric compounds |
JP4151751B2 (ja) | 1999-07-22 | 2008-09-17 | 第一三共株式会社 | 新規ビシクロヌクレオシド類縁体 |
WO2002094250A2 (en) * | 2001-05-18 | 2002-11-28 | Cureon A/S | Therapeutic uses of lna-modified oligonucleotides in infectious diseases |
US7407943B2 (en) * | 2001-08-01 | 2008-08-05 | Isis Pharmaceuticals, Inc. | Antisense modulation of apolipoprotein B expression |
US7888324B2 (en) * | 2001-08-01 | 2011-02-15 | Genzyme Corporation | Antisense modulation of apolipoprotein B expression |
US7569575B2 (en) | 2002-05-08 | 2009-08-04 | Santaris Pharma A/S | Synthesis of locked nucleic acid derivatives |
US20040219565A1 (en) | 2002-10-21 | 2004-11-04 | Sakari Kauppinen | Oligonucleotides useful for detecting and analyzing nucleic acids of interest |
AU2003291755A1 (en) | 2002-11-05 | 2004-06-07 | Isis Pharmaceuticals, Inc. | Oligomers comprising modified bases for binding cytosine and uracil or thymine and their use |
AU2003291753B2 (en) | 2002-11-05 | 2010-07-08 | Isis Pharmaceuticals, Inc. | Polycyclic sugar surrogate-containing oligomeric compounds and compositions for use in gene modulation |
EP1569695B1 (en) | 2002-11-13 | 2013-05-15 | Genzyme Corporation | Antisense modulation of apolipoprotein b expression |
EP2752488B1 (en) | 2002-11-18 | 2020-02-12 | Roche Innovation Center Copenhagen A/S | Antisense design |
MXPA05008319A (es) | 2003-02-10 | 2006-02-28 | Santaris Pharma As | Compuestos oligomericos para la modulacion de la expresion de survivina. |
WO2004106356A1 (en) | 2003-05-27 | 2004-12-09 | Syddansk Universitet | Functionalized nucleotide derivatives |
US7457046B2 (en) * | 2003-07-01 | 2008-11-25 | Canon Kabushiki Kaisha | Zoom lens system and image-taking apparatus |
US7427672B2 (en) | 2003-08-28 | 2008-09-23 | Takeshi Imanishi | Artificial nucleic acids of n-o bond crosslinkage type |
US20050053981A1 (en) * | 2003-09-09 | 2005-03-10 | Swayze Eric E. | Gapped oligomeric compounds having linked bicyclic sugar moieties at the termini |
US20050074801A1 (en) * | 2003-09-09 | 2005-04-07 | Monia Brett P. | Chimeric oligomeric compounds comprising alternating regions of northern and southern conformational geometry |
PE20050469A1 (es) * | 2003-09-18 | 2005-09-10 | Lilly Co Eli | Modulacion de la expresion de eif4e |
AU2004303464B2 (en) | 2003-12-23 | 2009-10-01 | Santaris Pharma A/S | Oligomeric compounds for the modulation of BCL-2 |
GB0407382D0 (en) * | 2004-03-31 | 2004-05-05 | Univ Cambridge Tech | Therapeutic methods and means |
JP2008501693A (ja) | 2004-06-03 | 2008-01-24 | アイシス ファーマシューティカルズ、インク. | 遺伝子調節で使用するための個別に調節された鎖を有する二本鎖組成物 |
JP5523705B2 (ja) * | 2005-08-29 | 2014-06-18 | レグルス・セラピューティクス・インコーポレイテッド | Mir−122aをモジュレートする使用方法 |
DK1931780T3 (en) | 2005-08-29 | 2016-01-25 | Regulus Therapeutics Inc | Antisense-forbindelser med forøget anti-microrna-aktivitet |
US20070299027A1 (en) | 2006-01-26 | 2007-12-27 | Gene Hung | Compositions and their uses directed to huntingtin |
AU2007211080B9 (en) | 2006-01-27 | 2012-05-03 | Isis Pharmaceuticals, Inc. | 6-modified bicyclic nucleic acid analogs |
ES2386578T3 (es) * | 2006-05-05 | 2012-08-23 | Isis Pharmaceuticals, Inc. | Compuestos y procedimientos para modular la expresión de PCSK9 |
ES2389737T3 (es) | 2006-05-11 | 2012-10-31 | Isis Pharmaceuticals, Inc. | Análogos de ácidos nucleicos bicíclicos modificados en 5' |
JP5665317B2 (ja) * | 2006-10-18 | 2015-02-04 | アイシス ファーマシューティカルズ, インコーポレーテッド | アンチセンス化合物 |
EP2134736A4 (en) | 2007-03-15 | 2013-05-29 | Jyoti Chattopadhyaya | FIVE- AND SIX-PIECE CONFORMATIVELY FIXED 2 ', 4'-CARBOCYCLIC RIBOTHYMIDINE FOR THE TREATMENT OF INFECTIONS AND CANCER |
EP2170917B1 (en) † | 2007-05-30 | 2012-06-27 | Isis Pharmaceuticals, Inc. | N-substituted-aminomethylene bridged bicyclic nucleic acid analogs |
EP2173760B2 (en) † | 2007-06-08 | 2015-11-04 | Isis Pharmaceuticals, Inc. | Carbocyclic bicyclic nucleic acid analogs |
US8088904B2 (en) † | 2007-08-15 | 2012-01-03 | Isis Pharmaceuticals, Inc. | Tetrahydropyran nucleic acid analogs |
US8389488B2 (en) | 2007-11-05 | 2013-03-05 | Isis Pharmaceuticals, Inc. | Antidotes to antisense compounds |
WO2009067647A1 (en) | 2007-11-21 | 2009-05-28 | Isis Pharmaceuticals, Inc. | Carbocyclic alpha-l-bicyclic nucleic acid analogs |
EP2265627A2 (en) | 2008-02-07 | 2010-12-29 | Isis Pharmaceuticals, Inc. | Bicyclic cyclohexitol nucleic acid analogs |
WO2009124295A2 (en) | 2008-04-04 | 2009-10-08 | Isis Pharmaceuticals, Inc. | Oligomeric compounds comprising bicyclic nucleosides and having reduced toxicity |
WO2010036698A1 (en) | 2008-09-24 | 2010-04-01 | Isis Pharmaceuticals, Inc. | Substituted alpha-l-bicyclic nucleosides |
WO2010108035A1 (en) | 2009-03-18 | 2010-09-23 | Isis Pharmaceuticals, Inc. | Compounds and methods for modulating toxic and proinflammatory effects |
WO2011017521A2 (en) | 2009-08-06 | 2011-02-10 | Isis Pharmaceuticals, Inc. | Bicyclic cyclohexose nucleic acid analogs |
WO2012027033A1 (en) | 2010-07-19 | 2012-03-01 | Isis Pharmaceuticals, Inc. | Compounds and methods for modulating target nuclear and sub-nuclear nucleic acid molecules in cells and animals |
EP2673361B1 (en) | 2011-02-08 | 2016-04-13 | Ionis Pharmaceuticals, Inc. | Oligomeric compounds comprising bicyclic nucleotides and uses thereof |
LT3505528T (lt) | 2011-04-21 | 2021-04-26 | Glaxo Group Limited | Hepatito b viruso (hbv) raiškos moduliacija |
US9752142B2 (en) | 2011-08-11 | 2017-09-05 | Ionis Pharmaceuticals, Inc. | Gapped oligomeric compounds comprising 5′-modified deoxyribonucleosides in the gap and uses thereof |
AU2014318580B2 (en) | 2013-09-13 | 2019-12-12 | Ionis Pharmaceuticals, Inc. | Modulators of Complement Factor B |
-
2007
- 2007-10-18 JP JP2009533545A patent/JP5665317B2/ja active Active
- 2007-10-18 EP EP21155022.3A patent/EP3916095A1/en active Pending
- 2007-10-18 CA CA2667055A patent/CA2667055C/en active Active
- 2007-10-18 WO PCT/US2007/081850 patent/WO2008049085A1/en active Application Filing
- 2007-10-18 ES ES11186113T patent/ES2526295T5/es active Active
- 2007-10-18 AU AU2007310989A patent/AU2007310989B2/en active Active
- 2007-10-18 EP EP07844422.1A patent/EP2092065B2/en active Active
- 2007-10-18 DK DK11186113.4T patent/DK2410053T4/da active
- 2007-10-18 EP EP11186203.3A patent/EP2410054B2/en active Active
- 2007-10-18 DK DK11186203.3T patent/DK2410054T4/da active
- 2007-10-18 AT AT07844422T patent/ATE540118T1/de active
- 2007-10-18 DK DK07844422.1T patent/DK2092065T4/da active
- 2007-10-18 US US12/445,851 patent/US9550988B2/en active Active
- 2007-10-18 EP EP16205317.7A patent/EP3202905A1/en not_active Withdrawn
- 2007-10-18 ES ES07844422T patent/ES2377327T5/es active Active
- 2007-10-18 ES ES11186203T patent/ES2620472T5/es active Active
- 2007-10-18 EP EP11186113.4A patent/EP2410053B2/en active Active
-
2012
- 2012-07-25 HK HK12107284.6A patent/HK1166643A1/xx active IP Right Maintenance
-
2014
- 2014-06-16 AU AU2014203243A patent/AU2014203243B2/en active Active
- 2014-07-24 JP JP2014150706A patent/JP2014221817A/ja active Pending
-
2016
- 2016-09-27 AU AU2016231660A patent/AU2016231660A1/en not_active Abandoned
- 2016-12-09 US US15/373,860 patent/US10493092B2/en active Active
-
2019
- 2019-10-21 US US16/659,368 patent/US20200276221A1/en not_active Abandoned
-
2023
- 2023-01-05 US US18/150,395 patent/US20240058370A1/en active Pending
Also Published As
Similar Documents
Publication | Publication Date | Title |
---|---|---|
ES2620472T3 (es) | Compuestos antisentido | |
ES2935658T3 (es) | Compuestos y métodos para la modulación de SMN2 | |
EP2640853B1 (en) | Modulation of alpha synuclein expression | |
BR122020024443B1 (pt) | Composto e composição farmacêutica para modulação da expressão de angptl3 | |
WO2012012443A2 (en) | Modulation of dystrophia myotonica-protein kinase (dmpk) expression | |
BR112016022742B1 (pt) | Composto químico, composição compreendendo o composto e uso dos mesmos | |
BR112016022593B1 (pt) | Compostos oligoméricos, composições que os compreendem, e usos dos mesmos |