EA202190581A1 - Антисмысловые олигонуклеотиды, нацеленные на scn2a, для лечения энцефалопатии scn1a - Google Patents
Антисмысловые олигонуклеотиды, нацеленные на scn2a, для лечения энцефалопатии scn1aInfo
- Publication number
- EA202190581A1 EA202190581A1 EA202190581A EA202190581A EA202190581A1 EA 202190581 A1 EA202190581 A1 EA 202190581A1 EA 202190581 A EA202190581 A EA 202190581A EA 202190581 A EA202190581 A EA 202190581A EA 202190581 A1 EA202190581 A1 EA 202190581A1
- Authority
- EA
- Eurasian Patent Office
- Prior art keywords
- scn2a
- scn1a
- encephalopathy
- treatment
- sense oligonucleotides
- Prior art date
Links
- 101000631760 Homo sapiens Sodium channel protein type 1 subunit alpha Proteins 0.000 title abstract 2
- 101000684826 Homo sapiens Sodium channel protein type 2 subunit alpha Proteins 0.000 title abstract 2
- 102100028910 Sodium channel protein type 1 subunit alpha Human genes 0.000 title abstract 2
- 102100023150 Sodium channel protein type 2 subunit alpha Human genes 0.000 title abstract 2
- 108020000948 Antisense Oligonucleotides Proteins 0.000 title 1
- 208000014644 Brain disease Diseases 0.000 title 1
- 208000032274 Encephalopathy Diseases 0.000 title 1
- 239000000074 antisense oligonucleotide Substances 0.000 title 1
- 238000012230 antisense oligonucleotides Methods 0.000 title 1
- 230000008685 targeting Effects 0.000 title 1
- 150000001875 compounds Chemical class 0.000 abstract 2
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 2
- 239000000203 mixture Substances 0.000 abstract 2
- 201000007547 Dravet syndrome Diseases 0.000 abstract 1
- 208000036572 Myoclonic epilepsy Diseases 0.000 abstract 1
- 206010073677 Severe myoclonic epilepsy of infancy Diseases 0.000 abstract 1
- 201000010099 disease Diseases 0.000 abstract 1
- 208000035475 disorder Diseases 0.000 abstract 1
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- 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
- C12N15/1138—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 against receptors or cell surface proteins
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/0012—Galenical forms characterised by the site of application
- A61K9/0085—Brain, e.g. brain implants; Spinal cord
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
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- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01K—ANIMAL HUSBANDRY; AVICULTURE; APICULTURE; PISCICULTURE; FISHING; REARING OR BREEDING ANIMALS, NOT OTHERWISE PROVIDED FOR; NEW BREEDS OF ANIMALS
- A01K2217/00—Genetically modified animals
- A01K2217/07—Animals genetically altered by homologous recombination
- A01K2217/075—Animals genetically altered by homologous recombination inducing loss of function, i.e. knock out
- A01K2217/077—Animals genetically altered by homologous recombination inducing loss of function, i.e. knock out heterozygous knock out animals displaying phenotype
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- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01K—ANIMAL HUSBANDRY; AVICULTURE; APICULTURE; PISCICULTURE; FISHING; REARING OR BREEDING ANIMALS, NOT OTHERWISE PROVIDED FOR; NEW BREEDS OF ANIMALS
- A01K2227/00—Animals characterised by species
- A01K2227/10—Mammal
- A01K2227/105—Murine
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- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01K—ANIMAL HUSBANDRY; AVICULTURE; APICULTURE; PISCICULTURE; FISHING; REARING OR BREEDING ANIMALS, NOT OTHERWISE PROVIDED FOR; NEW BREEDS OF ANIMALS
- A01K2267/00—Animals characterised by purpose
- A01K2267/03—Animal model, e.g. for test or diseases
- A01K2267/035—Animal model for multifactorial diseases
- A01K2267/0356—Animal model for processes and diseases of the central nervous system, e.g. stress, learning, schizophrenia, pain, epilepsy
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- C12N2310/00—Structure or type of the nucleic acid
- C12N2310/10—Type of nucleic acid
- C12N2310/11—Antisense
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- C12N2310/00—Structure or type of the nucleic acid
- C12N2310/30—Chemical structure
- C12N2310/31—Chemical structure of the backbone
- C12N2310/314—Phosphoramidates
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- C12N2310/00—Structure or type of the nucleic acid
- C12N2310/30—Chemical structure
- C12N2310/31—Chemical structure of the backbone
- C12N2310/315—Phosphorothioates
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- 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
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- C12N2310/00—Structure or type of the nucleic acid
- C12N2310/30—Chemical structure
- C12N2310/32—Chemical structure of the sugar
- C12N2310/322—2'-R Modification
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- 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
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- 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
- C12N2310/3233—Morpholino-type ring
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- 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
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- 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 ===---===
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- 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
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- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
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- C12N2320/00—Applications; Uses
- C12N2320/30—Special therapeutic applications
- C12N2320/32—Special delivery means, e.g. tissue-specific
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- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Biomedical Technology (AREA)
- Genetics & Genomics (AREA)
- Chemical & Material Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Organic Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Molecular Biology (AREA)
- General Engineering & Computer Science (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Biotechnology (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Biochemistry (AREA)
- Microbiology (AREA)
- Plant Pathology (AREA)
- Biophysics (AREA)
- Physics & Mathematics (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Psychology (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Abstract
В данном документе предложены способы, соединения и композиции для снижения экспрессии SCN2A у субъекта. Такие способы, соединения и композиции применимы для лечения, предотвращения, отсрочки или облегчения связанного с SCN1А заболевания или расстройства (например, синдрома Драве) у нуждающегося в этом субъекта.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US201862765344P | 2018-08-20 | 2018-08-20 | |
PCT/US2019/047313 WO2020041348A1 (en) | 2018-08-20 | 2019-08-20 | Antisense oligonucleotides targeting scn2a for the treatment of scn1a encephalopathies |
Publications (1)
Publication Number | Publication Date |
---|---|
EA202190581A1 true EA202190581A1 (ru) | 2021-07-13 |
Family
ID=69591162
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EA202190581A EA202190581A1 (ru) | 2018-08-20 | 2019-08-20 | Антисмысловые олигонуклеотиды, нацеленные на scn2a, для лечения энцефалопатии scn1a |
Country Status (9)
Country | Link |
---|---|
US (1) | US11939582B2 (ru) |
EP (1) | EP3840733A4 (ru) |
JP (1) | JP7476199B2 (ru) |
CN (1) | CN113329739A (ru) |
AU (1) | AU2019325255A1 (ru) |
BR (1) | BR112021003224A2 (ru) |
CA (1) | CA3110211A1 (ru) |
EA (1) | EA202190581A1 (ru) |
WO (1) | WO2020041348A1 (ru) |
Families Citing this family (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
AU2016334804B2 (en) | 2015-10-09 | 2022-03-31 | University Of Southampton | Modulation of gene expression and screening for deregulated protein expression |
AU2016370653A1 (en) | 2015-12-14 | 2018-06-21 | Cold Spring Harbor Laboratory | Antisense oligomers for treatment of Autosomal Dominant Mental Retardation-5 and Dravet Syndrome |
EP4303321A2 (en) | 2017-08-25 | 2024-01-10 | Stoke Therapeutics, Inc. | Antisense oligomers for treatment of conditions and diseases |
EP4110919A4 (en) * | 2020-02-28 | 2024-06-05 | Ionis Pharmaceuticals Inc | COMPOUNDS AND METHODS FOR MODULATING SCN1A EXPRESSION |
WO2021231107A1 (en) | 2020-05-11 | 2021-11-18 | Stoke Therapeutics, Inc. | Opa1 antisense oligomers for treatment of conditions and diseases |
CA3186935A1 (en) * | 2020-08-07 | 2022-02-10 | Paymaan JAFAR-NEJAD | Compounds and methods for modulating scn2a |
EP4155402A1 (en) | 2021-09-22 | 2023-03-29 | Royal College of Surgeons in Ireland | Modulation of microrna-335 for the treatment of sodium channelopathies |
WO2024026122A2 (en) * | 2022-07-29 | 2024-02-01 | Stoke Therapeutics, Inc. | Compounds for treatment of conditions and diseases |
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2019
- 2019-08-20 US US17/269,706 patent/US11939582B2/en active Active
- 2019-08-20 WO PCT/US2019/047313 patent/WO2020041348A1/en unknown
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- 2019-08-20 AU AU2019325255A patent/AU2019325255A1/en active Pending
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- 2019-08-20 CA CA3110211A patent/CA3110211A1/en active Pending
- 2019-08-20 CN CN201980068868.6A patent/CN113329739A/zh active Pending
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CN113329739A (zh) | 2021-08-31 |
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BR112021003224A2 (pt) | 2021-07-20 |
JP7476199B2 (ja) | 2024-04-30 |
JP2021535204A (ja) | 2021-12-16 |
WO2020041348A1 (en) | 2020-02-27 |
EP3840733A1 (en) | 2021-06-30 |
EP3840733A4 (en) | 2022-07-20 |
CA3110211A1 (en) | 2020-02-27 |
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