EA201100810A1 - Фармацевтическая композиция - Google Patents
Фармацевтическая композицияInfo
- Publication number
- EA201100810A1 EA201100810A1 EA201100810A EA201100810A EA201100810A1 EA 201100810 A1 EA201100810 A1 EA 201100810A1 EA 201100810 A EA201100810 A EA 201100810A EA 201100810 A EA201100810 A EA 201100810A EA 201100810 A1 EA201100810 A1 EA 201100810A1
- Authority
- EA
- Eurasian Patent Office
- Prior art keywords
- oligonucleotides
- formation
- short
- pharmaceutical composition
- mechanisms
- Prior art date
Links
Classifications
-
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/16—Drugs for disorders of the alimentary tract or the digestive system for liver or gallbladder disorders, e.g. hepatoprotective agents, cholagogues, litholytics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/06—Antihyperlipidemics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
- A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
- A61P31/14—Antivirals for RNA viruses
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P7/00—Drugs for disorders of the blood or the extracellular fluid
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
-
- 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
- C12N2310/113—Antisense targeting other non-coding nucleic acids, e.g. antagomirs
-
- 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
- C12N2310/322—2'-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
- C12N2310/35—Nature of the modification
- C12N2310/351—Conjugate
- C12N2310/3515—Lipophilic moiety, e.g. cholesterol
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Bioinformatics & Cheminformatics (AREA)
- General Health & Medical Sciences (AREA)
- Genetics & Genomics (AREA)
- Public Health (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Veterinary Medicine (AREA)
- Pharmacology & Pharmacy (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Animal Behavior & Ethology (AREA)
- Biomedical Technology (AREA)
- Diabetes (AREA)
- Molecular Biology (AREA)
- Zoology (AREA)
- General Engineering & Computer Science (AREA)
- Biotechnology (AREA)
- Wood Science & Technology (AREA)
- Virology (AREA)
- Hematology (AREA)
- Oncology (AREA)
- Microbiology (AREA)
- Obesity (AREA)
- Plant Pathology (AREA)
- Communicable Diseases (AREA)
- Biochemistry (AREA)
- Physics & Mathematics (AREA)
- Biophysics (AREA)
- Vascular Medicine (AREA)
- Urology & Nephrology (AREA)
- Gastroenterology & Hepatology (AREA)
- Endocrinology (AREA)
- Emergency Medicine (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
Abstract
Настоящее изобретение относится к фармацевтическим композициям, включающим короткие одноцепочечные олигонуклеотиды длиной 8-26 нуклеотидов, комплементарных человеческим микроРНК, выбранным из группы, состоящей из miR19b, miR21, miR122a, miR155 и miR375. Короткие олигонуклеотиды особенно эффективно способствуют подавлению миРНК in vivo. Было обнаружено, что включение высокоаффинных нуклеотидных аналогов в олигонуклеотиды приводит к образованию высокоэффективных молекул, которые подавляют микроРНК и, очевидно, действуют посредством образования почти необратимых дуплексов с миРНК-мишенью, но не посредством механизмов на основе расщепления РНК, таких как механизмы, ассоциированные с действием РНКазы Н или RISC.
Applications Claiming Priority (6)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US78899506P | 2006-04-03 | 2006-04-03 | |
DKPA200600478 | 2006-04-03 | ||
US79681306P | 2006-05-01 | 2006-05-01 | |
DKPA200600615 | 2006-05-01 | ||
US83871006P | 2006-08-18 | 2006-08-18 | |
DKPA200601401 | 2006-10-30 |
Publications (1)
Publication Number | Publication Date |
---|---|
EA201100810A1 true EA201100810A1 (ru) | 2012-06-29 |
Family
ID=43062722
Family Applications (4)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EA201100812A EA201100812A1 (ru) | 2006-04-03 | 2007-03-30 | Фармацевтическая композиция |
EA201100813A EA201100813A1 (ru) | 2006-04-03 | 2007-03-30 | Фармацевтическая композиция |
EA201100811A EA201100811A1 (ru) | 2006-04-03 | 2007-03-30 | Фармацевтическая композиция |
EA201100810A EA201100810A1 (ru) | 2006-04-03 | 2007-03-30 | Фармацевтическая композиция |
Family Applications Before (3)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EA201100812A EA201100812A1 (ru) | 2006-04-03 | 2007-03-30 | Фармацевтическая композиция |
EA201100813A EA201100813A1 (ru) | 2006-04-03 | 2007-03-30 | Фармацевтическая композиция |
EA201100811A EA201100811A1 (ru) | 2006-04-03 | 2007-03-30 | Фармацевтическая композиция |
Country Status (9)
Country | Link |
---|---|
US (1) | US8163708B2 (ru) |
EP (4) | EP3502255A1 (ru) |
CN (1) | CN102851291B (ru) |
EA (4) | EA201100812A1 (ru) |
ES (1) | ES2569558T3 (ru) |
MY (1) | MY162210A (ru) |
NZ (1) | NZ571569A (ru) |
PL (1) | PL2666859T3 (ru) |
SG (2) | SG170773A1 (ru) |
Families Citing this family (47)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
ES2406686T3 (es) * | 2007-10-04 | 2013-06-07 | Santaris Pharma A/S | Micromirs |
WO2009091972A2 (en) * | 2008-01-18 | 2009-07-23 | Alnylam Pharmaceuticals, Inc. | Chemically modified oligonucleotides and small molecules for use in reducing micro rna activity levels and uses thereof |
US8361980B2 (en) * | 2008-03-07 | 2013-01-29 | Santaris Pharma A/S | Pharmaceutical compositions for treatment of microRNA related diseases |
ES2541442T3 (es) | 2008-08-01 | 2015-07-20 | Roche Innovation Center Copenhagen A/S | Modulación mediada por microARN de factores estimulantes de colonias |
US8796443B2 (en) | 2008-09-22 | 2014-08-05 | Rxi Pharmaceuticals Corporation | Reduced size self-delivering RNAi compounds |
ES2599979T3 (es) * | 2009-04-24 | 2017-02-06 | Roche Innovation Center Copenhagen A/S | Composiciones farmacéuticas para el tratamiento de pacientes de VHC que no responden al interferón |
ES2574625T3 (es) * | 2009-11-25 | 2016-06-21 | Elitechgroup B.V. | Antagonistas de miARN de oligonucleótido conjugado con aglutinante del surco menor (MGB) |
US9624491B2 (en) | 2010-02-26 | 2017-04-18 | Memorial Sloan Kettering Cancer Center | Methods and compositions for the detection and treatment of cancer involving miRNAs and miRNA inhibitors and targets |
IL265674B2 (en) | 2010-03-24 | 2024-05-01 | Phio Pharm Corp | Rana disorder in cutaneous and fibrotic symptoms |
US9095504B2 (en) | 2010-03-24 | 2015-08-04 | Rxi Pharmaceuticals Corporation | RNA interference in ocular indications |
JP5931050B2 (ja) * | 2010-03-26 | 2016-06-08 | ジ・オハイオ・ステート・ユニバーシティ | miR−155によるミスマッチ修復およびゲノム安定性の調節に関連する材料および方法 |
EP2638163B1 (en) * | 2010-11-12 | 2017-05-17 | 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 |
PL3211082T3 (pl) * | 2011-04-25 | 2021-08-02 | Sanofi | Związki mikroRNA i sposoby modulowania aktywności miR-21 |
WO2013013165A2 (en) * | 2011-07-21 | 2013-01-24 | The Trustees Of The University Of Pennsylvania | Use of lna compounds for therapeutic inhibition of mir-21 in systemic lupus erythematosus |
BR112014008925A2 (pt) * | 2011-10-11 | 2020-10-27 | The Brigham And Women's Hospital, Inc. | micro rnas em distúrbios de neurodegenerativos |
CA3077746A1 (en) | 2011-10-19 | 2013-04-25 | Council Of Scientific And Industrial Research (C.S.I.R.) | Biomarkers useful for detection of types, grades and stages of human breast cancer |
KR20220028183A (ko) | 2012-04-25 | 2022-03-08 | 사노피 | 마이크로rna 화합물 및 mir-21 활성 조절 방법 |
EP2850188A4 (en) | 2012-05-16 | 2016-01-20 | Rana Therapeutics Inc | COMPOSITIONS AND METHOD FOR MODULATING THE EXPRESSION OF THE HEMOGLOBIN GENE FAMILIES |
US10837014B2 (en) | 2012-05-16 | 2020-11-17 | Translate Bio Ma, Inc. | Compositions and methods for modulating SMN gene family expression |
BR112014028644A2 (pt) | 2012-05-16 | 2017-08-15 | Rana Therapeutics Inc | Composições e métodos para modulação da expressão de atp2a2 |
EA201492116A1 (ru) | 2012-05-16 | 2015-05-29 | Рана Терапьютикс, Инк. | Композиции и способы для модулирования экспрессии mecp2 |
UA116639C2 (uk) | 2012-10-09 | 2018-04-25 | Рег'Юлес Терап'Ютікс Інк. | Способи лікування синдрому альпорта |
NZ708171A (en) | 2012-11-15 | 2019-11-29 | Roche Innovation Ct Copenhagen As | Oligonucleotide conjugates |
JP6649248B2 (ja) | 2013-05-01 | 2020-02-19 | レグルス セラピューティクス インコーポレイテッド | 細胞取り込みの向上のための化合物および方法 |
NZ630890A (en) | 2013-05-01 | 2017-09-29 | Regulus Therapeutics Inc | Microrna compounds and methods for modulating mir-122 |
CN104031987B (zh) * | 2014-05-12 | 2016-08-31 | 贵州省人民医院 | miRNA在心肌纤维化疾病治疗中的应用 |
US10858650B2 (en) | 2014-10-30 | 2020-12-08 | The General Hospital Corporation | Methods for modulating ATRX-dependent gene repression |
CR20170192A (es) * | 2014-11-10 | 2017-09-29 | Glaxosmithkline Intellectual Property N 2 Ltd | Composiciones de acción prolongada de combinación y procedimientos para hepatitis c |
WO2016149455A2 (en) | 2015-03-17 | 2016-09-22 | The General Hospital Corporation | The rna interactome of polycomb repressive complex 1 (prc1) |
CN105087477A (zh) * | 2015-05-21 | 2015-11-25 | 王松灵 | miR-21反义核苷酸修饰的骨髓间充质干细胞的用途 |
CA2986949C (en) | 2015-06-05 | 2020-07-21 | MiRagen Therapeutics, Inc. | Mir-155 inhibitors for treating cutaneous t cell lymphoma (ctcl) |
KR102048165B1 (ko) * | 2015-08-26 | 2019-11-22 | 카오슝 메디칼 유니버시티 | 마이크로rna-328 안티-센스 조성물 및 치료 용도 |
JP6666002B2 (ja) | 2015-10-07 | 2020-03-13 | 国立大学法人京都大学 | Tdp−43プロテノパシーの予防又は治療用組成物 |
CN107034216A (zh) * | 2016-02-04 | 2017-08-11 | 中国科学技术大学 | miRancer分子的设计与应用 |
US11584932B2 (en) | 2016-11-01 | 2023-02-21 | The Research Foundation For The State University Of New York | 5-halouracil-modified microRNAs and their use in the treatment of cancer |
WO2018170759A1 (zh) * | 2017-03-22 | 2018-09-27 | 深圳市博奥康生物科技有限公司 | 重组Ad-140-148a-185-Tud腺病毒及其构建和应用 |
WO2019000151A1 (zh) * | 2017-06-26 | 2019-01-03 | 深圳市博奥康生物科技有限公司 | 用于同步抑制三种微小rna表达的重组腺相关病毒 |
WO2019000143A1 (zh) * | 2017-06-26 | 2019-01-03 | 深圳市博奥康生物科技有限公司 | 一种敲减miRNA表达的重组腺相关病毒 |
WO2019000147A1 (zh) * | 2017-06-26 | 2019-01-03 | 深圳市博奥康生物科技有限公司 | 一种有效抑制人mir-148a、mir-152和mir-185表达的tud rna及其应用 |
JP7279081B2 (ja) | 2018-05-08 | 2023-05-22 | レグルス セラピューティクス インコーポレイテッド | Mir-122を調節するためのマイクロrna化合物及び方法 |
BR112020022620A2 (pt) * | 2018-05-11 | 2021-02-17 | Alpha Anomeric Sas | conjugados de oligonucleotídeos que compreendem nucleosídeos de açúcar 7'-5'-alfa-anomérico-bicíclicos |
WO2020230108A1 (en) | 2019-05-16 | 2020-11-19 | Aptatargets, S.L. | Treatment of ischemic stroke with aptamers targeting tlr-4 |
EP3990028B1 (en) | 2019-06-26 | 2025-06-04 | Biorchestra Co., Ltd. | Micellar nanoparticles and uses thereof |
WO2021262919A2 (en) | 2020-06-26 | 2021-12-30 | The Research Foundation For The State University Of New York | 5-halouracil-modified micrornas and their use in the treatment of cancer |
CN119866224A (zh) | 2022-07-28 | 2025-04-22 | 加拿大干细胞技术公司 | 编码连接抗原的多核苷酸以及其用途 |
WO2024240750A1 (en) | 2023-05-22 | 2024-11-28 | Aptatargets, S.L. | New tlr-4 antagonist aptamers |
Family Cites Families (91)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4914210A (en) | 1987-10-02 | 1990-04-03 | Cetus Corporation | Oligonucleotide functionalizing reagents |
US4962029A (en) | 1987-10-02 | 1990-10-09 | Cetus Corporation | Covalent oligonucleotide-horseradish peroxidase conjugate |
US4920115A (en) | 1988-12-28 | 1990-04-24 | Virginia Commonwealth University | Method of lowering LDL cholesterol in blood |
WO2002081494A1 (en) | 2001-03-26 | 2002-10-17 | Sirna Therapeutics, Inc. | Oligonucleotide mediated inhibition of hepatitis b virus and hepatitis c virus replication |
JPH06311885A (ja) | 1992-08-25 | 1994-11-08 | Mitsubishi Kasei Corp | C型肝炎ウイルス遺伝子に相補的なアンチセンス化合物 |
US6423489B1 (en) | 1992-09-10 | 2002-07-23 | Isis Pharmaceuticals, Inc. | Compositions and methods for treatment of Hepatitis C virus-associated diseases |
ATE202383T1 (de) | 1992-09-10 | 2001-07-15 | Isis Pharmaceuticals Inc | Zusammensetzungen und verfahren für die behandlung von mit hepatitis c viren assoziierten krankheiten |
US6433159B1 (en) | 1992-09-10 | 2002-08-13 | Isis Pharmaceuticals, Inc. | Compositions and methods for treatment of Hepatitis C virus associated diseases |
JPH10503364A (ja) | 1994-05-10 | 1998-03-31 | ザ ジェネラル ホスピタル コーポレーション | C型肝炎ウイルスのアンチセンス阻害 |
DK0832069T3 (da) | 1995-06-07 | 2003-04-22 | Pfizer | Biphenyl-2-carboxylsyre-tetrahydroisoquinolin-6-ylamidderivater, deres fremstilling og deres anvendelse som inhibitorer af sekretion af mikrosomalt triglyceridoverførselsprotein og/eller apolipoprotein B (Apo B) |
CN1238764A (zh) | 1996-11-27 | 1999-12-15 | 美国辉瑞有限公司 | 可抑制ApoB-分泌物/MTP的酰胺 |
NZ337703A (en) | 1997-03-05 | 2001-05-25 | Univ Washington | A screening method to identify agents that selectively inhibit Hepatitis C virus replication in viruses that contain an ISDR region |
CA2303299C (en) | 1997-09-12 | 2016-02-23 | Exiqon A/S | Oligonucleotide analogues |
DE60044241D1 (de) | 1999-03-18 | 2010-06-02 | Exiqon As | Xylo-lna analoge |
DE60029314T2 (de) | 1999-03-24 | 2007-07-12 | Exiqon A/S | Verbesserte Synthese für -2.2.1. I Bicyclo-Nukleoside |
KR100782896B1 (ko) | 1999-05-04 | 2007-12-06 | 엑시콘 에이/에스 | L-리보-lna 유사체 |
US6617442B1 (en) | 1999-09-30 | 2003-09-09 | Isis Pharmaceuticals, Inc. | Human Rnase H1 and oligonucleotide compositions thereof |
AU7406600A (en) * | 1999-10-04 | 2001-05-10 | Exiqon A/S | A method of increasing the specificity of oxy-lna oligonucleotides |
AU7406700A (en) | 1999-10-04 | 2001-05-10 | Exiqon A/S | Design of high affinity rnase h recruiting oligonucleotide |
IL139450A0 (en) | 1999-11-10 | 2001-11-25 | Pfizer Prod Inc | Methods of administering apo b-secretion/mtp inhibitors |
EP1334109B1 (en) | 2000-10-04 | 2006-05-10 | Santaris Pharma A/S | Improved synthesis of purine locked nucleic acid analogues |
AU2002322478A1 (en) | 2001-03-02 | 2002-12-16 | Medimmune, Inc. | Methods of administering/dosing cd2 antagonists for the prevention and treatment of autoimmune disorders or inflammatory disorders |
US20030125241A1 (en) | 2001-05-18 | 2003-07-03 | Margit Wissenbach | Therapeutic uses of LNA-modified oligonucleotides in infectious diseases |
DE60202681T2 (de) | 2001-07-12 | 2006-01-12 | Santaris Pharma A/S | Verfahren zur herstellung des lna phosphoramidite |
US7407943B2 (en) | 2001-08-01 | 2008-08-05 | Isis Pharmaceuticals, Inc. | Antisense modulation of apolipoprotein B expression |
JP4371812B2 (ja) | 2001-09-28 | 2009-11-25 | マックス−プランク−ゲゼルシャフト・ツア・フェルデルング・デア・ヴィッセンシャフテン・エー・ファオ | マイクロrna分子 |
EP1430157B1 (en) | 2002-02-20 | 2011-08-10 | Sirna Therapeutics, Inc. | RNA INTERFERENCE MEDIATED INHIBITION OF HEPATITIS C VIRUS (HCV) GENE EXPRESSION USING SHORT INTERFERING NUCLEIC ACID (siNA) |
DK1501848T3 (da) | 2002-05-08 | 2007-10-22 | Santaris Pharma As | Syntese af låst nukleinsyrederivater |
UA79300C2 (en) | 2002-08-12 | 2007-06-11 | Janssen Pharmaceutica Nv | N-aryl piperidine substituted biphenylcarboxamides as inhibitors of apolipoprotein b secretion |
US7183302B2 (en) | 2002-08-12 | 2007-02-27 | Bristol-Myers Squibb Company | Iminothiazolidinones as inhibitors of HCV replication |
US7087229B2 (en) | 2003-05-30 | 2006-08-08 | Enzon Pharmaceuticals, Inc. | Releasable polymeric conjugates based on aliphatic biodegradable linkers |
WO2004044181A2 (en) | 2002-11-13 | 2004-05-27 | Isis Pharmaceuticals, Inc. | Antisense modulation of apolipoprotein b expression |
DK2284269T3 (en) | 2002-11-18 | 2017-10-23 | Roche Innovation Ct Copenhagen As | Antisense design |
US8124582B2 (en) | 2002-12-06 | 2012-02-28 | Fibrogen, Inc. | Treatment of diabetes |
FR2848572B1 (fr) | 2002-12-12 | 2005-12-09 | Univ Joseph Fourier | Molecules inhibitrices de la synthese proteique du virus de l'hepatite c et procede de criblage desdites molecules inhibitrices |
JP4503590B2 (ja) | 2003-02-10 | 2010-07-14 | サンタリス ファーマ アー/エス | サバイビン発現を調整するためのオリゴマー化合物 |
AU2004215097A1 (en) | 2003-02-10 | 2004-09-10 | National Institute Of Advanced Industrial Science And Technology | Regulation of gene expression by DNA interference |
EP2530157B1 (en) * | 2003-07-31 | 2016-09-28 | Regulus Therapeutics Inc. | Oligomeric compounds and compositions for use in modulation of miRNAs |
AU2004263124B2 (en) | 2003-08-07 | 2009-01-15 | Avi Biopharma, Inc. | Sense antiviral compound and method for treating ssRNA viral infection |
US20050142581A1 (en) | 2003-09-04 | 2005-06-30 | Griffey Richard H. | Microrna as ligands and target molecules |
JP5654722B2 (ja) | 2003-11-26 | 2015-01-14 | ユニバーシティ オブ マサチューセッツ | 短鎖rna機能の配列特異的阻害法 |
UA83510C2 (en) | 2003-12-09 | 2008-07-25 | Янссен Фармацевтика Н.В. | N-aryl piperidine substituted biphenylcarboxamides as inhibitors of apolipoprotein b |
DE602004027163D1 (de) * | 2003-12-23 | 2010-06-24 | Santaris Pharma As | Oligomere verbindungen zur modulation von bcl-2 |
CA2554818A1 (en) | 2004-02-09 | 2005-08-25 | Thomas Jefferson University | Diagnosis and treatment of cancers with microrna located in or near cancer-associated chromosomal features |
US20050182005A1 (en) | 2004-02-13 | 2005-08-18 | Tuschl Thomas H. | Anti-microRNA oligonucleotide molecules |
WO2005079397A2 (en) * | 2004-02-13 | 2005-09-01 | Rockefeller University | Anti-microrna oligonucleotide molecules |
CN1961081B (zh) | 2004-04-07 | 2012-09-05 | 埃克斯魁恩公司 | 用于定量微rna和小干扰rna的新方法 |
US7365058B2 (en) | 2004-04-13 | 2008-04-29 | The Rockefeller University | MicroRNA and methods for inhibiting same |
BRPI0509979A (pt) | 2004-04-20 | 2007-10-16 | Genaco Biomedical Products Inc | método para detectar ncrna |
DE602005025751D1 (de) | 2004-05-04 | 2011-02-17 | Univ R | Verfahren und zusammensetzungen zur verringerung von hcv virusgenommengen in einer zielzelle |
EP1828215A2 (en) | 2004-07-21 | 2007-09-05 | Alnylam Pharmaceuticals Inc. | Oligonucleotides comprising a modified or non-natural nucleobase |
US20080213891A1 (en) | 2004-07-21 | 2008-09-04 | Alnylam Pharmaceuticals, Inc. | RNAi Agents Comprising Universal Nucleobases |
FR2873694B1 (fr) | 2004-07-27 | 2006-12-08 | Merck Sante Soc Par Actions Si | Nouveaux aza-indoles inhibiteurs de la mtp et apob |
EP1913011B1 (en) | 2004-08-04 | 2016-11-02 | Alnylam Pharmaceuticals Inc. | Oligonucleotides comprising a ligand tethered to a modified or non-natural nucleobase |
WO2006020676A2 (en) | 2004-08-10 | 2006-02-23 | Isis Pharmaceuticals, Inc. | Antisense modulation of apolipoprotein b expression |
JP5192234B2 (ja) | 2004-08-10 | 2013-05-08 | 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 | 化学修飾オリゴヌクレオチド |
EP1791954A1 (en) | 2004-09-07 | 2007-06-06 | Yissum Research Development Company Of The Hebrew University Of Jerusalem | Agents, compositions and methods for treating pathologies in which regulating an ache-associated biological pathway is beneficial |
AU2005289588B2 (en) | 2004-09-24 | 2011-12-22 | Alnylam Pharmaceuticals, Inc. | RNAi modulation of ApoB and uses thereof |
JP2008519606A (ja) | 2004-11-12 | 2008-06-12 | アンビオン インコーポレーティッド | miRNAおよびmiRNA阻害分子に関する方法および組成物 |
EP1828219A4 (en) | 2004-11-17 | 2008-07-23 | Protiva Biotherapeutics Inc | ARNSI SILENCE OF APOLIPOPROTEIN B |
US20060185027A1 (en) | 2004-12-23 | 2006-08-17 | David Bartel | Systems and methods for identifying miRNA targets and for altering miRNA and target expression |
EP1959012A3 (en) | 2004-12-29 | 2009-12-30 | Exiqon A/S | Novel oligonucleotide compositions and probe sequences useful for detection and analysis of microRNAs and their target mRNAs |
KR20080015792A (ko) | 2005-04-19 | 2008-02-20 | 서피스 로직스, 인크. | 미소체 트리글리세리드 전달 단백질 및 apo-b 분비의저해 |
US20060265771A1 (en) | 2005-05-17 | 2006-11-23 | Lewis David L | Monitoring microrna expression and function |
EP1904111A4 (en) | 2005-06-03 | 2009-08-19 | Univ Johns Hopkins | COMPOSITIONS AND METHODS FOR REDUCING MICRORNA EXPRESSION FOR THE TREATMENT OF NEOPLASIA |
US20070213292A1 (en) | 2005-08-10 | 2007-09-13 | The Rockefeller University | Chemically modified oligonucleotides for use in modulating micro RNA and uses thereof |
AU2006279906B2 (en) | 2005-08-10 | 2012-05-10 | Alnylam Pharmaceuticals, Inc. | Chemically modified oligonucleotides for use in modulating micro RNA and uses thereof |
WO2007027894A2 (en) | 2005-08-29 | 2007-03-08 | Isis Pharmaceuticals, Inc. | Antisense compounds having enhanced anti-microrna activity |
CA2620856C (en) | 2005-08-29 | 2017-11-28 | Isis Pharmaceuticals, Inc. | Methods for use in modulating mir-122a |
JP2009507499A (ja) | 2005-09-15 | 2009-02-26 | サンタリス ファーマ アー/エス | Apo−b100発現の抑制のためのrnaアンタゴニスト化合物 |
WO2007031091A2 (en) | 2005-09-15 | 2007-03-22 | Santaris Pharma A/S | Rna antagonist compounds for the modulation of p21 ras expression |
EP2388328A1 (en) | 2006-01-27 | 2011-11-23 | Isis Pharmaceuticals, Inc. | Oligomeric compounds and compositions for the use in modulation of micrornas |
EP2007889A2 (en) | 2006-04-03 | 2008-12-31 | Santaris Pharma A/S | Pharmaceutical compositions comprising anti-mirna antisense oligonucleotides |
EP2397551A1 (en) | 2006-05-05 | 2011-12-21 | Isis Pharmaceuticals, Inc. | Compounds and methods for modulating expression of PCSK9 |
WO2007134181A2 (en) | 2006-05-11 | 2007-11-22 | Isis Pharmaceuticals, Inc. | 5'-modified bicyclic nucleic acid analogs |
US20080199961A1 (en) | 2006-08-25 | 2008-08-21 | Avi Biopharma, Inc. | ANTISENSE COMPOSITION AND METHOD FOR INHIBITION OF miRNA BIOGENESIS |
CN101534643A (zh) | 2006-09-15 | 2009-09-16 | 安佐制药股份有限公司 | 用于递送寡核苷酸的基于位阻酯的生物可降解连接体 |
KR20090054438A (ko) | 2006-09-15 | 2009-05-29 | 엔존 파마슈티컬즈, 인코포레이티드 | 양전하를 띄는 부분을 포함하는 고분자 컨쥬게이트 |
WO2008046911A2 (en) | 2006-10-20 | 2008-04-24 | Exiqon A/S | Novel human micrornas associated with cancer |
US7803784B2 (en) | 2006-10-24 | 2010-09-28 | The Board Of Trustees Of The Leland Stanford Junior University | Modulation of T cell signaling threshold and T cell sensitivity to antigens |
JP2010509923A (ja) | 2006-11-23 | 2010-04-02 | ミルクス セラピューティクス アンパーツゼルスカブ | 標的rnaの活性を変化させるためのオリゴヌクレオチド |
WO2008074328A2 (en) | 2006-12-21 | 2008-06-26 | Exiqon A/S | Microrna target site blocking oligos and uses thereof |
WO2008113832A2 (en) | 2007-03-22 | 2008-09-25 | Santaris Pharma A/S | SHORT RNA ANTAGONIST COMPOUNDS FOR THE MODULATION OF TARGET mRNA |
WO2008124384A2 (en) | 2007-04-03 | 2008-10-16 | Aegerion Pharmaceuticals, Inc. | Combinations of mtp inhibitors with cholesterol absorption inhibitors or interferon for treating hepatitis c |
CA2688321A1 (en) | 2007-05-30 | 2008-12-11 | Isis Pharmaceuticals, Inc. | N-substituted-aminomethylene bridged bicyclic nucleic acid analogs |
ES2386492T3 (es) | 2007-06-08 | 2012-08-21 | Isis Pharmaceuticals, Inc. | Análogos de ácidos nucleicos bicíclicos carbocíclicos |
US20090082297A1 (en) | 2007-06-25 | 2009-03-26 | Lioy Daniel T | Compositions and Methods for Regulating Gene Expression |
WO2009032083A1 (en) | 2007-08-29 | 2009-03-12 | President And Fellows Of Harvard College | Methods of increasing gene expression through rna protection |
ES2406686T3 (es) | 2007-10-04 | 2013-06-07 | Santaris Pharma A/S | Micromirs |
US8361980B2 (en) | 2008-03-07 | 2013-01-29 | Santaris Pharma A/S | Pharmaceutical compositions for treatment of microRNA related diseases |
ES2599979T3 (es) | 2009-04-24 | 2017-02-06 | Roche Innovation Center Copenhagen A/S | Composiciones farmacéuticas para el tratamiento de pacientes de VHC que no responden al interferón |
-
2007
- 2007-03-30 ES ES10173208.9T patent/ES2569558T3/es active Active
- 2007-03-30 EP EP18203866.1A patent/EP3502255A1/en not_active Withdrawn
- 2007-03-30 SG SG201102154-0A patent/SG170773A1/en unknown
- 2007-03-30 PL PL13172958T patent/PL2666859T3/pl unknown
- 2007-03-30 CN CN201210247597.0A patent/CN102851291B/zh not_active Expired - Fee Related
- 2007-03-30 EA EA201100812A patent/EA201100812A1/ru unknown
- 2007-03-30 EA EA201100813A patent/EA201100813A1/ru unknown
- 2007-03-30 NZ NZ571569A patent/NZ571569A/en not_active IP Right Cessation
- 2007-03-30 US US12/295,960 patent/US8163708B2/en not_active Expired - Fee Related
- 2007-03-30 SG SG10201406016SA patent/SG10201406016SA/en unknown
- 2007-03-30 EA EA201100811A patent/EA201100811A1/ru unknown
- 2007-03-30 EA EA201100810A patent/EA201100810A1/ru unknown
- 2007-03-30 EP EP13172958.4A patent/EP2666859B1/en active Active
- 2007-03-30 EP EP10173208.9A patent/EP2261333B1/en active Active
- 2007-03-30 EP EP18177355.7A patent/EP3431602A1/en not_active Withdrawn
- 2007-03-30 MY MYPI20083769A patent/MY162210A/en unknown
Also Published As
Publication number | Publication date |
---|---|
EP2261333A2 (en) | 2010-12-15 |
EP2666859A2 (en) | 2013-11-27 |
PL2666859T3 (pl) | 2019-09-30 |
CN102851291B (zh) | 2016-03-09 |
EA201100812A1 (ru) | 2012-06-29 |
ES2569558T3 (es) | 2016-05-11 |
EP2666859A3 (en) | 2014-05-07 |
SG170773A1 (en) | 2011-05-30 |
MY162210A (en) | 2017-05-31 |
EA201100813A1 (ru) | 2012-06-29 |
CN102851291A (zh) | 2013-01-02 |
EP2261333A3 (en) | 2014-03-19 |
US8163708B2 (en) | 2012-04-24 |
EP3431602A1 (en) | 2019-01-23 |
EA201100811A1 (ru) | 2012-06-29 |
NZ571569A (en) | 2011-09-30 |
EP3502255A1 (en) | 2019-06-26 |
EP2261333B1 (en) | 2016-03-30 |
EP2666859B1 (en) | 2019-01-02 |
US20100286234A1 (en) | 2010-11-11 |
SG10201406016SA (en) | 2014-11-27 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
EA201100813A1 (ru) | Фармацевтическая композиция | |
EA200870402A1 (ru) | Фармацевтическая композиция | |
WO2009142822A3 (en) | 2-f modified rna interference agents | |
WO2011056005A3 (ko) | 안티센스 가닥에 의한 오프-타겟 효과를 최소화한 신규한 siRNA 구조 및 그 용도 | |
EP2495248A4 (en) | BRIDGED ARTIFICIAL NUCLEOSIDE AND NUCLEOTIDE | |
WO2008116860A3 (en) | Dsrna compositions and methods for treating hpv infections | |
WO2014154835A3 (en) | Modified tgf-beta oligonucleotides | |
SG171676A1 (en) | Compositions and methods for inhibiting expression of the pcsk9 gene | |
MX2010004452A (es) | Acido ribonucleico de doble cadena modificado con lipidos que tienen un potente efecto de interferencia de acido ribonucleico. | |
WO2004007718A3 (en) | Rna-interference by single-stranded rna molecules | |
EA200870401A1 (ru) | КОМПОЗИЦИИ И СПОСОБЫ ИНГИБИРОВАНИЯ ЭКСПРЕССИИ ГЕНА Eg5 | |
JP2014527401A5 (ru) | ||
WO2008036933A3 (en) | Compositions and methods for inhibiting expression of the hamp gene | |
NO20053465D0 (no) | Pavisning av sma nukleinsyrer | |
AU2014219019A8 (en) | Short interfering nucleic acid (siNA) molecules containing a 2' internucleoside linkage | |
WO2010111503A3 (en) | RNA INTERFERENCE MEDIATED INHIBITION OF THE HIGH AFFINITY IGE RECEPTOR ALPHA CHAIN (FCεRLα) GENE EXPRESSION USING SHORT INTERFERING NUCLEIC ACID (SINA) | |
WO2004092383A3 (en) | RNA INTERFERENCE MEDIATED INHIBITION OF SEVERE ACUTE RESPIRATORY SYNDROME (SARS) VIRUS GENE EXPRESSION USING SHORT INTERFERING NUCLEIC ACID (siNA) | |
WO2012083005A3 (en) | Microrna inhibitors comprising locked nucleotides | |
WO2005028650A3 (en) | RNA INTERFERENCE MEDIATED INHIBITION OF HEPATITIS C VIRUS (HCV) EXPRESSION USING SHORT INTERFERING NUCLEIC ACID (siNA) | |
WO2007127919A3 (en) | Compositions and methods for inhibiting expression of a gene from the jc virus | |
WO2012178033A3 (en) | Serpina1 sirnas: compositions of matter and methods of treatment | |
WO2006032041A3 (en) | Compositions and methods for inhibiting expression of anti-apoptotic genes | |
EA201100847A1 (ru) | Опосредованное рнк-интерференцией ингибирование экспрессии генов эпителиального натриевого канала (enac) c использованием малой интерферирующей нуклеиновой кислоты (минк) | |
JP6137484B2 (ja) | 遺伝子発現抑制用二本鎖核酸分子 | |
WO2007137220A3 (en) | Compositions and methods for inhibiting expression of ikk-b gene |