HK1160484A1 - Irna agents targeting vegf irna - Google Patents
Irna agents targeting vegf irnaInfo
- Publication number
- HK1160484A1 HK1160484A1 HK12100722.1A HK12100722A HK1160484A1 HK 1160484 A1 HK1160484 A1 HK 1160484A1 HK 12100722 A HK12100722 A HK 12100722A HK 1160484 A1 HK1160484 A1 HK 1160484A1
- Authority
- HK
- Hong Kong
- Prior art keywords
- irna
- agents targeting
- targeting vegf
- vegf
- irna agents
- 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
- C12N15/1136—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 growth factors, growth regulators, cytokines, lymphokines or hormones
-
- 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
-
- 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
- A61K31/713—Double-stranded nucleic acids or oligonucleotides
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
- A61K47/50—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates
- A61K47/51—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent
- A61K47/54—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an organic compound
- A61K47/549—Sugars, nucleosides, nucleotides or nucleic acids
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
- A61K47/50—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates
- A61K47/51—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent
- A61K47/54—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an organic compound
- A61K47/55—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an organic compound the modifying agent being also a pharmacologically or therapeutically active agent, i.e. the entire conjugate being a codrug, i.e. a dimer, oligomer or polymer of pharmacologically or therapeutically active compounds
- A61K47/551—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an organic compound the modifying agent being also a pharmacologically or therapeutically active agent, i.e. the entire conjugate being a codrug, i.e. a dimer, oligomer or polymer of pharmacologically or therapeutically active compounds one of the codrug's components being a vitamin, e.g. niacinamide, vitamin B3, cobalamin, vitamin B12, folate, vitamin A or retinoic acid
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
- A61K47/50—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates
- A61K47/51—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent
- A61K47/56—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an organic macromolecular compound, e.g. an oligomeric, polymeric or dendrimeric molecule
- A61K47/59—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an organic macromolecular compound, e.g. an oligomeric, polymeric or dendrimeric molecule obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds, e.g. polyureas or polyurethanes
- A61K47/60—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an organic macromolecular compound, e.g. an oligomeric, polymeric or dendrimeric molecule obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds, e.g. polyureas or polyurethanes the organic macromolecular compound being a polyoxyalkylene oligomer, polymer or dendrimer, e.g. PEG, PPG, PEO or polyglycerol
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K48/00—Medicinal preparations containing genetic material which is inserted into cells of the living body to treat genetic diseases; Gene therapy
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
- A61P11/06—Antiasthmatics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
- A61P17/06—Antipsoriatics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
- A61P19/02—Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P27/00—Drugs for disorders of the senses
- A61P27/02—Ophthalmic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P27/00—Drugs for disorders of the senses
- A61P27/02—Ophthalmic agents
- A61P27/06—Antiglaucoma agents or miotics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- 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
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
- A61P35/04—Antineoplastic agents specific for metastasis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
- A61P37/06—Immunosuppressants, e.g. drugs for graft rejection
-
- 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
-
- 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
-
- 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
- A61P9/14—Vasoprotectives; Antihaemorrhoidals; Drugs for varicose therapy; Capillary stabilisers
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- C07K14/435—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
- C07K14/475—Growth factors; Growth regulators
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
- A61K47/02—Inorganic compounds
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
- A61K47/06—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite
- A61K47/08—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite containing oxygen, e.g. ethers, acetals, ketones, quinones, aldehydes, peroxides
- A61K47/10—Alcohols; Phenols; Salts thereof, e.g. glycerol; Polyethylene glycols [PEG]; Poloxamers; PEG/POE alkyl ethers
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
- A61K47/06—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite
- A61K47/08—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite containing oxygen, e.g. ethers, acetals, ketones, quinones, aldehydes, peroxides
- A61K47/12—Carboxylic acids; Salts or anhydrides thereof
-
- 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
- A61K9/0019—Injectable compositions; Intramuscular, intravenous, arterial, subcutaneous administration; Compositions to be administered through the skin in an invasive manner
-
- 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
- C12N2310/14—Type of nucleic acid interfering N.A.
-
- 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
-
- 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
- C12N2310/50—Physical structure
- C12N2310/53—Physical structure partially self-complementary or closed
- C12N2310/533—Physical structure partially self-complementary or closed having a mismatch or nick in at least one of the strands
-
- 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
- C12N2320/30—Special therapeutic applications
-
- 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
- C12N2320/30—Special therapeutic applications
- C12N2320/32—Special delivery means, e.g. tissue-specific
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US55262004P | 2004-03-12 | 2004-03-12 | |
US55982404P | 2004-04-05 | 2004-04-05 | |
US64719105P | 2005-01-25 | 2005-01-25 |
Publications (1)
Publication Number | Publication Date |
---|---|
HK1160484A1 true HK1160484A1 (en) | 2012-08-17 |
Family
ID=34994206
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
HK12100722.1A HK1160484A1 (en) | 2004-03-12 | 2012-01-20 | Irna agents targeting vegf irna |
Country Status (8)
Country | Link |
---|---|
US (5) | US7947659B2 (fr) |
EP (4) | EP2365077B1 (fr) |
JP (4) | JP4937899B2 (fr) |
AU (2) | AU2005222902B2 (fr) |
CA (1) | CA2559161C (fr) |
ES (1) | ES2423060T3 (fr) |
HK (1) | HK1160484A1 (fr) |
WO (1) | WO2005089224A2 (fr) |
Families Citing this family (111)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2832154B1 (fr) | 2001-11-09 | 2007-03-16 | Centre Nat Rech Scient | Oligonucleotides inhibiteurs et leur utilisation pour reprimer specifiquement un gene |
AU2003222820A1 (en) * | 2002-04-18 | 2003-10-27 | Acuity Pharmaceuticals, Inc. | Means and methods for the specific modulation of target genes in the cns and the eye and methods for their identification |
US7148342B2 (en) | 2002-07-24 | 2006-12-12 | The Trustees Of The University Of Pennyslvania | Compositions and methods for sirna inhibition of angiogenesis |
DK3222724T3 (en) | 2002-08-05 | 2018-12-03 | Silence Therapeutics Gmbh | ADDITIONALLY UNKNOWN FORMS OF INTERFERRING RNA MOLECULES |
US9719092B2 (en) | 2002-11-14 | 2017-08-01 | Thermo Fisher Scientific Inc. | RNAi targeting CNTD2 |
US7691998B2 (en) | 2002-11-14 | 2010-04-06 | Dharmacon, Inc. | siRNA targeting nucleoporin 62kDa (Nup62) |
EP2305813A3 (fr) | 2002-11-14 | 2012-03-28 | Dharmacon, Inc. | SIRNA fonctionnel et hyperfonctionnel |
US9719094B2 (en) | 2002-11-14 | 2017-08-01 | Thermo Fisher Scientific Inc. | RNAi targeting SEC61G |
US7612196B2 (en) | 2002-11-14 | 2009-11-03 | Dharmacon, Inc. | siRNA targeting cyclin-dependent kinase inhibitor 1B (p27, Kip1) (CDKN1B) |
US7619081B2 (en) | 2002-11-14 | 2009-11-17 | Dharmacon, Inc. | siRNA targeting coatomer protein complex, subunit beta 2 (COPB2) |
US7951935B2 (en) | 2002-11-14 | 2011-05-31 | Dharmacon, Inc. | siRNA targeting v-myc myelocytomatosis viral oncogene homolog (MYC) |
US9228186B2 (en) | 2002-11-14 | 2016-01-05 | Thermo Fisher Scientific Inc. | Methods and compositions for selecting siRNA of improved functionality |
US7977471B2 (en) | 2002-11-14 | 2011-07-12 | Dharmacon, Inc. | siRNA targeting TNFα |
WO2006006948A2 (fr) | 2002-11-14 | 2006-01-19 | Dharmacon, Inc. | Methodes et compositions permettant de selectionner des arnsi presentant une fonctionnalite amelioree |
US9879266B2 (en) | 2002-11-14 | 2018-01-30 | Thermo Fisher Scientific Inc. | Methods and compositions for selecting siRNA of improved functionality |
US9771586B2 (en) | 2002-11-14 | 2017-09-26 | Thermo Fisher Scientific Inc. | RNAi targeting ZNF205 |
US7781575B2 (en) | 2002-11-14 | 2010-08-24 | Dharmacon, Inc. | siRNA targeting tumor protein 53 (p53) |
US7635770B2 (en) | 2002-11-14 | 2009-12-22 | Dharmacon, Inc. | siRNA targeting protein kinase N-3 (PKN-3) |
US8198427B1 (en) | 2002-11-14 | 2012-06-12 | Dharmacon, Inc. | SiRNA targeting catenin, beta-1 (CTNNB1) |
US7592442B2 (en) | 2002-11-14 | 2009-09-22 | Dharmacon, Inc. | siRNA targeting ribonucleotide reductase M2 polypeptide (RRM2 or RNR-R2) |
US9839649B2 (en) | 2002-11-14 | 2017-12-12 | Thermo Fisher Scientific Inc. | Methods and compositions for selecting siRNA of improved functionality |
US10011836B2 (en) | 2002-11-14 | 2018-07-03 | Thermo Fisher Scientific Inc. | Methods and compositions for selecting siRNA of improved functionality |
US20090280567A1 (en) * | 2004-02-06 | 2009-11-12 | Dharmacon, Inc. | Stabilized sirnas as transfection controls and silencing reagents |
EP2365077B1 (fr) | 2004-03-12 | 2013-05-08 | Alnylam Pharmaceuticals, Inc. | Agents ARNi ciblant le facteur de croissance de l'endothélium vasculaire (VEGF) |
KR101147147B1 (ko) * | 2004-04-01 | 2012-05-25 | 머크 샤프 앤드 돔 코포레이션 | Rna 간섭의 오프 타겟 효과 감소를 위한 변형된폴리뉴클레오타이드 |
US7605250B2 (en) | 2004-05-12 | 2009-10-20 | Dharmacon, Inc. | siRNA targeting cAMP-specific phosphodiesterase 4D |
SI1781787T1 (sl) * | 2004-08-23 | 2017-08-31 | Sylentis S.A.U. | Zdravljenje očesnih nepravilnosti, kakakterističnih za povišan očesni tlak s sirna |
US20060223777A1 (en) * | 2005-03-29 | 2006-10-05 | Dharmacon, Inc. | Highly functional short hairpin RNA |
US7893244B2 (en) * | 2005-04-12 | 2011-02-22 | Intradigm Corporation | Composition and methods of RNAi therapeutics for treatment of cancer and other neovascularization diseases |
WO2006110813A2 (fr) * | 2005-04-12 | 2006-10-19 | Intradigm Corporation | Composition d'agents therapeutiques a arn interferent (arni) et procedes pour traiter le cancer et d'autres maladies de neovascularisation |
WO2006124726A2 (fr) * | 2005-05-12 | 2006-11-23 | The General Hospital Corporation | Nouvelles compositions biotinylatees |
GB0521351D0 (en) * | 2005-10-20 | 2005-11-30 | Genomica Sau | Modulation of TRPV expression levels |
GB0521716D0 (en) * | 2005-10-25 | 2005-11-30 | Genomica Sau | Modulation of 11beta-hydroxysteriod dehydrogenase 1 expression for the treatment of ocular diseases |
US7320965B2 (en) | 2005-10-28 | 2008-01-22 | Alnylam Pharmaceuticals, Inc. | Compositions and methods for inhibiting expression of Huntingtin gene |
EP2008274B1 (fr) * | 2006-03-31 | 2015-05-27 | Alnylam Pharmaceuticals Inc. | Compositions et methodes destinees a inhiber l'expression du gene eg5 |
US20090130212A1 (en) * | 2006-05-15 | 2009-05-21 | Physical Pharmaceutica, Llc | Composition and improved method for preparation of small particles |
US8598333B2 (en) * | 2006-05-26 | 2013-12-03 | Alnylam Pharmaceuticals, Inc. | SiRNA silencing of genes expressed in cancer |
WO2007146953A2 (fr) * | 2006-06-12 | 2007-12-21 | Exegenics, Inc., D/B/A Opko Health, Inc. | COMPOSITIONS ET PROCÉDÉS DESTINÉS À UNE INHIBITION DE L'ANGIOGENÈSE PAR LES ARNsi |
US7872118B2 (en) * | 2006-09-08 | 2011-01-18 | Opko Ophthalmics, Llc | siRNA and methods of manufacture |
EP2064223B1 (fr) * | 2006-09-22 | 2013-04-24 | Dharmacon, Inc. | Complexes d'oligonucléotides bicaténaires et procédés de silençage de gènes par interférence ARN |
WO2008109377A1 (fr) * | 2007-03-02 | 2008-09-12 | Mdrna, Inc. | Composés d'acide nucléique permettant d'inhiber l'expression de gène de la famille vegf et utilisations de ceux-ci |
EP2121923A1 (fr) * | 2007-03-02 | 2009-11-25 | MDRNA, Inc. | Composes d'acide nucleique permettant d'inhiber l'expression de gene de la famille erbb et utilisations de ceux-ci |
US20110046206A1 (en) * | 2007-06-22 | 2011-02-24 | Isis Pharmaceuticals, Inc. | Double strand compositions comprising differentially modified strands for use in gene modulation |
JP5273740B2 (ja) * | 2007-09-07 | 2013-08-28 | 国立大学法人徳島大学 | p53の発現促進方法およびそれに用いるp53発現促進剤 |
US8188060B2 (en) | 2008-02-11 | 2012-05-29 | Dharmacon, Inc. | Duplex oligonucleotides with enhanced functionality in gene regulation |
CA2716793A1 (fr) * | 2008-03-05 | 2009-09-11 | Alnylam Pharmaceuticals, Inc. | Compositions et procedes pour inhiber l'expression des genes eg5 et vegf |
DE102008014318B4 (de) * | 2008-03-14 | 2021-02-04 | Premark Feg L.L.C. | Transportspülmaschine und Verfahren zum Betreiben einer Transportspülmaschine |
US20100009451A1 (en) * | 2008-05-30 | 2010-01-14 | Sigma Aldrich Company | Compositions and methods for specifically silencing a target nucleic acid |
JP2011526892A (ja) | 2008-06-30 | 2011-10-20 | アンジオブラスト システムズ,インコーポレーテッド | 併用療法を使用した眼疾患及び過剰血管新生の治療 |
WO2010042751A2 (fr) * | 2008-10-08 | 2010-04-15 | Chimeros Inc. | Agents thérapeutiques chimères, compositions et procédés permettant de les utiliser |
CA2739672C (fr) * | 2008-10-15 | 2017-03-28 | F. Hoffmann-La Roche Ag | Methode de detection des oligonucleotides a l'aide d'une sonde d'acide nucleique peptidique |
WO2010065834A1 (fr) * | 2008-12-04 | 2010-06-10 | Opko Ophthalmics, Llc | Compositions et procédés pour l'inhibition sélective d'isoformes pro-angiogéniques de vegf |
JP5875976B2 (ja) | 2009-06-01 | 2016-03-02 | ヘイロー−バイオ アールエヌエーアイ セラピューティクス, インコーポレイテッド | 多価rna干渉のためのポリヌクレオチド、組成物およびそれらの使用方法 |
WO2011017548A1 (fr) * | 2009-08-05 | 2011-02-10 | Alnylam Pharmaceuticals, Inc. | Compositions à formulation lipidique et procédés pour inhiber l'expression de gènes eg5 et vegf |
WO2011034798A1 (fr) | 2009-09-15 | 2011-03-24 | Alnylam Pharmaceuticals, Inc. | Compositions à base de formulations lipidiques et méthodes pour inhiber l'expression des gènes eg5 et vegf |
US20110104154A1 (en) * | 2009-10-30 | 2011-05-05 | Alcon Research, Ltd. | Single nucleotide polymorphisms and genes associated with age-related macular degeneration |
WO2011073521A1 (fr) | 2009-12-15 | 2011-06-23 | Petri Salven | Méthodes pour l'enrichissement de cellules progénitrices endothéliales adultes et leurs utilisations |
WO2011119852A1 (fr) | 2010-03-24 | 2011-09-29 | Rxi Pharmaceuticals Corporation | Composés d'arni de taille réduite s'auto-administrant |
CN106074591B (zh) | 2010-03-24 | 2020-01-14 | 菲奥医药公司 | 眼部症候中的rna干扰 |
JP2013538191A (ja) | 2010-07-23 | 2013-10-10 | トラスティーズ オブ ボストン ユニバーシティ | 病的血管新生および腫瘍細胞侵襲性の阻害のための治療法としてならびに分子イメージングおよび標的化送達のための抗DEsupR阻害剤 |
US9290760B2 (en) * | 2010-09-15 | 2016-03-22 | Alnylam Pharmaceuticals, Inc. | Modified iRNA agents |
EP2622075B1 (fr) * | 2010-09-27 | 2016-03-02 | Sabanci Universitesi | Utilisation d'arnmi pour diagnostiquer, prévenir, traiter et suivre les maladies impliquant des anomalies de type macro-autophagie |
DK2631291T3 (da) | 2010-10-22 | 2019-06-11 | Olix Pharmaceuticals Inc | Nukleinsyremolekyler, der inducerer rna-interferens, og anvendelser deraf |
CN110123830A (zh) | 2010-11-09 | 2019-08-16 | 阿尔尼拉姆医药品有限公司 | 用于抑制Eg5和VEGF基因的表达的脂质配制的组合物和方法 |
EP3693025B1 (fr) | 2011-04-22 | 2021-10-13 | The Regents of The University of California | Virions de virus adéno-associé avec capside variant et procédés d'utilisation de ceux-ci |
EP2704745B1 (fr) | 2011-05-05 | 2016-12-14 | Duke University | Procédés pour mettre au point un pronostic du cancer du pancréas et prédire la réponse à une thérapie contre le cancer |
EP3919620A1 (fr) | 2012-05-02 | 2021-12-08 | Sirna Therapeutics, Inc. | Compositions d'acide nucléique interférent court (sina) |
JP6139671B2 (ja) | 2012-05-22 | 2017-05-31 | オリックス ファーマシューティカルズ インコーポレイテッドOlix Pharmaceuticals Inc. | 細胞内貫通能を持ってrna干渉を誘導する核酸分子およびその用途 |
AU2013308519A1 (en) | 2012-08-31 | 2015-04-09 | The General Hospital Corporation | Biotin complexes for treatment and diagnosis of Alzheimer's disease |
BR112015004452A2 (pt) | 2012-09-05 | 2017-08-08 | Sylentis Sau | sirna e seu uso em métodos e composições para o tratamento e/ou prevenção de condições oculares |
GB201215857D0 (en) | 2012-09-05 | 2012-10-24 | Sylentis Sau | siRNA and their use in methods and compositions for the treatment and/or prevention of eye conditions |
SG11201505272QA (en) * | 2013-01-08 | 2015-08-28 | Benitec Biopharma Ltd | Age-related macular degeneration treatment |
TW201515650A (zh) | 2013-05-06 | 2015-05-01 | 艾爾妮蘭製藥公司 | 遞送經脂質調配之核酸分子之劑量及方法 |
EP2865756A1 (fr) * | 2013-10-22 | 2015-04-29 | Sylentis, S.A.U. | ARNsi et leur utilisation dans des procédés et des compositions pour inhiber l'expression du gène FLAP |
EA201691587A1 (ru) | 2014-02-11 | 2017-01-30 | Элнилэм Фармасьютикалз, Инк. | КОМПОЗИЦИИ НА ОСНОВЕ iRNA ДЛЯ КЕТОГЕКСОКИНАЗЫ (KHK) И СПОСОБЫ ИХ ПРИМЕНЕНИЯ |
GB201403684D0 (en) | 2014-03-03 | 2014-04-16 | King S College London | Vector |
WO2015132303A1 (fr) | 2014-03-04 | 2015-09-11 | Sylentis Sau | Arnsi et leur utilisation dans des méthodes et des compositions pour le traitement et/ou la prévention d'affections oculaires |
CN104038000B (zh) * | 2014-07-03 | 2016-08-24 | 雷勃电气(无锡)有限公司 | 可拆装铜笼转子铁心叠压热套工艺 |
CN107073050A (zh) | 2014-09-07 | 2017-08-18 | 西莱克塔生物科技公司 | 用于减弱基因治疗抗病毒转移载体免疫应答的方法和组合物 |
EP3277814B1 (fr) | 2015-04-03 | 2020-06-03 | University of Massachusetts | Composés oligonucléotidiques pour le ciblage de l'arnm de l'huntingtine |
HUE057431T2 (hu) | 2015-04-03 | 2022-05-28 | Univ Massachusetts | Oligonukleotid vegyületek preeklampszia és más angiogén rendellenességek kezelésére |
JP6715325B2 (ja) * | 2015-06-26 | 2020-07-01 | スーチョウ リボ ライフ サイエンス カンパニー、リミテッドSuzhou Ribo Life Science Co., Ltd. | siRNA、siRNAを含む医薬組成物及び結合体、並びにそれらの応用 |
WO2017030973A1 (fr) | 2015-08-14 | 2017-02-23 | University Of Massachusetts | Conjugués bioactifs pour l'administration d'oligonucléotides |
CN108366966A (zh) | 2015-08-24 | 2018-08-03 | 光环生物干扰疗法公司 | 用于调节基因表达的多核苷酸纳米颗粒及其用途 |
CN108699556B (zh) | 2015-11-16 | 2023-02-17 | 奥利克斯医药有限公司 | 使用靶向myd88或tlr3的rna复合物治疗老年性黄斑变性 |
US10358647B2 (en) | 2015-12-13 | 2019-07-23 | Nitto Denko Corporation | siRNA structures for high activity and reduced off target |
JP2019503394A (ja) | 2016-01-31 | 2019-02-07 | ユニバーシティ・オブ・マサチューセッツUniversity Of Massachusetts | 分岐オリゴヌクレオチド |
EP3411480A4 (fr) | 2016-02-02 | 2020-01-22 | Olix Pharmaceuticals, Inc. | Traitement de la dermatite atopique et de l'asthme en utilisant des complexes d'arn qui ciblent l'll4r , trpa1, ou f2rl1 |
CN108779464B (zh) | 2016-02-02 | 2022-05-17 | 奥利克斯医药有限公司 | 使用靶向angpt2和pdgfb的rna复合物治疗血管生成相关性疾病 |
JP7049262B2 (ja) | 2016-04-11 | 2022-04-06 | オリックス ファーマシューティカルズ,インコーポレーテッド | 結合組織成長因子を標的とするrna複合体を用いた特発性肺胞線維症の治療 |
EP4049683A1 (fr) | 2016-04-29 | 2022-08-31 | Adverum Biotechnologies, Inc. | Évasion d'anticorps neutralisants par un virus adéno-associé recombinant |
US11499973B2 (en) | 2016-05-17 | 2022-11-15 | Duke University | Methods of predicting responsiveness of a cancer to a VEGF targeting agent and methods of prognosing and treating cancer |
KR101916652B1 (ko) | 2016-06-29 | 2018-11-08 | 올릭스 주식회사 | 작은 간섭 rna의 rna 간섭효과 증진용 화합물 및 이의 용도 |
KR101961332B1 (ko) * | 2016-07-28 | 2019-03-22 | 기초과학연구원 | Cas9 단백질 및 가이드 RNA를 포함하는 안질환 치료용 약학 조성물 |
US11554180B2 (en) | 2016-07-29 | 2023-01-17 | The Regents Of The University Of California | Adeno-associated virus virions with variant capsid and methods of use thereof |
WO2018031933A2 (fr) | 2016-08-12 | 2018-02-15 | University Of Massachusetts | Oligonucléotides conjugués |
AU2017313616B2 (en) * | 2016-08-19 | 2022-12-08 | Institute For Basic Science | Artificially engineered angiogenesis regulatory system |
WO2018075798A1 (fr) | 2016-10-19 | 2018-04-26 | Adverum Biotechnologies, Inc. | Capsides d'aav modifiées et leurs utilisations |
KR20190090836A (ko) * | 2016-11-28 | 2019-08-02 | 나파젠 파마, 인크. | 화학 수식 siRNA |
WO2018146557A2 (fr) | 2017-02-10 | 2018-08-16 | Dong Ki Lee | Arn double brin long pour interférence arn |
JPWO2019022250A1 (ja) * | 2017-07-28 | 2020-07-09 | 国立大学法人九州大学 | 水溶性有効成分の放出が制御された経皮吸収組成物 |
CA3078705A1 (fr) | 2017-10-13 | 2019-04-18 | Selecta Biosciences, Inc. | Methodes et compositions permettant d'attenuer les reponses en igm anti-vecteur de transfert viral |
WO2020033899A1 (fr) | 2018-08-10 | 2020-02-13 | University Of Massachusetts | Oligonucléotides modifiés ciblant des snp |
JP2022534741A (ja) | 2019-05-28 | 2022-08-03 | セレクタ バイオサイエンシーズ インコーポレーテッド | 減弱化された抗ウイルス導入ベクター免疫応答のための方法および組成物 |
KR20220035161A (ko) * | 2019-07-12 | 2022-03-21 | 오레곤 헬스 앤드 사이언스 유니버시티 | 유사분열 키나제 억제제 및 면역 체크포인트 억제제의 공동-전달을 위한 치료 구축물 |
WO2021117009A2 (fr) * | 2019-12-11 | 2021-06-17 | Moore Tara | Silençage spécifique d'allèle de gène induit par le facteur de croissance transformant bêta avec mutation r124h à l'aide d'arn interférant court |
KR102324428B1 (ko) * | 2020-04-16 | 2021-11-09 | 건국대학교 산학협력단 | 혈관내피 성장인자 발현을 억제하는 shRNA 및 이의 용도 |
US20230190956A1 (en) | 2020-04-24 | 2023-06-22 | INSERM (Institut National de la Santé et de la Recherche Médicale) | Methods for preventing induction of immune responses to the transduced cells expressing a transgene product after ocular gene therapy |
IL309334A (en) | 2021-06-23 | 2024-02-01 | Univ Massachusetts | Anti-FLT1 optimized oligonucleotide compounds for the treatment of preeclampsia and other angiogenic disorders |
US20230141563A1 (en) | 2021-10-12 | 2023-05-11 | Selecta Biosciences, Inc. | Methods and compositions for attenuating anti-viral transfer vector igm responses |
WO2023172624A1 (fr) | 2022-03-09 | 2023-09-14 | Selecta Biosciences, Inc. | Immunosuppresseurs en association avec des agents anti-igm et dosage associé |
Family Cites Families (132)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4426330A (en) | 1981-07-20 | 1984-01-17 | Lipid Specialties, Inc. | Synthetic phospholipid compounds |
US4534899A (en) | 1981-07-20 | 1985-08-13 | Lipid Specialties, Inc. | Synthetic phospholipid compounds |
KR840001915A (ko) * | 1981-10-13 | 1984-06-07 | 그레이험 워커 존 | 자동 조절 돛 세트 |
WO1987000201A1 (fr) | 1985-07-05 | 1987-01-15 | Whitehead Institute For Biomedical Research | Cellules epitheliales exprimant un materiau genetique etranger |
US4980286A (en) | 1985-07-05 | 1990-12-25 | Whitehead Institute For Biomedical Research | In vivo introduction and expression of foreign genetic material in epithelial cells |
US5139941A (en) | 1985-10-31 | 1992-08-18 | University Of Florida Research Foundation, Inc. | AAV transduction vectors |
US4837028A (en) | 1986-12-24 | 1989-06-06 | Liposome Technology, Inc. | Liposomes with enhanced circulation time |
US4888116A (en) * | 1987-01-15 | 1989-12-19 | The Dow Chemical Company | Method of improving membrane properties via reaction of diazonium compounds or precursors |
WO1989002468A1 (fr) | 1987-09-11 | 1989-03-23 | Whitehead Institute For Biomedical Research | Fibroblastes transduits et leurs applications |
EP0391960B1 (fr) | 1987-12-11 | 1994-08-17 | Whitehead Institute For Biomedical Research | Modification genetique de cellules endotheliales |
WO1989007136A2 (fr) | 1988-02-05 | 1989-08-10 | Whitehead Institute For Biomedical Research | Hepatocytes modifies et leurs utilisations |
GB8824593D0 (en) | 1988-10-20 | 1988-11-23 | Royal Free Hosp School Med | Liposomes |
US5328470A (en) | 1989-03-31 | 1994-07-12 | The Regents Of The University Of Michigan | Treatment of diseases by site-specific instillation of cells or site-specific transformation of cells and kits therefor |
EP0451221B1 (fr) | 1989-08-31 | 1994-10-12 | City Of Hope | Sequences catalytiques chimeriques d'adn/arn |
US5225212A (en) | 1989-10-20 | 1993-07-06 | Liposome Technology, Inc. | Microreservoir liposome composition and method |
US5013556A (en) | 1989-10-20 | 1991-05-07 | Liposome Technology, Inc. | Liposomes with enhanced circulation time |
US5356633A (en) | 1989-10-20 | 1994-10-18 | Liposome Technology, Inc. | Method of treatment of inflamed tissues |
US5665710A (en) | 1990-04-30 | 1997-09-09 | Georgetown University | Method of making liposomal oligodeoxynucleotide compositions |
US5962219A (en) | 1990-06-11 | 1999-10-05 | Nexstar Pharmaceuticals, Inc. | Systematic evolution of ligands by exponential enrichment: chemi-selex |
CA2093664C (fr) | 1990-10-12 | 2003-07-29 | Fritz Eckstein | Ribozymes modifies |
CA2095153C (fr) | 1990-10-31 | 2007-01-09 | Lori F. Rafield | Modification genetique de cellules endotheliales |
JP3220180B2 (ja) | 1991-05-23 | 2001-10-22 | 三菱化学株式会社 | 薬剤含有タンパク質結合リポソーム |
DE4216134A1 (de) | 1991-06-20 | 1992-12-24 | Europ Lab Molekularbiolog | Synthetische katalytische oligonukleotidstrukturen |
US5252479A (en) | 1991-11-08 | 1993-10-12 | Research Corporation Technologies, Inc. | Safe vector for gene therapy |
US5652094A (en) | 1992-01-31 | 1997-07-29 | University Of Montreal | Nucleozymes |
AU687736B2 (en) | 1992-05-11 | 1998-03-05 | Ribozyme Pharmaceuticals, Inc. | Method and reagent for inhibiting viral replication |
US5587308A (en) | 1992-06-02 | 1996-12-24 | The United States Of America As Represented By The Department Of Health & Human Services | Modified adeno-associated virus vector capable of expression from a novel promoter |
EP0654077A4 (fr) | 1992-07-17 | 1996-03-13 | Ribozyme Pharm Inc | Procede et reactif pour le traitement de maladies chez les animaux. |
US5478745A (en) | 1992-12-04 | 1995-12-26 | University Of Pittsburgh | Recombinant viral vector system |
US5672659A (en) | 1993-01-06 | 1997-09-30 | Kinerton Limited | Ionic molecular conjugates of biodegradable polyesters and bioactive polypeptides |
EP0681482B1 (fr) | 1993-01-22 | 2005-12-07 | University Research Corporation | Localisation d'agents therapeutiques |
JP3351476B2 (ja) | 1993-01-22 | 2002-11-25 | 三菱化学株式会社 | リン脂質誘導体及びそれを含有するリポソーム |
RU2143903C1 (ru) | 1993-02-19 | 2000-01-10 | Ниппон Синяку Ко., Лтд. | Фармацевтическая композиция, содержащая сополимер нуклеиновой кислоты |
US5395619A (en) | 1993-03-03 | 1995-03-07 | Liposome Technology, Inc. | Lipid-polymer conjugates and liposomes |
US5731294A (en) * | 1993-07-27 | 1998-03-24 | Hybridon, Inc. | Inhibition of neovasularization using VEGF-specific oligonucleotides |
CA2137297C (fr) | 1993-12-06 | 2000-04-18 | Tsuyoshi Miyazaki | Vesicule reactive et vesicule fonctionnelle fixee a une substance |
US5902880A (en) | 1994-08-19 | 1999-05-11 | Ribozyme Pharmaceuticals, Inc. | RNA polymerase III-based expression of therapeutic RNAs |
US5627053A (en) | 1994-03-29 | 1997-05-06 | Ribozyme Pharmaceuticals, Inc. | 2'deoxy-2'-alkylnucleotide containing nucleic acid |
US6054299A (en) | 1994-04-29 | 2000-04-25 | Conrad; Charles A. | Stem-loop cloning vector and method |
WO2000022114A1 (fr) | 1998-10-09 | 2000-04-20 | Ingene, Inc. | PRODUCTION D'ADN SIMPLE BRIN $i(IN VIVO) |
US5543152A (en) | 1994-06-20 | 1996-08-06 | Inex Pharmaceuticals Corporation | Sphingosomes for enhanced drug delivery |
EP0769552A4 (fr) * | 1994-06-27 | 1997-06-18 | Toagosei Co Ltd | Compose d'acide nucleique antisens |
US6146886A (en) | 1994-08-19 | 2000-11-14 | Ribozyme Pharmaceuticals, Inc. | RNA polymerase III-based expression of therapeutic RNAs |
US5595760A (en) | 1994-09-02 | 1997-01-21 | Delab | Sustained release of peptides from pharmaceutical compositions |
US5820873A (en) | 1994-09-30 | 1998-10-13 | The University Of British Columbia | Polyethylene glycol modified ceramide lipids and liposome uses thereof |
US5885613A (en) | 1994-09-30 | 1999-03-23 | The University Of British Columbia | Bilayer stabilizing components and their use in forming programmable fusogenic liposomes |
US5753613A (en) | 1994-09-30 | 1998-05-19 | Inex Pharmaceuticals Corporation | Compositions for the introduction of polyanionic materials into cells |
US5716824A (en) | 1995-04-20 | 1998-02-10 | Ribozyme Pharmaceuticals, Inc. | 2'-O-alkylthioalkyl and 2-C-alkylthioalkyl-containing enzymatic nucleic acids (ribozymes) |
US5756122A (en) | 1995-06-07 | 1998-05-26 | Georgetown University | Liposomally encapsulated nucleic acids having high entrapment efficiencies, method of manufacturer and use thereof for transfection of targeted cells |
US7422902B1 (en) | 1995-06-07 | 2008-09-09 | The University Of British Columbia | Lipid-nucleic acid particles prepared via a hydrophobic lipid-nucleic acid complex intermediate and use for gene transfer |
EP0832271B8 (fr) | 1995-06-07 | 2005-03-02 | INEX Pharmaceuticals Corp. | Particules d'acides nucleiques et de lipides preparees au moyen d'un intermediaire de complexe hydrophobe d'acides nucleiques et de lipides et utilisation pour transferer des genes |
US5981501A (en) | 1995-06-07 | 1999-11-09 | Inex Pharmaceuticals Corp. | Methods for encapsulating plasmids in lipid bilayers |
WO1997004787A1 (fr) | 1995-08-01 | 1997-02-13 | Novartis Ag | Compositions d'oligonucleotides et de liposomes |
US5858397A (en) | 1995-10-11 | 1999-01-12 | University Of British Columbia | Liposomal formulations of mitoxantrone |
EP1108724B1 (fr) | 1996-01-16 | 2007-09-19 | Sirna Therpeutics, Inc. | Synthèse de methoxy nucléosides et de molécules d'acide nucléique enzymatique |
US5994316A (en) | 1996-02-21 | 1999-11-30 | The Immune Response Corporation | Method of preparing polynucleotide-carrier complexes for delivery to cells |
US5849902A (en) | 1996-09-26 | 1998-12-15 | Oligos Etc. Inc. | Three component chimeric antisense oligonucleotides |
US6001311A (en) | 1997-02-05 | 1999-12-14 | Protogene Laboratories, Inc. | Apparatus for diverse chemical synthesis using two-dimensional array |
US6127533A (en) * | 1997-02-14 | 2000-10-03 | Isis Pharmaceuticals, Inc. | 2'-O-aminooxy-modified oligonucleotides |
US6395713B1 (en) | 1997-07-23 | 2002-05-28 | Ribozyme Pharmaceuticals, Inc. | Compositions for the delivery of negatively charged molecules |
US6506559B1 (en) | 1997-12-23 | 2003-01-14 | Carnegie Institute Of Washington | Genetic inhibition by double-stranded RNA |
EP3214177A3 (fr) | 1998-04-08 | 2017-11-22 | Commonwealth Scientific and Industrial Research Organisation | Procédés et moyens pour obtenir des phénotypes modifiés |
WO1999054459A2 (fr) | 1998-04-20 | 1999-10-28 | Ribozyme Pharmaceuticals, Inc. | Molecules d'acides nucleiques presentant de nouvelles compositions chimiques capables de moduler l'expression genique |
AR020078A1 (es) | 1998-05-26 | 2002-04-10 | Syngenta Participations Ag | Metodo para alterar la expresion de un gen objetivo en una celula de planta |
DE69906977T2 (de) | 1998-07-20 | 2004-05-19 | Protiva Biotherapeutics Inc., Burnaby | In liposomen verkapselte nukleinsäurekomplexe |
KR20010099682A (ko) | 1998-10-09 | 2001-11-09 | 추후보충 | 단일가닥 dna의 효소 합성 |
DE19956568A1 (de) | 1999-01-30 | 2000-08-17 | Roland Kreutzer | Verfahren und Medikament zur Hemmung der Expression eines vorgegebenen Gens |
CA2365625A1 (fr) | 1999-03-10 | 2000-09-14 | Phogen Limited | Administration de substances a des cellules |
US20050112141A1 (en) | 2000-08-30 | 2005-05-26 | Terman David S. | Compositions and methods for treatment of neoplastic disease |
DE10100586C1 (de) | 2001-01-09 | 2002-04-11 | Ribopharma Ag | Verfahren zur Hemmung der Expression eines Ziegens |
WO2001053345A1 (fr) * | 2000-01-20 | 2001-07-26 | North Bristol Nhs Trust | Isoforme de vegf 148, variant d'epissage tronque de vegf, heterodimeres de vegf et utilisations therapeutiques de ces derniers |
WO2001057064A2 (fr) | 2000-02-07 | 2001-08-09 | Roche Diagnostics Corporation | Nouveaux amphiphiles cationiques |
US20070026394A1 (en) | 2000-02-11 | 2007-02-01 | Lawrence Blatt | Modulation of gene expression associated with inflammation proliferation and neurite outgrowth using nucleic acid based technologies |
WO2003070918A2 (fr) | 2002-02-20 | 2003-08-28 | Ribozyme Pharmaceuticals, Incorporated | Inhibition mediee par interference arn d'une expression genique faisant appel a des acides nucleiques interferants courts chimiquement modifies (sina) |
SE0003665D0 (sv) | 2000-10-11 | 2000-10-11 | Astrazeneca Ab | A delivery device |
WO2002033094A1 (fr) * | 2000-10-19 | 2002-04-25 | Kyowa Hakko Kogyo Co., Ltd. | Anticorps inhibant l'activite vplf |
WO2002044321A2 (fr) | 2000-12-01 | 2002-06-06 | MAX-PLANCK-Gesellschaft zur Förderung der Wissenschaften e.V. | Petites molecules d'arn mediant l'interference arn |
US20030170891A1 (en) | 2001-06-06 | 2003-09-11 | Mcswiggen James A. | RNA interference mediated inhibition of epidermal growth factor receptor gene expression using short interfering nucleic acid (siNA) |
WO2003070910A2 (fr) * | 2002-02-20 | 2003-08-28 | Ribozyme Pharmaceuticals, Incorporated | Inhibition induite par interference d'arn du facteur de croissance endothelial vasculaire et expression genetique du recepteur de facteur de croissance endothelial vasculaire au moyen d'acides nucleiques interferents courts (sina) |
US20040209832A1 (en) * | 2001-11-30 | 2004-10-21 | Mcswiggen James | RNA interference mediated inhibition of vascular endothelial growth factor and vascular endothelial growth factor receptor gene expression using short interfering nucleic acid (siNA) |
US7981863B2 (en) | 2001-09-19 | 2011-07-19 | Neuronova Ab | Treatment of Parkinson's disease with PDGF |
FR2832154B1 (fr) * | 2001-11-09 | 2007-03-16 | Centre Nat Rech Scient | Oligonucleotides inhibiteurs et leur utilisation pour reprimer specifiquement un gene |
EP1448590A4 (fr) | 2002-02-20 | 2004-12-15 | Sirna Therapeutics Inc | Inhibition induite par l'interference de l'arn des genes myc et myb ou de genes intervenant dans leurs voies respectives |
EP1432724A4 (fr) * | 2002-02-20 | 2006-02-01 | Sirna Therapeutics Inc | Inhibition a mediation par interference d'arn de genes de map kinase |
US7199107B2 (en) | 2002-05-23 | 2007-04-03 | Isis Pharmaceuticals, Inc. | Antisense modulation of kinesin-like 1 expression |
NO20023047A (no) | 2002-06-21 | 2003-09-01 | Hydralift Asa | Kompenseringsanordning |
JP4222792B2 (ja) | 2002-06-26 | 2009-02-12 | シャープ株式会社 | 測距センサおよびそれを用いた電子機器ならびに測距センサの製造方法 |
CN1156336C (zh) | 2002-07-12 | 2004-07-07 | 清华大学 | 柔性基底材料表面负载二氧化钛薄膜光催化剂的制备方法 |
US6679120B1 (en) | 2002-07-15 | 2004-01-20 | Gas Research Institute | System and method for guided boring obstacle detection |
US7148342B2 (en) * | 2002-07-24 | 2006-12-12 | The Trustees Of The University Of Pennyslvania | Compositions and methods for sirna inhibition of angiogenesis |
WO2004011822A1 (fr) | 2002-07-29 | 2004-02-05 | The Gates Corporation | Courroie |
US7036793B2 (en) | 2002-07-31 | 2006-05-02 | Brass-Craft Manufacturing Company | Stop valve |
JP2005534696A (ja) * | 2002-08-06 | 2005-11-17 | イントラディグム、コーポレイション | 干渉性rnaの導入によるターゲット遺伝子発現のイン・ビボでのダウンレギュレーション方法 |
US7923547B2 (en) | 2002-09-05 | 2011-04-12 | Sirna Therapeutics, Inc. | RNA interference mediated inhibition of gene expression using chemically modified short interfering nucleic acid (siNA) |
US20040115201A1 (en) | 2002-09-25 | 2004-06-17 | Paz Einat | Mitotic kinesin-like protein-1, MKLP1, and uses thereof |
EP2305813A3 (fr) * | 2002-11-14 | 2012-03-28 | Dharmacon, Inc. | SIRNA fonctionnel et hyperfonctionnel |
WO2004064737A2 (fr) | 2003-01-17 | 2004-08-05 | Alnylam Pharmaceuticals | Compositions therapeutiques |
DE10302421A1 (de) | 2003-01-21 | 2004-07-29 | Ribopharma Ag | Doppelsträngige Ribonukleinsäure mit verbesserter Wirksamkeit |
AR050920A1 (es) | 2003-03-07 | 2006-12-06 | Astrazeneca Ab | Enantiomeros de heterociclos fusionados seleccionados y usos de los mismos |
WO2004080406A2 (fr) | 2003-03-07 | 2004-09-23 | Alnylam Pharmaceuticals | Compositions therapeutiques |
JP2006522158A (ja) | 2003-04-03 | 2006-09-28 | 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 | iRNA複合体 |
EP2664672A1 (fr) | 2003-04-17 | 2013-11-20 | Alnylam Pharmaceuticals Inc. | Agents iARN modifiés |
EP1625138A4 (fr) | 2003-04-17 | 2010-06-23 | Alnylam Pharmaceuticals Inc | Monomeres proteges |
US7919103B2 (en) * | 2003-05-09 | 2011-04-05 | Transfert Plus | Compound and method for regulating plasminogen activation and cell migration |
EP2336317B1 (fr) | 2003-06-13 | 2019-09-11 | Alnylam Europe AG | Acide ribonucléique à double brin avec une meilleure efficacité dans un organisme |
WO2005007196A2 (fr) | 2003-07-16 | 2005-01-27 | Protiva Biotherapeutics, Inc. | Arn interférant encapsulé dans un lipide |
JP2007505634A (ja) | 2003-09-22 | 2007-03-15 | ロゼッタ インファーマティクス エルエルシー | Rna干渉を用いる合成致死スクリーニング |
EP2365077B1 (fr) | 2004-03-12 | 2013-05-08 | Alnylam Pharmaceuticals, Inc. | Agents ARNi ciblant le facteur de croissance de l'endothélium vasculaire (VEGF) |
CA2569664C (fr) | 2004-06-07 | 2013-07-16 | Protiva Biotherapeutics, Inc. | Arn interferant encapsule dans des lipides |
JP4764426B2 (ja) | 2004-06-07 | 2011-09-07 | プロチバ バイオセラピューティクス インコーポレイティッド | カチオン性脂質および使用方法 |
AU2006336384B2 (en) | 2005-02-14 | 2010-12-16 | Sirna Therapeutics, Inc. | Lipid nanoparticle based compositions and methods for the delivery of biologically active molecules |
TWI335352B (en) | 2005-03-31 | 2011-01-01 | Calando Pharmaceuticals Inc | Inhibitors of ribonucleotide reductase subunit 2 and uses thereof |
US7915230B2 (en) | 2005-05-17 | 2011-03-29 | Molecular Transfer, Inc. | Reagents for transfection of eukaryotic cells |
EP1893625A4 (fr) | 2005-06-22 | 2012-12-26 | Biocryst Pharm Inc | Procédés destinés à la préparation de dérivés de la 9-déazapurine |
CN101267805A (zh) | 2005-07-27 | 2008-09-17 | 普洛体维生物治疗公司 | 制造脂质体的系统和方法 |
WO2007051303A1 (fr) | 2005-11-02 | 2007-05-10 | Protiva Biotherapeutics, Inc. | Molecules d'arnsi modifiees et utilisations de celles-ci |
EP2008274B1 (fr) | 2006-03-31 | 2015-05-27 | Alnylam Pharmaceuticals Inc. | Compositions et methodes destinees a inhiber l'expression du gene eg5 |
US8598333B2 (en) | 2006-05-26 | 2013-12-03 | Alnylam Pharmaceuticals, Inc. | SiRNA silencing of genes expressed in cancer |
MX363224B (es) | 2006-10-03 | 2019-03-15 | Alnylam Pharmaceuticals Inc | Formulaciones que contienen lipidos. |
US20080213350A1 (en) | 2007-02-20 | 2008-09-04 | Texas Tech University System | Encapsulation of nucleic acids in liposomes |
US7858592B2 (en) | 2007-02-26 | 2010-12-28 | The Board Of Regents Of The University Of Texas System | Interfering RNAs against the promoter region of P53 |
ES2535419T3 (es) | 2007-12-27 | 2015-05-11 | Protiva Biotherapeutics Inc. | Silenciamiento de expresión de quinasa tipo polo usando ARN interferente |
AU2009241591A1 (en) | 2008-01-31 | 2009-11-05 | Alnylam Pharmaceuticals, Inc. | Optimized methods for delivery of DSRNA targeting the PCSK9 gene |
CA2716793A1 (fr) | 2008-03-05 | 2009-09-11 | Alnylam Pharmaceuticals, Inc. | Compositions et procedes pour inhiber l'expression des genes eg5 et vegf |
ES2638448T3 (es) | 2008-04-15 | 2017-10-20 | Protiva Biotherapeutics Inc. | Novedosas formulaciones de lípidos para la administración de ácidos nucleicos |
KR20210158864A (ko) | 2008-11-10 | 2021-12-31 | 알닐람 파마슈티칼스 인코포레이티드 | 치료제 운반용 신규 지질 및 조성물 |
AU2010208035B2 (en) | 2009-01-29 | 2016-06-23 | Arbutus Biopharma Corporation | Improved lipid formulation for the delivery of nucleic acids |
WO2010105209A1 (fr) | 2009-03-12 | 2010-09-16 | Alnylam Pharmaceuticals, Inc. | COMPOSITIONS FORMULÉES DE LIPIDES ET PROCÉDÉS D'INHIBITION DE L'EXPRESSION DE GÈNES DE Eg5 ET DE VEGF |
EP3097908A1 (fr) | 2009-05-05 | 2016-11-30 | Arbutus Biopharma Corporation | Compositions lipidiques |
PT3431076T (pt) | 2009-06-10 | 2021-10-26 | Arbutus Biopharma Corp | Formulação lipídica melhorada |
WO2011017548A1 (fr) | 2009-08-05 | 2011-02-10 | Alnylam Pharmaceuticals, Inc. | Compositions à formulation lipidique et procédés pour inhiber l'expression de gènes eg5 et vegf |
WO2011034798A1 (fr) | 2009-09-15 | 2011-03-24 | Alnylam Pharmaceuticals, Inc. | Compositions à base de formulations lipidiques et méthodes pour inhiber l'expression des gènes eg5 et vegf |
-
2005
- 2005-03-11 EP EP11001330.7A patent/EP2365077B1/fr not_active Not-in-force
- 2005-03-11 JP JP2007503050A patent/JP4937899B2/ja active Active
- 2005-03-11 EP EP14197031.9A patent/EP2899278A1/fr not_active Withdrawn
- 2005-03-11 CA CA2559161A patent/CA2559161C/fr not_active Expired - Fee Related
- 2005-03-11 US US11/078,073 patent/US7947659B2/en active Active
- 2005-03-11 EP EP13156812.3A patent/EP2636739B1/fr not_active Not-in-force
- 2005-03-11 AU AU2005222902A patent/AU2005222902B2/en not_active Ceased
- 2005-03-11 ES ES11001330T patent/ES2423060T3/es active Active
- 2005-03-11 WO PCT/US2005/008182 patent/WO2005089224A2/fr active Application Filing
- 2005-03-11 EP EP05725384A patent/EP1735009A4/fr not_active Withdrawn
-
2006
- 2006-01-25 US US11/340,080 patent/US7919473B2/en active Active
-
2010
- 2010-08-19 AU AU2010212443A patent/AU2010212443B8/en not_active Ceased
-
2011
- 2011-03-08 US US13/043,228 patent/US8293719B2/en active Active
- 2011-05-30 JP JP2011121050A patent/JP5502025B2/ja active Active
-
2012
- 2012-01-20 HK HK12100722.1A patent/HK1160484A1/xx unknown
- 2012-09-14 US US13/620,212 patent/US20130018085A1/en not_active Abandoned
-
2014
- 2014-02-13 JP JP2014025057A patent/JP2014094020A/ja not_active Withdrawn
- 2014-07-07 US US14/325,087 patent/US20150011608A1/en not_active Abandoned
-
2016
- 2016-04-27 JP JP2016088971A patent/JP2016135144A/ja active Pending
Also Published As
Publication number | Publication date |
---|---|
AU2010212443A1 (en) | 2010-09-09 |
JP2014094020A (ja) | 2014-05-22 |
EP1735009A4 (fr) | 2011-03-30 |
AU2005222902B2 (en) | 2010-06-10 |
AU2005222902A1 (en) | 2005-09-29 |
JP4937899B2 (ja) | 2012-05-23 |
WO2005089224A3 (fr) | 2007-03-01 |
AU2010212443B2 (en) | 2013-08-29 |
EP2365077A1 (fr) | 2011-09-14 |
ES2423060T3 (es) | 2013-09-17 |
JP5502025B2 (ja) | 2014-05-28 |
US20150011608A1 (en) | 2015-01-08 |
JP2011188866A (ja) | 2011-09-29 |
JP2016135144A (ja) | 2016-07-28 |
CA2559161C (fr) | 2013-06-11 |
EP2636739A1 (fr) | 2013-09-11 |
US8293719B2 (en) | 2012-10-23 |
EP2636739B1 (fr) | 2014-12-10 |
CA2559161A1 (fr) | 2005-09-29 |
AU2010212443A8 (en) | 2013-09-12 |
US20060094032A1 (en) | 2006-05-04 |
WO2005089224A2 (fr) | 2005-09-29 |
US20110224282A1 (en) | 2011-09-15 |
US20130018085A1 (en) | 2013-01-17 |
EP1735009A2 (fr) | 2006-12-27 |
JP2007528736A (ja) | 2007-10-18 |
US20060223770A1 (en) | 2006-10-05 |
EP2365077B1 (fr) | 2013-05-08 |
EP2899278A1 (fr) | 2015-07-29 |
AU2010212443B8 (en) | 2013-09-12 |
US7947659B2 (en) | 2011-05-24 |
US7919473B2 (en) | 2011-04-05 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
HK1160484A1 (en) | Irna agents targeting vegf irna | |
IL227215A (en) | Vegf antagonists | |
ZA200807253B (en) | Targeted mobile device advertisements | |
EP1620544A4 (fr) | Agents modifies d'arni | |
GB0609492D0 (en) | Therapeutic agents | |
GB0608928D0 (en) | Therapeutic agents | |
GB0601962D0 (en) | Therapeutic agents | |
IL191850A0 (en) | Targeting vector-phospholipid conjugates | |
GB0616214D0 (en) | Therapeutic Agents | |
IL192996A0 (en) | Targeted mobile device advertisements | |
HK1137587A1 (zh) | 移動貨幣化 | |
GB0611152D0 (en) | Therapeutic agents | |
GB0620818D0 (en) | Therapeutic agents | |
GB0620059D0 (en) | Therapeutic agents | |
GB0609676D0 (en) | Therapeutic agents | |
GB0503509D0 (en) | An improved delivery agent | |
GB0601098D0 (en) | Vegf variants | |
GB0622195D0 (en) | Therapeutic agents | |
GB0419983D0 (en) | Improved targeting device | |
GB0402471D0 (en) | Improved targeting device | |
GB0410763D0 (en) | Cellular targeting agents | |
GB0406786D0 (en) | Cellular targeting agents | |
GB0410816D0 (en) | Targeting GCP-2 | |
GB0410702D0 (en) | Targeting GCP-2 | |
GB0619011D0 (en) | Targeting device |