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WO2004043977A3 - Composes oligomeres substitues par fluoro en position 2' et compositions a utiliser dans des modulations geniques - Google Patents

Composes oligomeres substitues par fluoro en position 2' et compositions a utiliser dans des modulations geniques Download PDF

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Publication number
WO2004043977A3
WO2004043977A3 PCT/US2003/034905 US0334905W WO2004043977A3 WO 2004043977 A3 WO2004043977 A3 WO 2004043977A3 US 0334905 W US0334905 W US 0334905W WO 2004043977 A3 WO2004043977 A3 WO 2004043977A3
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WIPO (PCT)
Prior art keywords
oligomer
compositions
oligomeric compounds
fluoro substituted
hybridizing
Prior art date
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Ceased
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PCT/US2003/034905
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English (en)
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WO2004043977A2 (fr
Inventor
Thazha P Prakush
Brenda F Baker
Anne B Eldrup
Muthiah Manoharan
Balkrishen Bhat
Richard H Griffey
Eric E Swayze
Stanley T Crooke
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Ionis Pharmaceuticals Inc
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Isis Pharmaceuticals Inc
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Priority to AU2003287464A priority Critical patent/AU2003287464A1/en
Publication of WO2004043977A2 publication Critical patent/WO2004043977A2/fr
Publication of WO2004043977A3 publication Critical patent/WO2004043977A3/fr
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

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    • C12N15/09Recombinant DNA-technology
    • C12N15/11DNA or RNA fragments; Modified forms thereof; Non-coding nucleic acids having a biological activity
    • C12N15/113Non-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
    • C12N15/1135Non-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 oncogenes or tumor suppressor genes
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    • C07HSUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
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    • C07HSUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
    • C07H21/00Compounds containing two or more mononucleotide units having separate phosphate or polyphosphate groups linked by saccharide radicals of nucleoside groups, e.g. nucleic acids
    • C07H21/02Compounds containing two or more mononucleotide units having separate phosphate or polyphosphate groups linked by saccharide radicals of nucleoside groups, e.g. nucleic acids with ribosyl as saccharide radical
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    • C07HSUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
    • C07H21/00Compounds containing two or more mononucleotide units having separate phosphate or polyphosphate groups linked by saccharide radicals of nucleoside groups, e.g. nucleic acids
    • C07H21/04Compounds containing two or more mononucleotide units having separate phosphate or polyphosphate groups linked by saccharide radicals of nucleoside groups, e.g. nucleic acids with deoxyribosyl as saccharide radical
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    • C12N15/09Recombinant DNA-technology
    • C12N15/11DNA or RNA fragments; Modified forms thereof; Non-coding nucleic acids having a biological activity
    • C12N15/113Non-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
    • C12N15/1137Non-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 enzymes
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    • C12N2310/00Structure or type of the nucleic acid
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    • C12N2310/14Type of nucleic acid interfering nucleic acids [NA]
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    • C12N2310/00Structure or type of the nucleic acid
    • C12N2310/30Chemical structure
    • C12N2310/31Chemical structure of the backbone
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    • C12N2310/00Structure or type of the nucleic acid
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    • C12N2310/32Chemical structure of the sugar
    • C12N2310/3212'-O-R Modification
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    • C12N2310/34Spatial arrangement of the modifications
    • C12N2310/341Gapmers, i.e. of the type ===---===
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    • C12N2310/30Chemical structure
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    • C12N2310/00Structure or type of the nucleic acid
    • C12N2310/50Physical structure
    • C12N2310/53Physical structure partially self-complementary or closed

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  • Oncology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Saccharide Compounds (AREA)

Abstract

L'invention concerne des compositions comprenant un premier oligomère et un second oligomère, dans lesquelles au moins une partie du premier oligomère permet une hybridation avec au moins une partie du second oligomère, au moins une partie du premier oligomère étant complémentaire à une hybridation et permettant une hybridation avec un acide nucléique cible sélectionné, et au moins un premier oligomère ou un second oligomère comprenant un sucre modifié et/ou une modification de squelette. Dans certains modes de réalisation, la modification est un groupe substituant 2'-F sur une fraction de sucre. Des compositions oligomères/protéiniques sont également décrites, elles comprennent un oligomère complémentaire à une hybridation et permettant une hybridation avec un acide nucléique cible sélectionné et au moins une protéine comprenant au moins une partie d'un complexe de silençage induit par ARN (RISC), au moins un nucléoside de l'oligomère présentant un sucre modifié et/ou une modification de squelette.
PCT/US2003/034905 2002-11-05 2003-11-04 Composes oligomeres substitues par fluoro en position 2' et compositions a utiliser dans des modulations geniques Ceased WO2004043977A2 (fr)

Priority Applications (1)

Application Number Priority Date Filing Date Title
AU2003287464A AU2003287464A1 (en) 2002-11-05 2003-11-04 2'-fluoro substituted oligomeric compounds and compositions for use in gene modulations

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
US42376002P 2002-11-05 2002-11-05
US60/423,760 2002-11-05
US50352103P 2003-09-16 2003-09-16
US60/503,521 2003-09-16

Publications (2)

Publication Number Publication Date
WO2004043977A2 WO2004043977A2 (fr) 2004-05-27
WO2004043977A3 true WO2004043977A3 (fr) 2005-01-20

Family

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Family Applications (3)

Application Number Title Priority Date Filing Date
PCT/US2003/034905 Ceased WO2004043977A2 (fr) 2002-11-05 2003-11-04 Composes oligomeres substitues par fluoro en position 2' et compositions a utiliser dans des modulations geniques
PCT/US2003/035087 Ceased WO2004044140A2 (fr) 2002-11-05 2003-11-04 Composes oligomeres 2'-substitues et compositions destinees a etre utilisees dans des modulations genetiques
PCT/US2003/034906 Ceased WO2004043978A2 (fr) 2002-11-05 2003-11-04 Composes oligomeres substitues par methoxy en position 2' et compositions a utiliser dans des modulations geniques

Family Applications After (2)

Application Number Title Priority Date Filing Date
PCT/US2003/035087 Ceased WO2004044140A2 (fr) 2002-11-05 2003-11-04 Composes oligomeres 2'-substitues et compositions destinees a etre utilisees dans des modulations genetiques
PCT/US2003/034906 Ceased WO2004043978A2 (fr) 2002-11-05 2003-11-04 Composes oligomeres substitues par methoxy en position 2' et compositions a utiliser dans des modulations geniques

Country Status (4)

Country Link
EP (1) EP1563070A4 (fr)
AU (4) AU2003295388A1 (fr)
CA (1) CA2504554A1 (fr)
WO (3) WO2004043977A2 (fr)

Cited By (7)

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US7176304B2 (en) 2002-02-20 2007-02-13 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)
US7456155B2 (en) 2002-06-28 2008-11-25 Idenix Pharmaceuticals, Inc. 2′-C-methyl-3′-O-L-valine ester ribofuranosyl cytidine for treatment of flaviviridae infections
US7517864B2 (en) 2001-05-18 2009-04-14 Sirna Therapeutics, Inc. RNA interference mediated inhibition of vascular endothelial growth factor and vascular endothelial growth factor receptor gene expression using short interfering nucleic acid (siNA)
US7582618B2 (en) 2002-06-28 2009-09-01 Idenix Pharmaceuticals, Inc. 2′-C-methyl-3′-O-L-valine ester ribofuranosyl cytidine for treatment of flaviviridae infections
US7598373B2 (en) 2002-12-12 2009-10-06 Idenix Pharmaceuticals, Inc. Process for the production of 2-C-methyl-D-ribonolactone
US7608597B2 (en) 2000-05-23 2009-10-27 Idenix Pharmaceuticals, Inc. Methods and compositions for treating hepatitis C virus
US7858625B2 (en) 2001-05-18 2010-12-28 Sirna Therapeutics, Inc. Conjugates and compositions for cellular delivery

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US5898031A (en) 1996-06-06 1999-04-27 Isis Pharmaceuticals, Inc. Oligoribonucleotides for cleaving RNA
US9096636B2 (en) 1996-06-06 2015-08-04 Isis Pharmaceuticals, Inc. Chimeric oligomeric compounds and their use in gene modulation
WO2002081628A2 (fr) 2001-04-05 2002-10-17 Ribozyme Pharmaceuticals, Incorporated Modulation de l'expression genique associee a la proliferation inflammatoire et a la croissance de neurites, par des procedes faisant intervenir l'acide nucleique
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WO2005078097A2 (fr) 2004-02-10 2005-08-25 Sirna Therapeutics, Inc. Inhibition induite par l'interference arn de l'expression genetique, a l'aide d'un acide nucleique interferant court multifonctionnel (sina multifonctionnel)
US9994853B2 (en) 2001-05-18 2018-06-12 Sirna Therapeutics, Inc. Chemically modified multifunctional short interfering nucleic acid molecules that mediate RNA interference
GB2413557B (en) * 2002-02-20 2006-08-16 Sirna Therapeutics Inc RNA interference mediated inhibtion of gene expression using chemically modified short interfering nucleic acid (siNA)
US9657294B2 (en) 2002-02-20 2017-05-23 Sirna Therapeutics, Inc. RNA interference mediated inhibition of gene expression using chemically modified short interfering nucleic acid (siNA)
GB2406568B (en) * 2002-02-20 2005-09-28 Sirna Therapeutics Inc RNA interference mediated inhibition of gene expression using chemically modified short interfering nucleic acid (siNA)
US9181551B2 (en) 2002-02-20 2015-11-10 Sirna Therapeutics, Inc. RNA interference mediated inhibition of gene expression using chemically modified short interfering nucleic acid (siNA)
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US10508277B2 (en) 2004-05-24 2019-12-17 Sirna Therapeutics, Inc. Chemically modified multifunctional short interfering nucleic acid molecules that mediate RNA interference
US8394947B2 (en) 2004-06-03 2013-03-12 Isis Pharmaceuticals, Inc. Positionally modified siRNA constructs
US7884086B2 (en) 2004-09-08 2011-02-08 Isis Pharmaceuticals, Inc. Conjugates for use in hepatocyte free uptake assays
WO2006036916A2 (fr) 2004-09-24 2006-04-06 Alnylam Pharmaceuticals, Inc. Modulation d'arni d'apob et utilisations correspondantes
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MA41795A (fr) 2015-03-18 2018-01-23 Sarepta Therapeutics Inc Exclusion d'un exon induite par des composés antisens dans la myostatine
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PT3554554T (pt) 2016-12-19 2022-11-08 Sarepta Therapeutics Inc Conjugaos oligoméricos de salto de exão para a distrofia mascular
EA201991450A1 (ru) 2017-09-22 2019-12-30 Сарепта Терапьютикс, Инк. Конъюгаты олигомеров для пропуска экзона при мышечной дистрофии
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US10758629B2 (en) 2018-05-29 2020-09-01 Sarepta Therapeutics, Inc. Exon skipping oligomer conjugates for muscular dystrophy
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AU2019397461A1 (en) 2018-12-13 2021-07-29 Sarepta Therapeutics, Inc. Exon skipping oligomer conjugates for muscular dystrophy
US20220193246A1 (en) 2019-04-18 2022-06-23 Sarepta Therapeutics, Inc. Compositions for treating muscular dystrophy
JP2024537711A (ja) 2021-09-30 2024-10-16 サレプタ セラピューティクス, インコーポレイテッド 1つ以上の脱塩基ユニットを有するアンチセンスオリゴヌクレオチド
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Citations (2)

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US20030143732A1 (en) * 2001-04-05 2003-07-31 Kathy Fosnaugh RNA interference mediated inhibition of adenosine A1 receptor (ADORA1) gene expression using short interfering RNA

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AU2003291682A1 (en) 2004-06-03
EP1563070A4 (fr) 2008-05-28
EP1563070A2 (fr) 2005-08-17
WO2004044140A2 (fr) 2004-05-27
WO2004043977A2 (fr) 2004-05-27
AU2003295388A1 (en) 2004-06-03
AU2003291682A8 (en) 2004-06-03
WO2004044140A3 (fr) 2005-04-14
AU2003287464A8 (en) 2004-06-03
CA2504554A1 (fr) 2004-05-27
AU2010201712B2 (en) 2012-05-31
WO2004043978A2 (fr) 2004-05-27
AU2010201712A1 (en) 2010-05-20
WO2004043978A3 (fr) 2005-04-07

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