BR112017001725A2 - tratamento de esclerose lateral amiotrófica - Google Patents

tratamento de esclerose lateral amiotrófica

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Publication number
BR112017001725A2
BR112017001725A2 BR112017001725A BR112017001725A BR112017001725A2 BR 112017001725 A2 BR112017001725 A2 BR 112017001725A2 BR 112017001725 A BR112017001725 A BR 112017001725A BR 112017001725 A BR112017001725 A BR 112017001725A BR 112017001725 A2 BR112017001725 A2 BR 112017001725A2
Authority
BR
Brazil
Prior art keywords
lateral sclerosis
amyotrophic lateral
sclerosis treatment
mrna
treatment
Prior art date
Application number
BR112017001725A
Other languages
English (en)
Inventor
Biferi Maria-Grazia
Barkats Martine
Voit Thomas
Original Assignee
Association Inst De Myologie
Centre Nat Rech Scient
Inst Nat Sante Rech Med
Univ Pierre Et Marie Curie Paris 6
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Association Inst De Myologie, Centre Nat Rech Scient, Inst Nat Sante Rech Med, Univ Pierre Et Marie Curie Paris 6 filed Critical Association Inst De Myologie
Publication of BR112017001725A2 publication Critical patent/BR112017001725A2/pt

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    • C12N15/00Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
    • 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/70Carbohydrates; Sugars; Derivatives thereof
    • A61K31/7088Compounds having three or more nucleosides or nucleotides
    • A61K31/713Double-stranded nucleic acids or oligonucleotides
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P21/00Drugs for disorders of the muscular or neuromuscular system
    • A61P21/02Muscle relaxants, e.g. for tetanus or cramps
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
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    • C12N15/09Recombinant DNA-technology
    • C12N15/63Introduction of foreign genetic material using vectors; Vectors; Use of hosts therefor; Regulation of expression
    • C12N15/79Vectors or expression systems specially adapted for eukaryotic hosts
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    • C12Y115/00Oxidoreductases acting on superoxide as acceptor (1.15)
    • C12Y115/01Oxidoreductases acting on superoxide as acceptor (1.15) with NAD or NADP as acceptor (1.15.1)
    • C12Y115/01001Superoxide dismutase (1.15.1.1)
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    • C12N2750/14111Dependovirus, e.g. adenoassociated viruses
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    • C12N2750/00011Details
    • C12N2750/14011Parvoviridae
    • C12N2750/14311Parvovirus, e.g. minute virus of mice
    • C12N2750/14341Use of virus, viral particle or viral elements as a vector
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    • C12N2799/00Uses of viruses
    • C12N2799/02Uses of viruses as vector
    • C12N2799/021Uses of viruses as vector for the expression of a heterologous nucleic acid
    • C12N2799/025Uses of viruses as vector for the expression of a heterologous nucleic acid where the vector is derived from a parvovirus

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  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Genetics & Genomics (AREA)
  • Organic Chemistry (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Biomedical Technology (AREA)
  • Wood Science & Technology (AREA)
  • Zoology (AREA)
  • General Engineering & Computer Science (AREA)
  • General Health & Medical Sciences (AREA)
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  • Biochemistry (AREA)
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  • Virology (AREA)
  • Microbiology (AREA)
  • Medicinal Chemistry (AREA)
  • Physics & Mathematics (AREA)
  • Plant Pathology (AREA)
  • Biophysics (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Animal Behavior & Ethology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Neurology (AREA)
  • Epidemiology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Neurosurgery (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Immunology (AREA)
  • Orthopedic Medicine & Surgery (AREA)
  • Pain & Pain Management (AREA)
  • Hospice & Palliative Care (AREA)
  • Physical Education & Sports Medicine (AREA)
  • Psychiatry (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Medicines Containing Material From Animals Or Micro-Organisms (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

Abstract

a invenção se refere a um método para o tratamento de esclerose lateral amiotrófica (als). especificamente, a invenção implementa o uso de uma sequência de antissentido adaptada para afetar a junção alternativa em um pré-mrna da sod1 humana, levando deste modo à destruição do mrna pulado pelo mecanismo celular.
BR112017001725A 2014-07-31 2015-07-31 tratamento de esclerose lateral amiotrófica BR112017001725A2 (pt)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
EP14306228 2014-07-31
PCT/EP2015/067722 WO2016016449A1 (en) 2014-07-31 2015-07-31 Treatment of amyotrophic lateral sclerosis

Publications (1)

Publication Number Publication Date
BR112017001725A2 true BR112017001725A2 (pt) 2018-02-14

Family

ID=51298679

Family Applications (1)

Application Number Title Priority Date Filing Date
BR112017001725A BR112017001725A2 (pt) 2014-07-31 2015-07-31 tratamento de esclerose lateral amiotrófica

Country Status (7)

Country Link
US (1) US10590420B2 (pt)
EP (1) EP3174981B1 (pt)
JP (1) JP6872479B2 (pt)
BR (1) BR112017001725A2 (pt)
CA (1) CA2955285C (pt)
ES (1) ES2806087T3 (pt)
WO (1) WO2016016449A1 (pt)

Families Citing this family (17)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP6756700B2 (ja) 2014-03-18 2020-09-16 ユニバーシティ オブ マサチューセッツ 筋萎縮性側索硬化症を処置するためのrAAVベースの組成物および方法
EP4137573A3 (en) 2014-04-01 2023-05-03 Biogen MA Inc. Compositions for modulating sod-1 expression
KR102599909B1 (ko) 2014-11-14 2023-11-09 보이저 테라퓨틱스, 인크. 근위축성 측삭 경화증(als)을 치료하는 조성물 및 방법
RU2749882C2 (ru) 2014-11-14 2021-06-18 Вояджер Терапьютикс, Инк. Модулирующие полинуклеотиды
WO2017136435A1 (en) 2016-02-01 2017-08-10 The Usa, As Represented By The Secretary, Department Of Health And Human Services Office Of Technology Transfer National Institute Of Health Compounds for modulating fc-epsilon-ri-beta expression and uses thereof
IL302748A (en) 2016-05-18 2023-07-01 Voyager Therapeutics Inc modulatory polynucleotides
WO2018204786A1 (en) 2017-05-05 2018-11-08 Voyager Therapeutics, Inc. Compositions and methods of treating amyotrophic lateral sclerosis (als)
AU2018264996A1 (en) 2017-05-09 2019-12-05 University Of Massachusetts Methods of treating Amyotrophic Lateral Sclerosis (ALS)
WO2019028246A2 (en) * 2017-08-03 2019-02-07 University Of Iowa Research Foundation METHODS OF TREATING GENETIC HEARING LOSS
CN111448321A (zh) * 2017-09-22 2020-07-24 马萨诸塞大学 Sod1双表达载体及其用途
EP3697908A1 (en) * 2017-10-16 2020-08-26 Voyager Therapeutics, Inc. Treatment of amyotrophic lateral sclerosis (als)
TWI804518B (zh) 2017-10-16 2023-06-11 美商航海家醫療公司 肌萎縮性脊髓側索硬化症(als)之治療
AU2020248392A1 (en) * 2019-03-26 2021-11-11 Rutgers, The State University Of New Jersey Compositions and methods for treating neurodegenerative disorders
JP2022530945A (ja) * 2019-05-01 2022-07-05 ブラック スワン ファーマシューティカルズ, インコーポレイテッド Sod1関連疾患に対する処置
WO2021089736A1 (en) 2019-11-06 2021-05-14 Association Institut De Myologie Combined therapy for muscular diseases
EP4291654A2 (en) 2021-02-12 2023-12-20 Alnylam Pharmaceuticals, Inc. Superoxide dismutase 1 (sod1) irna compositions and methods of use thereof for treating or preventing superoxide dismutase 1- (sod1-) associated neurodegenerative diseases
WO2023201300A2 (en) * 2022-04-14 2023-10-19 Shift Pharmaceuticals Holding Inc. Polynucleotide treatments for charcot-marie-tooth disease

Family Cites Families (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2003000707A2 (en) * 2001-06-21 2003-01-03 Isis Pharmaceuticals, Inc. Antisense modulation of superoxide dismutase 1, soluble expression
FR2874384B1 (fr) 2004-08-17 2010-07-30 Genethon Vecteur viral adeno-associe pour realiser du saut d'exons dans un gene codant une proteine a domaines dispensables
EP2058401A1 (en) 2007-10-05 2009-05-13 Genethon Widespread gene delivery to motor neurons using peripheral injection of AAV vectors
GB0816778D0 (en) 2008-09-12 2008-10-22 Isis Innovation Gene silencing
US9080170B2 (en) 2010-03-17 2015-07-14 Association Institut De Myologie Modified U7 snRNAs for treatment of neuromuscular diseases
EP2581448B1 (en) 2011-10-13 2015-01-28 Association Institut de Myologie Tricyclo-phosphorothioate DNA
WO2013184209A1 (en) * 2012-06-04 2013-12-12 Ludwig Institute For Cancer Research Ltd. Mif for use in methods of treating subjects with a neurodegenerative disorder
CA2877428A1 (en) 2012-06-21 2013-12-27 Association Institut De Myologie Widespread gene delivery of gene therapy vectors
WO2014172698A1 (en) 2013-04-19 2014-10-23 Isis Pharmaceuticals, Inc. Compositions and methods for modulation nucleic acids through nonsense mediated decay
EP4137573A3 (en) * 2014-04-01 2023-05-03 Biogen MA Inc. Compositions for modulating sod-1 expression

Also Published As

Publication number Publication date
CA2955285A1 (en) 2016-02-04
WO2016016449A1 (en) 2016-02-04
EP3174981A1 (en) 2017-06-07
ES2806087T3 (es) 2021-02-16
EP3174981B1 (en) 2020-03-25
JP2017527276A (ja) 2017-09-21
JP6872479B2 (ja) 2021-05-19
US10590420B2 (en) 2020-03-17
US20170152517A1 (en) 2017-06-01
CA2955285C (en) 2023-09-26

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B25A Requested transfer of rights approved

Owner name: CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE (FR)

Owner name: CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE (FR) ; INSTITUT NATIONAL DE LA SANTE ET DE LA RECHERCHE MEDICALE (FR) ; SORBONNE UNIVERSITE (FR) ; ASSOCIATION INSTITUT DE MYOLOGIE (FR)

B07D Technical examination (opinion) related to article 229 of industrial property law [chapter 7.4 patent gazette]

Free format text: DE ACORDO COM O ARTIGO 229-C DA LEI NO 10196/2001, QUE MODIFICOU A LEI NO 9279/96, A CONCESSAO DA PATENTE ESTA CONDICIONADA A ANUENCIA PREVIA DA ANVISA. CONSIDERANDO A APROVACAO DOS TERMOS DO PARECER NO 337/PGF/EA/2010, BEM COMO A PORTARIA INTERMINISTERIAL NO 1065 DE 24/05/2012, ENCAMINHA-SE O PRESENTE PEDIDO PARA AS PROVIDENCIAS CABIVEIS.

B07E Notification of approval relating to section 229 industrial property law [chapter 7.5 patent gazette]
B06U Preliminary requirement: requests with searches performed by other patent offices: procedure suspended [chapter 6.21 patent gazette]
B25A Requested transfer of rights approved

Owner name: INSTITUT NATIONAL DE LA SANTE ET DE LA RECHERCHE MEDICALE (FR) ; SORBONNE UNIVERSITE (FR) ; ASSOCIATION INSTITUT DE MYOLOGIE (FR)

B07A Application suspended after technical examination (opinion) [chapter 7.1 patent gazette]
B09B Patent application refused [chapter 9.2 patent gazette]
B12B Appeal against refusal [chapter 12.2 patent gazette]