JP2022185052A5 - - Google Patents

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Publication number
JP2022185052A5
JP2022185052A5 JP2022156496A JP2022156496A JP2022185052A5 JP 2022185052 A5 JP2022185052 A5 JP 2022185052A5 JP 2022156496 A JP2022156496 A JP 2022156496A JP 2022156496 A JP2022156496 A JP 2022156496A JP 2022185052 A5 JP2022185052 A5 JP 2022185052A5
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JP
Japan
Prior art keywords
rna molecule
vector
synthetic rna
seq
sequence
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Legal status (The legal status 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 status listed.)
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JP2022156496A
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English (en)
Japanese (ja)
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JP7642211B2 (ja
JP2022185052A (ja
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Priority claimed from PCT/US2017/020289 external-priority patent/WO2017151823A1/en
Application filed filed Critical
Publication of JP2022185052A publication Critical patent/JP2022185052A/ja
Publication of JP2022185052A5 publication Critical patent/JP2022185052A5/ja
Priority to JP2024168632A priority Critical patent/JP2025016451A/ja
Application granted granted Critical
Publication of JP7642211B2 publication Critical patent/JP7642211B2/ja
Active legal-status Critical Current
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JP2022156496A 2016-03-01 2022-09-29 優性網膜色素変性の治療のためのaavベクター Active JP7642211B2 (ja)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2024168632A JP2025016451A (ja) 2016-03-01 2024-09-27 優性網膜色素変性の治療のためのaavベクター

Applications Claiming Priority (6)

Application Number Priority Date Filing Date Title
US201662302122P 2016-03-01 2016-03-01
US62/302,122 2016-03-01
US201662398451P 2016-09-22 2016-09-22
US62/398,451 2016-09-22
PCT/US2017/020289 WO2017151823A1 (en) 2016-03-01 2017-03-01 Aav vectors for treatment of dominant retinitis pigmentosa
JP2018545818A JP7272795B2 (ja) 2016-03-01 2017-03-01 優性網膜色素変性の治療のためのaavベクター

Related Parent Applications (1)

Application Number Title Priority Date Filing Date
JP2018545818A Division JP7272795B2 (ja) 2016-03-01 2017-03-01 優性網膜色素変性の治療のためのaavベクター

Related Child Applications (1)

Application Number Title Priority Date Filing Date
JP2024168632A Division JP2025016451A (ja) 2016-03-01 2024-09-27 優性網膜色素変性の治療のためのaavベクター

Publications (3)

Publication Number Publication Date
JP2022185052A JP2022185052A (ja) 2022-12-13
JP2022185052A5 true JP2022185052A5 (https=) 2023-05-01
JP7642211B2 JP7642211B2 (ja) 2025-03-10

Family

ID=59743213

Family Applications (3)

Application Number Title Priority Date Filing Date
JP2018545818A Active JP7272795B2 (ja) 2016-03-01 2017-03-01 優性網膜色素変性の治療のためのaavベクター
JP2022156496A Active JP7642211B2 (ja) 2016-03-01 2022-09-29 優性網膜色素変性の治療のためのaavベクター
JP2024168632A Pending JP2025016451A (ja) 2016-03-01 2024-09-27 優性網膜色素変性の治療のためのaavベクター

Family Applications Before (1)

Application Number Title Priority Date Filing Date
JP2018545818A Active JP7272795B2 (ja) 2016-03-01 2017-03-01 優性網膜色素変性の治療のためのaavベクター

Family Applications After (1)

Application Number Title Priority Date Filing Date
JP2024168632A Pending JP2025016451A (ja) 2016-03-01 2024-09-27 優性網膜色素変性の治療のためのaavベクター

Country Status (9)

Country Link
US (2) US11118185B2 (https=)
EP (2) EP3423582B1 (https=)
JP (3) JP7272795B2 (https=)
CN (2) CN115896106A (https=)
AU (2) AU2017227776C1 (https=)
CA (1) CA3014671A1 (https=)
ES (1) ES2923877T3 (https=)
IL (2) IL302455A (https=)
WO (1) WO2017151823A1 (https=)

Families Citing this family (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN115896106A (zh) 2016-03-01 2023-04-04 佛罗里达大学研究基金会有限公司 用于治疗显性视网膜色素变性的aav载体
JP7385282B2 (ja) * 2017-11-07 2023-11-22 ザ・ユニヴァーシティ・オヴ・ノース・キャロライナ・アト・チャペル・ヒル 環状rna分子のための方法及び組成物
BR112020023298A2 (pt) * 2018-05-15 2021-03-09 University Of Washington composições e métodos para reduzir a spliceopatia e tratamento de distúrbios de dominância de rna
CN112204145B (zh) * 2018-06-01 2024-03-26 佛罗里达大学研究基金会有限公司 用于治疗显性视网膜色素变性的组合物和方法
GB201817469D0 (en) * 2018-10-26 2018-12-12 Univ Oxford Innovation Ltd Gene therapy for retinal disease
CN111518813B (zh) * 2019-02-03 2023-04-28 武汉纽福斯生物科技有限公司 视紫红质的编码序列、其表达载体构建及其应用
EP4013414A4 (en) * 2019-08-15 2023-09-27 The Children's Hospital of Philadelphia COMBINED INTRON-DERIVED MIRNA AND TRANSGENE THERAPY FOR THE TREATMENT OF SCA1
US20230149439A1 (en) * 2020-04-21 2023-05-18 Chigenovo Co., Ltd. Rho-adrp gene editing-based methods and compositions
CN111926044B (zh) * 2020-10-12 2021-01-22 北京大学第三医院(北京大学第三临床医学院) 结合突变rho基因的核酸分子和试剂盒
WO2022165313A1 (en) 2021-02-01 2022-08-04 Regenxbio Inc. Gene therapy for neuronal ceroid lipofuscinoses
WO2025231487A1 (en) * 2024-05-03 2025-11-06 The Trustees Of The University Of Pennsylvania Photoreceptor specific promotors for use in gene therapies for treatment of retinal degeneration

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US5795587A (en) 1995-01-23 1998-08-18 University Of Pittsburgh Stable lipid-comprising drug delivery complexes and methods for their production
US8551970B2 (en) 1996-04-02 2013-10-08 Optigen Patents Limited Genetic suppression and replacement
US20040234999A1 (en) 1996-04-02 2004-11-25 Farrar Gwenyth Jane Genetic suppression and replacement
GB9606961D0 (en) 1996-04-02 1996-06-05 Farrar Gwyneth J Genetic strategy III
AU2003274397A1 (en) 2002-06-05 2003-12-22 University Of Florida Production of pseudotyped recombinant aav virions
AU2004233043A1 (en) 2003-04-18 2004-11-04 The Trustees Of The University Of Pennsylvania Compositions and methods for siRNA inhibition of angiopoietin 1 and 2 and their receptor Tie2
US20070009899A1 (en) * 2003-10-02 2007-01-11 Mounts William M Nucleic acid arrays for detecting gene expression in animal models of inflammatory diseases
GB0403600D0 (en) * 2004-02-18 2004-03-24 Trinity College Dublin Methods and reagents for treating disease
CN1977044A (zh) 2004-03-24 2007-06-06 肿瘤疗法科学股份有限公司 治疗胰腺癌的组合物和方法
US20080221057A1 (en) 2007-02-16 2008-09-11 Wyeth Secreted protein ccdc80 regulates adipocyte differentiation
US20120322861A1 (en) 2007-02-23 2012-12-20 Barry John Byrne Compositions and Methods for Treating Diseases
EP2140004B1 (en) * 2007-04-12 2022-01-12 The Provost, Fellows, Foundation Scholars, & the other members of Board, of the College of the Holy & Undiv. Trinity of Queen Elizabeth near Dublin Genetic suppression and replacement
WO2009035792A1 (en) * 2007-08-03 2009-03-19 Melba Ketchum Compositions, methods and systems for the simultaneous determination of parentage, identity, sex, genotype and/or phenotype and breed determination in animals
WO2010127209A2 (en) * 2009-04-30 2010-11-04 The Research Foundation Of State University Of New York Compositions and methods for therapy of macular degeneration
SG10201800541SA (en) * 2010-04-23 2018-03-28 Univ Florida Raav-guanylate cyclase compositions and methods for treating leber's congenital amaurosis-1 (lca1)
KR101761388B1 (ko) 2010-07-30 2017-07-25 큐어백 아게 트랜스펙션 및 면역 자극을 위한 이황화-크로스링크된 양이온 성분 및 핵산의 복합체
CN102061308B (zh) 2010-10-29 2013-05-08 北京未名凯拓作物设计中心有限公司 一种用百草枯筛选转基因植物的方法
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US11180760B2 (en) * 2012-03-09 2021-11-23 The Johns Hopkins University Identification of molecular pathways and methods of use thereof for treating retinal neurodegeneration and other neurodegenerative disorders
US9163259B2 (en) * 2012-05-04 2015-10-20 Novartis Ag Viral vectors for the treatment of retinal dystrophy
US9695443B2 (en) 2012-05-25 2017-07-04 Commissariat A L'energie Atomique Et Aux Energies Alternatives Vector for the selective silencing of a gene in astrocytes
WO2014138792A1 (en) 2013-03-14 2014-09-18 Commonwealth Scientific And Industrial Research Organisation Double-stranded rna
PL3628334T3 (pl) * 2014-03-21 2023-12-18 Genzyme Corporation Terapia genowa w retinopatii barwnikowej
AU2016222546B2 (en) 2015-02-26 2020-01-23 Ionis Pharmaceuticals, Inc. Allele specific modulators of P23H rhodopsin
EP3289080B1 (en) 2015-04-30 2021-08-25 The Trustees of Columbia University in the City of New York Gene therapy for autosomal dominant diseases
WO2017137493A1 (en) 2016-02-09 2017-08-17 Fondazione Telethon Synthetic promoters and uses thereof
US20170348387A1 (en) 2016-02-29 2017-12-07 The Trustees Of The University Of Pennsylvania Aav-mediated gene therapy for nphp5 lca-ciliopathy
CN115896106A (zh) 2016-03-01 2023-04-04 佛罗里达大学研究基金会有限公司 用于治疗显性视网膜色素变性的aav载体

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