JP2023088902A5 - - Google Patents

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Publication number
JP2023088902A5
JP2023088902A5 JP2023020149A JP2023020149A JP2023088902A5 JP 2023088902 A5 JP2023088902 A5 JP 2023088902A5 JP 2023020149 A JP2023020149 A JP 2023020149A JP 2023020149 A JP2023020149 A JP 2023020149A JP 2023088902 A5 JP2023088902 A5 JP 2023088902A5
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JP
Japan
Prior art keywords
raav
promoter
seq
cep290
syndrome
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JP2023020149A
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English (en)
Japanese (ja)
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JP7535332B2 (ja
JP2023088902A (ja
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Priority claimed from PCT/US2018/026230 external-priority patent/WO2018187552A1/en
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Publication of JP2023088902A publication Critical patent/JP2023088902A/ja
Publication of JP2023088902A5 publication Critical patent/JP2023088902A5/ja
Application granted granted Critical
Publication of JP7535332B2 publication Critical patent/JP7535332B2/ja
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JP2023020149A 2017-04-05 2023-02-13 ミニ遺伝子療法 Active JP7535332B2 (ja)

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
US201762481727P 2017-04-05 2017-04-05
US62/481,727 2017-04-05
PCT/US2018/026230 WO2018187552A1 (en) 2017-04-05 2018-04-05 Minigene therapy
JP2019555010A JP7307480B2 (ja) 2017-04-05 2018-04-05 ミニ遺伝子療法

Related Parent Applications (1)

Application Number Title Priority Date Filing Date
JP2019555010A Division JP7307480B2 (ja) 2017-04-05 2018-04-05 ミニ遺伝子療法

Publications (3)

Publication Number Publication Date
JP2023088902A JP2023088902A (ja) 2023-06-27
JP2023088902A5 true JP2023088902A5 (enExample) 2023-10-31
JP7535332B2 JP7535332B2 (ja) 2024-08-16

Family

ID=63712901

Family Applications (2)

Application Number Title Priority Date Filing Date
JP2019555010A Active JP7307480B2 (ja) 2017-04-05 2018-04-05 ミニ遺伝子療法
JP2023020149A Active JP7535332B2 (ja) 2017-04-05 2023-02-13 ミニ遺伝子療法

Family Applications Before (1)

Application Number Title Priority Date Filing Date
JP2019555010A Active JP7307480B2 (ja) 2017-04-05 2018-04-05 ミニ遺伝子療法

Country Status (7)

Country Link
US (2) US11739346B2 (enExample)
EP (1) EP3606544B1 (enExample)
JP (2) JP7307480B2 (enExample)
CN (2) CN110709095B (enExample)
AU (2) AU2018248304C1 (enExample)
CA (1) CA3059112A1 (enExample)
WO (1) WO2018187552A1 (enExample)

Families Citing this family (10)

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Publication number Priority date Publication date Assignee Title
ES2925049T3 (es) * 2015-11-16 2022-10-13 Synlogic Operating Co Inc Bacterias manipuladas para reducir la hiperfenilalaninemia
CN110709095B (zh) 2017-04-05 2024-05-03 马萨诸塞大学 小基因治疗
EP3956453A4 (en) 2019-04-19 2023-02-22 University of Massachusetts GENE THERAPIES FOR USHER SYNDROME (USH1B)
EP3956452A4 (en) * 2019-04-19 2023-03-15 University of Massachusetts GENE THERAPIES FOR USHER SYNDROME (USH2A)
WO2020236815A1 (en) * 2019-05-20 2020-11-26 University Of Massachusetts Minigene therapy
KR20220128607A (ko) 2019-09-18 2022-09-21 인터갈락틱 테라퓨틱스, 인크. 합성 dna 벡터 및 사용 방법
JP2023535632A (ja) 2020-07-27 2023-08-18 アンジャリウム バイオサイエンシズ エージー Dna分子の組成物、その作製方法、及びその使用方法
CN112062827B (zh) * 2020-09-16 2022-10-21 中国人民解放军军事科学院军事医学研究院 Cep55蛋白在调控纤毛去组装和制备纤毛相关疾病模型中的应用
KR20230117177A (ko) * 2020-12-03 2023-08-07 유니버시티 오브 매사추세츠 진행성 골화성 섬유이형성증을 위한 신규 유전자 치료제의개발
US11926842B2 (en) * 2021-02-02 2024-03-12 University Of Massachusetts Use of inverted terminal repeats (ITRS) from adeno-associated virus serotypes 8 and RH.39 in gene therapy vectors

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US5399363A (en) 1991-01-25 1995-03-21 Eastman Kodak Company Surface modified anticancer nanoparticles
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AU2009231171A1 (en) 2008-04-02 2009-10-08 Fondazione Telethon Method of treating genetic disorders
US10266845B2 (en) 2013-02-08 2019-04-23 The Trustees Of The University Of Pennsylvania Enhanced AAV-mediated gene transfer for retinal therapies
AU2014255665B2 (en) 2013-04-18 2018-08-02 Fondazione Telethon Effective delivery of large genes by dual AAV vectors
US10155794B2 (en) 2013-07-16 2018-12-18 The Trustees Of The University Of Pennsylvania Compositions and methods for treatment of disorders related to CEP290
AU2014305218B2 (en) * 2013-08-05 2020-01-16 Academisch Ziekenhuis Leiden H.O.D.N. Leids Universitair Medisch Centrum Recombinant AAV-Crumbs homologue composition and methods for treating LCA-8 and progressive RP
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CA3005474A1 (en) 2015-11-19 2017-05-26 The Trustees Of The University Of Pennsylvania Compositions and methods for correction of heritable ocular disease
JP7007273B2 (ja) 2015-12-22 2022-01-24 アンセルム(アンスティチュート・ナシオナル・ドゥ・ラ・サンテ・エ・ドゥ・ラ・ルシェルシュ・メディカル) 遺伝子治療用の改良された複合型二重組換えaavベクターシステム
US20170348387A1 (en) * 2016-02-29 2017-12-07 The Trustees Of The University Of Pennsylvania Aav-mediated gene therapy for nphp5 lca-ciliopathy
BR112019001887A2 (pt) 2016-08-02 2019-07-09 Editas Medicine Inc composições e métodos para o tratamento de doença associada a cep290
CN110709095B (zh) 2017-04-05 2024-05-03 马萨诸塞大学 小基因治疗
CA3053154A1 (en) 2017-06-30 2019-01-03 The Regents Of The University Of California Adeno-associated virus virions with variant capsids and methods of use thereof
CN111867635A (zh) 2017-10-20 2020-10-30 法国国家卫生及研究医学协会 包括视网膜下递送治疗有效量的重组aav9衍生载体的在对象的视锥细胞光感受器中表达目的多核苷酸的方法
WO2020236815A1 (en) 2019-05-20 2020-11-26 University Of Massachusetts Minigene therapy

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