JP2022536495A5 - - Google Patents

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Publication number
JP2022536495A5
JP2022536495A5 JP2021573441A JP2021573441A JP2022536495A5 JP 2022536495 A5 JP2022536495 A5 JP 2022536495A5 JP 2021573441 A JP2021573441 A JP 2021573441A JP 2021573441 A JP2021573441 A JP 2021573441A JP 2022536495 A5 JP2022536495 A5 JP 2022536495A5
Authority
JP
Japan
Prior art keywords
composition according
antisense oligomer
pharmaceutically acceptable
acceptable salt
administered
Prior art date
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.)
Withdrawn
Application number
JP2021573441A
Other languages
English (en)
Japanese (ja)
Other versions
JP2022536495A (ja
Filing date
Publication date
Application filed filed Critical
Priority claimed from PCT/US2020/038483 external-priority patent/WO2020257489A1/en
Publication of JP2022536495A publication Critical patent/JP2022536495A/ja
Publication of JP2022536495A5 publication Critical patent/JP2022536495A5/ja
Priority to JP2025113283A priority Critical patent/JP2025174961A/ja
Withdrawn legal-status Critical Current

Links

JP2021573441A 2019-06-19 2020-06-18 筋ジストロフィーを治療する方法 Withdrawn JP2022536495A (ja)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2025113283A JP2025174961A (ja) 2019-06-19 2025-07-03 筋ジストロフィーを治療する方法

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US201962863456P 2019-06-19 2019-06-19
US62/863,456 2019-06-19
PCT/US2020/038483 WO2020257489A1 (en) 2019-06-19 2020-06-18 Methods for treating muscular dystrophy

Related Child Applications (1)

Application Number Title Priority Date Filing Date
JP2025113283A Division JP2025174961A (ja) 2019-06-19 2025-07-03 筋ジストロフィーを治療する方法

Publications (2)

Publication Number Publication Date
JP2022536495A JP2022536495A (ja) 2022-08-17
JP2022536495A5 true JP2022536495A5 (https=) 2023-06-19

Family

ID=74040497

Family Applications (2)

Application Number Title Priority Date Filing Date
JP2021573441A Withdrawn JP2022536495A (ja) 2019-06-19 2020-06-18 筋ジストロフィーを治療する方法
JP2025113283A Pending JP2025174961A (ja) 2019-06-19 2025-07-03 筋ジストロフィーを治療する方法

Family Applications After (1)

Application Number Title Priority Date Filing Date
JP2025113283A Pending JP2025174961A (ja) 2019-06-19 2025-07-03 筋ジストロフィーを治療する方法

Country Status (4)

Country Link
US (1) US20220296633A1 (https=)
EP (1) EP3987029A1 (https=)
JP (2) JP2022536495A (https=)
WO (1) WO2020257489A1 (https=)

Families Citing this family (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20200131231A1 (en) 2017-02-17 2020-04-30 Oxford University Innovation Limited Cell penetrating peptides
SG11202100928QA (en) 2018-08-02 2021-02-25 Dyne Therapeutics Inc Muscle targeting complexes and uses thereof for treating facioscapulohumeral muscular dystrophy
US12018087B2 (en) 2018-08-02 2024-06-25 Dyne Therapeutics, Inc. Muscle-targeting complexes comprising an anti-transferrin receptor antibody linked to an oligonucleotide and methods of delivering oligonucleotide to a subject
US11168141B2 (en) 2018-08-02 2021-11-09 Dyne Therapeutics, Inc. Muscle targeting complexes and uses thereof for treating dystrophinopathies
CA3108282A1 (en) 2018-08-02 2020-02-06 Dyne Therapeutics, Inc. Muscle targeting complexes and uses thereof for treating dystrophinopathies
GB201812980D0 (en) 2018-08-09 2018-09-26 Univ Oxford Innovation Ltd Cell-penetrating peptides
GB201812972D0 (en) 2018-08-09 2018-09-26 Univ Oxford Innovation Ltd Cell-penetrating peptides
US12465646B2 (en) 2018-12-07 2025-11-11 Oxford University Innovation Limited Linkers
WO2022171972A1 (en) * 2021-02-12 2022-08-18 Oxford University Innovation Limited Cell-penetrating peptide conjugates and methods of their use
US11771776B2 (en) 2021-07-09 2023-10-03 Dyne Therapeutics, Inc. Muscle targeting complexes and uses thereof for treating dystrophinopathies
US11969475B2 (en) 2021-07-09 2024-04-30 Dyne Therapeutics, Inc. Muscle targeting complexes and uses thereof for treating facioscapulohumeral muscular dystrophy

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