JPWO2020223762A5 - - Google Patents

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Publication number
JPWO2020223762A5
JPWO2020223762A5 JP2021566041A JP2021566041A JPWO2020223762A5 JP WO2020223762 A5 JPWO2020223762 A5 JP WO2020223762A5 JP 2021566041 A JP2021566041 A JP 2021566041A JP 2021566041 A JP2021566041 A JP 2021566041A JP WO2020223762 A5 JPWO2020223762 A5 JP WO2020223762A5
Authority
JP
Japan
Prior art keywords
pharmaceutical composition
subject
cd49d
dosing
oligonucleotide
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.)
Pending
Application number
JP2021566041A
Other languages
English (en)
Japanese (ja)
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JP2022532098A (ja
Publication date
Application filed filed Critical
Priority claimed from PCT/AU2020/050445 external-priority patent/WO2020223762A1/en
Publication of JP2022532098A publication Critical patent/JP2022532098A/ja
Publication of JPWO2020223762A5 publication Critical patent/JPWO2020223762A5/ja
Ceased legal-status Critical Current

Links

JP2021566041A 2019-05-06 2020-05-06 CD49dに対する阻害オリゴヌクレオチドを使用して筋ジストロフィーを治療する方法 Ceased JP2022532098A (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
AU2019901540A AU2019901540A0 (en) 2019-05-06 Therapeutic uses and methods
AU2019901540 2019-05-06
PCT/AU2020/050445 WO2020223762A1 (en) 2019-05-06 2020-05-06 Methods for treating muscular dystrophy using inhibitory oligonucleotides to cd49d

Publications (2)

Publication Number Publication Date
JP2022532098A JP2022532098A (ja) 2022-07-13
JPWO2020223762A5 true JPWO2020223762A5 (enExample) 2023-05-16

Family

ID=73050454

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2021566041A Ceased JP2022532098A (ja) 2019-05-06 2020-05-06 CD49dに対する阻害オリゴヌクレオチドを使用して筋ジストロフィーを治療する方法

Country Status (9)

Country Link
US (1) US20220296631A1 (enExample)
EP (1) EP3965778A4 (enExample)
JP (1) JP2022532098A (enExample)
KR (1) KR20220061915A (enExample)
CN (1) CN114555095A (enExample)
AU (1) AU2020269078A1 (enExample)
BR (1) BR112021022208A2 (enExample)
CA (1) CA3138945A1 (enExample)
WO (1) WO2020223762A1 (enExample)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
IT202100014333A1 (it) * 2021-06-01 2022-12-01 Materias S R L Nuovo impiego terapeutico di inibitori della iodiotironina deiodinasi di tipo 2 (D2)
WO2024159266A1 (en) * 2023-02-01 2024-08-08 Antisense Therapeutics Ltd Combination compositions and methods for treatment of muscular dystrophy
CN119113214B (zh) * 2024-11-14 2025-02-11 四川大学 一种肌肉修复材料及其制备方法和用途

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2010008474A2 (en) * 2008-06-23 2010-01-21 Teva Pharmaceutical Industries, Ltd. Methods for treating multiple sclerosis using antisense oligonucleotides
CA2761248C (en) * 2009-05-08 2023-03-14 Joseph Collard Treatment of dystrophin family related diseases by inhibition of natural antisense transcript to dmd family
EP2467159A1 (en) * 2009-08-20 2012-06-27 INSERM (Institut National de la Santé et de la Recherche Médicale) Vla-4 as a biomarker for prognosis and target for therapy in duchenne muscular dystrophy
WO2017062835A2 (en) * 2015-10-09 2017-04-13 Sarepta Therapeutics, Inc. Compositions and methods for treating duchenne muscular dystrophy and related disorders
CA3067193A1 (en) * 2017-06-16 2018-12-20 Antisense Therapeutics Ltd Methods for treating multiple sclerosis using antisense oligonucleotides
EP3787639A4 (en) * 2018-05-04 2022-02-23 Antisense Therapeutics Ltd THERAPEUTIC USES AND PROCESSES

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