JP2020518556A5 - - Google Patents

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Publication number
JP2020518556A5
JP2020518556A5 JP2019555219A JP2019555219A JP2020518556A5 JP 2020518556 A5 JP2020518556 A5 JP 2020518556A5 JP 2019555219 A JP2019555219 A JP 2019555219A JP 2019555219 A JP2019555219 A JP 2019555219A JP 2020518556 A5 JP2020518556 A5 JP 2020518556A5
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JP
Japan
Prior art keywords
seq
peptide
amino acid
disorders
group
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
JP2019555219A
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English (en)
Japanese (ja)
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JP2020518556A (ja
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Publication date
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Priority claimed from PCT/EP2018/061547 external-priority patent/WO2018202870A1/en
Publication of JP2020518556A publication Critical patent/JP2020518556A/ja
Publication of JP2020518556A5 publication Critical patent/JP2020518556A5/ja
Priority to JP2023051477A priority Critical patent/JP2023082076A/ja
Priority to JP2025037548A priority patent/JP2025090703A/ja
Pending legal-status Critical Current

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JP2019555219A 2017-05-04 2018-05-04 糖尿病の処置のためのペプチド Pending JP2020518556A (ja)

Priority Applications (2)

Application Number Priority Date Filing Date Title
JP2023051477A JP2023082076A (ja) 2017-05-04 2023-03-28 糖尿病の処置のためのペプチド
JP2025037548A JP2025090703A (ja) 2017-05-04 2025-03-10 糖尿病の処置のためのペプチド

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
EP17169500.0 2017-05-04
EP17169500 2017-05-04
PCT/EP2018/061547 WO2018202870A1 (en) 2017-05-04 2018-05-04 Peptides for treatment of diabetes

Related Child Applications (1)

Application Number Title Priority Date Filing Date
JP2023051477A Division JP2023082076A (ja) 2017-05-04 2023-03-28 糖尿病の処置のためのペプチド

Publications (2)

Publication Number Publication Date
JP2020518556A JP2020518556A (ja) 2020-06-25
JP2020518556A5 true JP2020518556A5 (enExample) 2021-06-17

Family

ID=58671461

Family Applications (3)

Application Number Title Priority Date Filing Date
JP2019555219A Pending JP2020518556A (ja) 2017-05-04 2018-05-04 糖尿病の処置のためのペプチド
JP2023051477A Ceased JP2023082076A (ja) 2017-05-04 2023-03-28 糖尿病の処置のためのペプチド
JP2025037548A Pending JP2025090703A (ja) 2017-05-04 2025-03-10 糖尿病の処置のためのペプチド

Family Applications After (2)

Application Number Title Priority Date Filing Date
JP2023051477A Ceased JP2023082076A (ja) 2017-05-04 2023-03-28 糖尿病の処置のためのペプチド
JP2025037548A Pending JP2025090703A (ja) 2017-05-04 2025-03-10 糖尿病の処置のためのペプチド

Country Status (17)

Country Link
US (2) US10815283B2 (enExample)
EP (1) EP3618845B1 (enExample)
JP (3) JP2020518556A (enExample)
KR (1) KR102700014B1 (enExample)
CN (1) CN110545834B (enExample)
AU (1) AU2018262805B2 (enExample)
BR (1) BR112019021886A2 (enExample)
CA (1) CA3061935A1 (enExample)
DK (1) DK3618845T3 (enExample)
EA (1) EA201992562A1 (enExample)
ES (1) ES2857749T3 (enExample)
IL (1) IL270199B2 (enExample)
MX (1) MX2019013096A (enExample)
PL (1) PL3618845T3 (enExample)
SG (1) SG11201908513RA (enExample)
WO (1) WO2018202870A1 (enExample)
ZA (1) ZA201905891B (enExample)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
SG11202104276YA (en) * 2018-11-07 2021-05-28 Follicum Ab Peptide fragments for treatment of diabetes
EP3958835B1 (en) * 2019-04-24 2023-05-24 Follicum AB Topical formulation
KR102816261B1 (ko) * 2022-03-24 2025-06-05 (주)케어젠 항당뇨 활성을 갖는 펩타이드 복합체 및 이의 용도
WO2023218095A1 (en) * 2022-05-13 2023-11-16 Coegin Pharma Ab Agents for stimulating tissue regeneration
KR20250010632A (ko) * 2022-05-13 2025-01-21 코에긴 파르마 아베 혈관신생 유도 제제

Family Cites Families (20)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1996008513A1 (en) * 1994-09-16 1996-03-21 The Scripps Research Institute Cytotactin derivatives that stimulate attachment and neurite outgrowth, and methods of making and using same
WO1999015904A1 (en) 1997-09-26 1999-04-01 University Of Washington Methods and compositions for diagnosing renal pathologies
US6551990B2 (en) 1998-12-07 2003-04-22 University Of Washington Methods of inhibiting ectopic calcification
AU4256901A (en) * 2000-03-23 2001-10-03 Glaxo Group Limited Method of screening for inhibitors of osteopontin
CA2411346A1 (en) 2000-06-13 2001-12-20 Children's Medical Center Corporation Biosynthetic oncolytic molecules and uses therefor
HRP20030840A2 (en) 2001-05-17 2005-08-31 Applied Research Systems Ars Holding N.V. Use of osteopontin for the treatment and/or prevention of neurologic diseases
AU2002312566A1 (en) 2001-07-09 2003-01-29 Elan Pharmaceuticals, Inc. Methods of inhibiting amyloid toxicity
US7205398B2 (en) 2002-05-24 2007-04-17 Schering-Plough Animal Health Corporation Eta-1 gene and methods for use
EP1637159A4 (en) * 2003-05-23 2009-01-21 Immuno Biological Lab Co Ltd IMMUNOCOMPETENT CELL ACTIVATION INHIBITOR AND USE THEREOF
WO2008086449A2 (en) 2007-01-09 2008-07-17 Oregon Health & Science University Synthetic osteopontin peptides and methods of use
JP2010520181A (ja) 2007-03-02 2010-06-10 ナショナル・ユニバーシティ・オブ・アイルランド・ゴルウェイ 心血管疾患の予測および治療のためのオステオポンチン
WO2008131094A1 (en) 2007-04-17 2008-10-30 Pfizer Inc. Method for controlling glucose uptake and insulin sensitivity
CN101293916A (zh) 2007-04-24 2008-10-29 上海国健生物技术研究院 骨桥蛋白的功能表位、与其特异性结合的单克隆抗体及用途
RU2010121967A (ru) * 2007-10-31 2011-12-10 Медиммун, Ллк (Us) Белковые каркасные структуры
CN101215324B (zh) * 2007-12-26 2010-11-24 吉林大学 艾塞那肽短肽模拟肽及其在制备糖尿病治疗药物中的应用
WO2011058182A1 (en) * 2009-11-13 2011-05-19 National University Of Ireland, Galway Osteopontin-conditioned medium for the treatment of vascular diseases
GB2493540A (en) * 2011-08-10 2013-02-13 Follicum Ab Agents for stimulating hair growth in mammals
EP2875134A1 (en) 2012-07-20 2015-05-27 Arla Foods amba Osteopontin peptide fragments for use in suppression or prevention of tumor growth
GB201406989D0 (en) * 2014-04-17 2014-06-04 Follicum Ab Novel treatments
CA3021994A1 (en) 2016-05-06 2017-11-09 Brett P. Monia Glp-1 receptor ligand moiety conjugated oligonucleotides and uses thereof

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