JP2018513142A5 - - Google Patents

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Publication number
JP2018513142A5
JP2018513142A5 JP2017551201A JP2017551201A JP2018513142A5 JP 2018513142 A5 JP2018513142 A5 JP 2018513142A5 JP 2017551201 A JP2017551201 A JP 2017551201A JP 2017551201 A JP2017551201 A JP 2017551201A JP 2018513142 A5 JP2018513142 A5 JP 2018513142A5
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JP
Japan
Prior art keywords
composition
composition according
subject
cancer
cage structure
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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.)
Pending
Application number
JP2017551201A
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English (en)
Japanese (ja)
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JP2018513142A (ja
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Publication date
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Priority claimed from PCT/US2016/025290 external-priority patent/WO2016161129A1/en
Publication of JP2018513142A publication Critical patent/JP2018513142A/ja
Publication of JP2018513142A5 publication Critical patent/JP2018513142A5/ja
Priority to JP2021062630A priority Critical patent/JP2021113196A/ja
Pending legal-status Critical Current

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JP2017551201A 2015-03-31 2016-03-31 標的型薬物デリバリーのための自己集合性分子 Pending JP2018513142A (ja)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2021062630A JP2021113196A (ja) 2015-03-31 2021-04-01 標的型薬物デリバリーのための自己集合性分子

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US201562140696P 2015-03-31 2015-03-31
US62/140,696 2015-03-31
PCT/US2016/025290 WO2016161129A1 (en) 2015-03-31 2016-03-31 Self assembling molecules for targeted drug delivery

Related Child Applications (1)

Application Number Title Priority Date Filing Date
JP2021062630A Division JP2021113196A (ja) 2015-03-31 2021-04-01 標的型薬物デリバリーのための自己集合性分子

Publications (2)

Publication Number Publication Date
JP2018513142A JP2018513142A (ja) 2018-05-24
JP2018513142A5 true JP2018513142A5 (https=) 2019-05-09

Family

ID=57007332

Family Applications (2)

Application Number Title Priority Date Filing Date
JP2017551201A Pending JP2018513142A (ja) 2015-03-31 2016-03-31 標的型薬物デリバリーのための自己集合性分子
JP2021062630A Pending JP2021113196A (ja) 2015-03-31 2021-04-01 標的型薬物デリバリーのための自己集合性分子

Family Applications After (1)

Application Number Title Priority Date Filing Date
JP2021062630A Pending JP2021113196A (ja) 2015-03-31 2021-04-01 標的型薬物デリバリーのための自己集合性分子

Country Status (10)

Country Link
US (2) US20180140719A1 (https=)
EP (2) EP3277268A4 (https=)
JP (2) JP2018513142A (https=)
CN (1) CN107613963A (https=)
AU (1) AU2016242920B2 (https=)
CA (1) CA2980329C (https=)
HK (1) HK1248540A1 (https=)
MA (1) MA41866A (https=)
MX (2) MX394468B (https=)
WO (1) WO2016161129A1 (https=)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
MA41866A (fr) * 2015-03-31 2018-02-06 Massachusetts Gen Hospital Molécules à auto-assemblage pour l'administration ciblée de médicaments
US20200338011A1 (en) * 2017-10-20 2020-10-29 The General Hospital Corporation Macrophage Targeted Immunotherapeutics
WO2021154709A1 (en) * 2020-01-28 2021-08-05 Nanotomer, Inc. Clathrin-chimeric antibody receptor constructs for immune cell activation therapy in vivo
WO2021160873A1 (en) * 2020-02-13 2021-08-19 Eth Zurich Nanoparticles encapsulating small molecules
CN112229887B (zh) * 2020-09-02 2022-07-22 中国科学院深圳先进技术研究院 一种可精准编辑酶/电极界面及其制备方法

Family Cites Families (40)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5679683A (en) 1994-01-25 1997-10-21 Warner-Lambert Company Tricyclic compounds capable of inhibiting tyrosine kinases of the epidermal growth factor receptor family
US5525625A (en) 1995-01-24 1996-06-11 Warner-Lambert Company 2-(2-Amino-3-methoxyphenyl)-4-oxo-4H-[1]benzopyran for treating proliferative disorders
WO1998037881A1 (en) 1997-02-28 1998-09-03 Warner Lambert Company Method of treating or preventing septic shock by administering a mek inhibitor
UA73073C2 (uk) 1997-04-03 2005-06-15 Уайт Холдінгз Корпорейшн Заміщені 3-ціанохіноліни, спосіб їх одержання та фармацевтична композиція
CA2290509A1 (en) 1997-07-01 1999-01-14 Warner-Lambert Company 2-(4-bromo or 4-iodo phenylamino) benzoic acid derivatives and their use as mek inhibitors
NZ501276A (en) 1997-07-01 2000-10-27 Warner Lambert Co 4-bromo or 4-iodo phenylamino benzhydroxamic acid derivatives and their use as MEK inhibitors in treating proliferative disorders
CA2349832A1 (en) 1999-01-13 2000-07-20 Warner-Lambert Company Benzenesulfonamide derivatives and their use as mek inhibitors
HUP0105092A3 (en) 1999-01-13 2003-12-29 Warner Lambert Co 1-heterocycle substituted diarylamines and medicaments containing them
EP1144372B1 (en) 1999-01-13 2005-11-30 Warner-Lambert Company Llc Sulphohydroxamic acids and sulphohydroxamates and their use as mek inhibitors
CA2355470C (en) 1999-01-13 2008-09-30 Warner-Lambert Company Benzoheterocycles and their use as mek inhibitors
CA2348236A1 (en) 1999-01-13 2000-07-20 Stephen Douglas Barrett 4-arylamino, 4-aryloxy, and 4-arylthio diarylamines and derivatives thereof as selective mek inhibitors
EP1150950A2 (en) 1999-01-13 2001-11-07 Warner-Lambert Company Anthranilic acid derivatives
GB9910577D0 (en) 1999-05-08 1999-07-07 Zeneca Ltd Chemical compounds
GB9910579D0 (en) 1999-05-08 1999-07-07 Zeneca Ltd Chemical compounds
EP1339702A1 (en) 2000-03-15 2003-09-03 Warner-Lambert Company 5-amide substituted diarylamines as mek inhibitors
BR0109188A (pt) 2000-03-15 2003-03-18 Warner Lambert Co Diarilaminas 5-amida substituìdas como inibidores de mex
DZ3401A1 (fr) 2000-07-19 2002-01-24 Warner Lambert Co Esters oxygenes d'acides 4-iodophenylamino benzhydroxamiques
ATE335737T1 (de) 2000-09-15 2006-09-15 Vertex Pharma Isoxazole und ihre verwendung als erk-inhibitoren
US20030049203A1 (en) * 2001-08-31 2003-03-13 Elmaleh David R. Targeted nucleic acid constructs and uses related thereto
SG2013013339A (en) 2002-03-13 2014-12-30 Array Biopharma Inc N3 alkylated benzimidazole derivatives as mek inhibitors
US7144907B2 (en) 2003-09-03 2006-12-05 Array Biopharma Inc. Heterocyclic inhibitors of MEK and methods of use thereof
US7732616B2 (en) 2003-11-19 2010-06-08 Array Biopharma Inc. Dihydropyridine and dihydropyridazine derivatives as inhibitors of MEK and methods of use thereof
CA2546353A1 (en) 2003-11-19 2005-06-09 Array Biopharma Inc. Bicyclic inhibitors of mek and methods of use thereof
US7393924B2 (en) * 2004-01-06 2008-07-01 Franco Vitaliano Smart bio-nanoparticle elements
US7429667B2 (en) 2005-01-20 2008-09-30 Ardea Biosciences, Inc. Phenylamino isothiazole carboxamidines as MEK inhibitors
RU2494107C2 (ru) * 2005-05-09 2013-09-27 Оно Фармасьютикал Ко., Лтд. Моноклональные антитела человека к белку программируемой смерти 1 (pd-1) и способы лечения рака с использованием анти-pd-1-антител самостоятельно или в комбинации с другими иммунотерапевтическими средствами
SG177981A1 (en) 2005-05-18 2012-02-28 Array Biopharma Inc 4-(phenylamino)-6-oxo-1, 6-dihydropyridazine-3-carboxamide derivatives as mek inhibitors for the treatment of hyperproliferative diseases
US8101799B2 (en) 2005-07-21 2012-01-24 Ardea Biosciences Derivatives of N-(arylamino) sulfonamides as inhibitors of MEK
WO2007025090A2 (en) 2005-08-25 2007-03-01 Kalypsys, Inc. Heterobicyclic and - tricyclic inhibitors of mapk/erk kinase
DE102005062440B4 (de) * 2005-12-27 2011-02-24 Lts Lohmann Therapie-Systeme Ag Proteinbasiertes Trägersystem zur Resistenzüberwindung von Tumorzellen
EP2069308B1 (en) 2006-09-12 2017-03-29 Government of the United States of America, Represented by the Secretary, Department of Health and Human Services Azonafide derived tumor and cancer targeting compounds
MX2009007661A (es) 2007-01-19 2009-12-14 Ardea Biosciences Inc Inhibidores de mek.
WO2008103920A2 (en) * 2007-02-23 2008-08-28 Specigen, Inc. Targeted protein cages
AU2008343065B2 (en) 2007-12-19 2012-04-05 Genentech, Inc. 5-anilinoimidazopyridines and methods of use
US11235062B2 (en) * 2009-03-06 2022-02-01 Metaqor Llc Dynamic bio-nanoparticle elements
CA2779843A1 (en) 2009-11-13 2011-05-19 Infinity Pharmaceuticals, Inc. Compositions, kits, and methods for identification, assessment, prevention, and therapy of cancer
WO2014141289A1 (en) * 2013-03-12 2014-09-18 Amrita Vishwa Vidyapeetham University Photo - chemo composition on the basis of microcapsules with a core -shell structure
WO2015108783A1 (en) 2014-01-16 2015-07-23 The Brigham And Women's Hospital, Inc. Targeted delivery of immunoregulatory drugs
TWI595006B (zh) * 2014-12-09 2017-08-11 禮納特神經系統科學公司 抗pd-1抗體類和使用彼等之方法
MA41866A (fr) 2015-03-31 2018-02-06 Massachusetts Gen Hospital Molécules à auto-assemblage pour l'administration ciblée de médicaments

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