MA39211B1 - Composés tricycliques comme agents anti-cancers - Google Patents

Composés tricycliques comme agents anti-cancers

Info

Publication number
MA39211B1
MA39211B1 MA39211A MA39211A MA39211B1 MA 39211 B1 MA39211 B1 MA 39211B1 MA 39211 A MA39211 A MA 39211A MA 39211 A MA39211 A MA 39211A MA 39211 B1 MA39211 B1 MA 39211B1
Authority
MA
Morocco
Prior art keywords
tricyclic compounds
cancer agents
compounds
tricyclic
treatment
Prior art date
Application number
MA39211A
Other languages
English (en)
Other versions
MA39211A1 (fr
Inventor
Ashvinikumar V Gavai
George V Delucca
Daniel O'malley
Patrice Gill
Claude A Quesnelle
Francis Y Lee
John S Tokarski
Derek J Norris
Wayne Vaccaro
Mikkel V Debenedetto
Andrew P Degnan
Haiquan Fang
Matthew D Hill
Hong Huang
William D Schmitz
John E Starrett
Wen-Ching Han
Sunil Kumar Mandal
Original Assignee
Bristol Myers Squibb Co
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Bristol Myers Squibb Co filed Critical Bristol Myers Squibb Co
Publication of MA39211A1 publication Critical patent/MA39211A1/fr
Publication of MA39211B1 publication Critical patent/MA39211B1/fr

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
    • C07D471/04—Ortho-condensed systems
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/4353—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems
    • A61K31/437—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a five-membered ring having nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
    • A61K31/444—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a six-membered ring with nitrogen as a ring heteroatom, e.g. amrinone
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/50—Pyridazines; Hydrogenated pyridazines
    • A61K31/501—Pyridazines; Hydrogenated pyridazines not condensed and containing further heterocyclic rings
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/506—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
    • A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • A61P35/02—Antineoplastic agents specific for leukemia
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K2300/00—Mixtures or combinations of active ingredients, wherein at least one active ingredient is fully defined in groups A61K31/00 - A61K41/00

Abstract

La présente invention concerne des composés tricycliques (i), des compositions pharmaceutiquement acceptables contenant des composés de l'invention et des procédés d'utilisation desdites compositions dans le traitement de divers troubles.
MA39211A 2013-12-24 2014-12-23 Composés tricycliques comme agents anti-cancers MA39211B1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US201361920500P 2013-12-24 2013-12-24
PCT/US2014/072031 WO2015100282A1 (fr) 2013-12-24 2014-12-23 Composés tricycliques comme agents anti-cancers

Publications (2)

Publication Number Publication Date
MA39211A1 MA39211A1 (fr) 2018-08-31
MA39211B1 true MA39211B1 (fr) 2019-01-31

Family

ID=52293305

Family Applications (1)

Application Number Title Priority Date Filing Date
MA39211A MA39211B1 (fr) 2013-12-24 2014-12-23 Composés tricycliques comme agents anti-cancers

Country Status (33)

Country Link
US (1) US20160318928A1 (fr)
EP (2) EP3087071B1 (fr)
JP (2) JP6466456B2 (fr)
KR (1) KR102457145B1 (fr)
CN (2) CN108558871B (fr)
AR (2) AR099379A1 (fr)
AU (1) AU2014369982B2 (fr)
BR (1) BR112016013744B1 (fr)
CA (1) CA2934953C (fr)
CL (1) CL2016001629A1 (fr)
CY (2) CY1121076T1 (fr)
DK (2) DK3087071T3 (fr)
EA (2) EA201990240A1 (fr)
ES (2) ES2857848T3 (fr)
HR (2) HRP20181849T1 (fr)
HU (2) HUE054183T2 (fr)
IL (1) IL246359B (fr)
LT (2) LT3087071T (fr)
MA (1) MA39211B1 (fr)
MX (1) MX369491B (fr)
MY (1) MY176489A (fr)
NZ (1) NZ722326A (fr)
PE (1) PE20160844A1 (fr)
PH (1) PH12016500953A1 (fr)
PL (2) PL3466949T3 (fr)
PT (2) PT3087071T (fr)
RS (2) RS58014B1 (fr)
SG (1) SG11201605097SA (fr)
SI (2) SI3466949T1 (fr)
TN (1) TN2016000238A1 (fr)
TW (2) TWI726544B (fr)
UY (1) UY35916A (fr)
WO (1) WO2015100282A1 (fr)

Families Citing this family (27)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US10053454B2 (en) 2013-02-27 2018-08-21 Bristol-Myers Squibb Company Carbazole compounds useful as bromodomain inhibitors
US11446309B2 (en) 2013-11-08 2022-09-20 Dana-Farber Cancer Institute, Inc. Combination therapy for cancer using bromodomain and extra-terminal (BET) protein inhibitors
US9458156B2 (en) 2014-12-23 2016-10-04 Bristol-Myers Squibb Company Tricyclic compounds as anticancer agents
LT3087071T (lt) * 2013-12-24 2018-11-12 Bristol-Myers Squibb Company Tricikliniai junginiai kaip priešvėžiniai agentai
CN107074861A (zh) * 2014-02-28 2017-08-18 密执安大学评议会 作为bet溴结构域抑制剂的9h嘧啶并[4，5‑b]吲哚和相关类似物
EP3307740B1 (fr) 2015-05-12 2019-12-18 Bristol-Myers Squibb Company Composés 5h-pyrido[3,2-b]indole en tant qu'agents anticancéreux
US9725449B2 (en) 2015-05-12 2017-08-08 Bristol-Myers Squibb Company Tricyclic compounds as anticancer agents
EP3322448A4 (fr) * 2015-07-16 2019-03-06 Bioxcel Therapeutics, Inc. Nouvelle approche pour le traitement du cancer par immunomodulation
WO2017059319A2 (fr) * 2015-10-02 2017-04-06 Dana-Farber Cancer Institute, Inc. Polythérapie par inhibiteurs de bromodomaine et blocage de point de contrôle
WO2017124934A1 (fr) * 2016-01-20 2017-07-27 宁波文达医药科技有限公司 Dérivé de carboline contenant de la phosphine servant d'inhibiteur de bromodomaine
JP6855505B2 (ja) * 2016-01-20 2021-04-07 ニンボー ウェンダ ファーマー テクノロジー エルティーディー． ブロモドメイン阻害剤としてのカルボリン誘導体
EP3412669A4 (fr) * 2016-02-05 2019-09-04 Chia Tai Tianqing Pharmaceutical Group Co.,Ltd Composé tricyclique pour inhibiteur de protéine contenant un bromodomaine et préparation, composition pharmaceutique et son utilisation
BR112018067330A2 (pt) * 2016-03-01 2019-01-22 Corcept Therapeutics Inc método para o tratamento de paciente com carga tumoral
AU2017357329A1 (en) 2016-11-10 2019-06-13 Luoxin Pharmaceutical (Shanghai) Co., Ltd. Nitrogenous macrocyclic compound, preparation method therefor, pharmaceutical composition and application thereof
CN109824693B (zh) * 2017-04-18 2020-12-08 四川大学 Brd4抑制剂及其在肿瘤治疗药物中的应用
WO2019080941A1 (fr) * 2017-10-27 2019-05-02 Jacobio-Beta Pharmaceuticals Co., Ltd. Nouveaux composés tricycliques
MX2020014111A (es) * 2018-06-25 2021-06-15 Jacobio Pharmaceuticals Co Ltd Compuestos triciclicos.
CN108840868B (zh) * 2018-08-01 2019-10-18 上海山的实业有限公司 具有抗肿瘤活性的吲哚并吡啶酮类化合物的制备方法及应用
WO2020132046A1 (fr) 2018-12-19 2020-06-25 Corcept Therapeutics Incorporated Méthodes de traitement du cancer comprenant l'administration d'un modulateur du récepteur des glucocorticoïdes et d'un agent chimiothérapeutique anticancéreux
US11234971B2 (en) 2018-12-19 2022-02-01 Corcept Therapeutics Incorporated Methods of treating cancer comprising administration of a glucocorticoid receptor modulator and a cancer chemotherapy agent
WO2020200284A1 (fr) * 2019-04-04 2020-10-08 上海华汇拓医药科技有限公司 Procédé de préparation de composé tricyclique et son utilisation dans le domaine de la médecine
CN110003204B (zh) * 2019-04-30 2020-08-11 上海勋和医药科技有限公司 一种bet蛋白抑制剂、其制备方法及用途
US10947253B2 (en) 2019-08-05 2021-03-16 Ankh Life Sciences Limited Fused polycyclic dimers
EP4039333A4 (fr) 2019-09-30 2024-02-14 Kyowa Kirin Co Ltd Agent de dégradation de bet
AU2022211285A1 (en) * 2021-01-22 2023-08-17 Jingrui Biopharma Co., Ltd. Tricyclic compounds as anticancer agents
EP4297750A1 (fr) * 2021-02-25 2024-01-03 Impact Biomedicines, Inc. Utilisation d'un inhibiteur de bet seul ou en combinaison avec du fedratinib ou du ruxolitinib pour le traitement d'une malignité hématologique telle que la myélofibrose
AU2022270984A1 (en) * 2021-05-06 2023-11-23 Raziel Therapeutics Ltd. Crystalline carbazole derivative

Family Cites Families (49)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AU3427093A (en) * 1992-01-15 1993-08-03 E.I. Du Pont De Nemours And Company Bridged heterocyclic fungicides
JP2007509045A (ja) 2003-10-18 2007-04-12 バイエル・ヘルスケア・アクチェンゲゼルシャフト 尿失禁および関連疾患の処置用のｇａｂａアゴニストとしての５−置換２−（フェニルメチル）チオ−４−フェニル−４ｈ−１，２，４−トリアゾール誘導体および関連化合物
US20070269420A1 (en) * 2003-11-24 2007-11-22 Chunduru Srinivas K Compounds, Compositions and Methods for Treatment and Prophylaxis of Hepatitis C Viral Infections and Associated Diseases
TWI380996B (zh) 2004-09-17 2013-01-01 Hoffmann La Roche 抗ｏｘ４０ｌ抗體
EP1866339B8 (fr) 2005-03-25 2021-12-01 GITR, Inc. Molecules de liaison gitr et leurs utilisations
GB0507298D0 (en) 2005-04-11 2005-05-18 Novartis Ag Organic compounds
AU2006244068B9 (en) 2005-05-10 2012-10-25 Incyte Holdings Corporation Modulators of indoleamine 2,3-dioxygenase and methods of using the same
CN105330741B (zh) 2005-07-01 2023-01-31 E.R.施贵宝&圣斯有限责任公司 抗程序性死亡配体1(pd-l1)的人单克隆抗体
US8450351B2 (en) 2005-12-20 2013-05-28 Incyte Corporation N-hydroxyamidinoheterocycles as modulators of indoleamine 2,3-dioxygenase
US7696166B2 (en) 2006-03-28 2010-04-13 Albany Molecular Research, Inc. Use of cyclosporin alkyne/alkene analogues for preventing or treating viral-induced disorders
WO2008036642A2 (fr) 2006-09-19 2008-03-27 Incyte Corporation N-hydroxyamidinohétérocycles en tant que modulateurs d'indoléamine 2,3-dioxygénase
CL2007002650A1 (es) 2006-09-19 2008-02-08 Incyte Corp Compuestos derivados de heterociclo n-hidroxiamino; composicion farmaceutica, util para tratar cancer, infecciones virales y desordenes neurodegenerativos entre otras.
UY30892A1 (es) 2007-02-07 2008-09-02 Smithkline Beckman Corp Inhibidores de la actividad akt
EP1987839A1 (fr) 2007-04-30 2008-11-05 I.N.S.E.R.M. Institut National de la Sante et de la Recherche Medicale Anticorps monoclonal cytotoxique anti-LAG-3 et son utilisation pour le traitement ou la prévention d'un rejet de greffe d'organe et de maladies auto-immunes
ES2591281T3 (es) 2007-07-12 2016-11-25 Gitr, Inc. Terapias de combinación que emplean moléculas de enlazamiento a GITR
EP2044949A1 (fr) 2007-10-05 2009-04-08 Immutep Utilisation de lag-3 recombinant ou ses dérivatifs pour déclencher la réponse immune des monocytes
WO2009073620A2 (fr) 2007-11-30 2009-06-11 Newlink Genetics Inhibiteurs de l'ido
FR2927330B1 (fr) 2008-02-07 2010-02-19 Sanofi Aventis Derives de 5,6-bisaryl-2-pyridine-carboxamide, leur preparation et leur application en therapeutique comme antagonistes des recepteurs a l'urotensine ii
AR072999A1 (es) 2008-08-11 2010-10-06 Medarex Inc Anticuerpos humanos que se unen al gen 3 de activacion linfocitaria (lag-3) y los usos de estos
SI2376535T1 (sl) 2008-12-09 2017-07-31 F. Hoffmann-La Roche Ag Protitelesa anti-pd-l1 in njihova uporaba za izboljšanje funkcije celic t
WO2010080474A1 (fr) * 2008-12-19 2010-07-15 Bristol-Myers Squibb Company Carbazole et inhibiteurs de la carboline kinase
LT3023438T (lt) 2009-09-03 2020-05-11 Merck Sharp & Dohme Corp. Anti-gitr antikūnai
US8722720B2 (en) 2009-10-28 2014-05-13 Newlink Genetics Corporation Imidazole derivatives as IDO inhibitors
ES2722300T3 (es) 2009-12-10 2019-08-09 Hoffmann La Roche Anticuerpos que se unen preferentemente al dominio extracelular 4 de CSF1R y su uso
EA201201191A1 (ru) 2010-02-26 2013-04-30 Бёрингер Ингельхайм Интернациональ Гмбх 4-[циклоалкилокси(гетеро)ариламино]тиено[2,3-d]пиримидины, обладающие ингибирующей активностью по отношению к mnkl/mnk2, предназначенные для фармацевтических композиций
ME03447B (fr) 2010-03-04 2020-01-20 Macrogenics Inc Anticorps réagissant avec b7-h3, fragments immunologiquement actifs associés et utilisations associées
BR112012022046A2 (pt) 2010-03-05 2017-02-14 F Hoffamann-La Roche Ag ''anticorpo,composição farmacêutica,ácido nucleico ,vetores de expressão,célula hospedeira e método para a produção de um anticorpo recombinante''.
CA2789076C (fr) 2010-03-05 2017-11-21 F. Hoffmann-La Roche Ag Anticorps contre les colonies humaines stimulant le recepteur du facteur-1 et ses utilisations
TWI503323B (zh) * 2010-03-29 2015-10-11 Oncotherapy Science Inc 三環化合物以及含此化合物之ｐｂｋ抑制劑
US8206715B2 (en) 2010-05-04 2012-06-26 Five Prime Therapeutics, Inc. Antibodies that bind colony stimulating factor 1 receptor (CSF1R)
JP5860042B2 (ja) 2010-06-16 2016-02-16 ヴァイティー ファーマシューティカルズ，インコーポレイテッド 置換５、６及び７員複素環、そのような化合物を含有する医薬及びそれらの使用
KR101527300B1 (ko) 2010-09-09 2015-06-09 화이자 인코포레이티드 4-1ｂｂ 결합 분자
AR084312A1 (es) * 2010-12-16 2013-05-08 Genentech Inc Compuestos triciclicos inhibidores de la pi3k y composiciones farmaceuticas
US8580399B2 (en) * 2011-04-08 2013-11-12 Universal Display Corporation Substituted oligoazacarbazoles for light emitting diodes
NO2694640T3 (fr) 2011-04-15 2018-03-17
LT2699264T (lt) 2011-04-20 2018-07-10 Medimmune, Llc Antikūnai ir kitos molekulės, kurios jungiasi prie b7-h1 ir pd-1
WO2013046635A1 (fr) 2011-09-28 2013-04-04 出光興産株式会社 Substance pour élément électroluminescent organique, et élément électroluminescent organique produit en utilisant celle-ci
KR101981873B1 (ko) 2011-11-28 2019-05-23 메르크 파텐트 게엠베하 항-ｐｄ-ｌ1 항체 및 그의 용도
CN104159921B (zh) 2011-12-15 2018-05-04 霍夫曼-拉罗奇有限公司 针对人csf-1r的抗体及其用途
KR20140127855A (ko) 2012-02-06 2014-11-04 제넨테크, 인크. Csf1r 억제제를 사용하는 조성물 및 방법
AR090263A1 (es) 2012-03-08 2014-10-29 Hoffmann La Roche Terapia combinada de anticuerpos contra el csf-1r humano y las utilizaciones de la misma
EP2847220A1 (fr) 2012-05-11 2015-03-18 Five Prime Therapeutics, Inc. Méthodes destinées à traiter des affections avec des anticorps qui se lient au récepteur du facteur 1 de stimulation des colonies (csf1r)
AR091649A1 (es) 2012-07-02 2015-02-18 Bristol Myers Squibb Co Optimizacion de anticuerpos que se fijan al gen de activacion de linfocitos 3 (lag-3) y sus usos
AU2013308635A1 (en) 2012-08-31 2015-03-12 Five Prime Therapeutics, Inc. Methods of treating conditions with antibodies that bind colony stimulating factor 1 receptor (CSF1R)
UA115576C2 (uk) * 2012-12-06 2017-11-27 Байєр Фарма Акцієнгезелльшафт Похідні бензимідазолу як антагоністи ер4
US10053454B2 (en) * 2013-02-27 2018-08-21 Bristol-Myers Squibb Company Carbazole compounds useful as bromodomain inhibitors
US9492460B2 (en) * 2013-02-27 2016-11-15 Bristol-Myers Squibb Company Carbazole compounds useful as bromodomain inhibitors
EP2970312B1 (fr) * 2013-03-11 2017-11-15 The Regents of The University of Michigan Inhibiteurs de bromodomaines bet et méthodes thérapeutiques les utilisant
LT3087071T (lt) * 2013-12-24 2018-11-12 Bristol-Myers Squibb Company Tricikliniai junginiai kaip priešvėžiniai agentai

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HRP20210212T1 (hr) 2021-07-09
JP6675501B2 (ja) 2020-04-01
EP3087071B1 (fr) 2018-09-05
SI3087071T1 (sl) 2018-11-30
EP3466949B1 (fr) 2020-12-23
JP2019070014A (ja) 2019-05-09
CA2934953C (fr) 2022-09-20
CN106029663A (zh) 2016-10-12
EP3466949A1 (fr) 2019-04-10
KR20160095168A (ko) 2016-08-10
DK3087071T3 (da) 2019-01-02
PE20160844A1 (es) 2016-09-03
BR112016013744B1 (pt) 2022-08-30
HUE054183T2 (hu) 2021-08-30
MY176489A (en) 2020-08-12
EA201990240A1 (ru) 2019-06-28
AU2014369982A1 (en) 2016-08-04
MX369491B (es) 2019-11-11
HUE041719T2 (hu) 2019-05-28
RS58014B1 (sr) 2019-02-28
AR123996A2 (es) 2023-02-01
PT3466949T (pt) 2021-02-25
TW201609725A (zh) 2016-03-16
MX2016007928A (es) 2016-08-03
SG11201605097SA (en) 2016-07-28
RS61479B1 (sr) 2021-03-31
PH12016500953A1 (en) 2016-06-27
IL246359B (en) 2020-04-30
JP6466456B2 (ja) 2019-02-06
JP2017505762A (ja) 2017-02-23
TW202028203A (zh) 2020-08-01
CN108558871A (zh) 2018-09-21
ES2698998T3 (es) 2019-02-06
IL246359A0 (en) 2016-08-31
DK3466949T3 (da) 2021-03-15
TWI726544B (zh) 2021-05-01
CY1124061T1 (el) 2022-05-27
CY1121076T1 (el) 2019-12-11
HRP20181849T1 (hr) 2018-12-28
WO2015100282A1 (fr) 2015-07-02
EA201691070A1 (ru) 2016-11-30
EP3087071A1 (fr) 2016-11-02
ES2857848T3 (es) 2021-09-29
TWI736517B (zh) 2021-08-21
PL3087071T3 (pl) 2019-03-29
US20160318928A1 (en) 2016-11-03
CA2934953A1 (fr) 2015-07-02
CL2016001629A1 (es) 2017-02-17
BR112016013744A2 (fr) 2017-10-03
UY35916A (es) 2015-06-30
TN2016000238A1 (en) 2017-10-06
EA032469B1 (ru) 2019-05-31
NZ722326A (en) 2019-09-27
PT3087071T (pt) 2018-11-29
KR102457145B1 (ko) 2022-10-19
HRP20210212T8 (hr) 2021-08-20
LT3087071T (lt) 2018-11-12
MA39211A1 (fr) 2018-08-31
LT3466949T (lt) 2021-03-25
AR099379A1 (es) 2016-07-20
CN108558871B (zh) 2022-02-18
PL3466949T3 (pl) 2021-05-31
AU2014369982B2 (en) 2019-04-18
CN106029663B (zh) 2018-06-01
SI3466949T1 (sl) 2021-03-31

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