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MX2017003114A - Derivados de piridona como inhibidores de cinasa ret (reorganizado durante la transfeccion). - Google Patents

Derivados de piridona como inhibidores de cinasa ret (reorganizado durante la transfeccion).

Info

Publication number
MX2017003114A
MX2017003114A MX2017003114A MX2017003114A MX2017003114A MX 2017003114 A MX2017003114 A MX 2017003114A MX 2017003114 A MX2017003114 A MX 2017003114A MX 2017003114 A MX2017003114 A MX 2017003114A MX 2017003114 A MX2017003114 A MX 2017003114A
Authority
MX
Mexico
Prior art keywords
cancer
functional
ret
constipation
ret kinase
Prior art date
Application number
MX2017003114A
Other languages
English (en)
Other versions
MX373863B (es
Inventor
Michael P Demartino
Amy Guan Huiping
Original Assignee
Glaxosmithkline Ip Dev Ltd
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 Glaxosmithkline Ip Dev Ltd filed Critical Glaxosmithkline Ip Dev Ltd
Publication of MX2017003114A publication Critical patent/MX2017003114A/es
Publication of MX373863B publication Critical patent/MX373863B/es

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435Heterocyclic 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
    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/4427Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
    • A61K31/4439Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435Heterocyclic 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
    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/4412Non condensed pyridines; Hydrogenated derivatives thereof having oxo groups directly attached to the heterocyclic ring
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435Heterocyclic 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
    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/4418Non condensed pyridines; Hydrogenated derivatives thereof having a carbocyclic group directly attached to the heterocyclic ring, e.g. cyproheptadine
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00Drugs for disorders of the alimentary tract or the digestive system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/04Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D213/00Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
    • C07D213/02Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/60Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D213/62Oxygen or sulfur atoms
    • C07D213/69Two or more oxygen atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/12Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D413/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/02Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
    • C07D413/12Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Epidemiology (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Pain & Pain Management (AREA)
  • Rheumatology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Pyridine Compounds (AREA)

Abstract

Esta invención se refiere a nuevos compuestos que son inhibidores de la cinasa RET (reorganizado durante la transfección), a composiciones farmacéuticas que los contienen, a procedimientos para su preparación, y a su uso para tratamientos, en monoterapia o en politerapia, para la normalización de la sensibilidad, movilidad y/o secreción gastrointestinal y/o trastornos o enfermedades abdominales y/o el tratamiento relacionado con enfermedades relacionadas con la disfunción de RET o en donde la modulación de la actividad de RET puede tener un beneficio terapéutico, que incluye, pero sin limitarse a ellos, todas las clasificaciones del síndrome del colon irritable (SCI), entre ellas el patrón de deposiciones donde predominan las diarreas, donde predomina el estreñimiento o su alternancia, meteorismo funcional, estreñimiento funcional, diarrea funcional, colon irritable funcional inespecífico, síndrome del dolor abdominal funcional, estreñimiento idiopático crónico, trastornos esofágicos funcionales, trastornos gastroduodenales funcionales, dolor anorrectal funcional, enteropatía inflamatoria, enfermedades proliferativas tales como cáncer de pulmón no microcítico, carcinoma hepatocelular, cáncer colorrectal, cáncer tiroideo medular, cáncer tiroideo folicular, cáncer tiroideo anaplásico, cáncer tiroideo papilar, tumores encefálicos, cáncer de la cavidad peritoneal, tumores sólidos, otro cáncer de pulmón, cáncer de cabeza y cuello, gliomas, neuroblastomas, síndrome de Von Hippel-Lindau y tumores de riñón, cáncer de mama, cáncer de las trompas de Falopio, cáncer de ovario, cáncer de las células de transición, cáncer de próstata, cáncer de esófago y de la unión gastroesofágica, cáncer biliar y adenocarcinoma, y cualquier neoplasia maligna con incremento de la actividad de la cinasa RET.
MX2017003114A 2014-09-10 2015-09-09 Derivados de piridona como inhibidores de cinasa ret (reorganizado durante la transfección). MX373863B (es)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
CN2014086197 2014-09-10
CN2015086995 2015-08-14
PCT/IB2015/056905 WO2016038552A1 (en) 2014-09-10 2015-09-09 Pyridone derivatives as rearranged during transfection (ret) kinase inhibitors

Publications (2)

Publication Number Publication Date
MX2017003114A true MX2017003114A (es) 2017-11-15
MX373863B MX373863B (es) 2020-03-26

Family

ID=54186249

Family Applications (1)

Application Number Title Priority Date Filing Date
MX2017003114A MX373863B (es) 2014-09-10 2015-09-09 Derivados de piridona como inhibidores de cinasa ret (reorganizado durante la transfección).

Country Status (36)

Country Link
US (4) US9918974B2 (es)
EP (2) EP3191450B1 (es)
JP (2) JP6538154B2 (es)
KR (1) KR20170045350A (es)
CN (1) CN107074768B (es)
AU (1) AU2015313841B2 (es)
BR (1) BR112017004900A2 (es)
CA (1) CA2960768A1 (es)
CL (1) CL2017000588A1 (es)
CO (1) CO2017002273A2 (es)
CR (1) CR20170093A (es)
CY (1) CY1121661T1 (es)
DK (1) DK3191450T3 (es)
DO (1) DOP2017000059A (es)
EA (1) EA033544B1 (es)
ES (2) ES2816453T3 (es)
HR (1) HRP20190815T1 (es)
HU (1) HUE044604T2 (es)
IL (1) IL250908B (es)
LT (1) LT3191450T (es)
MA (1) MA40581A (es)
ME (1) ME03432B (es)
MX (1) MX373863B (es)
MY (1) MY181913A (es)
PE (1) PE20170705A1 (es)
PH (1) PH12017500425A1 (es)
PL (1) PL3191450T3 (es)
PT (1) PT3191450T (es)
RS (1) RS58813B1 (es)
SG (1) SG11201701694QA (es)
SI (1) SI3191450T1 (es)
SM (1) SMT201900304T1 (es)
TW (1) TWI683807B (es)
UA (1) UA122213C2 (es)
UY (1) UY36293A (es)
WO (1) WO2016038552A1 (es)

Families Citing this family (25)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
ES2628418T3 (es) 2010-05-20 2017-08-02 Array Biopharma, Inc. Compuestos macrocíclicos como inhibidores de la TRK cinasa
SG11201701694QA (en) 2014-09-10 2017-04-27 Glaxosmithkline Ip Dev Ltd Pyridone derivatives as rearranged during transfection (ret) kinase inhibitors
DK3191449T3 (da) * 2014-09-10 2020-08-03 Glaxosmithkline Ip Dev Ltd Forbindelser som ret- (rearranged during transfection) hæmmere
WO2016127074A1 (en) 2015-02-06 2016-08-11 Blueprint Medicines Corporation 2-(pyridin-3-yl)-pyrimidine derivatives as ret inhibitors
WO2017011776A1 (en) 2015-07-16 2017-01-19 Array Biopharma, Inc. Substituted pyrazolo[1,5-a]pyridine compounds as ret kinase inhibitors
WO2017079140A1 (en) 2015-11-02 2017-05-11 Blueprint Medicines Corporation Inhibitors of ret
UY37155A (es) 2016-03-17 2017-10-31 Blueprint Medicines Corp Inhibidores de ret
WO2018017983A1 (en) 2016-07-22 2018-01-25 Blueprint Medicines Corporation Compounds useful for treating disorders related to ret
JP2018052878A (ja) * 2016-09-29 2018-04-05 第一三共株式会社 ピリジン化合物
TWI704148B (zh) 2016-10-10 2020-09-11 美商亞雷生物製藥股份有限公司 作為ret激酶抑制劑之經取代吡唑并[1,5-a]吡啶化合物
JOP20190077A1 (ar) 2016-10-10 2019-04-09 Array Biopharma Inc مركبات بيرازولو [1، 5-a]بيريدين بها استبدال كمثبطات كيناز ret
EP3571203B1 (en) 2017-01-18 2023-06-07 Array BioPharma Inc. Substituted pyrazolo[1,5-a]pyrazine compounds as ret kinase inhibitors
WO2018136663A1 (en) 2017-01-18 2018-07-26 Array Biopharma, Inc. Ret inhibitors
JOP20190213A1 (ar) 2017-03-16 2019-09-16 Array Biopharma Inc مركبات حلقية ضخمة كمثبطات لكيناز ros1
JP2020519672A (ja) 2017-05-15 2020-07-02 ブループリント メディシンズ コーポレイション RET阻害剤とmTORC1阻害剤との組合せ及び異常なRET活性によって媒介されるがんを処置するためのその使用
TWI876442B (zh) 2017-10-10 2025-03-11 美商絡速藥業公司 6-(2-羥基-2-甲基丙氧基)-4-(6-(6-((6-甲氧基吡啶-3-基)甲基)-3,6-二氮雜雙環[3.1.1]庚-3-基)吡啶-3-基)吡唑并[1,5-a]吡啶-3-甲腈之調配物
TWI791053B (zh) 2017-10-10 2023-02-01 美商亞雷生物製藥股份有限公司 6-(2-羥基-2-甲基丙氧基)-4-(6-(6-((6-甲氧基吡啶-3-基)甲基)-3,6-二氮雜雙環[3.1.1]庚-3-基)吡啶-3-基)吡唑并[1,5-a]吡啶-3-甲腈之結晶形式及其醫藥組合物
WO2019143994A1 (en) 2018-01-18 2019-07-25 Array Biopharma Inc. Substituted pyrazolyl[4,3-c]pyridinecompounds as ret kinase inhibitors
EP3740490A1 (en) 2018-01-18 2020-11-25 Array Biopharma, Inc. Substituted pyrazolo[3,4-d]pyrimidine compounds as ret kinase inhibitors
WO2019143977A1 (en) 2018-01-18 2019-07-25 Array Biopharma Inc. Substituted pyrrolo[2,3-d]pyrimidines compounds as ret kinase inhibitors
MX2020010417A (es) 2018-04-03 2021-01-08 Blueprint Medicines Corp Inhibidor de ret para uso en tratar cancer que tiene una alteracion de ret.
EP3849986B1 (en) 2018-09-10 2022-06-08 Array Biopharma, Inc. Fused heterocyclic compounds as ret kinase inhibitors
MX2022014858A (es) 2020-05-29 2023-02-23 Blueprint Medicines Corp Formas solidas de pralsetinib.
CN115803316B (zh) * 2020-07-23 2024-12-06 深圳晶泰科技有限公司 吡啶酮类化合物及其制备方法和应用
AU2023329563A1 (en) 2022-08-24 2025-02-27 Toray Industries, Inc. Medicament for treatment and/or prevention of cancer

Family Cites Families (26)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20070244120A1 (en) 2000-08-18 2007-10-18 Jacques Dumas Inhibition of raf kinase using substituted heterocyclic ureas
US20120046290A1 (en) 1997-12-22 2012-02-23 Jacques Dumas Inhibition of p38 kinase activity using substituted heterocyclic ureas
EP1041982B1 (en) 1997-12-22 2011-10-19 Bayer HealthCare LLC INHIBITION OF p38 KINASE ACTIVITY USING SUBSTITUTED HETEROCYCLIC UREAS
IL136767A0 (en) 1997-12-22 2001-06-14 Bayer Ag Inhibition of raf kinase using substituted heterocyclic ureas
EA005373B1 (ru) 1999-08-12 2005-02-24 Фармация Италия С.П.А. Производные 3(5)-аминопиразола, способ их получения и их применение в качестве противоопухолевых средств
AU2002215053A1 (en) * 2000-11-27 2002-06-24 Pharmacia Italia S.P.A. Phenylacetamido- pyrazole derivatives and their use as antitumor agents
DE10201764A1 (de) 2002-01-18 2003-07-31 Bayer Cropscience Ag Substituierte 4-Aminopyridin-Derivate
PE20040522A1 (es) 2002-05-29 2004-09-28 Novartis Ag Derivados de diarilurea dependientes de la cinasa de proteina
WO2004024694A1 (ja) 2002-09-10 2004-03-25 Kyorin Pharmaceutical Co., Ltd. 4-置換アリール-5-ヒドロキシイソキノリノン誘導体
CN1838958A (zh) 2003-08-22 2006-09-27 贝林格尔·英格海姆药物公司 治疗慢性阻塞性肺病和肺动脉高血压的方法
TW200530236A (en) * 2004-02-23 2005-09-16 Chugai Pharmaceutical Co Ltd Heteroaryl phenylurea
EP1836169B9 (en) * 2004-12-28 2012-07-04 Kinex Pharmaceuticals, LLC Compositions and methods of treating cell proliferation disorders
US7968574B2 (en) 2004-12-28 2011-06-28 Kinex Pharmaceuticals, Llc Biaryl compositions and methods for modulating a kinase cascade
GB0507575D0 (en) * 2005-04-14 2005-05-18 Novartis Ag Organic compounds
US8247556B2 (en) * 2005-10-21 2012-08-21 Amgen Inc. Method for preparing 6-substituted-7-aza-indoles
TW200804349A (en) * 2005-12-23 2008-01-16 Kalypsys Inc Novel substituted pyrimidinyloxy ureas as inhibitors of protein kinases
WO2008002676A2 (en) 2006-06-29 2008-01-03 Kinex Pharmaceuticals, Llc Biaryl compositions and methods for modulating a kinase cascade
WO2008033562A2 (en) * 2006-09-15 2008-03-20 Xcovery, Inc. Kinase inhibitor compounds
KR20090064602A (ko) * 2006-10-16 2009-06-19 노파르티스 아게 단백질 키나제 억제제로서 유용한 페닐아세트아미드
US8461161B2 (en) * 2006-11-15 2013-06-11 Ym Biosciences Australia Pty Ltd Substituted pyrazines as inhibitors of kinase activity
EP2467137A1 (en) 2009-08-19 2012-06-27 Ambit Biosciences Corporation Biaryl compounds and methods of use thereof
JP6097998B2 (ja) 2010-12-16 2017-03-22 ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング ロイコトリエン生成のビアリールアミドインヒビター
PE20151538A1 (es) 2013-03-15 2015-11-18 Glaxosmithkline Ip Dev Ltd Nuevos compuestos como inhibidores de reorganizado durante la transfeccion (ret)
MA38394B1 (fr) 2013-03-15 2018-04-30 Glaxosmithkline Ip Dev Ltd Dérivés pyridine utilisés comme inhibiteurs de la kinase réarrangée au cours de la transfection (ret)
DK3191449T3 (da) 2014-09-10 2020-08-03 Glaxosmithkline Ip Dev Ltd Forbindelser som ret- (rearranged during transfection) hæmmere
SG11201701694QA (en) * 2014-09-10 2017-04-27 Glaxosmithkline Ip Dev Ltd Pyridone derivatives as rearranged during transfection (ret) kinase inhibitors

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SMT201900304T1 (it) 2019-07-11
US20170340617A1 (en) 2017-11-30
IL250908A0 (en) 2017-04-30
EP3517526A1 (en) 2019-07-31
MY181913A (en) 2021-01-14
CR20170093A (es) 2017-07-17
RS58813B1 (sr) 2019-07-31
KR20170045350A (ko) 2017-04-26
MX373863B (es) 2020-03-26
US10709695B2 (en) 2020-07-14
TW201625534A (en) 2016-07-16
UY36293A (es) 2016-04-01
HUE044604T2 (hu) 2019-11-28
CO2017002273A2 (es) 2017-06-20
LT3191450T (lt) 2019-06-10
CN107074768B (zh) 2019-12-10
EA033544B1 (ru) 2019-10-31
JP6538154B2 (ja) 2019-07-03
PE20170705A1 (es) 2017-05-21
BR112017004900A2 (pt) 2017-12-12
US20190022078A1 (en) 2019-01-24
TWI683807B (zh) 2020-02-01
AU2015313841A1 (en) 2017-03-23
PH12017500425B1 (en) 2017-07-31
US20180147194A1 (en) 2018-05-31
JP2019163316A (ja) 2019-09-26
CA2960768A1 (en) 2016-03-17
PL3191450T3 (pl) 2019-08-30
EP3191450A1 (en) 2017-07-19
ES2816453T3 (es) 2021-04-05
MA40581A (fr) 2019-04-10
SG11201701694QA (en) 2017-04-27
US20190247382A1 (en) 2019-08-15
WO2016038552A1 (en) 2016-03-17
DOP2017000059A (es) 2017-03-31
AU2015313841B2 (en) 2018-03-08
EA201790546A1 (ru) 2017-07-31
SI3191450T1 (sl) 2019-07-31
CY1121661T1 (el) 2020-07-31
EP3191450B1 (en) 2019-04-10
DK3191450T3 (da) 2019-05-20
JP6728447B2 (ja) 2020-07-22
PH12017500425A1 (en) 2017-07-31
CN107074768A (zh) 2017-08-18
CL2017000588A1 (es) 2017-10-06
UA122213C2 (uk) 2020-10-12
US10292975B2 (en) 2019-05-21
ES2725704T3 (es) 2019-09-26
US10111866B2 (en) 2018-10-30
US9918974B2 (en) 2018-03-20
JP2017527578A (ja) 2017-09-21
PT3191450T (pt) 2019-05-29
HRP20190815T1 (hr) 2019-07-12
ME03432B (me) 2020-01-20
EP3517526B1 (en) 2020-08-19
IL250908B (en) 2020-11-30

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