IN2014MN02497A - - Google Patents
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- Publication number
- IN2014MN02497A IN2014MN02497A IN2497MUN2014A IN2014MN02497A IN 2014MN02497 A IN2014MN02497 A IN 2014MN02497A IN 2497MUN2014 A IN2497MUN2014 A IN 2497MUN2014A IN 2014MN02497 A IN2014MN02497 A IN 2014MN02497A
- Authority
- IN
- India
- Prior art keywords
- acceptable salt
- pharmacologically acceptable
- inhibitory action
- kinase enzyme
- compound
- Prior art date
Links
- 150000001875 compounds Chemical class 0.000 abstract 3
- 230000002401 inhibitory effect Effects 0.000 abstract 2
- 150000003839 salts Chemical class 0.000 abstract 2
- 101000686031 Homo sapiens Proto-oncogene tyrosine-protein kinase ROS Proteins 0.000 abstract 1
- 206010028980 Neoplasm Diseases 0.000 abstract 1
- 108091000080 Phosphotransferase Proteins 0.000 abstract 1
- 102100023347 Proto-oncogene tyrosine-protein kinase ROS Human genes 0.000 abstract 1
- 230000000694 effects Effects 0.000 abstract 1
- UTCSSFWDNNEEBH-UHFFFAOYSA-N imidazo[1,2-a]pyridine Chemical compound C1=CC=CC2=NC=CN21 UTCSSFWDNNEEBH-UHFFFAOYSA-N 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- 102000020233 phosphotransferase Human genes 0.000 abstract 1
- PBMFSQRYOILNGV-UHFFFAOYSA-N pyridazine Chemical group C1=CC=NN=C1 PBMFSQRYOILNGV-UHFFFAOYSA-N 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
-
- 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
- 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
- A61K31/5025—Pyridazines; Hydrogenated pyridazines ortho- or peri-condensed with heterocyclic ring systems
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Veterinary Medicine (AREA)
- Pharmacology & Pharmacy (AREA)
- Public Health (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Hematology (AREA)
- Oncology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Abstract
The present invention provides a compound useful in treating tumors by ROS1 kinase enzyme activity inhibitory action and NTRK kinase enzyme inhibitory action or a pharmacologically acceptable salt thereof. A compound having an imidazo[1 2 b]pyridazine structure represented by general formula (I) a pharmacologically acceptable salt thereof or pharmaceutical compositions comprising such compounds. (In the formula R G T Y Y Y and Y are as defined in the present description.)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2012127079 | 2012-06-04 | ||
| PCT/JP2013/065328 WO2013183578A1 (en) | 2012-06-04 | 2013-06-03 | IMIDAZO[1,2-b]PYRIDAZINE DERIVATIVE AS KINASE INHIBITOR |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| IN2014MN02497A true IN2014MN02497A (en) | 2015-07-17 |
Family
ID=49711970
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| IN2497MUN2014 IN2014MN02497A (en) | 2012-06-04 | 2013-06-03 |
Country Status (32)
| Country | Link |
|---|---|
| US (2) | US9187489B2 (en) |
| EP (1) | EP2857404B1 (en) |
| JP (1) | JP5814467B2 (en) |
| KR (1) | KR101781255B1 (en) |
| CN (1) | CN104520300B (en) |
| AU (1) | AU2013272701B2 (en) |
| BR (1) | BR112014029851B1 (en) |
| CA (1) | CA2874819C (en) |
| CO (1) | CO7160119A2 (en) |
| CY (1) | CY1119607T1 (en) |
| DK (1) | DK2857404T3 (en) |
| ES (1) | ES2648228T3 (en) |
| HR (1) | HRP20171724T1 (en) |
| HU (1) | HUE037221T2 (en) |
| IL (1) | IL236075A (en) |
| IN (1) | IN2014MN02497A (en) |
| LT (1) | LT2857404T (en) |
| MX (1) | MX357021B (en) |
| MY (1) | MY170326A (en) |
| NO (1) | NO2857404T3 (en) |
| NZ (1) | NZ702574A (en) |
| PH (1) | PH12014502721A1 (en) |
| PL (1) | PL2857404T3 (en) |
| PT (1) | PT2857404T (en) |
| RS (1) | RS56625B1 (en) |
| RU (1) | RU2635917C2 (en) |
| SG (1) | SG11201408052WA (en) |
| SI (1) | SI2857404T1 (en) |
| SM (1) | SMT201700539T1 (en) |
| TW (1) | TWI585088B (en) |
| WO (1) | WO2013183578A1 (en) |
| ZA (1) | ZA201408843B (en) |
Families Citing this family (57)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| SI2350075T1 (en) | 2008-09-22 | 2014-06-30 | Array Biopharma, Inc. | Substituted imidazoš1,2bćpyridazine compounds as trk kinase inhibitors |
| CN102264736B (en) | 2008-10-22 | 2013-08-14 | 阵列生物制药公司 | Substituted pyrazolo[1,5-a]pyrimidine compounds as TRK kinase inhibitors |
| AR077468A1 (en) | 2009-07-09 | 2011-08-31 | Array Biopharma Inc | PIRAZOLO COMPOUNDS (1,5-A) PYRIMIDINE SUBSTITUTED AS TRK-QUINASA INHIBITORS |
| BR122019024201B1 (en) | 2010-05-20 | 2021-08-03 | Array Biopharma Inc | MACROCYCLIC COMPOUND AS TRK KINASE INHIBITORS, ITS USE, AND PHARMACEUTICAL COMPOSITION |
| WO2013180183A1 (en) | 2012-05-30 | 2013-12-05 | 日本新薬株式会社 | Aromatic heterocyclic derivative and pharmaceutical |
| US10342795B2 (en) * | 2014-03-27 | 2019-07-09 | Janssen Pharmaceutica Nv | Substituted 4,5,6,7-tetrahydro-pyrazolo[1,5-a]pyrimidine derivatives and 2,3-dihydro-1H-imidazo[1,2-b]pyrazole derivatives as ROS1 inhibitors |
| EP3129376B1 (en) * | 2014-03-27 | 2018-12-26 | Janssen Pharmaceutica NV | Substituted 4,5,6,7-tetrahydro-pyrazolo[1,5-a]pyrazine derivatives and 5,6,7,8-tetrahydro-4h-pyrazolo[1,5-a][1,4]diazepine derivatives as ros1 inhibitors |
| JP6696908B2 (en) * | 2014-04-25 | 2020-05-20 | エグゼリクシス， インコーポレイテッド | How to treat lung adenocarcinoma |
| TWI746426B (en) | 2014-11-16 | 2021-11-21 | 美商亞雷生物製藥股份有限公司 | Crystalline form of (s)-n-(5-((r)-2-(2,5-difluorophenyl)-pyrrolidin-1-yl)-pyrazolo[1,5-a]pyrimidin-3-yl)-3-hydroxypyrrolidine-1-carboxamide hydrogen sulfate |
| HK1253093A1 (en) | 2015-06-01 | 2019-06-06 | Loxo Oncology Inc. | Methods of diagnosing and treating cancer |
| EP3310773B1 (en) | 2015-06-18 | 2020-12-02 | 89Bio Ltd. | Substituted 4-benzyl and 4-benzoyl piperidine derivatives |
| PE20180572A1 (en) | 2015-06-18 | 2018-04-04 | Cephalon Inc | 1,4-SUBSTITUTED PIPERIDINE DERIVATIVES |
| CA2992586A1 (en) | 2015-07-16 | 2017-01-19 | Array Biopharma, Inc. | Substituted pyrazolo[1,5-a]pyridine compounds as ret kinase inhibitors |
| EP3368039A1 (en) | 2015-10-26 | 2018-09-05 | The Regents of The University of Colorado, A Body Corporate | Point mutations in trk inhibitor-resistant cancer and methods relating to the same |
| CN106854174A (en) * | 2015-12-08 | 2017-06-16 | 湖南华腾制药有限公司 | A kind of preparation method of 4 substituted piperidine derivatives |
| UA125025C2 (en) | 2016-04-04 | 2021-12-29 | Локсо Онколоджі, Інк. | Methods of treating pediatric cancers |
| UA125026C2 (en) | 2016-04-04 | 2021-12-29 | Локсо Онколоджі, Інк. | Liquid formulations of (s)-n-(5-(r)-2-(2,5-difluorophenyl)-pyrrolidin-1-yl)-pyrazolo[1,5-a]pyrimidin-3-yl)-3-hydroxypyrrolidine-1-carboxamide |
| MX392604B (en) | 2016-05-18 | 2025-03-24 | Array Biopharma Inc | Preparation of (s)-n-(5-((r)-2-(2,5-difluorophenyl)pyrrolidin-1-yl)pyrazolo[1,5-a]pyrimidin-3-y l)-3-hydroxypyrrolidine-1-carboxamide |
| CN107400082A (en) * | 2016-05-19 | 2017-11-28 | 湖南华腾制药有限公司 | A kind of preparation method of substituted piperidine derivative |
| TWI752098B (en) | 2016-10-10 | 2022-01-11 | 美商亞雷生物製藥股份有限公司 | Substituted pyrazolo[1,5-a]pyridine compounds as ret kinase inhibitors |
| TWI704148B (en) | 2016-10-10 | 2020-09-11 | 美商亞雷生物製藥股份有限公司 | Substituted pyrazolo[1,5-a]pyridine compounds as ret kinase inhibitors |
| JOP20190072A1 (en) * | 2016-10-13 | 2019-04-07 | Glaxosmithkline Ip Dev Ltd | 1,3 di-substituted cyclobutane or azetidine derivatives as hematopoietic prostaglandin d synthase inhibitors |
| JOP20190092A1 (en) | 2016-10-26 | 2019-04-25 | Array Biopharma Inc | PROCESS FOR THE PREPARATION OF PYRAZOLO[1,5-a]PYRIMIDINES AND SALTS THEREOF |
| WO2018136663A1 (en) | 2017-01-18 | 2018-07-26 | Array Biopharma, Inc. | Ret inhibitors |
| JP6888101B2 (en) | 2017-01-18 | 2021-06-16 | アレイ バイオファーマ インコーポレイテッド | Substituted pyrazolo [1,5-a] pyrazine compounds as RET kinase inhibitors |
| SMT202300269T1 (en) * | 2017-03-14 | 2023-09-06 | Daiichi Sankyo Co Ltd | Method for producing 3, 6-disubstituted imidazo[1, 2-b]pyridazine derivative |
| JOP20190213A1 (en) | 2017-03-16 | 2019-09-16 | Array Biopharma Inc | Macrocyclic compounds as ros1 kinase inhibitors |
| US10180422B1 (en) | 2017-08-22 | 2019-01-15 | Scripps Health | Methods of treating a neuroendocrine tumor |
| TWI876442B (en) | 2017-10-10 | 2025-03-11 | 美商絡速藥業公司 | Formulations of 6-(2-hydroxy-2-methylpropoxy)-4-(6-(6-((6-methoxypyridin-3-yl)methyl)-3,6-diazabicyclo[3.1.1]heptan-3-yl)pyridin-3-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile |
| TWI791053B (en) | 2017-10-10 | 2023-02-01 | 美商亞雷生物製藥股份有限公司 | Crystalline forms of 6-(2-hydroxy-2-methylpropoxy)-4-(6-(6-((6-methoxypyridin-3-yl)methyl)-3,6-diazabicyclo[3.1.1]heptan-3-yl)pyridin-3-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile and pharmaceutical composition thereof |
| CA3080157A1 (en) | 2017-10-26 | 2019-05-02 | Array Biopharma Inc. | Formulations of a macrocyclic trk kinase inhibitor |
| CN109748902B (en) * | 2017-11-02 | 2020-11-06 | 杭州科巢生物科技有限公司 | A kind of preparation method of Anlotinib hydrochloride |
| WO2019107671A1 (en) | 2017-11-29 | 2019-06-06 | 서울대학교 산학협력단 | Anti-ros1 antibody and use thereof |
| CN108129288B (en) * | 2017-12-27 | 2021-01-22 | 上海毕得医药科技股份有限公司 | Synthesis method of trans-3-hydroxycyclobutylformic acid |
| CN111630054B (en) | 2018-01-18 | 2023-05-09 | 奥瑞生物药品公司 | Substituted pyrazolo [3,4-d ] pyrimidine compounds as RET kinase inhibitors |
| EP3740486A1 (en) | 2018-01-18 | 2020-11-25 | Array Biopharma, Inc. | Substituted pyrazolyl[4,3-c]pyridinecompounds as ret kinase inhibitors |
| EP3740491A1 (en) | 2018-01-18 | 2020-11-25 | Array Biopharma, Inc. | Substituted pyrrolo[2,3-d]pyrimidines compounds as ret kinase inhibitors |
| EP3773725A1 (en) | 2018-03-29 | 2021-02-17 | Loxo Oncology Inc. | Treatment of trk-associated cancers |
| MA53395A (en) | 2018-07-24 | 2021-06-02 | Otsuka Pharma Co Ltd | HETEROBICYCLIC COMPOUNDS TO INHIBIT SHP2 ACTIVITY |
| CA3108065C (en) | 2018-07-31 | 2025-10-07 | Loxo Oncology, Inc. | Spray-dried dispersions, formulations, and polymorphs of (s)-5-amino-3-(4-((5-fluoro-2-methoxybenzamido)methyl)phenyl)-1-(1,1,1-trifluoropropan-2-yl)-1h-pyrazole-4-carboxamide |
| ES2922314T3 (en) | 2018-09-10 | 2022-09-13 | Array Biopharma Inc | Fused Heterocyclic Compounds as RET Kinase Inhibitors |
| WO2020131627A1 (en) | 2018-12-19 | 2020-06-25 | Array Biopharma Inc. | Substituted pyrazolo[1,5-a]pyridine compounds as inhibitors of fgfr tyrosine kinases |
| US12351571B2 (en) | 2018-12-19 | 2025-07-08 | Array Biopharma Inc. | Substituted quinoxaline compounds as inhibitors of FGFR tyrosine kinases |
| US12240855B2 (en) | 2019-03-06 | 2025-03-04 | Daiichi Sankyo Company, Limited | Pyrrolopyrazole derivative |
| CA3129665A1 (en) | 2019-03-21 | 2020-09-24 | Onxeo | A dbait molecule in combination with kinase inhibitor for the treatment of cancer |
| BR112021022255A2 (en) * | 2019-05-08 | 2022-01-18 | Tyk Medicines Inc | Compound used as a kinase inhibitor and its application |
| GB201911928D0 (en) | 2019-08-20 | 2019-10-02 | Otsuka Pharma Co Ltd | Pharmaceutical compounds |
| KR20220098759A (en) | 2019-11-08 | 2022-07-12 | 인쎄름 (엥스띠뛰 나씨오날 드 라 쌍떼 에 드 라 흐쉐르슈 메디깔) | A method of treating cancer that has acquired resistance to a kinase inhibitor |
| WO2021148581A1 (en) | 2020-01-22 | 2021-07-29 | Onxeo | Novel dbait molecule and its use |
| AR122159A1 (en) * | 2020-05-28 | 2022-08-17 | Novartis Ag | MLL1 INHIBITORS AND ANTINEOPLASTIC AGENTS |
| CN114957259A (en) * | 2021-02-25 | 2022-08-30 | 南京明德新药研发有限公司 | Cyano-substituted aromatic bicyclic compound and application thereof |
| CA3223035A1 (en) * | 2021-07-01 | 2023-01-05 | Anheart Therapeutics (Hangzhou) Co., Ltd. | Crystalline forms of 3-{4-[(2r)-2-aminopropoxy]phenyl}-n-[(1r)- 1-(3-fluorophenyl) ethyl]imidazo[1,2-b]pyridazin-6-amine and salts thereof |
| KR20250012111A (en) * | 2022-05-18 | 2025-01-23 | 안허트 테라퓨틱스 (항저우) 컴퍼니 리미티드 | Method for preparing 3,6-disubstituted-imidazo[1,2-B]pyridazine compounds |
| CN114989176B (en) * | 2022-07-08 | 2024-08-27 | 深圳市新樾生物科技有限公司 | Imidazopyridazine derivative and application thereof |
| CN115197115B (en) * | 2022-08-25 | 2024-11-08 | 成都金博汇康医药科技有限公司 | Preparation method and application of chiral 5-oxo pyrrolidine-3-carboxylic acid |
| CN117659020A (en) * | 2022-09-07 | 2024-03-08 | 苏州朗睿生物医药有限公司 | An imidazo[1,2-b]pyridazine derivative and its preparation method and use |
| AU2023339247A1 (en) * | 2022-09-07 | 2025-03-27 | Suzhou Langrui Biopharmaceutical Co., Ltd. | Macrocyclic imidazo[1,2-b]pyridazine derivative, preparation method therefor, and use thereof |
Family Cites Families (23)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6399780B1 (en) | 1999-08-20 | 2002-06-04 | Cephalon, Inc. | Isomeric fused pyrrolocarbazoles and isoindolones |
| WO2002020513A1 (en) | 2000-09-01 | 2002-03-14 | Glaxo Group Limited | Oxindole derivatives |
| US7071217B2 (en) | 2000-09-01 | 2006-07-04 | Smithkline Beecham Corporation | Substituted oxindole derivatives as tyrosine kinase inhibitors |
| JP2003231687A (en) | 2002-02-04 | 2003-08-19 | Japan Tobacco Inc | Pyrazolyl fused ring compounds and their pharmaceutical uses |
| MY141220A (en) | 2003-11-17 | 2010-03-31 | Astrazeneca Ab | Pyrazole derivatives as inhibitors of receptor tyrosine kinases |
| EP1742921A2 (en) | 2004-04-21 | 2007-01-17 | AstraZeneca AB | Pyrazole derivatives useful for the treatment of cancer |
| JPWO2006070943A1 (en) | 2004-12-28 | 2008-06-12 | 武田薬品工業株式会社 | Condensed imidazole compounds and uses thereof |
| DK2383268T3 (en) | 2005-02-04 | 2015-09-14 | Astrazeneca Ab | PYRAZOLYLAMINOPYRIDINDERIVATER useful as kinase inhibitors |
| KR20070104936A (en) | 2005-02-16 | 2007-10-29 | 아스트라제네카 아베 | compound |
| KR101362621B1 (en) | 2005-02-16 | 2014-02-13 | 아스트라제네카 아베 | Chemical compouns |
| US20100216798A1 (en) | 2005-07-29 | 2010-08-26 | Astellas Pharma Inc | Fused heterocycles as lck inhibitors |
| EP1912987A1 (en) * | 2005-08-01 | 2008-04-23 | F. Hoffmann-Roche AG | Heterocyclic benzylamino derivatives, their manufacture and use as pharmaceutical agents |
| DE102005042742A1 (en) | 2005-09-02 | 2007-03-08 | Schering Ag | Substituted imidazo [1,2b] pyridazines as kinase inhibitors, their production and use as pharmaceuticals |
| DE102006029447A1 (en) * | 2006-06-21 | 2007-12-27 | Bayer Schering Pharma Ag | Oxo-substituted imidazo [1,2b] pyridazines, their preparation and use as pharmaceuticals |
| BRPI0718266A2 (en) | 2006-10-30 | 2014-01-07 | Novartis Ag | HETEROCYCLIC COMPOUNDS AS ANTI-INFLAMMATORY AGENTS. |
| US7750007B2 (en) * | 2006-11-06 | 2010-07-06 | Supergen, Inc. | Imidazo[1,2-beta]pyridazine and pyrazolo[1,5-alpha]pyrimidine derivatives and their use as protein kinase inhibitors |
| WO2008072682A1 (en) * | 2006-12-15 | 2008-06-19 | Daiichi Sankyo Company, Limited | Imidazo[1,2-b]pyridazine derivative |
| JP2009227599A (en) | 2008-03-21 | 2009-10-08 | Daiichi Sankyo Co Ltd | Imidazopyridazine derivative |
| CA2722418C (en) | 2008-05-13 | 2013-09-17 | Irm Llc | Fused nitrogen containing heterocycles and compositions thereof as kinase inhibitors |
| SI2350075T1 (en) | 2008-09-22 | 2014-06-30 | Array Biopharma, Inc. | Substituted imidazoš1,2bćpyridazine compounds as trk kinase inhibitors |
| KR101147550B1 (en) | 2009-10-22 | 2012-05-17 | 한국과학기술연구원 | 2,7-Substituted thieno[3,2-d]pyrimidine compounds as protein kinase inhibitors |
| WO2012005299A1 (en) | 2010-07-07 | 2012-01-12 | 日本新薬株式会社 | Ros tyrosine kinase inhibitor |
| WO2012125667A1 (en) | 2011-03-17 | 2012-09-20 | Merck Sharp & Dohme Corp. | TrkA KINASE INHIBITORS, COMPOSITIONS AND METHODS THEREOF |
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2013
- 2013-05-31 TW TW102119261A patent/TWI585088B/en active
- 2013-06-03 RU RU2014153627A patent/RU2635917C2/en active
- 2013-06-03 CA CA2874819A patent/CA2874819C/en active Active
- 2013-06-03 ES ES13801320.6T patent/ES2648228T3/en active Active
- 2013-06-03 SG SG11201408052WA patent/SG11201408052WA/en unknown
- 2013-06-03 NZ NZ702574A patent/NZ702574A/en unknown
- 2013-06-03 SM SM20170539T patent/SMT201700539T1/en unknown
- 2013-06-03 MX MX2014014803A patent/MX357021B/en active IP Right Grant
- 2013-06-03 PL PL13801320T patent/PL2857404T3/en unknown
- 2013-06-03 EP EP13801320.6A patent/EP2857404B1/en active Active
- 2013-06-03 LT LTEP13801320.6T patent/LT2857404T/en unknown
- 2013-06-03 HU HUE13801320A patent/HUE037221T2/en unknown
- 2013-06-03 JP JP2014519977A patent/JP5814467B2/en active Active
- 2013-06-03 PT PT138013206T patent/PT2857404T/en unknown
- 2013-06-03 US US14/378,318 patent/US9187489B2/en active Active
- 2013-06-03 WO PCT/JP2013/065328 patent/WO2013183578A1/en not_active Ceased
- 2013-06-03 BR BR112014029851-3A patent/BR112014029851B1/en active IP Right Grant
- 2013-06-03 MY MYPI2014003346A patent/MY170326A/en unknown
- 2013-06-03 DK DK13801320.6T patent/DK2857404T3/en active
- 2013-06-03 RS RS20171198A patent/RS56625B1/en unknown
- 2013-06-03 HR HRP20171724TT patent/HRP20171724T1/en unknown
- 2013-06-03 IN IN2497MUN2014 patent/IN2014MN02497A/en unknown
- 2013-06-03 SI SI201330798T patent/SI2857404T1/en unknown
- 2013-06-03 AU AU2013272701A patent/AU2013272701B2/en active Active
- 2013-06-03 KR KR1020147033351A patent/KR101781255B1/en active Active
- 2013-06-03 CN CN201380041498.XA patent/CN104520300B/en active Active
- 2013-06-03 NO NO13801320A patent/NO2857404T3/no unknown
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2014
- 2014-12-02 ZA ZA2014/08843A patent/ZA201408843B/en unknown
- 2014-12-04 PH PH12014502721A patent/PH12014502721A1/en unknown
- 2014-12-04 IL IL236075A patent/IL236075A/en active IP Right Grant
- 2014-12-30 CO CO14286593A patent/CO7160119A2/en unknown
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2015
- 2015-10-29 US US14/926,973 patent/US9751887B2/en active Active
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2017
- 2017-11-15 CY CY20171101204T patent/CY1119607T1/en unknown
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