MA33849B1 - Formes cristallines de la 3-(2,6-dichloro-3,5-diméthoxy-phényl)-1- {6-[4-(4-éthyl-pipérazin-1-yl) -phénylamino] -pyrimidin-4-yl} -1-méthyl-urée et de ses sels - Google Patents
Formes cristallines de la 3-(2,6-dichloro-3,5-diméthoxy-phényl)-1- {6-[4-(4-éthyl-pipérazin-1-yl) -phénylamino] -pyrimidin-4-yl} -1-méthyl-urée et de ses selsInfo
- Publication number
- MA33849B1 MA33849B1 MA35005A MA35005A MA33849B1 MA 33849 B1 MA33849 B1 MA 33849B1 MA 35005 A MA35005 A MA 35005A MA 35005 A MA35005 A MA 35005A MA 33849 B1 MA33849 B1 MA 33849B1
- Authority
- MA
- Morocco
- Prior art keywords
- piperazin
- phenylamino
- pyrimidin
- dimethoxy
- dichloro
- Prior art date
Links
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
- C07D239/46—Two or more oxygen, sulphur or nitrogen atoms
- C07D239/48—Two nitrogen atoms
-
- 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
- A61K31/4965—Non-condensed pyrazines
- A61K31/497—Non-condensed pyrazines 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
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P15/00—Drugs for genital or sexual disorders; Contraceptives
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
- A61P17/06—Antipsoriatics
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/10—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a carbon chain containing aromatic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
- C07B2200/00—Indexing scheme relating to specific properties of organic compounds
- C07B2200/13—Crystalline forms, e.g. polymorphs
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (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)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Epidemiology (AREA)
- Oncology (AREA)
- Hematology (AREA)
- Dermatology (AREA)
- Endocrinology (AREA)
- Reproductive Health (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Abstract
La présente technologie concerne de nouvelles formes cristallines anhydres et hydratées de 3-(2,6-dichloro-3,5-diméthoxy-phényl)-1-{6-[4-(4-éthyl-pipérazin-1-yl)-phénylamino]-pyrimidin-4-yl}-1-méthyl-urée, des polymorphes amorphes et cristallines anhydres de son sel d'acide monophosphorique, et le sel chlorhydrate, incluant son dihydrate. La présente technologie concerne également des procédés de préparation de diverses formes, des compositions les contenant et des procédés de traitement les employant.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US26715509P | 2009-12-07 | 2009-12-07 | |
PCT/US2010/059108 WO2011071821A1 (fr) | 2009-12-07 | 2010-12-06 | Formes cristallines de la 3-(2,6-dichloro-3,5-diméthoxy-phényl)-1-{6-[4-(4-éthyl-pipérazin-1-yl)-phénylamino]-pyrimidin-4-yl}-1-méthyl-urée et de ses sels |
Publications (1)
Publication Number | Publication Date |
---|---|
MA33849B1 true MA33849B1 (fr) | 2012-12-03 |
Family
ID=43983750
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
MA35005A MA33849B1 (fr) | 2009-12-07 | 2012-06-26 | Formes cristallines de la 3-(2,6-dichloro-3,5-diméthoxy-phényl)-1- {6-[4-(4-éthyl-pipérazin-1-yl) -phénylamino] -pyrimidin-4-yl} -1-méthyl-urée et de ses sels |
Country Status (33)
Country | Link |
---|---|
US (1) | US9067896B2 (fr) |
EP (1) | EP2509963B1 (fr) |
JP (2) | JP5714024B2 (fr) |
KR (1) | KR101787784B1 (fr) |
CN (5) | CN111100078A (fr) |
AR (2) | AR079257A1 (fr) |
AU (1) | AU2010328391B2 (fr) |
BR (1) | BR112012013784B1 (fr) |
CA (1) | CA2781431C (fr) |
CL (1) | CL2012001480A1 (fr) |
DK (1) | DK2509963T3 (fr) |
EC (1) | ECSP12012026A (fr) |
ES (1) | ES2562462T3 (fr) |
GT (1) | GT201200181A (fr) |
HK (1) | HK1171016A1 (fr) |
HR (1) | HRP20160126T1 (fr) |
HU (1) | HUE026983T2 (fr) |
IL (1) | IL220012B (fr) |
JO (1) | JO3061B1 (fr) |
MA (1) | MA33849B1 (fr) |
MX (1) | MX2012006562A (fr) |
MY (1) | MY158333A (fr) |
NZ (3) | NZ600070A (fr) |
PE (1) | PE20121499A1 (fr) |
PH (1) | PH12014502593A1 (fr) |
PL (1) | PL2509963T3 (fr) |
RU (1) | RU2572848C2 (fr) |
SG (1) | SG10201408063SA (fr) |
SI (1) | SI2509963T1 (fr) |
TN (1) | TN2012000263A1 (fr) |
TW (1) | TWI526440B (fr) |
WO (1) | WO2011071821A1 (fr) |
ZA (1) | ZA201203612B (fr) |
Families Citing this family (49)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB0512324D0 (en) * | 2005-06-16 | 2005-07-27 | Novartis Ag | Organic compounds |
AR079257A1 (es) * | 2009-12-07 | 2012-01-04 | Novartis Ag | Formas cristalinas de 3-(2,6-dicloro-3-5-dimetoxi-fenil)-1-{6-[4-(4-etil-piperazin-1-il)-fenil-amino]-pirimidin-4-il}-1-metil-urea y sales de las mismas |
WO2012088266A2 (fr) | 2010-12-22 | 2012-06-28 | Incyte Corporation | Imidazopyridazines et benzimidazoles substitués en tant qu'inhibiteurs de fgfr3 |
RU2643326C2 (ru) * | 2012-03-30 | 2018-01-31 | Новартис Аг | Ингибитор рецептора фрф для применения в лечении гипофосфатемических заболеваний |
WO2014007951A2 (fr) | 2012-06-13 | 2014-01-09 | Incyte Corporation | Composés tricycliques substitués utilisés comme inhibiteurs de fgfr |
WO2014026125A1 (fr) | 2012-08-10 | 2014-02-13 | Incyte Corporation | Dérivés de pyrazine en tant qu'inhibiteurs de fgfr |
US9266892B2 (en) | 2012-12-19 | 2016-02-23 | Incyte Holdings Corporation | Fused pyrazoles as FGFR inhibitors |
AR094812A1 (es) | 2013-02-20 | 2015-08-26 | Eisai R&D Man Co Ltd | Derivado de piridina monocíclico como inhibidor del fgfr |
EP2968337B1 (fr) | 2013-03-15 | 2021-07-21 | Celgene CAR LLC | Composés hétéroaryle et utilisations associées |
TWI647220B (zh) | 2013-03-15 | 2019-01-11 | 美商西建卡爾有限責任公司 | 雜芳基化合物及其用途 |
KR102350704B1 (ko) | 2013-03-15 | 2022-01-13 | 셀젠 카르 엘엘씨 | 헤테로아릴 화합물 및 이의 용도 |
WO2014155268A2 (fr) | 2013-03-25 | 2014-10-02 | Novartis Ag | Inhibiteurs de kinase tyrosine fgf-r et leur utilisation dans le traitement de maladies associées à un manque ou à une absence d'activité snf5 |
DK2986610T5 (en) | 2013-04-19 | 2018-12-10 | Incyte Holdings Corp | BICYCLIC HETEROCYCLES AS FGFR INHIBITORS |
CA2917667A1 (fr) * | 2013-07-09 | 2015-01-15 | Dana-Farber Cancer Institute, Inc. | Inhibiteurs de kinase pour le traitement d'une maladie |
RS57444B1 (sr) * | 2013-10-18 | 2018-09-28 | Eisai R&D Man Co Ltd | Pirimidin fgfr4 inhibitori |
SI3079667T1 (sl) | 2013-12-13 | 2019-10-30 | Novartis Ag | Farmacevtske dozirne oblike |
WO2016027781A1 (fr) | 2014-08-18 | 2016-02-25 | エーザイ・アール・アンド・ディー・マネジメント株式会社 | Sel de dérivé de pyridine monocyclique et son cristal |
US20170304313A1 (en) | 2014-10-06 | 2017-10-26 | Novartis Ag | Therapeutic Combination For The Treatment Of Cancer |
US10851105B2 (en) | 2014-10-22 | 2020-12-01 | Incyte Corporation | Bicyclic heterocycles as FGFR4 inhibitors |
NZ773116A (en) | 2015-02-20 | 2024-05-31 | Incyte Holdings Corp | Bicyclic heterocycles as fgfr inhibitors |
US9580423B2 (en) | 2015-02-20 | 2017-02-28 | Incyte Corporation | Bicyclic heterocycles as FGFR4 inhibitors |
MA41551A (fr) | 2015-02-20 | 2017-12-26 | Incyte Corp | Hétérocycles bicycliques utilisés en tant qu'inhibiteurs de fgfr4 |
JP2018509448A (ja) * | 2015-03-25 | 2018-04-05 | ノバルティス アーゲー | 組合せ医薬 |
EP3283465B1 (fr) | 2015-04-14 | 2021-01-06 | Eisai R&D Management Co., Ltd. | Composé inhibiteur de fgfr4 cristallin et utilisations de celui-ci |
CN104803925B (zh) * | 2015-04-16 | 2018-01-12 | 温州医科大学 | 一类以fgfr为靶点的2,4,5‑三取代嘧啶类化合物及其制备方法和用途 |
WO2016189472A1 (fr) | 2015-05-28 | 2016-12-01 | Novartis Ag | Inhibiteur de fgfr destiné à être utilisé dans le traitement de la tumeur mésenchymateuse phosphaturique |
WO2017196854A1 (fr) | 2016-05-10 | 2017-11-16 | Eisai R&D Management Co., Ltd. | Associations médicamenteuses permettant de réduire la viabilité et/ou la prolifération cellulaire |
EP3459952B1 (fr) * | 2016-05-20 | 2022-01-05 | Zhejiang Hisun Pharmaceutical Co., Ltd. | Dérivé pyrimidine, procédé de préparation et utilisation associée en médecine |
CN109803684B (zh) * | 2016-08-23 | 2022-08-23 | 卫材 R&D 管理有限公司 | 用于治疗肝细胞癌的组合疗法 |
AR111960A1 (es) | 2017-05-26 | 2019-09-04 | Incyte Corp | Formas cristalinas de un inhibidor de fgfr y procesos para su preparación |
CN107176954B (zh) | 2017-06-02 | 2019-01-11 | 无锡双良生物科技有限公司 | 一种egfr抑制剂的药用盐及其晶型、制备方法和应用 |
US11440903B2 (en) | 2017-11-01 | 2022-09-13 | Guangdong Zhongsheng Pharmaceutical Co., Ltd | Salt form and crystal form of compound as FGFR4 inhibitor and preparation method thereof |
CA3091153A1 (fr) | 2018-03-28 | 2019-10-03 | Eisai R&D Management Co., Ltd. | Agent therapeutique pour le carcinome hepatocellulaire |
SG11202010636VA (en) | 2018-05-04 | 2020-11-27 | Incyte Corp | Solid forms of an fgfr inhibitor and processes for preparing the same |
BR112020022373A2 (pt) | 2018-05-04 | 2021-02-02 | Incyte Corporation | sais de um inibidor de fgfr |
US11628162B2 (en) | 2019-03-08 | 2023-04-18 | Incyte Corporation | Methods of treating cancer with an FGFR inhibitor |
WO2021007269A1 (fr) | 2019-07-09 | 2021-01-14 | Incyte Corporation | Hétérocycles bicycliques en tant qu'inhibiteurs de fgfr |
WO2021067374A1 (fr) | 2019-10-01 | 2021-04-08 | Incyte Corporation | Hétérocycles bicycliques en tant qu'inhibiteurs de fgfr |
BR112022007163A2 (pt) | 2019-10-14 | 2022-08-23 | Incyte Corp | Heterociclos bicíclicos como inibidores de fgfr |
US11566028B2 (en) | 2019-10-16 | 2023-01-31 | Incyte Corporation | Bicyclic heterocycles as FGFR inhibitors |
US11407750B2 (en) | 2019-12-04 | 2022-08-09 | Incyte Corporation | Derivatives of an FGFR inhibitor |
JP2023505258A (ja) | 2019-12-04 | 2023-02-08 | インサイト・コーポレイション | Fgfr阻害剤としての三環式複素環 |
US12012409B2 (en) | 2020-01-15 | 2024-06-18 | Incyte Corporation | Bicyclic heterocycles as FGFR inhibitors |
WO2022221170A1 (fr) | 2021-04-12 | 2022-10-20 | Incyte Corporation | Polythérapie comprenant un inhibiteur de fgfr et un agent de ciblage de nectine-4 |
EP4352059A1 (fr) | 2021-06-09 | 2024-04-17 | Incyte Corporation | Hétérocycles tricycliques en tant qu'inhibiteurs de fgfr |
WO2022271933A1 (fr) | 2021-06-23 | 2022-12-29 | Kimtron, Inc. | Système et procédé d'irradiation à proximité ultra-étroite d'une biomasse rotative |
CN116768856A (zh) * | 2022-03-18 | 2023-09-19 | 上海润石医药科技有限公司 | 一种取代的氨基六元氮杂环类化合物的盐及其晶型、制备方法和应用 |
CN115785001B (zh) * | 2022-11-23 | 2023-09-15 | 斯坦德药典标准物质研发(湖北)有限公司 | 一种英菲格拉替尼的制备方法 |
WO2024186882A1 (fr) | 2023-03-06 | 2024-09-12 | Qed Therapeutics, Inc. | Méthodes de traitement de dysplasies squelettiques |
Family Cites Families (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB0512324D0 (en) | 2005-06-16 | 2005-07-27 | Novartis Ag | Organic compounds |
CN101242843A (zh) * | 2005-06-10 | 2008-08-13 | 詹森药业有限公司 | 作为激酶调节剂的氨基嘧啶类化合物 |
KR101486490B1 (ko) * | 2005-11-08 | 2015-01-27 | 제이더블유중외제약 주식회사 | α-헬릭스 유사체 및 암 줄기세포의 치료에 관한 방법 |
ME00011A (fr) * | 2005-12-21 | 2009-02-10 | Novartis Ag | Derives pyrimidinyl-aryluree constituant des inhibiteurs des facteurs de croissance des fibroblastes (fgf) |
CN102016592A (zh) * | 2008-04-29 | 2011-04-13 | 诺瓦提斯公司 | 监测成纤维细胞生长因子受体的激酶活性的调节的方法及所述方法的应用 |
AR079257A1 (es) * | 2009-12-07 | 2012-01-04 | Novartis Ag | Formas cristalinas de 3-(2,6-dicloro-3-5-dimetoxi-fenil)-1-{6-[4-(4-etil-piperazin-1-il)-fenil-amino]-pirimidin-4-il}-1-metil-urea y sales de las mismas |
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2010
- 2010-12-03 AR ARP100104472A patent/AR079257A1/es not_active Application Discontinuation
- 2010-12-05 JO JOP/2010/0433A patent/JO3061B1/ar active
- 2010-12-06 CN CN201911273119.5A patent/CN111100078A/zh active Pending
- 2010-12-06 BR BR112012013784-0A patent/BR112012013784B1/pt active IP Right Grant
- 2010-12-06 RU RU2012128351/04A patent/RU2572848C2/ru active
- 2010-12-06 CA CA2781431A patent/CA2781431C/fr active Active
- 2010-12-06 ES ES10788479.3T patent/ES2562462T3/es active Active
- 2010-12-06 PE PE2012000772A patent/PE20121499A1/es active IP Right Grant
- 2010-12-06 HU HUE10788479A patent/HUE026983T2/en unknown
- 2010-12-06 CN CN2010800550783A patent/CN102639510A/zh active Pending
- 2010-12-06 KR KR1020127017618A patent/KR101787784B1/ko active IP Right Grant
- 2010-12-06 PL PL10788479T patent/PL2509963T3/pl unknown
- 2010-12-06 TW TW099142438A patent/TWI526440B/zh active
- 2010-12-06 SI SI201031119A patent/SI2509963T1/sl unknown
- 2010-12-06 CN CN201911272657.2A patent/CN111100077A/zh active Pending
- 2010-12-06 EP EP10788479.3A patent/EP2509963B1/fr active Active
- 2010-12-06 MX MX2012006562A patent/MX2012006562A/es active IP Right Grant
- 2010-12-06 AU AU2010328391A patent/AU2010328391B2/en active Active
- 2010-12-06 WO PCT/US2010/059108 patent/WO2011071821A1/fr active Application Filing
- 2010-12-06 US US13/514,308 patent/US9067896B2/en active Active
- 2010-12-06 SG SG10201408063SA patent/SG10201408063SA/en unknown
- 2010-12-06 DK DK10788479.3T patent/DK2509963T3/en active
- 2010-12-06 NZ NZ600070A patent/NZ600070A/en unknown
- 2010-12-06 PH PH12014502593A patent/PH12014502593A1/en unknown
- 2010-12-06 MY MYPI2012002222A patent/MY158333A/en unknown
- 2010-12-06 JP JP2012543183A patent/JP5714024B2/ja active Active
- 2010-12-06 CN CN201911278014.9A patent/CN111269186A/zh active Pending
- 2010-12-06 CN CN201510484635.8A patent/CN105061332A/zh active Pending
- 2010-12-06 NZ NZ700778A patent/NZ700778A/en unknown
- 2010-12-06 NZ NZ624315A patent/NZ624315A/en unknown
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2012
- 2012-05-17 ZA ZA2012/03612A patent/ZA201203612B/en unknown
- 2012-05-24 IL IL220012A patent/IL220012B/en active IP Right Grant
- 2012-05-25 TN TNP2012000263A patent/TN2012000263A1/en unknown
- 2012-06-06 CL CL2012001480A patent/CL2012001480A1/es unknown
- 2012-06-07 GT GT201200181A patent/GT201200181A/es unknown
- 2012-06-26 MA MA35005A patent/MA33849B1/fr unknown
- 2012-07-05 EC ECSP12012026 patent/ECSP12012026A/es unknown
- 2012-11-19 HK HK12111776.3A patent/HK1171016A1/zh unknown
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2015
- 2015-01-20 JP JP2015008550A patent/JP6019142B2/ja active Active
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2016
- 2016-02-04 HR HRP20160126T patent/HRP20160126T1/hr unknown
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2019
- 2019-01-07 AR ARP190100029A patent/AR114946A2/es unknown
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