MA40581A - Dérivés pyridone utilisés comme inhibiteurs de la kinase réarrangée au cours de la transfection (ret) - Google Patents
Dérivés pyridone utilisés comme inhibiteurs de la kinase réarrangée au cours de la transfection (ret)Info
- Publication number
- MA40581A MA40581A MA040581A MA40581A MA40581A MA 40581 A MA40581 A MA 40581A MA 040581 A MA040581 A MA 040581A MA 40581 A MA40581 A MA 40581A MA 40581 A MA40581 A MA 40581A
- Authority
- MA
- Morocco
- Prior art keywords
- cancer
- functional
- ret
- thyroid
- disorders
- Prior art date
Links
Classifications
-
- 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
- A61K31/4439—Non 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
-
- 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
- A61K31/4412—Non condensed pyridines; Hydrogenated derivatives thereof having oxo groups directly attached to the heterocyclic ring
-
- 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
- A61K31/4418—Non condensed pyridines; Hydrogenated derivatives thereof having a carbocyclic group directly attached to the heterocyclic ring, e.g. cyproheptadine
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/04—Drugs 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- 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
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic 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
- C07D213/02—Heterocyclic 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
- C07D213/04—Heterocyclic 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
- C07D213/60—Heterocyclic 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
- C07D213/62—Oxygen or sulfur atoms
- C07D213/69—Two or more oxygen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic 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
- C07D401/02—Heterocyclic 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
- C07D401/12—Heterocyclic 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic 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
- C07D413/12—Heterocyclic 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
La présente invention concerne de nouveaux composés qui sont des inhibiteurs de la kinase réarrangée au cours de la transfection (ret), des compositions pharmaceutiques les contenant, des procédés pour leur préparation et leur utilisation en thérapie, seule ou en combinaison, pour la normalisation de la sensibilité gastro-intestinale. Troubles de la motilité et / ou de la sécrétion et / ou de l'abdomen et / ou traitements associés à des affections liées à un dysfonctionnement de la ret ou dans lesquels la modulation de l'activité de la ret peut avoir un bénéfice thérapeutique, y compris, sans limitation, toutes les classifications du syndrome du côlon irritable (sci), y compris la diarrhée - selles dominantes, constipation prédominante ou en alternance, ballonnements fonctionnels, constipation fonctionnelle, diarrhée fonctionnelle, troubles intestinaux fonctionnels non précisés, syndrome de la douleur abdominale fonctionnelle, constipation idiopathique chronique, troubles œsophagiens fonctionnels, troubles gastroduodénaux fonctionnels, douleurs anorectales fonctionnelles, maladie intestinale inflammatoire, maladie évolutive de l'intestin, prolifération maladies telles cancer du poumon non à petites cellules, carcinome hépatocellulaire, cancer colorectal, cancer médullaire de la thyroïde, cancer de la thyroïde folliculaire, cancer de la thyroïde anaplasique, cancer de la thyroïde papillaire, tumeurs au cerveau, cancer de la cavité péritonéale, tumeurs solides, autres cancers du poumon, cancers de la tête et du cou, gliomes , neuroblastomes, syndrome de von hippel-lindau et tumeurs du rein, cancer du sein, cancer de la trompe de fallope, cancer de l'ovaire, cancer à cellules transitionnelles, cancer de la prostate, cancer de l'œsophage et de la jonction gastro-œsophagienne, cancer des voies biliaires, adénocarcinome et tout cancer avec une activité accrue de la kinase ret .
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN2014086197 | 2014-09-10 | ||
| CN2015086995 | 2015-08-14 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| MA40581A true MA40581A (fr) | 2019-04-10 |
Family
ID=54186249
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MA040581A MA40581A (fr) | 2014-09-10 | 2015-09-09 | Dérivés pyridone utilisés comme inhibiteurs de la kinase réarrangée au cours de la transfection (ret) |
Country Status (35)
| Country | Link |
|---|---|
| US (4) | US9918974B2 (fr) |
| EP (2) | EP3191450B1 (fr) |
| JP (2) | JP6538154B2 (fr) |
| KR (1) | KR20170045350A (fr) |
| CN (1) | CN107074768B (fr) |
| AU (1) | AU2015313841B2 (fr) |
| BR (1) | BR112017004900A2 (fr) |
| CA (1) | CA2960768A1 (fr) |
| CL (1) | CL2017000588A1 (fr) |
| CO (1) | CO2017002273A2 (fr) |
| CR (1) | CR20170093A (fr) |
| CY (1) | CY1121661T1 (fr) |
| DK (1) | DK3191450T3 (fr) |
| DO (1) | DOP2017000059A (fr) |
| EA (1) | EA033544B1 (fr) |
| ES (2) | ES2816453T3 (fr) |
| HR (1) | HRP20190815T1 (fr) |
| HU (1) | HUE044604T2 (fr) |
| IL (1) | IL250908B (fr) |
| LT (1) | LT3191450T (fr) |
| MA (1) | MA40581A (fr) |
| ME (1) | ME03432B (fr) |
| MX (1) | MX2017003114A (fr) |
| MY (1) | MY181913A (fr) |
| PE (1) | PE20170705A1 (fr) |
| PH (1) | PH12017500425B1 (fr) |
| PL (1) | PL3191450T3 (fr) |
| PT (1) | PT3191450T (fr) |
| RS (1) | RS58813B1 (fr) |
| SG (1) | SG11201701694QA (fr) |
| SI (1) | SI3191450T1 (fr) |
| TW (1) | TWI683807B (fr) |
| UA (1) | UA122213C2 (fr) |
| UY (1) | UY36293A (fr) |
| WO (1) | WO2016038552A1 (fr) |
Families Citing this family (23)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| PL3205654T3 (pl) | 2010-05-20 | 2019-08-30 | Array Biopharma, Inc. | Związki makrocykliczne jako inhibitory kinazy TRK |
| DK3191449T3 (da) | 2014-09-10 | 2020-08-03 | Glaxosmithkline Ip Dev Ltd | Forbindelser som ret- (rearranged during transfection) hæmmere |
| US9918974B2 (en) | 2014-09-10 | 2018-03-20 | Glaxosmithkline Intellectual Property Development Limited | Pyridone derivatives as rearranged during transfection (RET) kinase inhibitors |
| US10202365B2 (en) | 2015-02-06 | 2019-02-12 | Blueprint Medicines Corporation | 2-(pyridin-3-yl)-pyrimidine derivatives as RET inhibitors |
| BR112018000808A2 (pt) | 2015-07-16 | 2018-09-04 | Array Biopharma Inc | compostos de pirazolo[1,5-a]piridina substituída como inibidores de ret cinase |
| EP4292594A3 (fr) | 2015-11-02 | 2024-03-27 | Blueprint Medicines Corporation | Inhibiteurs de ret |
| TW201738228A (zh) | 2016-03-17 | 2017-11-01 | 藍圖醫藥公司 | Ｒｅｔ之抑制劑 |
| US10227329B2 (en) | 2016-07-22 | 2019-03-12 | 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 |
| WO2018136661A1 (fr) | 2017-01-18 | 2018-07-26 | Andrews Steven W | Composés de pyrazolo[1,5-a]pyrazine substitués utilisés en tant qu'inhibiteurs de la kinase ret |
| WO2018136663A1 (fr) | 2017-01-18 | 2018-07-26 | Array Biopharma, Inc. | Inhibiteurs de ret |
| JOP20190213A1 (ar) | 2017-03-16 | 2019-09-16 | Array Biopharma Inc | مركبات حلقية ضخمة كمثبطات لكيناز ros1 |
| WO2018213329A1 (fr) | 2017-05-15 | 2018-11-22 | Blueprint Medicines Corporation | Associations d'inhibiteurs de ret et d'inhibiteurs de mtorc1, et utilisations de celles-ci pour le traitement de cancers liés à une activité ret aberrante |
| 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 |
| TW202410896A (zh) | 2017-10-10 | 2024-03-16 | 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 |
| CN111971286B (zh) | 2018-01-18 | 2023-04-14 | 阿雷生物药品公司 | 作为RET激酶抑制剂的取代的吡咯并[2,3-d]嘧啶化合物 |
| WO2019143994A1 (fr) | 2018-01-18 | 2019-07-25 | Array Biopharma Inc. | Composés de pyrazolyl[4,3-c]pyridine substitués utilisés en tant qu'inhibiteurs de la kinase ret |
| US11524963B2 (en) | 2018-01-18 | 2022-12-13 | Array Biopharma Inc. | Substituted pyrazolo[3,4-d]pyrimidines as RET kinase inhibitors |
| RS65127B1 (sr) | 2018-04-03 | 2024-02-29 | Blueprint Medicines Corp | Ret inhibitor za primenu u lečenju kancera koji ima ret alteraciju |
| WO2020055672A1 (fr) | 2018-09-10 | 2020-03-19 | Array Biopharma Inc. | Composés hétérocycliques condensés comme inhibiteurs de kinases ret |
| TWI786742B (zh) * | 2020-07-23 | 2022-12-11 | 大陸商深圳晶泰科技有限公司 | 吡啶酮類化合物及其製備方法和應用 |
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| US20120046290A1 (en) | 1997-12-22 | 2012-02-23 | Jacques Dumas | Inhibition of p38 kinase activity using substituted heterocyclic ureas |
| MXPA00006233A (es) | 1997-12-22 | 2002-09-18 | Bayer Ag | Inhibicion de la actividad de la cinasa p38 utilizando ureas heterociclicas sustituidas. |
| BR9814374B1 (pt) | 1997-12-22 | 2013-09-17 | "urÉias heterocÍclicas substituÍdas e composiÇÕes compreendendo as mesmas" | |
| US20070244120A1 (en) | 2000-08-18 | 2007-10-18 | Jacques Dumas | Inhibition of raf kinase using substituted heterocyclic ureas |
| KR20020060160A (ko) | 1999-08-12 | 2002-07-16 | 파마시아 이탈리아 에스.피.에이. | 3(5)-아미노-피라졸 유도체, 이의 제조 방법 및항종양제로서의 이의 용도 |
| CA2430151A1 (fr) * | 2000-11-27 | 2002-06-20 | Pharmacia Italia S.P.A. | Derives phenylacetamido-pyrazole et leur utilisation comme agents antitumoraux |
| 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 (fr) | 2002-09-10 | 2004-03-25 | Kyorin Pharmaceutical Co., Ltd. | Derive de 4-(aryle substitue)-5-hydroxyisoquinolinone |
| WO2005018624A2 (fr) | 2003-08-22 | 2005-03-03 | Boehringer Ingelheim Pharmaceuticals, Inc. | Procedes pour traiter la bronchopneumopathie chronique obstructive et l'hypertension pulmonaire |
| TW200530236A (en) * | 2004-02-23 | 2005-09-16 | Chugai Pharmaceutical Co Ltd | Heteroaryl phenylurea |
| US7968574B2 (en) | 2004-12-28 | 2011-06-28 | Kinex Pharmaceuticals, Llc | Biaryl compositions and methods for modulating a kinase cascade |
| WO2006071960A2 (fr) * | 2004-12-28 | 2006-07-06 | Kinex Pharmaceuticals, Llc | Compositions et procedes de traitement de troubles de la proliferation cellulaire |
| 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 (fr) | 2006-06-29 | 2008-01-03 | Kinex Pharmaceuticals, Llc | Compositions de biaryle et procédés de modulation d'une cascade de kinases |
| KR101507375B1 (ko) * | 2006-09-15 | 2015-04-07 | 엑스커버리 홀딩 컴퍼니 엘엘씨 | 키나아제 억제제 화합물 |
| US7977338B2 (en) * | 2006-10-16 | 2011-07-12 | Novartis Ag | Phenylacetamides being FLT3 inhibitors |
| EP2099774A4 (fr) | 2006-11-15 | 2010-11-24 | Ym Biosciences Australia Pty L | Inhibiteurs de l'activité kinase |
| US20130035326A1 (en) | 2009-08-19 | 2013-02-07 | Ambit Biosciences Corporation | Biaryl compounds and methods of use thereof |
| WO2012082817A1 (fr) | 2010-12-16 | 2012-06-21 | Boehringer Ingelheim International Gmbh | Inhibiteurs biarylamide de production de leukotriènes |
| EP2970191B1 (fr) | 2013-03-15 | 2016-12-21 | GlaxoSmithKline Intellectual Property Development Limited | Dérivés des pyridines comme inhibiteurs de la kinase arrangé pendant transfection (ret) |
| US8937071B2 (en) | 2013-03-15 | 2015-01-20 | Glaxosmithkline Intellectual Property Development Limited | Compounds as rearranged during transfection (RET) inhibitors |
| US9918974B2 (en) | 2014-09-10 | 2018-03-20 | Glaxosmithkline Intellectual Property Development Limited | 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 |
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2015
- 2015-09-09 US US15/509,613 patent/US9918974B2/en not_active Expired - Fee Related
- 2015-09-09 ME MEP-2019-136A patent/ME03432B/fr unknown
- 2015-09-09 SI SI201530720T patent/SI3191450T1/sl unknown
- 2015-09-09 CN CN201580058320.5A patent/CN107074768B/zh not_active Expired - Fee Related
- 2015-09-09 PE PE2017000417A patent/PE20170705A1/es unknown
- 2015-09-09 SG SG11201701694QA patent/SG11201701694QA/en unknown
- 2015-09-09 ES ES19160650T patent/ES2816453T3/es active Active
- 2015-09-09 LT LTEP15767599.2T patent/LT3191450T/lt unknown
- 2015-09-09 CR CR20170093A patent/CR20170093A/es unknown
- 2015-09-09 DK DK15767599.2T patent/DK3191450T3/da active
- 2015-09-09 UA UAA201703478A patent/UA122213C2/uk unknown
- 2015-09-09 AU AU2015313841A patent/AU2015313841B2/en not_active Ceased
- 2015-09-09 EP EP15767599.2A patent/EP3191450B1/fr active Active
- 2015-09-09 BR BR112017004900A patent/BR112017004900A2/pt not_active IP Right Cessation
- 2015-09-09 EP EP19160650.8A patent/EP3517526B1/fr active Active
- 2015-09-09 PL PL15767599T patent/PL3191450T3/pl unknown
- 2015-09-09 ES ES15767599T patent/ES2725704T3/es active Active
- 2015-09-09 WO PCT/IB2015/056905 patent/WO2016038552A1/fr active Application Filing
- 2015-09-09 CA CA2960768A patent/CA2960768A1/fr not_active Abandoned
- 2015-09-09 RS RS20190559A patent/RS58813B1/sr unknown
- 2015-09-09 KR KR1020177009237A patent/KR20170045350A/ko not_active Application Discontinuation
- 2015-09-09 MY MYPI2017700782A patent/MY181913A/en unknown
- 2015-09-09 MA MA040581A patent/MA40581A/fr unknown
- 2015-09-09 HU HUE15767599 patent/HUE044604T2/hu unknown
- 2015-09-09 MX MX2017003114A patent/MX2017003114A/es active IP Right Grant
- 2015-09-09 PT PT15767599T patent/PT3191450T/pt unknown
- 2015-09-09 EA EA201790546A patent/EA033544B1/ru not_active IP Right Cessation
- 2015-09-09 JP JP2017513450A patent/JP6538154B2/ja not_active Expired - Fee Related
- 2015-09-10 UY UY0001036293A patent/UY36293A/es unknown
- 2015-09-10 TW TW104129876A patent/TWI683807B/zh not_active IP Right Cessation
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2017
- 2017-03-02 IL IL250908A patent/IL250908B/en active IP Right Grant
- 2017-03-07 CO CONC2017/0002273A patent/CO2017002273A2/es unknown
- 2017-03-07 DO DO2017000059A patent/DOP2017000059A/es unknown
- 2017-03-07 PH PH12017500425A patent/PH12017500425B1/en unknown
- 2017-03-09 CL CL2017000588A patent/CL2017000588A1/es unknown
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2018
- 2018-01-23 US US15/877,524 patent/US10111866B2/en not_active Expired - Fee Related
- 2018-09-28 US US16/145,271 patent/US10292975B2/en not_active Expired - Fee Related
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2019
- 2019-04-05 US US16/376,858 patent/US10709695B2/en not_active Expired - Fee Related
- 2019-05-02 HR HRP20190815TT patent/HRP20190815T1/hr unknown
- 2019-05-09 CY CY20191100502T patent/CY1121661T1/el unknown
- 2019-05-31 JP JP2019102776A patent/JP6728447B2/ja not_active Expired - Fee Related
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