MX336723B - Combinacion de (a) un inhibidor de fosfoinositido 3-cinasa y (b) un modulador de la ruta de ras/raf/mek. - Google Patents
Combinacion de (a) un inhibidor de fosfoinositido 3-cinasa y (b) un modulador de la ruta de ras/raf/mek.Info
- Publication number
- MX336723B MX336723B MX2013005357A MX2013005357A MX336723B MX 336723 B MX336723 B MX 336723B MX 2013005357 A MX2013005357 A MX 2013005357A MX 2013005357 A MX2013005357 A MX 2013005357A MX 336723 B MX336723 B MX 336723B
- Authority
- MX
- Mexico
- Prior art keywords
- combination
- phosphoinositide
- raf
- ras
- kinase inhibitor
- 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
- A61K31/47—Quinolines; Isoquinolines
- A61K31/4738—Quinolines; Isoquinolines ortho- or peri-condensed with heterocyclic ring systems
- A61K31/4745—Quinolines; Isoquinolines ortho- or peri-condensed with heterocyclic ring systems condensed with ring systems having nitrogen as a ring hetero atom, e.g. phenantrolines
-
- 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
- A61K31/16—Amides, e.g. hydroxamic acids
- A61K31/165—Amides, e.g. hydroxamic acids having aromatic rings, e.g. colchicine, atenolol, progabide
- A61K31/166—Amides, e.g. hydroxamic acids having aromatic rings, e.g. colchicine, atenolol, progabide having the carbon of a carboxamide group directly attached to the aromatic ring, e.g. procainamide, procarbazine, metoclopramide, labetalol
-
- 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
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/4164—1,3-Diazoles
- A61K31/4188—1,3-Diazoles condensed with other heterocyclic ring systems, e.g. biotin, sorbinil
-
- 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
- A61K31/4439—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
- A61K31/535—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
- A61K31/5375—1,4-Oxazines, e.g. morpholine
- A61K31/5377—1,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
-
- 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
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/18—Drugs for disorders of the alimentary tract or the digestive system for pancreatic disorders, e.g. pancreatic enzymes
-
- 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
- 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
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Epidemiology (AREA)
- Organic Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Hematology (AREA)
- Oncology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Abstract
La invención se refiere a una combinación farmacéutica que comprende (a) un compuesto inhibidor de fosfoinosítido 3-cinasa y (b) un compuesto que modula la ruta de Ras/Raf/Mek para el tratamiento de una enfermedad proliferativa, en especial una enfermedad de tumor sólido; a una composición farmacéutica que comprende dicha combinación; al uso de dicha combinación para la preparación de un medicamento para el tratamiento de una enfermedad proliferativa; a un paquete o producto comercial que comprende dicha combinación como una preparación combinada para uso simultáneo, separado o secuencial; y a un método de tratamiento de un animal de sangre caliente, en especial un humano.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP08160218 | 2008-07-11 | ||
PCT/US2009/050192 WO2010006225A1 (en) | 2008-07-11 | 2009-07-10 | Combination of (a) a phosphoinositide 3-kinase inhibitor and (b) a modulator of ras/raf/mek pathway |
Publications (1)
Publication Number | Publication Date |
---|---|
MX336723B true MX336723B (es) | 2016-01-28 |
Family
ID=39739487
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
MX2011000440A MX2011000440A (es) | 2008-07-11 | 2009-07-10 | Combinacion de (a) un inhibidor de fosfoinositido 3-cinasa y (b) un modulador de la ruta de ras/raf/mek. |
MX2013005357A MX336723B (es) | 2008-07-11 | 2009-07-10 | Combinacion de (a) un inhibidor de fosfoinositido 3-cinasa y (b) un modulador de la ruta de ras/raf/mek. |
Family Applications Before (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
MX2011000440A MX2011000440A (es) | 2008-07-11 | 2009-07-10 | Combinacion de (a) un inhibidor de fosfoinositido 3-cinasa y (b) un modulador de la ruta de ras/raf/mek. |
Country Status (11)
Country | Link |
---|---|
US (3) | US20110105521A1 (es) |
EP (1) | EP2310050A1 (es) |
JP (2) | JP2011527703A (es) |
KR (1) | KR20110028651A (es) |
CN (1) | CN102089007B (es) |
AU (1) | AU2009268469B2 (es) |
BR (1) | BRPI0915901A2 (es) |
CA (1) | CA2729914A1 (es) |
MX (2) | MX2011000440A (es) |
RU (2) | RU2508110C2 (es) |
WO (1) | WO2010006225A1 (es) |
Families Citing this family (47)
Publication number | Priority date | Publication date | Assignee | Title |
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ATE428421T1 (de) | 2004-09-17 | 2009-05-15 | Eisai R&D Man Co Ltd | Medizinische zusammensetzung mit verbesserter stabilität und reduzierten gelierungseigenschaften |
EP1925676A4 (en) | 2005-08-02 | 2010-11-10 | Eisai R&D Man Co Ltd | TEST METHOD FOR THE EFFECT OF A VASCULARIZATION INHIBITOR |
ES2556173T3 (es) | 2006-05-18 | 2016-01-13 | Eisai R&D Management Co., Ltd. | Agente antitumoral para un cáncer de tiroides |
JP2011527703A (ja) | 2008-07-11 | 2011-11-04 | ノバルティス アーゲー | (a)ホスホイノシタイド3−キナーゼ阻害剤および(b)Ras/Raf/Mek経路のモジュレーターの配合物 |
KR20120096869A (ko) * | 2009-05-15 | 2012-08-31 | 노파르티스 아게 | 포스포이노시티드 3-키나제 억제제 및 항당뇨병 화합물의 조합물 |
US20130217710A1 (en) * | 2010-11-05 | 2013-08-22 | Glaxosmithkline Intellectual Property (No.2) Limited | Methods for treating cancer |
WO2012066451A1 (en) * | 2010-11-15 | 2012-05-24 | Pfizer Inc. | Prognostic and predictive gene signature for colon cancer |
JP2013545757A (ja) * | 2010-11-17 | 2013-12-26 | グラクソスミスクライン、インテレクチュアル、プロパティー、ナンバー2、リミテッド | 癌の治療方法 |
WO2012068562A2 (en) * | 2010-11-19 | 2012-05-24 | The Regents Of The University Of California | Compositions and methods for detection and treatment of b-raf inhibitor-resistant melanomas |
ES2688809T3 (es) | 2011-04-01 | 2018-11-07 | Genentech, Inc. | Combinaciones de compuestos inhibidores de AKT y MEK para tratar el cáncer |
RU2580609C2 (ru) * | 2011-04-18 | 2016-04-10 | Эйсай Ар Энд Ди Менеджмент Ко., Лтд. | Противоопухолевое терапевтическое средство |
ES2705950T3 (es) | 2011-06-03 | 2019-03-27 | Eisai R&D Man Co Ltd | Biomarcadores para predecir y valorar la capacidad de respuesta de sujetos con cáncer de tiroides y de riñón a compuestos de lenvatinib |
WO2013019906A1 (en) | 2011-08-01 | 2013-02-07 | Genentech, Inc. | Methods of treating cancer using pd-1 axis binding antagonists and mek inhibitors |
US9675595B2 (en) | 2011-08-31 | 2017-06-13 | Novartis Ag | Synergistic combinations of PI3K- and MEK-inhibitors |
SG11201401815XA (en) * | 2011-10-28 | 2014-05-29 | Genentech Inc | Therapeutic combinations and methods of treating melanoma |
US20140341916A1 (en) * | 2011-10-28 | 2014-11-20 | Genentech, Inc. | Therapeutic combinations and methods of treating melanoma |
WO2013082511A1 (en) | 2011-12-02 | 2013-06-06 | Genentech, Inc. | Methods for overcoming tumor resistance to vegf antagonists |
WO2013106683A1 (en) * | 2012-01-11 | 2013-07-18 | Duke University | Methods of treating and preventing cancer by disrupting the binding of copper in the map kinase pathway |
WO2013109142A1 (en) | 2012-01-16 | 2013-07-25 | Stichting Het Nederlands Kanker Instituut | Combined pdk and mapk/erk pathway inhibition in neoplasia |
AR091876A1 (es) | 2012-07-26 | 2015-03-04 | Novartis Ag | Combinaciones farmaceuticas para el tratamiento de enfermedades proliferativas |
CN104797270A (zh) | 2012-08-02 | 2015-07-22 | 基因泰克公司 | 抗etbr抗体和免疫偶联物 |
MX2015001399A (es) | 2012-08-02 | 2015-09-07 | Genentech Inc | Anticuerpos anti-etbr e inmunoconjugados. |
BR112015002528A2 (pt) * | 2012-08-16 | 2018-05-22 | Novartis Ag | combinação de inibidor de pi3k e inibidor de c-met, seus usos, composição farmacêutica e embalagem comercial |
JPWO2014098176A1 (ja) | 2012-12-21 | 2017-01-12 | エーザイ・アール・アンド・ディー・マネジメント株式会社 | キノリン誘導体のアモルファス及びその製造方法 |
EP2943199A1 (en) * | 2013-01-09 | 2015-11-18 | Glaxosmithkline Intellectual Property (No. 2) Limited | Combination |
US9611258B2 (en) * | 2013-03-13 | 2017-04-04 | The Regents Of The University Of Michigan | Dual MEK/PI3K inhibitors and therapeutic methods using the same |
US9522130B2 (en) | 2013-03-14 | 2016-12-20 | Thomas Cooper Woods | Use of miR-221 and 222 lowering agents to prevent cardiovascular disease in diabetic subjects |
WO2014160358A1 (en) * | 2013-03-14 | 2014-10-02 | Thomas Cooper Woods | Use of mir-221 and 222 lowering agents to prevent cardiovascular disease in diabetic subjects |
AU2014230098A1 (en) * | 2013-03-15 | 2015-10-01 | Sanofi | Anti-tumoral composition comprising a PI3kbeta inhibitor and a RAF inhibitor, to overcome cancer cells resistance |
KR102204279B1 (ko) | 2013-05-14 | 2021-01-15 | 에자이 알앤드디 매니지먼트 가부시키가이샤 | 자궁내막암 대상의 렌바티닙 화합물에 대한 반응성을 예측 및 평가하기 위한 생체표지 |
KR20160020502A (ko) * | 2013-06-18 | 2016-02-23 | 노파르티스 아게 | 제약 조합물 |
US9227969B2 (en) | 2013-08-14 | 2016-01-05 | Novartis Ag | Compounds and compositions as inhibitors of MEK |
WO2015041534A1 (en) | 2013-09-20 | 2015-03-26 | Stichting Het Nederlands Kanker Instituut | P90rsk in combination with raf/erk/mek |
US9629851B2 (en) | 2013-09-20 | 2017-04-25 | Stitching Het Nederlands Kanker Institut—Antoni Van Leeuwenhoek Ziekenhuis | ROCK in combination with MAPK pathway |
CN105745207A (zh) * | 2013-10-03 | 2016-07-06 | 千年药物公司 | 使用PI3Kα抑制剂的增强的治疗方案 |
US20170027940A1 (en) | 2014-04-10 | 2017-02-02 | Stichting Het Nederlands Kanker Instituut | Method for treating cancer |
WO2015178770A1 (en) | 2014-05-19 | 2015-11-26 | Stichting Het Nederlands Kanker Instituut | Compositions for cancer treatment |
EP3563870A1 (en) | 2014-07-15 | 2019-11-06 | F. Hoffmann-La Roche AG | Methods of treating cancer using pd-1 axis binding antagonists and mek inhibitors |
EP3825305A1 (en) | 2014-08-28 | 2021-05-26 | Eisai R&D Management Co., Ltd. | Process for preparing lenvatinib |
WO2016136745A1 (ja) | 2015-02-25 | 2016-09-01 | エーザイ・アール・アンド・ディー・マネジメント株式会社 | キノリン誘導体の苦味抑制方法 |
AU2015384801B2 (en) | 2015-03-04 | 2022-01-06 | Eisai R&D Management Co., Ltd. | Combination of a PD-1 antagonist and a VEGFR/FGFR/RET tyrosine kinase inhibitor for treating cancer |
KR20160129609A (ko) | 2015-04-30 | 2016-11-09 | 삼성전자주식회사 | Braf 저해제를 포함하는 세포 또는 개체의 노화를 감소시키기 위한 조성물 및 그의 용도 |
BR112017027227B1 (pt) | 2015-06-16 | 2023-12-12 | Eisai R&D Management Co., Ltd | Agente anti-câncer |
WO2018134254A1 (en) | 2017-01-17 | 2018-07-26 | Heparegenix Gmbh | Protein kinase inhibitors for promoting liver regeneration or reducing or preventing hepatocyte death |
CN107802838A (zh) * | 2017-09-25 | 2018-03-16 | 石河子大学 | PLCE1抑制剂与NF‑κB通路抑制剂联合在制备治疗食管鳞癌的药物中的应用 |
CN110760582A (zh) * | 2019-07-10 | 2020-02-07 | 中山大学 | 二甲双胍在治疗kras突变型结直肠癌中的应用 |
CN114053416A (zh) * | 2021-10-11 | 2022-02-18 | 中山大学附属第一医院 | Pi3k抑制剂在制备用于治疗对flt3抑制剂耐药的药物中的应用 |
Family Cites Families (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
RU2192861C1 (ru) * | 2001-06-29 | 2002-11-20 | Новосибирский институт биоорганической химии СО РАН | Композиция для антибластической терапии |
US20030133903A1 (en) | 2001-07-19 | 2003-07-17 | Wenbin Dang | Compositions for treatment of prostate cancers and methods of making and using the same |
US7235537B2 (en) * | 2002-03-13 | 2007-06-26 | Array Biopharma, Inc. | N3 alkylated benzimidazole derivatives as MEK inhibitors |
US7378423B2 (en) * | 2004-06-11 | 2008-05-27 | Japan Tobacco Inc. | Pyrimidine compound and medical use thereof |
ATE539064T1 (de) | 2005-05-18 | 2012-01-15 | Array Biopharma Inc | Heterozyklische inhibitoren von mek und verwendungsverfahren damit |
GB0510390D0 (en) * | 2005-05-20 | 2005-06-29 | Novartis Ag | Organic compounds |
PE20070335A1 (es) * | 2005-08-30 | 2007-04-21 | Novartis Ag | Benzimidazoles sustituidos y metodos para su preparacion |
JO2660B1 (en) * | 2006-01-20 | 2012-06-17 | نوفارتيس ايه جي | Pi-3 inhibitors and methods of use |
EP2074122B9 (en) * | 2006-09-15 | 2013-09-11 | Pfizer Products Inc. | Pyrido (2, 3-d) pyrimidin0ne compounds and their use as pi3 inhibitors |
JP2011527703A (ja) | 2008-07-11 | 2011-11-04 | ノバルティス アーゲー | (a)ホスホイノシタイド3−キナーゼ阻害剤および(b)Ras/Raf/Mek経路のモジュレーターの配合物 |
UA104147C2 (uk) | 2008-09-10 | 2014-01-10 | Новартис Аг | Похідна піролідиндикарбонової кислоти та її застосування у лікуванні проліферативних захворювань |
TWI428336B (zh) | 2009-10-12 | 2014-03-01 | Hoffmann La Roche | Pi3k抑制劑及mek抑制劑之組合 |
-
2009
- 2009-07-10 JP JP2011517641A patent/JP2011527703A/ja active Pending
- 2009-07-10 RU RU2011104570/15A patent/RU2508110C2/ru not_active IP Right Cessation
- 2009-07-10 WO PCT/US2009/050192 patent/WO2010006225A1/en active Application Filing
- 2009-07-10 KR KR1020117003118A patent/KR20110028651A/ko not_active Application Discontinuation
- 2009-07-10 CA CA 2729914 patent/CA2729914A1/en not_active Abandoned
- 2009-07-10 EP EP20090795223 patent/EP2310050A1/en not_active Withdrawn
- 2009-07-10 MX MX2011000440A patent/MX2011000440A/es active IP Right Grant
- 2009-07-10 BR BRPI0915901A patent/BRPI0915901A2/pt not_active IP Right Cessation
- 2009-07-10 US US13/003,581 patent/US20110105521A1/en not_active Abandoned
- 2009-07-10 CN CN2009801265844A patent/CN102089007B/zh not_active Withdrawn - After Issue
- 2009-07-10 MX MX2013005357A patent/MX336723B/es unknown
- 2009-07-10 AU AU2009268469A patent/AU2009268469B2/en not_active Ceased
-
2013
- 2013-07-05 RU RU2013131004/15A patent/RU2013131004A/ru not_active Application Discontinuation
- 2013-10-30 US US14/066,734 patent/US20140057904A1/en not_active Abandoned
-
2014
- 2014-09-08 JP JP2014181858A patent/JP5931982B2/ja active Active
- 2014-12-19 US US14/576,314 patent/US9241939B2/en not_active Expired - Fee Related
Also Published As
Publication number | Publication date |
---|---|
JP5931982B2 (ja) | 2016-06-08 |
EP2310050A1 (en) | 2011-04-20 |
BRPI0915901A2 (pt) | 2015-10-27 |
RU2508110C2 (ru) | 2014-02-27 |
RU2011104570A (ru) | 2012-08-20 |
CN102089007B (zh) | 2013-05-15 |
WO2010006225A1 (en) | 2010-01-14 |
US9241939B2 (en) | 2016-01-26 |
CN102089007A (zh) | 2011-06-08 |
MX2011000440A (es) | 2011-02-24 |
US20110105521A1 (en) | 2011-05-05 |
US20150105417A1 (en) | 2015-04-16 |
AU2009268469A1 (en) | 2010-01-14 |
AU2009268469B2 (en) | 2013-02-28 |
JP2015007110A (ja) | 2015-01-15 |
KR20110028651A (ko) | 2011-03-21 |
RU2013131004A (ru) | 2015-01-10 |
JP2011527703A (ja) | 2011-11-04 |
CA2729914A1 (en) | 2010-01-14 |
US20140057904A1 (en) | 2014-02-27 |
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