MA28880B1 - Forme thermodynamiquement stable de tosylate de bay 43-9006 - Google Patents

Forme thermodynamiquement stable de tosylate de bay 43-9006

Info

Publication number
MA28880B1
MA28880B1 MA29784A MA29784A MA28880B1 MA 28880 B1 MA28880 B1 MA 28880B1 MA 29784 A MA29784 A MA 29784A MA 29784 A MA29784 A MA 29784A MA 28880 B1 MA28880 B1 MA 28880B1
Authority
MA
Morocco
Prior art keywords
tosylate
bay
thermodynamically stable
stable form
thermodynamically
Prior art date
Application number
MA29784A
Other languages
English (en)
Inventor
Alfons Grunenberg
Jana Lenz
Original Assignee
Bayer Schering Pharma Ag
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
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=35482258&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=MA28880(B1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Bayer Schering Pharma Ag filed Critical Bayer Schering Pharma Ag
Publication of MA28880B1 publication Critical patent/MA28880B1/fr

Links

Classifications

    • 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
    • C07D213/78—Carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen, e.g. ester or nitrile radicals
    • C07D213/81—Amides; Imides
    • 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
    • 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
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P7/00—Drugs for disorders of the blood or the extracellular fluid
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Hematology (AREA)
  • Cardiology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Diabetes (AREA)
  • Oncology (AREA)
  • Epidemiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Pyridine Compounds (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Analysing Materials By The Use Of Radiation (AREA)
  • Medicinal Preparation (AREA)
  • Paper (AREA)
  • Catalysts (AREA)
  • Glass Compositions (AREA)
MA29784A 2004-09-29 2007-03-29 Forme thermodynamiquement stable de tosylate de bay 43-9006 MA28880B1 (fr)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
EP04023130 2004-09-29

Publications (1)

Publication Number Publication Date
MA28880B1 true MA28880B1 (fr) 2007-09-03

Family

ID=35482258

Family Applications (1)

Application Number Title Priority Date Filing Date
MA29784A MA28880B1 (fr) 2004-09-29 2007-03-29 Forme thermodynamiquement stable de tosylate de bay 43-9006

Country Status (32)

Country Link
US (1) US8877933B2 (fr)
EP (1) EP1797038B1 (fr)
JP (2) JP5215666B2 (fr)
KR (4) KR101381454B1 (fr)
CN (1) CN101065360B (fr)
AR (1) AR051301A1 (fr)
AU (1) AU2005289100B2 (fr)
BR (1) BRPI0515946A (fr)
CA (1) CA2581843C (fr)
CU (1) CU20070068A7 (fr)
CY (1) CY1113598T1 (fr)
DK (1) DK1797038T3 (fr)
EC (1) ECSP077356A (fr)
ES (1) ES2387812T3 (fr)
GT (1) GT200500270A (fr)
HN (1) HN2005000722A (fr)
HR (1) HRP20120662T1 (fr)
IL (1) IL181734A (fr)
MA (1) MA28880B1 (fr)
MY (1) MY176929A (fr)
NO (1) NO344272B1 (fr)
NZ (1) NZ553804A (fr)
PE (3) PE20060699A1 (fr)
PL (1) PL1797038T3 (fr)
PT (1) PT1797038E (fr)
SG (1) SG155996A1 (fr)
SI (1) SI1797038T1 (fr)
TW (1) TWI382016B (fr)
UA (1) UA91520C2 (fr)
UY (1) UY29144A1 (fr)
WO (1) WO2006034797A1 (fr)
ZA (1) ZA200702510B (fr)

Families Citing this family (57)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8124630B2 (en) 1999-01-13 2012-02-28 Bayer Healthcare Llc ω-carboxyaryl substituted diphenyl ureas as raf kinase inhibitors
ATE538794T1 (de) 1999-01-13 2012-01-15 Bayer Healthcare Llc Gamma carboxyarylsubstituierte diphenylharnstoffverbindungen als p38 kinasehemmer
MXPA04007832A (es) 2002-02-11 2005-09-08 Bayer Pharmaceuticals Corp Aril-ureas con actividad inhibitoria de angiogenesis.
US10653684B2 (en) 2002-02-11 2020-05-19 Bayer Healthcare Llc Aryl ureas with angiogenisis inhibiting activity
US7557129B2 (en) 2003-02-28 2009-07-07 Bayer Healthcare Llc Cyanopyridine derivatives useful in the treatment of cancer and other disorders
WO2004113274A2 (fr) 2003-05-20 2004-12-29 Bayer Pharmaceuticals Corporation Diaryl-urees presentant une activite d'inhibition des kinases
EA010485B1 (ru) 2003-07-23 2008-10-30 Байер Фамэсьютиклс Копэрейшн Производное n,n'-дифенилмочевины, фармацевтическая композиция (варианты) и способ лечения и предупреждения заболеваний и состояний с его использованием (варианты)
KR101381454B1 (ko) 2004-09-29 2014-04-04 바이엘 인텔렉쳐 프로퍼티 게엠베하 열역학적으로 안정한 형태의 ｂａｙ 43-9006 토실레이트
SG160364A1 (en) 2005-03-07 2010-04-29 Bayer Schering Pharma Ag Pharmaceutical composition comprising an omega-carboxyaryl substituted diphenyl urea for the treatment of cancer
CA2627875A1 (fr) * 2005-10-31 2007-05-10 Bayer Pharmaceuticals Corporation Diaryle-urees et combinaisons
AR062927A1 (es) * 2006-10-11 2008-12-17 Bayer Healthcare Ag 4- [4-( [ [ 4- cloro-3-( trifluorometil) fenil) carbamoil] amino] -3- fluorofenoxi) -n- metilpiridin-2- carboxamida monohidratada
US20100113533A1 (en) * 2006-11-14 2010-05-06 Bayer Schering Pharma Aktiengesellschaft Polymorph II of 4-[4-(Amino)-3- Fluorophenoxy]-N-Methylpyridine-2-Carboxamide
CN101220024A (zh) * 2007-12-11 2008-07-16 杜晓敏 一组抑制激酶的抗癌化合物
WO2009092070A1 (fr) * 2008-01-17 2009-07-23 Sicor Inc. Polymorphes de forme iii de tosylate de sorafénib, solvate de méthanol tosylate de sorafénib et solvate d'éthanol tosylate de sorafénib, et procédés de préparation associés
WO2009106825A1 (fr) * 2008-02-27 2009-09-03 Cipla Limited Polymorphes de sorafénib et leurs sels
WO2010079498A2 (fr) * 2009-01-12 2010-07-15 Hetero Research Foundation Nouveau polymorphe de tosylate de sorafénib
JP2012524058A (ja) * 2009-04-15 2012-10-11 フォンダツィオーネ アイアールシーシーエス イスティトゥト ナツィオナーレ デイ トゥモリ 血管透過性亢進の治療におけるマルチキナーゼ阻害剤の使用
WO2010142678A2 (fr) * 2009-06-12 2010-12-16 Ratiopharm Gmbh Polymorphes de 4-[4-[[4-chloro-3-(trifluorométhyl)phényl]carbamoylamino]phénoxy]-n-méthyl-pyridine-2-carboxamide
US8604208B2 (en) 2009-09-24 2013-12-10 Ranbaxy Laboratories Limited Polymorphs of sorafenib acid addition salts
WO2011036647A1 (fr) 2009-09-24 2011-03-31 Ranbaxy Laboratories Limited Procédé de préparation de tosylate de sorafénib
WO2011058522A1 (fr) 2009-11-12 2011-05-19 Ranbaxy Laboratories Limited Sel d'ethylsulfonate de sorafenib et son procede de preparation
WO2011076711A2 (fr) 2009-12-23 2011-06-30 Ratiopharm Gmbh Polymorphes de 4-[4-[[4-chloro-3-(trifluorométhyl)phényl]carbamoylamino]phénoxy]-n-méthylpyridine-2-carboxamide
AU2011210326B2 (en) 2010-01-29 2014-10-09 Sun Pharmaceutical Industries Limited Sorafenib dimethyl sulphoxide solvate
AR081060A1 (es) 2010-04-15 2012-06-06 Bayer Schering Pharma Ag Procedimiento para preparar 4-{4-[({[4-cloro-3-(trifluorometil)fenil]amino}carbonil)amino]-3-fluorofenoxi}-n-metilpiridin-2-carboxamida
MA34553B1 (fr) 2010-10-01 2013-09-02 Bayer Ip Gmbh Combinaisons contenant du n-(2-arylamino)arylsulfonamide substitué
WO2012071425A1 (fr) 2010-11-22 2012-05-31 Teva Pharmaceutical Industries Ltd. Formes à l'état solide de bésylate de sorafénib et procédés de préparation
WO2013000909A1 (fr) 2011-06-28 2013-01-03 Bayer Intellectual Property Gmbh Composition pharmaceutique topique ophtalmologique contenant du sorafénib
EP2559431A1 (fr) 2011-08-17 2013-02-20 Ratiopharm GmbH Composition pharmaceutique comportant du 4-[4-[[4-Chloro-3-(trifluoromethyl)phényl]carbamoylamino]phénoxy]-N-méthyl-pyridine-2-carboxamide
IN2014KN01490A (fr) 2012-01-23 2015-10-23 Sandoz Ag
EP2852574B1 (fr) * 2012-05-21 2020-02-05 Hetero Research Foundation Procédé de préparation du polymorphe iii de tosylate de sorafénib
US20150111929A1 (en) * 2012-05-23 2015-04-23 Shilpa Medicare Limited Process for preparing crystalline sorafenib tosylate
CN103570613B (zh) * 2012-07-18 2016-06-15 苏州泽璟生物制药有限公司 氘代ω-二苯基脲或其盐的多晶型物
CN103896833B (zh) * 2012-12-27 2016-12-28 上海创诺制药有限公司 索拉非尼对甲苯磺酸盐溶剂化物多晶型物及其制法和用途
WO2014118807A1 (fr) * 2013-02-04 2014-08-07 Intas Pharmaceuticals Limited Nouveau procédé de préparation de tosylate de sorafénib de forme iii
WO2014138905A1 (fr) * 2013-03-14 2014-09-18 Apotex Technologies Inc. Formes de tosylate de sorafénib et procédés pour les préparer
WO2014181549A1 (fr) 2013-05-10 2014-11-13 株式会社デンソー Dispositif de commande d'injection de carburant et système d'injection de carburant
CN104761492A (zh) * 2014-01-03 2015-07-08 正大天晴药业集团股份有限公司 对甲苯磺酸索拉非尼的晶型及其制备方法
US20170114323A1 (en) * 2014-06-19 2017-04-27 Whitehead Institute For Biomedical Research Uses of kinase inhibitors for inducing and maintaining pluripotency
CN104177292A (zh) * 2014-08-08 2014-12-03 亿腾药业（泰州）有限公司 一种工业化生产甲苯磺酸索拉非尼多晶型ⅰ的方法
CN105439947A (zh) * 2014-12-01 2016-03-30 石药集团中奇制药技术（石家庄）有限公司 一种甲苯磺酸索拉非尼新晶型及其制备方法
RU2568638C1 (ru) * 2015-02-26 2015-11-20 Индивидуальный предприниматель Михайлов Олег Ростиславович КРИСТАЛЛИЧЕСКАЯ β-МОДИФИКАЦИЯ 4-[4-({ [4-ХЛОРО-3-(ТРИФТОРОМЕТИЛ) ФЕНИЛ]КАРБАМОИЛ} АМИНО)ФЕНОКСИ]-N-МЕТИЛ-ПИРИДИН-2-КАРБОКСАМИДА п-ТОЛУОЛСУЛЬФОНАТА, СПОСОБ ЕЁ ПОЛУЧЕНИЯ И ФАРМАЦЕВТИЧЕСКАЯ КОМПОЗИЦИЯ НА ЕЁ ОСНОВЕ
EP3109236B1 (fr) 2015-06-23 2017-08-09 F.I.S.- Fabbrica Italiana Sintetici S.p.A. Procédé évolutif pour la préparation de solvate d'éthanol tosylate de sorafénibe et tosylate de sorafénibe forme iii
CN106336377A (zh) * 2015-07-17 2017-01-18 苏州亚宝药物研发有限公司 一种甲苯磺酸索拉非尼晶型ⅱ的制备方法
CN105503715A (zh) * 2015-12-03 2016-04-20 神威药业集团有限公司 一种索拉非尼半甲苯磺酸盐多晶型及其制备方法
CN105585523A (zh) * 2015-12-29 2016-05-18 上海北卡医药技术有限公司 一种对甲苯磺酸索拉非尼的新晶型及其制备方法和用途
CN107759517A (zh) * 2016-08-23 2018-03-06 广州白云山医药集团股份有限公司白云山制药总厂 一种甲苯磺酸索拉非尼晶型ⅰ的制备方法
CN107840823B (zh) * 2016-09-20 2021-08-17 意大利合成制造有限公司 用于制备甲苯磺酸索拉非尼乙醇溶剂化物和iii型甲苯磺酸索拉非尼的可变规模的方法
CN108164459B (zh) * 2016-12-07 2021-07-27 上海创诺制药有限公司 甲苯磺酸索拉非尼晶型iii的制备方法
KR102707399B1 (ko) 2017-01-05 2024-09-13 래디어스 파마슈티컬스, 인코포레이티드 Rad1901-2hcl의 다형 형태
CN109796400B (zh) * 2017-11-16 2022-07-29 四川科伦药物研究院有限公司 一种甲苯磺酸索拉菲尼晶型及其制备方法
US11179322B2 (en) 2018-07-10 2021-11-23 Novocure Gmbh Methods and compositions for treating tumors with TTFields and sorafenib
WO2018211336A2 (fr) 2018-09-07 2018-11-22 Alvogen Malta Operations (Row) Ltd Forme galénique solide contenant du tosylate de sorafénib
CN113677346A (zh) 2018-11-01 2021-11-19 希洛斯医药品股份有限公司 周期蛋白依赖性激酶7(cdk7)的抑制剂
CN110156671A (zh) * 2019-06-06 2019-08-23 杭州中美华东制药有限公司 新型的索拉非尼共晶及其制备方法
EP4725489A2 (fr) 2019-08-02 2026-04-15 OneHealthCompany, Inc. Traitement de cancers canins
KR102887639B1 (ko) * 2019-10-25 2025-11-18 한미약품 주식회사 생산성 및 용출성이 개선된 소라페닙 토실레이트염의 제제 및 그 제조 방법
CN117088809A (zh) * 2022-05-12 2023-11-21 浙江工业大学 一种索拉非尼-丙二酸共晶及其制备方法

Family Cites Families (53)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5629425A (en) * 1994-09-19 1997-05-13 Eli Lilly And Company Haloalkyl hemisolvates of 6-hydroxy-2-(4-hydroxyphenyl)-3-[4-piperidinoethoxy)-benzoyl]benzo[b]thiophene
CO4410191A1 (es) 1994-09-19 1997-01-09 Lilly Co Eli SINTESIS DE 3-[4-(2-AMINOETOXI)BENZOIL]-2-ARIL-6- HIDROXIBENZO [b] TIOFENOS
AU1153097A (en) * 1996-06-07 1998-01-05 Eisai Co. Ltd. Stable polymorphs of donepezil (1-benzyl-4-{(5,6-dimethoxy-1-indanon)-2-yl}methylpiperidine ) hydrochloride and process for production
CZ299247B6 (cs) 1996-09-23 2008-05-28 Eli Lilly And Company Olanzapin dihydrát D
US6187799B1 (en) * 1997-05-23 2001-02-13 Onyx Pharmaceuticals Inhibition of raf kinase activity using aryl ureas
US6344476B1 (en) * 1997-05-23 2002-02-05 Bayer Corporation Inhibition of p38 kinase activity by aryl ureas
US7329670B1 (en) * 1997-12-22 2008-02-12 Bayer Pharmaceuticals Corporation Inhibition of RAF kinase using aryl and heteroaryl substituted heterocyclic ureas
US7517880B2 (en) * 1997-12-22 2009-04-14 Bayer Pharmaceuticals Corporation Inhibition of p38 kinase using symmetrical and unsymmetrical diphenyl ureas
US7351834B1 (en) 1999-01-13 2008-04-01 Bayer Pharmaceuticals Corporation ω-Carboxyaryl substituted diphenyl ureas as raf kinase inhibitors
WO2000042012A1 (fr) 1999-01-13 2000-07-20 Bayer Corporation DIPHENYLUREES A SUBSTITUANTS φ-CARBOXYARYLES, INHIBITRICES DE KINASE RAF
ATE538794T1 (de) 1999-01-13 2012-01-15 Bayer Healthcare Llc Gamma carboxyarylsubstituierte diphenylharnstoffverbindungen als p38 kinasehemmer
US8124630B2 (en) * 1999-01-13 2012-02-28 Bayer Healthcare Llc ω-carboxyaryl substituted diphenyl ureas as raf kinase inhibitors
US7928239B2 (en) * 1999-01-13 2011-04-19 Bayer Healthcare Llc Inhibition of RAF kinase using quinolyl, isoquinolyl or pyridyl ureas
US7235576B1 (en) * 2001-01-12 2007-06-26 Bayer Pharmaceuticals Corporation Omega-carboxyaryl substituted diphenyl ureas as raf kinase inhibitors
US7371763B2 (en) 2001-04-20 2008-05-13 Bayer Pharmaceuticals Corporation Inhibition of raf kinase using quinolyl, isoquinolyl or pyridyl ureas
JP4982685B2 (ja) * 2001-12-03 2012-07-25 バイエル、ファーマシューテイカルズ、コーポレイション ヒトがんを処置するための他の細胞毒剤又は細胞増殖抑制剤と組合わせたアリール尿素化合物
GB0129876D0 (en) 2001-12-13 2002-02-06 Smithkline Beecham Plc Novel pharmaceutical
US20030207872A1 (en) * 2002-01-11 2003-11-06 Bayer Corporation Omega-carboxyaryl substituted diphenyl ureas as raf kinase inhibitors
MXPA04007830A (es) * 2002-02-11 2005-07-01 Bayer Pharmaceuticals Corp Arilureas como inhibidores de cinasa.
WO2003068229A1 (fr) * 2002-02-11 2003-08-21 Bayer Pharmaceuticals Corporation N-oxydes de pyridine, de quinoline, et d'isoquinoline en tant qu'inhibiteurs de kinase
MXPA04007832A (es) * 2002-02-11 2005-09-08 Bayer Pharmaceuticals Corp Aril-ureas con actividad inhibitoria de angiogenesis.
GB0203412D0 (en) 2002-02-13 2002-04-03 Pharmagene Lab Ltd 5-HT 2B receptor antagonists
CN1716417A (zh) 2002-03-29 2006-01-04 索尼株式会社 光盘识别装置和方法、光盘记录装置和光盘再现装置
CN1290893C (zh) * 2002-05-03 2006-12-20 詹森药业有限公司 聚合物微乳状液
US7351534B2 (en) * 2003-01-27 2008-04-01 Oregon Health & Sciences University Gene mutation associated with age-related macular degeneration
US7557129B2 (en) * 2003-02-28 2009-07-07 Bayer Healthcare Llc Cyanopyridine derivatives useful in the treatment of cancer and other disorders
US7378233B2 (en) * 2003-04-12 2008-05-27 The Johns Hopkins University BRAF mutation T1796A in thyroid cancers
WO2004113274A2 (fr) * 2003-05-20 2004-12-29 Bayer Pharmaceuticals Corporation Diaryl-urees presentant une activite d'inhibition des kinases
EA010485B1 (ru) * 2003-07-23 2008-10-30 Байер Фамэсьютиклс Копэрейшн Производное n,n'-дифенилмочевины, фармацевтическая композиция (варианты) и способ лечения и предупреждения заболеваний и состояний с его использованием (варианты)
CN101010315A (zh) * 2004-04-30 2007-08-01 拜耳制药公司 用于治疗癌症的取代的吡唑基脲衍生物
MY191349A (en) * 2004-08-27 2022-06-17 Bayer Pharmaceuticals Corp New pharmaceutical compositions for the treatment of hyper-proliferative disorders
WO2006026501A1 (fr) * 2004-08-27 2006-03-09 Bayer Pharmaceuticals Corporation Nouvelles compositions pharmaceutiques pour le traitement du cancer
AU2005289099B2 (en) * 2004-09-29 2012-07-19 Bayer Healthcare Llc Process for the preparation of 4-{4-[({[4-chloro-3-(trifluoromethyl)phenyl]amino}carbonyl)amino]phenoxy}-N-methylpyridine-2-carboxamide
KR101381454B1 (ko) 2004-09-29 2014-04-04 바이엘 인텔렉쳐 프로퍼티 게엠베하 열역학적으로 안정한 형태의 ｂａｙ 43-9006 토실레이트
US7271763B2 (en) * 2005-03-03 2007-09-18 The United States Of America As Represented By The Secretary Of The Army Hybrid-phased communication array
SG160364A1 (en) 2005-03-07 2010-04-29 Bayer Schering Pharma Ag Pharmaceutical composition comprising an omega-carboxyaryl substituted diphenyl urea for the treatment of cancer
US8329408B2 (en) * 2005-10-31 2012-12-11 Bayer Healthcare Llc Methods for prognosis and monitoring cancer therapy
CA2627873A1 (fr) * 2005-10-31 2007-05-10 Scott Wilhelm Traitement du cancer au moyen de sorafenib
CA2628849A1 (fr) * 2005-11-10 2007-05-18 Bayer Healthcare Ag Diaryle-uree permettant de traiter l'hypertension pulmonaire
WO2007059154A2 (fr) * 2005-11-14 2007-05-24 Bayer Healthcare Llc Traitement de cancers a resistance acquise a des inhibiteurs de kit
AR062927A1 (es) * 2006-10-11 2008-12-17 Bayer Healthcare Ag 4- [4-( [ [ 4- cloro-3-( trifluorometil) fenil) carbamoil] amino] -3- fluorofenoxi) -n- metilpiridin-2- carboxamida monohidratada
CA2668748A1 (fr) * 2006-11-09 2008-05-15 Bayer Schering Pharma Aktiengesellschaft Polymorphe iii de 4-[4-({[4-chloro-3-(trifluoromethyl)phenyl]carbamoyl}amino)-3-fluorophenoxy]-n-methylpyridine-2-carboxamide
US20100113533A1 (en) * 2006-11-14 2010-05-06 Bayer Schering Pharma Aktiengesellschaft Polymorph II of 4-[4-(Amino)-3- Fluorophenoxy]-N-Methylpyridine-2-Carboxamide
DK2111401T3 (da) * 2006-12-20 2011-05-30 Bayer Healthcare Llc 4-{4-[({3-tert-butyl-1-[3-(hydroxymethyl)phenyl]-1H-pyrazol-5-yl}carbamoyl)-amino]-3-fluorphenoxy}-N-methylpyridin-2-carboxamid samt prodrug og salte heraf til behandling af cancer
US20100173954A1 (en) * 2007-01-19 2010-07-08 Bayer Healthcare Llc Treatment of cancers having resistance to chemotherapeutic agents
JP5885012B2 (ja) * 2007-01-19 2016-03-15 バイエル・ヘルスケア・エルエルシーＢａｙｅｒ ＨｅａｌｔｈＣａｒｅＬＬＣ Ｋｉｔ阻害剤に対して獲得した抵抗性を有する癌の処置
WO2009092070A1 (fr) * 2008-01-17 2009-07-23 Sicor Inc. Polymorphes de forme iii de tosylate de sorafénib, solvate de méthanol tosylate de sorafénib et solvate d'éthanol tosylate de sorafénib, et procédés de préparation associés
JP5439494B2 (ja) * 2008-10-21 2014-03-12 バイエル ヘルスケア エルエルシー 肝細胞癌と関連するシグネチャ遺伝子の同定
AR081060A1 (es) * 2010-04-15 2012-06-06 Bayer Schering Pharma Ag Procedimiento para preparar 4-{4-[({[4-cloro-3-(trifluorometil)fenil]amino}carbonil)amino]-3-fluorofenoxi}-n-metilpiridin-2-carboxamida
CA2805874A1 (fr) * 2010-07-19 2012-01-26 Bayer Healthcare Llc Associations medicamenteuses contenant une omega-carboxyaryl diphenyluree fluorosubstituee utilisees pour le traitement et la prevention de maladies et d'affections
MA34553B1 (fr) * 2010-10-01 2013-09-02 Bayer Ip Gmbh Combinaisons contenant du n-(2-arylamino)arylsulfonamide substitué
WO2013000909A1 (fr) 2011-06-28 2013-01-03 Bayer Intellectual Property Gmbh Composition pharmaceutique topique ophtalmologique contenant du sorafénib
KR20140048218A (ko) 2011-06-28 2014-04-23 바이엘 헬스케어 엘엘씨 레고라페닙을 함유하는 국소 안과용 약학 조성물

Also Published As

Publication number Publication date
PL1797038T3 (pl) 2012-11-30
CA2581843A1 (fr) 2006-04-06
ES2387812T3 (es) 2012-10-02
PE20060699A1 (es) 2006-08-12
TW200626552A (en) 2006-08-01
IL181734A0 (en) 2007-07-04
SI1797038T1 (sl) 2012-10-30
HK1114605A1 (en) 2008-11-07
PE20100445A1 (es) 2010-07-04
NO20071508L (no) 2007-06-22
KR20130004385A (ko) 2013-01-09
BRPI0515946A (pt) 2008-08-12
KR20090018224A (ko) 2009-02-19
WO2006034797A1 (fr) 2006-04-06
CY1113598T1 (el) 2016-06-22
JP2008514658A (ja) 2008-05-08
KR101381454B1 (ko) 2014-04-04
JP5215666B2 (ja) 2013-06-19
UY29144A1 (es) 2006-04-28
KR20100061869A (ko) 2010-06-09
JP2013100302A (ja) 2013-05-23
CN101065360A (zh) 2007-10-31
HN2005000722A (es) 2010-08-19
HRP20120662T1 (hr) 2012-09-30
EP1797038A1 (fr) 2007-06-20
DK1797038T3 (da) 2012-09-03
CA2581843C (fr) 2012-05-15
AU2005289100B2 (en) 2011-11-03
TWI382016B (zh) 2013-01-11
AU2005289100A1 (en) 2006-04-06
KR101239489B1 (ko) 2013-03-06
IL181734A (en) 2015-10-29
PE20142042A1 (es) 2014-12-03
PT1797038E (pt) 2012-08-14
ECSP077356A (es) 2007-04-26
KR20070058537A (ko) 2007-06-08
NO344272B1 (no) 2019-10-21
SG155996A1 (en) 2009-10-29
UA91520C2 (en) 2010-08-10
US20090215833A1 (en) 2009-08-27
US8877933B2 (en) 2014-11-04
ZA200702510B (en) 2008-07-30
NZ553804A (en) 2010-07-30
GT200500270A (es) 2006-04-25
CN101065360B (zh) 2011-08-03
AR051301A1 (es) 2007-01-03
MY176929A (en) 2020-08-27
CU20070068A7 (es) 2010-01-22
EP1797038B1 (fr) 2012-06-13

Similar Documents

Publication Publication Date Title
MA28880B1 (fr) Forme thermodynamiquement stable de tosylate de bay 43-9006
CY2013035I1 (el) Μεθοδοι χρησης συνθεσεων αμινοπυριδινης παρατεταμενης αποδεσμευσης
DK1830869T3 (da) Fremgangsmåde til behandling eller profylakse
DK1720866T3 (da) Fremgangsmåde
EP1888055A4 (fr) Huile de poisson sous forme stabilisee
EP1788874A4 (fr) Sels de 5-azacytidine
CR9144A (es) Formulaciones de benzoxazoles sustituidos
NO20043305D0 (no) Preparation of lodixanol
DK2119472T3 (da) Hud-/hårbehandlingssystem
DE112005003431A5 (de) Neuartige Inhibitoren der Lysyloxidase
EP1772148A4 (fr) Inhibiteurs de la lipase
PT1763520E (pt) Utilização de benzopiranonas trissubstituídas
EP1767205A4 (fr) Inhibiteurs de la lipase
EP1781286A4 (fr) Inhibiteurs de la kinesine mitotique
ITMI20041143A1 (it) Polimorfi di fexofenadina e procedimento per la loro preparazione
EP1773326A4 (fr) Inhibiteurs de la kinesine mitotique
FR2870675B1 (fr) Petrin malaxeur fermenteur de pates viscoelastiques
EP1791972A4 (fr) Rapporteurs camp
ITMI20040586A1 (it) Emulsioni complesse di perfluoropolieteri
ITMI20042239A1 (it) Additivi per fluoropolieterei
ITMI20042139A1 (it) Procedimento per la produzione di cefepime e cefaposporine analoghe
FR2877833B1 (fr) Correcteur de lordoses
ITTO20050018A1 (it) Struttura per la disposizione di cuscinetti.
FR2878522B1 (fr) Nouveaux inhibiteurs specifiques de la caspas-10
ITMI20041086A1 (it) Procedimento per la preparazione di idrocarbilalogenuri