MA29378B1 - Composition pharmaceutique comprenant une diphenyluree substituee par un omega-carboxyaryle pour le traitement du cancer - Google Patents

Composition pharmaceutique comprenant une diphenyluree substituee par un omega-carboxyaryle pour le traitement du cancer

Info

Publication number
MA29378B1
MA29378B1 MA30267A MA30267A MA29378B1 MA 29378 B1 MA29378 B1 MA 29378B1 MA 30267 A MA30267 A MA 30267A MA 30267 A MA30267 A MA 30267A MA 29378 B1 MA29378 B1 MA 29378B1
Authority
MA
Morocco
Prior art keywords
cancer
treatment
pharmaceutical composition
diphenyluree
carboxyaryl
Prior art date
Application number
MA30267A
Other languages
English (en)
Inventor
Fritz Schueckler
Axel Wollenschlaeger
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=36507604&utm_source=***_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=MA29378(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 MA29378B1 publication Critical patent/MA29378B1/fr

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435Heterocyclic 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
    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/20Pills, tablets, discs, rods
    • A61K9/2004Excipients; Inactive ingredients
    • A61K9/2013Organic compounds, e.g. phospholipids, fats
    • A61K9/2018Sugars, or sugar alcohols, e.g. lactose, mannitol; Derivatives thereof, e.g. polysorbates
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435Heterocyclic 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
    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/4409Non condensed pyridines; Hydrogenated derivatives thereof only substituted in position 4, e.g. isoniazid, iproniazid
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435Heterocyclic 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
    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/4412Non condensed pyridines; Hydrogenated derivatives thereof having oxo groups directly attached to the heterocyclic ring
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/20Pills, tablets, discs, rods
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/20Pills, tablets, discs, rods
    • A61K9/2004Excipients; Inactive ingredients
    • A61K9/2022Organic macromolecular compounds
    • A61K9/205Polysaccharides, e.g. alginate, gums; Cyclodextrin
    • A61K9/2054Cellulose; Cellulose derivatives, e.g. hydroxypropyl methylcellulose
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/20Pills, tablets, discs, rods
    • A61K9/28Dragees; Coated pills or tablets, e.g. with film or compression coating
    • A61K9/2806Coating materials
    • A61K9/2813Inorganic compounds
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/20Pills, tablets, discs, rods
    • A61K9/28Dragees; Coated pills or tablets, e.g. with film or compression coating
    • A61K9/2806Coating materials
    • A61K9/2833Organic macromolecular compounds
    • A61K9/284Organic macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds, e.g. polyvinyl pyrrolidone
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/20Pills, tablets, discs, rods
    • A61K9/28Dragees; Coated pills or tablets, e.g. with film or compression coating
    • A61K9/2806Coating materials
    • A61K9/2833Organic macromolecular compounds
    • A61K9/286Polysaccharides, e.g. gums; Cyclodextrin
    • A61K9/2866Cellulose; Cellulose derivatives, e.g. hydroxypropyl methylcellulose
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • A61P35/02Antineoplastic agents specific for leukemia
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • A61P35/04Antineoplastic agents specific for metastasis
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Epidemiology (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • General Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Inorganic Chemistry (AREA)
  • Biophysics (AREA)
  • Molecular Biology (AREA)
  • Oncology (AREA)
  • Hematology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Medicinal Preparation (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)

Abstract

LA PRÉSENTE INVENTION CONCERNE UNE COMPOSITION PHARMACEUTIQUE QUI COMPREND LE COMPOSÉ DE LA FORMULE (I) À UNE CONCENTRATION ÉLEVÉE ET AU MOINS UN EXCIPIENT PHARMACEUTIQUEMENT ACCEPTABLE, L'UTILISATION DE LA COMPOSITION POUR LE TRAITEMENT DE MALADIES HYPERPROLIFÉRATIVES, TELLES QUE LE CANCER, SOIT COMME SEUL AGENT OU EN COMBINAISON AVEC D¿AUTRES THÉRAPIES ANTICANCÉREUSES, AINSI QUE LE PROCÉDÉ DE PRÉPARATION DE LADITE COMPOSITION.
MA30267A 2005-03-07 2007-10-02 Composition pharmaceutique comprenant une diphenyluree substituee par un omega-carboxyaryle pour le traitement du cancer MA29378B1 (fr)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US65882705P 2005-03-07 2005-03-07

Publications (1)

Publication Number Publication Date
MA29378B1 true MA29378B1 (fr) 2008-04-01

Family

ID=36507604

Family Applications (1)

Application Number Title Priority Date Filing Date
MA30267A MA29378B1 (fr) 2005-03-07 2007-10-02 Composition pharmaceutique comprenant une diphenyluree substituee par un omega-carboxyaryle pour le traitement du cancer

Country Status (38)

Country Link
US (2) US9737488B2 (fr)
EP (1) EP1868579B1 (fr)
JP (1) JP5304241B2 (fr)
KR (1) KR101335932B1 (fr)
CN (2) CN104688697A (fr)
AR (1) AR054234A1 (fr)
AT (1) ATE482693T1 (fr)
AU (1) AU2006222365B2 (fr)
BR (1) BRPI0608840B8 (fr)
CA (1) CA2601955C (fr)
CR (1) CR9348A (fr)
CU (1) CU23821A3 (fr)
CY (1) CY1111065T1 (fr)
DE (1) DE602006017188D1 (fr)
DK (1) DK1868579T3 (fr)
DO (1) DOP2006000057A (fr)
ES (1) ES2351612T3 (fr)
GT (1) GT200600096A (fr)
HK (2) HK1118019A1 (fr)
HN (1) HN2006009702A (fr)
HR (1) HRP20100674T1 (fr)
IL (1) IL185517A (fr)
MA (1) MA29378B1 (fr)
MX (1) MX2007010856A (fr)
MY (1) MY162319A (fr)
NO (1) NO343834B1 (fr)
NZ (1) NZ561178A (fr)
PE (1) PE20061345A1 (fr)
PL (1) PL1868579T3 (fr)
PT (1) PT1868579E (fr)
SG (1) SG160364A1 (fr)
SI (1) SI1868579T1 (fr)
TN (1) TNSN07341A1 (fr)
TW (1) TWI324928B (fr)
UA (1) UA93673C2 (fr)
UY (1) UY29410A1 (fr)
WO (1) WO2006094626A1 (fr)
ZA (1) ZA200707638B (fr)

Families Citing this family (30)

* 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
ATE556713T1 (de) 1999-01-13 2012-05-15 Bayer Healthcare Llc Omega-carboxyarylsubstituierte-diphenyl- harnstoffe als p38-kinasehemmer
AU2003209116A1 (en) 2002-02-11 2003-09-04 Bayer Pharmaceuticals Corporation Aryl ureas with angiogenesis inhibiting activity
US7557129B2 (en) 2003-02-28 2009-07-07 Bayer Healthcare Llc Cyanopyridine derivatives useful in the treatment of cancer and other disorders
JP4860474B2 (ja) 2003-05-20 2012-01-25 バイエル、ファーマシューテイカルズ、コーポレイション Pdgfrによって仲介される病気のためのジアリール尿素
DK1663978T3 (da) 2003-07-23 2008-04-07 Bayer Pharmaceuticals Corp Fluorsubstitueret omega-carboxyaryl-diphenylurinstof til behandling og forebyggelse af sygdomme og lidelser
UA91520C2 (en) 2004-09-29 2010-08-10 Баер Шеринг Фарма Акциенгезельшафт Thermodynamically stable form of tosylate
UA93673C2 (ru) 2005-03-07 2011-03-10 Баер Шеринг Фарма Акциенгезельшафт Фармацевтическая композиция, которая содержит омега-карбоксиарилзамещенную дифенилмочевину, для лечения paka
US20090068146A1 (en) 2005-10-31 2009-03-12 Scott Wilhelm Diaryl ureas and combinations
TW200820991A (en) * 2006-07-10 2008-05-16 Elan Pharma Int Ltd Nanoparticulate sorafenib formulations
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
CA2675980C (fr) 2007-01-19 2016-06-21 Bayer Healthcare Llc Utilisation de dast dans le traitement des cancers a resistance acquise a des inhibiteurs de kit
WO2009106825A1 (fr) * 2008-02-27 2009-09-03 Cipla Limited Polymorphes de sorafénib et leurs sels
ES2969144T3 (es) 2008-05-15 2024-05-16 Celgene Corp Formulaciones orales de análogos de citidina y métodos de uso de los mismos
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
WO2011092663A2 (fr) 2010-01-29 2011-08-04 Ranbaxy Laboratories Limited Solvate de diméthylsulfoxyde du 4-(4-{3-[4-chloro-3-(trifluorométhyl)phényl]uréido}phénoxy)-n2-méthylpyridine-2-carboxamide
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
WO2012041987A1 (fr) 2010-10-01 2012-04-05 Bayer Pharma Aktiengesellschaft Combinaisons contenant du n-(2-arylamino)arylsulfonamide substitué
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
EP2806860B1 (fr) 2012-01-23 2023-04-19 Sandoz AG Composition pharmaceutique contenant du tosylate sorafenib cristallin
CA2875986C (fr) 2012-06-04 2020-06-09 Pharmacyclics, Inc. Formes cristallines d'un inhibiteur de tyrosine kinase de bruton
US9545407B2 (en) 2014-08-07 2017-01-17 Pharmacyclics Llc Formulations of a bruton's tyrosine kinase inhibitor
MD3265084T2 (ro) 2015-03-03 2024-05-31 Pharmacyclics Llc Formulări farmaceutice ale inhibitorului tirozin kinazei Bruton
US10597820B2 (en) * 2015-05-14 2020-03-24 DuPont Nutrition USA, Inc. Method of making bleached microcrystalline cellulose
CA3016809C (fr) * 2016-03-14 2024-03-12 Santen Pharmaceutical Co., Ltd. Agent antiseptique contenant de la meglumine ou un sel correspondant
CN106344530B (zh) * 2016-09-30 2019-03-19 京津冀联创药物研究(北京)有限公司 一种索拉非尼组合物及其制备方法
US11712418B2 (en) 2017-05-26 2023-08-01 Bruin Biosciences, Inc. Chemoembolization agents
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
CA3118324A1 (fr) 2018-11-01 2020-05-07 Syros Pharmaceuticals, Inc. Methodes de traitement du cancer chez des patients identifies par biomarqueurs avec des inhibiteurs non covalents de la kinase cycline-dependante 7 (cdk7)

Family Cites Families (89)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3125359A (en) * 1964-03-17 Push-pull breakaway coupling
NL282262A (fr) * 1961-11-08
AU594098B2 (en) 1985-12-11 1990-03-01 Ishihara Sangyo Kaisha Ltd. N-benzoyl urea compounds, antitumorous compositions containing them, and process for their preparation
DK607188A (da) 1987-11-02 1989-06-22 Merck & Co Inc Tablet indeholdende en phthalazineddikesyreforbindelse
US5547966A (en) * 1993-10-07 1996-08-20 Bristol-Myers Squibb Company Aryl urea and related compounds
US6106865A (en) * 1995-01-09 2000-08-22 Edward Mendell Co., Inc. Pharmaceutical excipient having improved compressibility
GB9501127D0 (en) 1995-01-20 1995-03-08 Wellcome Found Tablet
US5773459A (en) 1995-06-07 1998-06-30 Sugen, Inc. Urea- and thiourea-type compounds
WO1997004765A1 (fr) 1995-07-25 1997-02-13 Smithkline Beecham Corporation INHIBITION D'UNE TRANSACYLASE INDEPENDANTE DE LA COENZYME A (CoA) ET APOPTOSE
AU723730B2 (en) 1996-04-23 2000-09-07 Vertex Pharmaceuticals Incorporated Urea derivatives as inhibitors of IMPDH enzyme
US6187799B1 (en) * 1997-05-23 2001-02-13 Onyx Pharmaceuticals Inhibition of raf kinase activity using aryl ureas
DE69826695T2 (de) 1997-05-23 2006-02-02 Bayer Pharmaceuticals Corp., West Haven Arylharnstoffderivate zur behandlung von inflammatorischen oder immunomodulatorischen erkrankungen
JP2002500650A (ja) 1997-05-23 2002-01-08 バイエル、コーポレイション Rafキナーゼ阻害剤
EP1041982B1 (fr) 1997-12-22 2011-10-19 Bayer HealthCare LLC Inhibition de l'activite de p38 kinase au moyen d'urees heterocycliques substituees
ES2153809T3 (es) 1997-12-22 2005-07-16 Bayer Pharmaceuticals Corporation Inhibicion de la cinasa raf por uso de difnil-ureas sustituidas simetrica y asimetricamente.
US20080300281A1 (en) * 1997-12-22 2008-12-04 Jacques Dumas Inhibition of p38 Kinase Activity Using Aryl and Heteroaryl Substituted Heterocyclic Ureas
ES2155817T3 (es) 1997-12-22 2007-06-16 Bayer Pharmaceuticals Corp. Inhibicion de la actividad de la quinasa p38 utilizando ureas heterociclicas sustituidas con arilo y heteroarilo.
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
US20070244120A1 (en) * 2000-08-18 2007-10-18 Jacques Dumas Inhibition of raf kinase using substituted heterocyclic ureas
PL341356A1 (en) 1997-12-22 2001-04-09 Bayer Ag Raf kinase inhibition employing aryl- and heteroaryl-substituted heterocyclic ureas
ATE300299T1 (de) 1997-12-22 2005-08-15 Bayer Pharmaceuticals Corp Inhibierung der raf-kinase durch substituierte heterocyclische harnstoffverbindungen
JP3887769B2 (ja) 1997-12-22 2007-02-28 バイエル コーポレイション 対称および非対称ジフェニル尿素を用いるp38キナーゼの阻害
US20010014352A1 (en) 1998-05-27 2001-08-16 Udit Batra Compressed tablet formulation
US20030087849A1 (en) 2001-07-03 2003-05-08 Isis Pharmaceuticals Inc. Antisense modulation of HKR1 expression
US6117451A (en) 1998-08-25 2000-09-12 Pharmalogix, Inc. Direct compression metformin hydrochloride tablets
US20080269265A1 (en) * 1998-12-22 2008-10-30 Scott Miller Inhibition Of Raf Kinase Using Symmetrical And Unsymmetrical Substituted Diphenyl Ureas
ATE556713T1 (de) * 1999-01-13 2012-05-15 Bayer Healthcare Llc Omega-carboxyarylsubstituierte-diphenyl- harnstoffe als p38-kinasehemmer
US7928239B2 (en) * 1999-01-13 2011-04-19 Bayer Healthcare Llc Inhibition of RAF kinase using quinolyl, isoquinolyl or pyridyl ureas
EP1140840B1 (fr) * 1999-01-13 2006-03-22 Bayer Pharmaceuticals Corp. Diphenylurees a substituants -g(v)-carboxyaryles, inhibitrices de kinase raf
US20020065296A1 (en) * 1999-01-13 2002-05-30 Bayer Corporation Heteroaryl ureas containing nitrogen hetero-atoms as p38 kinase inhibitors
ME00275B (fr) * 1999-01-13 2011-02-10 Bayer Corp DIPHENYLUREES A SUBSTITUANTS ω-CARBOXYARYLES, INHIBITRICES DE KINASE RAF
US8124630B2 (en) 1999-01-13 2012-02-28 Bayer Healthcare Llc ω-carboxyaryl substituted diphenyl ureas as raf kinase inhibitors
KR100787254B1 (ko) * 1999-01-22 2007-12-20 기린 홀딩스 가부시키가이샤 퀴놀린유도체 및 퀴나졸린유도체
US20020071857A1 (en) * 2000-08-18 2002-06-13 Kararli Tugrul T. Rapidly disintegrating oral formulation of a cyclooxygenase-2 inhibitor
US7235576B1 (en) * 2001-01-12 2007-06-26 Bayer Pharmaceuticals Corporation Omega-carboxyaryl substituted diphenyl ureas as raf kinase inhibitors
ATE353889T1 (de) 2001-03-23 2007-03-15 Bayer Pharmaceuticals Corp Rho-kinase inhibitoren
US7371763B2 (en) * 2001-04-20 2008-05-13 Bayer Pharmaceuticals Corporation Inhibition of raf kinase using quinolyl, isoquinolyl or pyridyl ureas
WO2002085857A2 (fr) 2001-04-20 2002-10-31 Bayer Corporation Inhibition de la kinase raf a l'aide d'urees de quinolyl, d'isoquinolyl ou de pyridyl
US20030207914A1 (en) * 2001-04-20 2003-11-06 Bayer Corporation Inhibition of raf kinase using quinolyl, isoquinolyl or pyridyl ureas
SI1450799T1 (sl) * 2001-12-03 2007-02-28 Bayer Pharmaceuticals Corp Aril secninske spojine v kombinaciji z drugimi citostaticnimi ali citotoksicnimi sredstvi za zdravljenje cloveskih rakov
CA2466762A1 (fr) 2001-12-04 2003-06-12 Onyx Pharmaceuticals, Inc. Inhibiteurs de la voie raf-mek-erk pour traiter le cancer
US20030207872A1 (en) * 2002-01-11 2003-11-06 Bayer Corporation Omega-carboxyaryl substituted diphenyl ureas as raf kinase inhibitors
US20080108672A1 (en) * 2002-01-11 2008-05-08 Bernd Riedl Omega-Carboxyaryl Substituted Diphenyl Ureas As Raf Kinase Inhibitors
US10653684B2 (en) 2002-02-11 2020-05-19 Bayer Healthcare Llc Aryl ureas with angiogenisis inhibiting activity
WO2003068223A1 (fr) 2002-02-11 2003-08-21 Bayer Corporation Urees aryliques a kinase de raf et activite inhibitrice d'angiogenese
AU2003209116A1 (en) * 2002-02-11 2003-09-04 Bayer Pharmaceuticals Corporation Aryl ureas with angiogenesis inhibiting activity
AU2003209119A1 (en) 2002-02-11 2003-09-04 Bayer Pharmaceuticals Corporation Pyridine, quinoline, and isoquinoline n-oxides as kinase inhibitors
ATE529406T1 (de) 2002-02-11 2011-11-15 Bayer Healthcare Llc Aryl-harnstoffe als kinase inhibitoren
GB0209265D0 (en) 2002-04-23 2002-06-05 Novartis Ag Organic compounds
WO2003101444A1 (fr) * 2002-05-29 2003-12-11 Millennium Pharmaceuticals, Inc. Composes et derives de diaryluree utilises comme inhibiteurs de chk-1 dans le traitement du cancer
CA2516624C (fr) 2003-02-28 2013-05-14 Bayer Pharmaceuticals Corporation Derives de 2-oxo-1,3,5-perhydrotriazapine destines au traitement de maladies hyperproliferatives, angiogeniques et inflammatoires
CA2516931C (fr) 2003-02-28 2014-09-09 Bayer Pharmaceuticals Corporation Nouveaux derives bicycliques d'uree utiles dans le traitement du cancer et d'autres troubles
CA2516627A1 (fr) 2003-02-28 2004-09-16 Bayer Pharmaceuticals Corporation Derives de pyridine substitues utilises pour traiter des cancers et d'autres troubles
US7557129B2 (en) * 2003-02-28 2009-07-07 Bayer Healthcare Llc Cyanopyridine derivatives useful in the treatment of cancer and other disorders
US6896863B2 (en) * 2003-04-01 2005-05-24 E. I. Du Pont De Nemours And Company Sodium cyanide process
JP4860474B2 (ja) 2003-05-20 2012-01-25 バイエル、ファーマシューテイカルズ、コーポレイション Pdgfrによって仲介される病気のためのジアリール尿素
US20060234931A1 (en) 2003-07-17 2006-10-19 Biggs William H Iii Treatment of diseases with kinase inhibitors
DK1663978T3 (da) 2003-07-23 2008-04-07 Bayer Pharmaceuticals Corp Fluorsubstitueret omega-carboxyaryl-diphenylurinstof til behandling og forebyggelse af sygdomme og lidelser
WO2005027972A2 (fr) * 2003-09-23 2005-03-31 Novartis Ag Polytherapie combinant un inhibiteur des recepteurs du facteur vegf avec un agent chimiotherapeutique
US7552093B2 (en) * 2003-12-04 2009-06-23 Black Duck Software, Inc. Resolving license dependencies for aggregations of legally-protectable content
WO2005059179A1 (fr) 2003-12-12 2005-06-30 Bayer Pharmaceutical Corporation Procede de prediction et de pronostic du cancer, et surveillance de traitement anticancereux
WO2005110994A2 (fr) 2004-04-30 2005-11-24 Bayer Pharmaceuticals Corporation Derives de pyrazolyl uree substitues utiles dans le traitement du cancer
JP2008503560A (ja) 2004-06-22 2008-02-07 ファイザー・プロダクツ・インク ジアザビシクロ系のヒスタミン−3受容体アンタゴニスト
MY191349A (en) 2004-08-27 2022-06-17 Bayer Pharmaceuticals Corp New pharmaceutical compositions for the treatment of hyper-proliferative disorders
EP1796642B1 (fr) 2004-08-27 2008-05-21 Bayer Pharmaceuticals Corporation Compositions pharmaceutiques sous forme de dispersions solides pour le traitement du cancer
UA91520C2 (en) 2004-09-29 2010-08-10 Баер Шеринг Фарма Акциенгезельшафт Thermodynamically stable form of tosylate
BRPI0515944B1 (pt) 2004-09-29 2021-11-09 Bayer Healthcare Llc Processo para a preparação de 4-{4-[({[4-cloro-3-(trifluorometil)fe-nil]amino}carbonil) amino]fenóxi}nmetilpiridina-2-carboxamida
UA93673C2 (ru) 2005-03-07 2011-03-10 Баер Шеринг Фарма Акциенгезельшафт Фармацевтическая композиция, которая содержит омега-карбоксиарилзамещенную дифенилмочевину, для лечения paka
US20090306020A1 (en) * 2005-05-27 2009-12-10 Bayer Healthcare Ag Combination therapy comprising diaryl ureas for treating diseases
CA2609389A1 (fr) 2005-05-27 2006-11-30 Bayer Healthcare Ag Traitement de combinaison comprenant un compose diaryluree et des inhibiteurs de pi3- ou akt-kinase ou de mtor (rapamycines) pour le traitement du cancer
WO2007015947A2 (fr) 2005-07-29 2007-02-08 Bayer Healthcare Llc Methodes et trousses pour la prediction du succes therapeutique, de la survie sans recidive et globale dans des therapies du cancer
AU2006304764A1 (en) 2005-10-21 2007-04-26 Bayer Healthcare Llc Methods for prediction and prognosis of cancer, and monitoring cancer therapy
WO2007053573A2 (fr) 2005-10-31 2007-05-10 Bayer Pharmaceuticals Corporation Traitement du cancer au moyen de sorafenib
US20090068146A1 (en) * 2005-10-31 2009-03-12 Scott Wilhelm Diaryl ureas and combinations
US8329408B2 (en) * 2005-10-31 2012-12-11 Bayer Healthcare Llc Methods for prognosis and monitoring cancer therapy
AU2006312059A1 (en) 2005-11-02 2007-05-18 Bayer Healthcare Llc Methods for prediction and prognosis of cancer, and monitoring cancer therapy
JP2009515166A (ja) 2005-11-02 2009-04-09 バイエル ヘルスケア エルエルシー がんの予測及び予後の検査方法、並びにがん治療のモニタリング
JP5075832B2 (ja) 2005-11-10 2012-11-21 バイエル・ファルマ・アクチェンゲゼルシャフト 肺高血圧を処置するためのジアリールウレア
WO2007059155A1 (fr) 2005-11-14 2007-05-24 Bayer Pharmaceuticals Corporation Traitement de cancers a resistance a des agents chimiotherapeutiques
EP1957069A2 (fr) 2005-11-14 2008-08-20 Bayer Healthcare, LLC Traitement de cancers a resistance acquise a des inhibiteurs de kit
CN101454668A (zh) 2005-11-14 2009-06-10 拜耳医药保健有限责任公司 癌症预测与预后以及监测癌症治疗的方法
WO2007064872A2 (fr) 2005-12-01 2007-06-07 Bayer Healthcare Llc Composes de l'uree utilises dans le traitement du cancer
US20090227637A1 (en) * 2005-12-15 2009-09-10 Olaf Weber Diaryl ureas for treating virus infections
DE602007012589D1 (de) 2006-12-20 2011-03-31 Bayer Healthcare Llc 4-ä4-Ä(ä3-TERT-BUTYL-1-Ä3-(HYDROXYMETHYL)-PHENYLÜ-1H-PYRAZOL-5-YLü-CARBAMOYL)-AMINOÜ-3-FLUOROPHENOXYü -N-METHYLPYRIDIN-2-CARBOXAMID SOWIE PRODRUGS UND
CA2675980C (fr) 2007-01-19 2016-06-21 Bayer Healthcare Llc Utilisation de dast dans le traitement des cancers a resistance acquise a des inhibiteurs de kit
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
JP2014518232A (ja) 2011-06-28 2014-07-28 バイエル・ヘルスケア・エルエルシー ソラフェニブを含有する眼科用局所医薬組成物
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

Also Published As

Publication number Publication date
EP1868579A1 (fr) 2007-12-26
EP1868579B1 (fr) 2010-09-29
DOP2006000057A (es) 2006-09-30
KR20070111513A (ko) 2007-11-21
DE602006017188D1 (de) 2010-11-11
AU2006222365B2 (en) 2011-07-14
ZA200707638B (en) 2009-08-26
AU2006222365A1 (en) 2006-09-14
HRP20100674T1 (hr) 2011-01-31
GT200600096A (es) 2007-01-12
MY162319A (en) 2017-05-31
SG160364A1 (en) 2010-04-29
BRPI0608840A2 (pt) 2010-02-02
US20080242707A1 (en) 2008-10-02
CA2601955C (fr) 2012-07-10
CY1111065T1 (el) 2015-06-11
CU23821A3 (es) 2012-06-21
CN104688697A (zh) 2015-06-10
CR9348A (es) 2008-02-13
PE20061345A1 (es) 2007-01-28
TNSN07341A1 (en) 2008-12-31
RU2420283C2 (ru) 2011-06-10
AR054234A1 (es) 2007-06-13
CA2601955A1 (fr) 2006-09-14
ES2351612T3 (es) 2011-02-08
US20180036249A1 (en) 2018-02-08
UY29410A1 (es) 2006-10-31
KR101335932B1 (ko) 2013-12-04
CN101132779B (zh) 2016-03-16
BRPI0608840B1 (pt) 2020-04-14
US9737488B2 (en) 2017-08-22
NO343834B1 (no) 2019-06-17
PL1868579T3 (pl) 2011-03-31
DK1868579T3 (da) 2011-01-10
JP5304241B2 (ja) 2013-10-02
ATE482693T1 (de) 2010-10-15
HK1209620A1 (en) 2016-04-08
RU2007136896A (ru) 2009-04-20
HK1118019A1 (zh) 2009-01-30
JP2008531741A (ja) 2008-08-14
BRPI0608840B8 (pt) 2021-05-25
SI1868579T1 (sl) 2011-02-28
CU20070203A7 (es) 2010-01-22
UA93673C2 (ru) 2011-03-10
IL185517A0 (en) 2008-01-06
WO2006094626A1 (fr) 2006-09-14
HN2006009702A (es) 2010-06-08
IL185517A (en) 2016-05-31
NO20075042L (no) 2007-10-05
MX2007010856A (es) 2007-11-12
TWI324928B (en) 2010-05-21
PT1868579E (pt) 2010-12-03
TW200700093A (en) 2007-01-01
CN101132779A (zh) 2008-02-27
NZ561178A (en) 2010-11-26

Similar Documents

Publication Publication Date Title
MA29378B1 (fr) Composition pharmaceutique comprenant une diphenyluree substituee par un omega-carboxyaryle pour le traitement du cancer
MA52492B1 (fr) Composés inhibiteurs de rip1, procédés de préparation et d'utilisation associés
MA31949B1 (fr) Dérivés d'aminotriazole comme agonistes d'alx
MA47399B1 (fr) Dérivés de 7-phényléthylamino-4h-pyrimido[4,5-d][1,3]oxazin-2-one en tant qu'inhibiteurs de la forme mutée des protéines idh1 et idh2
MA30085B1 (fr) Traitement du diabete de type 2 avec une association d'un inhibiteur de dpiv et de metformine ou d'une thiazolidinedione
MA29550B1 (fr) Derives de n- (pyridine-2-yl) - sulfonamide
MA34903B1 (fr) Derives de type azaindazole ou diazaindazole utilises comme medicaments
MA29213B1 (fr) Quinolones a substitution macrolones - amino
MA31496B1 (fr) Inhibiteurs macrocycliques innovants de la replication du virus de l'hepatite c
MA29692B1 (fr) Derives de la xanthine en tant qu'agonistes selectifs du hm74a
MA34655B1 (fr) Dérivés de 2,3- dihydroimidazo[1,2-c]quinazoléine substitués par un aminoalcool utiles pour traiter des troubles hyperprolifératifs et des maladies associées à l'angiogenèse
MA30333B1 (fr) Aminotetrahydropyranes utiles en tant qu'inhibiteurs de la dipeptidyle peptidase-iv pour le traitement ou la prevention du diabete.
MA29543B1 (fr) Procedes pour traiter un cancer pharmacoresistant
MA30906B1 (fr) Composes et compositions en tant quinhibiteurs des proteines kinases
MA27427A1 (fr) Composes de benzimidazole-1-yl-thiophene utilises en cancerotherapie
MA30911B1 (fr) Nouveaux derives de sulfonamide en tant qu'antagonistes de bradykinine
MA34308B1 (fr) Triazolopyridines substituées
CA2407100A1 (fr) 1-aroyle-piperidinyle benzamidines
MA29170B1 (fr) Derives puriniques agissant comme des agonistes du recepteur a2a
ATE449081T1 (de) Fluoralkoxy-substituierte 1, 3-dihydro-isoindolyl-verbindungen und ihre pharmazeutischen verwendungen
NO20042596L (no) Inbibitorer av 11-beta-hydroksy steroid dehydrogenase type 1
MA31867B1 (fr) Agonistes nouveaux des recepteurs de glucocorticoides
MA28269A1 (fr) Arylpyrazoles substitués servant d'agents parasiticides
MY145074A (en) Thiazolidin-4-one derivatives
TNSN06440A1 (fr) Derives de pyrido-pyrimidine, leur preparation, leur application dans le traitement du cancer