[go: up one dir, main page]

MA33581B1 - Composition pharmaceutique contenant un dérivé de quinoléine - Google Patents

Composition pharmaceutique contenant un dérivé de quinoléine

Info

Publication number
MA33581B1
MA33581B1 MA34683A MA34683A MA33581B1 MA 33581 B1 MA33581 B1 MA 33581B1 MA 34683 A MA34683 A MA 34683A MA 34683 A MA34683 A MA 34683A MA 33581 B1 MA33581 B1 MA 33581B1
Authority
MA
Morocco
Prior art keywords
pharmaceutical composition
composition containing
quinoline derivatives
containing quinoline
formula
Prior art date
Application number
MA34683A
Other languages
Arabic (ar)
English (en)
Inventor
Masashi Bando
Original Assignee
Eisai R&D Man Co Ltd
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=43607048&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=MA33581(B1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Eisai R&D Man Co Ltd filed Critical Eisai R&D Man Co Ltd
Publication of MA33581B1 publication Critical patent/MA33581B1/fr

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K47/00Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
    • A61K47/02Inorganic compounds
    • 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
    • A61K31/47Quinolines; Isoquinolines
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K47/00Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
    • A61K47/30Macromolecular organic or inorganic compounds, e.g. inorganic polyphosphates
    • A61K47/36Polysaccharides; Derivatives thereof, e.g. gums, starch, alginate, dextrin, hyaluronic acid, chitosan, inulin, agar or pectin
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/14Particulate form, e.g. powders, Processes for size reducing of pure drugs or the resulting products, Pure drug nanoparticles
    • A61K9/16Agglomerates; Granulates; Microbeadlets ; Microspheres; Pellets; Solid products obtained by spray drying, spray freeze drying, spray congealing,(multiple) emulsion solvent evaporation or extraction
    • A61K9/1605Excipients; Inactive ingredients
    • A61K9/1611Inorganic compounds
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/14Particulate form, e.g. powders, Processes for size reducing of pure drugs or the resulting products, Pure drug nanoparticles
    • A61K9/16Agglomerates; Granulates; Microbeadlets ; Microspheres; Pellets; Solid products obtained by spray drying, spray freeze drying, spray congealing,(multiple) emulsion solvent evaporation or extraction
    • A61K9/1605Excipients; Inactive ingredients
    • A61K9/1629Organic macromolecular compounds
    • A61K9/1652Polysaccharides, e.g. alginate, cellulose derivatives; Cyclodextrin
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/48Preparations in capsules, e.g. of gelatin, of chocolate
    • A61K9/4841Filling excipients; Inactive ingredients
    • A61K9/485Inorganic compounds
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/48Preparations in capsules, e.g. of gelatin, of chocolate
    • A61K9/4841Filling excipients; Inactive ingredients
    • A61K9/4866Organic macromolecular compounds
    • 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
    • A61P35/04Antineoplastic 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D215/00Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
    • C07D215/02Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom
    • C07D215/16Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms 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
    • C07D215/48Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Medicinal Chemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Epidemiology (AREA)
  • Organic Chemistry (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Inorganic Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Oncology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Medicinal Preparation (AREA)
  • Quinoline Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)

Abstract

La présente invention concerne une composition pharmaceutique qui contient : un composé représenté par la formule (i), un sel pharmacologiquement acceptable de celui-ci, ou un solvate du composé ou un sel ; et une substance basique. La composition pharmaceutique a une excellente aptitude à la dissolution, est stable même après une conservation à long terme, et est utile en tant qu'agent prophylactique/thérapeutique pour des tumeurs. (dans la formule, r1 représente un atome d'hydrogène, un groupe alkyle en c1-6 ou un groupe cycloalkyle en c3-8 ; et r2 représente un atome d'hydrogène ou un groupe méthoxy.)
MA34683A 2009-08-19 2012-03-12 Composition pharmaceutique contenant un dérivé de quinoléine MA33581B1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP2009190145 2009-08-19
PCT/JP2010/063804 WO2011021597A1 (fr) 2009-08-19 2010-08-16 Composition pharmaceutique contenant un dérivé de quinoléine

Publications (1)

Publication Number Publication Date
MA33581B1 true MA33581B1 (fr) 2012-09-01

Family

ID=43607048

Family Applications (1)

Application Number Title Priority Date Filing Date
MA34683A MA33581B1 (fr) 2009-08-19 2012-03-12 Composition pharmaceutique contenant un dérivé de quinoléine

Country Status (32)

Country Link
US (3) US20120077842A1 (fr)
EP (1) EP2468281B1 (fr)
JP (1) JP5048871B2 (fr)
KR (1) KR101496395B1 (fr)
CN (1) CN102470133B (fr)
AU (1) AU2010285740C1 (fr)
BR (1) BR112012003592B8 (fr)
CA (1) CA2771403C (fr)
CL (1) CL2012000412A1 (fr)
CO (1) CO6440512A2 (fr)
CY (1) CY1117481T1 (fr)
DK (1) DK2468281T3 (fr)
ES (1) ES2564797T3 (fr)
HR (1) HRP20160283T1 (fr)
HU (1) HUE026957T2 (fr)
IL (1) IL217197A (fr)
MA (1) MA33581B1 (fr)
ME (1) ME02359B (fr)
MX (2) MX2012002011A (fr)
MY (1) MY162940A (fr)
NZ (1) NZ598291A (fr)
PE (1) PE20121030A1 (fr)
PL (1) PL2468281T3 (fr)
RS (1) RS54686B1 (fr)
RU (1) RU2548673C3 (fr)
SG (1) SG178009A1 (fr)
SI (1) SI2468281T1 (fr)
SM (1) SMT201600077B (fr)
TH (1) TH121482A (fr)
UA (1) UA105671C2 (fr)
WO (1) WO2011021597A1 (fr)
ZA (1) ZA201108697B (fr)

Families Citing this family (38)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1797881B1 (fr) 2004-09-17 2009-04-15 Eisai R&D Management Co., Ltd. Composition medicamenteuse avec une stabilite amelioree et une tendence de gelification reduite
US9006240B2 (en) 2005-08-02 2015-04-14 Eisai R&D Management Co., Ltd. Method for assay on the effect of vascularization inhibitor
AU2006285673B2 (en) * 2005-09-01 2010-12-02 Eisai R&D Management Co., Ltd. Method for preparation of pharmaceutical composition having improved disintegratability
KR101353763B1 (ko) 2005-11-07 2014-01-21 에자이 알앤드디 매니지먼트 가부시키가이샤 혈관 신생 저해 물질과 c―kit 키나아제 저해 물질의병용
CA2652442C (fr) 2006-05-18 2014-12-09 Eisai R & D Management Co., Ltd. Agent antitumoral destine au cancer de la thyroide
CN101511793B (zh) * 2006-08-28 2011-08-03 卫材R&D管理有限公司 针对未分化型胃癌的抗肿瘤剂
US8962655B2 (en) * 2007-01-29 2015-02-24 Eisai R&D Management Co., Ltd. Composition for treatment of undifferentiated gastric cancer
EP2218712B1 (fr) 2007-11-09 2015-07-01 Eisai R&D Management Co., Ltd. Combinaison d'une substance antiangiogénique et d'un complexe de platine antitumoral
CA2771403C (fr) 2009-08-19 2015-02-24 Eisai R&D Management Co. Ltd. Composition pharmaceutique contenant un derive de quinoleine
BR112012032462A2 (pt) 2010-06-25 2016-11-08 Eisai R&D Man Co Ltd agente antitumoral empregando compostos que, em combinação, têm efeito inibidor de quinase.
MX2013009931A (es) 2011-04-18 2013-10-01 Eisai R&D Man Co Ltd Agentes terapeuticos contra tumores.
EP2714937B1 (fr) 2011-06-03 2018-11-14 Eisai R&D Management Co., Ltd. Biomarqueurs pour la prédiction et l'estimation de la sensibilité de sujets atteints d'un cancer de la thyroïde et du rein vis-à-vis de composés lenvatinib
RU2015115397A (ru) 2012-12-21 2017-01-25 Эйсай Ар Энд Ди Менеджмент Ко., Лтд. Аморфная форма производного хинолина и способ его получения
CN105264380B (zh) 2013-05-14 2017-09-05 卫材R&D管理有限公司 用于预测和评价子宫内膜癌受试者对乐伐替尼化合物响应性的生物标志
LT3524595T (lt) 2014-08-28 2022-09-26 Eisai R&D Management Co., Ltd. Aukšto grynumo chinolino darinys ir jo gamybos būdas
CN106139156B (zh) * 2014-11-14 2019-01-29 江苏恒瑞医药股份有限公司 一种含有喹啉衍生物或其盐的药物组合物
US20180028662A1 (en) * 2015-02-25 2018-02-01 Eisai R&D Management Co., Ltd. Method for Suppressing Bitterness of Quinoline Derivative
WO2016140717A1 (fr) 2015-03-04 2016-09-09 Merck Sharp & Dohme Corp. Association d'un antagoniste de pd-1 et d'un inhibiteur des tyrosines kinases vegfr/fgfr/ret pour traiter le cancer
CN106075456A (zh) * 2015-04-27 2016-11-09 南京圣和药业股份有限公司 一种含乐伐替尼的药物组合物及其应用
WO2016184436A1 (fr) * 2015-05-21 2016-11-24 苏州晶云药物科技有限公司 Nouvelle forme cristalline de sel de méthanesulfonate de lenvatinib et son procédé de préparation
MX373231B (es) 2015-06-16 2020-05-08 Eisai R&D Man Co Ltd Agente anticancerigeno.
CN106999483B (zh) * 2015-08-17 2019-05-03 江苏恒瑞医药股份有限公司 一种含有喹啉衍生物或其盐的药物组合物
CN108135894B (zh) 2015-08-20 2021-02-19 卫材R&D管理有限公司 肿瘤治疗剂
RU2606592C1 (ru) * 2015-10-07 2017-01-10 Открытое Акционерное Общество "Татхимфармпрепараты" Фармацевтическая композиция, содержащая кальциевую соль розувастатина (варианты)
CZ2016240A3 (cs) 2016-04-27 2017-11-08 Zentiva, K.S. Soli lenvatinibu
JP6581320B2 (ja) 2017-02-08 2019-09-25 エーザイ・アール・アンド・ディー・マネジメント株式会社 腫瘍治療用医薬組成物
HUE069392T2 (hu) 2017-04-04 2025-03-28 Synthon Bv Lenvatinib-mezilátot tartalmazó gyógyszerkészítmény
RU2019134940A (ru) 2017-05-16 2021-06-16 Эйсай Ар Энд Ди Менеджмент Ко., Лтд. Лечение гепатоцеллюлярной карциномы
US10583133B2 (en) 2018-03-12 2020-03-10 Shilpa Medicare Limited Pharmaceutical compositions of lenvatinib
CN110404079B (zh) * 2018-04-27 2023-01-24 北京睿创康泰医药研究院有限公司 一种不含碳酸盐、低基因毒性杂质含量的喹啉衍生物或其盐的药物组合物
US12102630B2 (en) 2018-10-04 2024-10-01 Synthon B.V. Crystalline forms and processes of lenvatinib besylate
EP3632436B1 (fr) 2018-10-04 2022-04-20 Synthon B.V. Composition pharmaceutique comprenant des sels de lenvatinib
CN113087666B (zh) * 2020-01-09 2021-12-14 南京正大天晴制药有限公司 无定形喹啉甲酰胺衍生物的制备方法
CN113491695A (zh) * 2020-03-18 2021-10-12 上海博志研新药物技术有限公司 一种仑伐替尼药物组合物、其制备方法及应用
EP4147689A1 (fr) 2021-09-13 2023-03-15 Lotus Pharmaceutical Co., Ltd. Formulation de lenvatinib
CN114306271B (zh) * 2021-11-24 2023-04-07 石药集团中奇制药技术(石家庄)有限公司 一种仑伐替尼组合物
CN115671074B (zh) * 2022-11-15 2024-06-04 郑州德迈药业有限公司 一种甲磺酸仑伐替尼制剂及其制备方法
EP4424303A1 (fr) 2023-02-28 2024-09-04 Stada Arzneimittel Ag Composition de lenvatinib présentant une biodisponibilité améliorée

Family Cites Families (329)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CU22545A1 (es) 1994-11-18 1999-03-31 Centro Inmunologia Molecular Obtención de un anticuerpo quimérico y humanizado contra el receptor del factor de crecimiento epidérmico para uso diagnóstico y terapéutico
GB1458148A (en) * 1974-04-19 1976-12-08 Wyeth John & Brother Ltd Carbocyclic-fused ring quinoline derivatives
JPS57123267A (en) 1981-01-23 1982-07-31 Kansai Paint Co Ltd Thermosetting paint composition
SE8103843L (sv) 1981-06-18 1982-12-19 Astra Laekemedel Ab Farmaceutisk mixtur
JPS59101423A (ja) 1982-12-02 1984-06-12 Takada Seiyaku Kk 新規なニフエジピン固形製剤
US4526988A (en) 1983-03-10 1985-07-02 Eli Lilly And Company Difluoro antivirals and intermediate therefor
EP0154434B1 (fr) 1984-02-17 1993-01-27 Genentech, Inc. Facteur humain de transformation de croissance et précurseur ou fragment de celui-ci, cellules, ADN, vecteurs et méthodes pour leur production, compositions et produits contenant ceux-ci et anticorps et méthodes diagnostiques en relation avec ceux-ci
US4582789A (en) 1984-03-21 1986-04-15 Cetus Corporation Process for labeling nucleic acids using psoralen derivatives
DE8411409U1 (de) 1984-04-11 1984-08-30 Dr.-Ing. Walter Frohn-Betriebe, 8000 München Entgasungsventil fuer lager- und/oder transportbehaelter
US4563417A (en) 1984-08-31 1986-01-07 Miles Laboratories, Inc. Nucleic acid hybridization assay employing antibodies to intercalation complexes
EP0183858B1 (fr) 1984-11-22 1988-09-14 Holsten-Brauerei AG Bière et son procédé de préparation
CA1264738A (fr) 1984-12-04 1990-01-23 Eli Lilly And Company Traitement des tumeurs chez les mammiferes
JPS62168137A (ja) 1985-12-20 1987-07-24 Fuji Photo Film Co Ltd ハロゲン化銀カラ−写真感光材料およびその処理方法
JPH07106295B2 (ja) 1986-07-22 1995-11-15 エーザイ株式会社 調湿剤
US4743450A (en) 1987-02-24 1988-05-10 Warner-Lambert Company Stabilized compositions
CA1339136C (fr) 1987-07-01 1997-07-29 Sailesh Amilal Varia Forme amorphe de l'aztreonam
US5009894A (en) * 1988-03-07 1991-04-23 Baker Cummins Pharmaceuticals, Inc. Arrangement for and method of administering a pharmaceutical preparation
AU4128089A (en) 1988-09-15 1990-03-22 Rorer International (Overseas) Inc. Monoclonal antibodies specific to human epidermal growth factor receptor and therapeutic methods employing same
US5143854A (en) 1989-06-07 1992-09-01 Affymax Technologies N.V. Large scale photolithographic solid phase synthesis of polypeptides and receptor binding screening thereof
US4983615A (en) 1989-06-28 1991-01-08 Hoechst-Roussel Pharmaceuticals Inc. Heteroarylamino- and heteroaryloxypyridinamine compounds which are useful in treating skin disorders
US5180818A (en) 1990-03-21 1993-01-19 The University Of Colorado Foundation, Inc. Site specific cleavage of single-stranded dna
US5210015A (en) 1990-08-06 1993-05-11 Hoffman-La Roche Inc. Homogeneous assay system using the nuclease activity of a nucleic acid polymerase
EP0834575B1 (fr) 1990-12-06 2001-11-28 Affymetrix, Inc. (a Delaware Corporation) Identification d'acides nucléiques dans des échantillons
GB9105677D0 (en) 1991-03-19 1991-05-01 Ici Plc Heterocyclic compounds
US5367057A (en) 1991-04-02 1994-11-22 The Trustees Of Princeton University Tyrosine kinase receptor flk-2 and fragments thereof
US5721237A (en) 1991-05-10 1998-02-24 Rhone-Poulenc Rorer Pharmaceuticals Inc. Protein tyrosine kinase aryl and heteroaryl quinazoline compounds having selective inhibition of HER-2 autophosphorylation properties
EP0584222B1 (fr) 1991-05-10 1997-10-08 Rhone-Poulenc Rorer International (Holdings) Inc. Composes aryle et heteroaryle bis monocycliques et/ou bicycliques qui inhibent la tyrosine kinase d'un recepteur du egf et/ou du pdgf
US5710158A (en) 1991-05-10 1998-01-20 Rhone-Poulenc Rorer Pharmaceuticals Inc. Aryl and heteroaryl quinazoline compounds which inhibit EGF and/or PDGF receptor tyrosine kinase
JPH04341454A (ja) 1991-05-16 1992-11-27 Canon Inc シート収納装置
US5750376A (en) 1991-07-08 1998-05-12 Neurospheres Holdings Ltd. In vitro growth and proliferation of genetically modified multipotent neural stem cells and their progeny
JPH05194259A (ja) 1991-08-30 1993-08-03 Mitsubishi Kasei Corp 抗消化性潰瘍剤
EP0648264A4 (fr) 1992-06-03 1997-10-01 Univ Case Western Reserve Bandage permettant l'application continue de produits biologiques.
TW271400B (fr) 1992-07-30 1996-03-01 Pfizer
GB9221220D0 (en) 1992-10-09 1992-11-25 Sandoz Ag Organic componds
JPH06153952A (ja) 1992-11-26 1994-06-03 Nobuaki Tamamaki 微量未知二重鎖dna分子の増幅、標識を行うための前処理方法
GB9323290D0 (en) 1992-12-10 1994-01-05 Zeneca Ltd Quinazoline derivatives
DE69324504T2 (de) 1993-01-19 1999-08-26 Warner-Lambert Co. Stabilisierte, oral anzuwendende zusammensetzung enthaltend die verbindung ci-981 und verfahren
US6027880A (en) 1995-08-02 2000-02-22 Affymetrix, Inc. Arrays of nucleic acid probes and methods of using the same for detecting cystic fibrosis
JPH07176103A (ja) 1993-12-20 1995-07-14 Canon Inc 光磁気記録再生システムならびにこれに用いる磁気ヘッド及び光磁気記録媒体
GB9326136D0 (en) 1993-12-22 1994-02-23 Erba Carlo Spa Biologically active 3-substituted oxindole derivatives useful as anti-angiogenic agents
IL112249A (en) 1994-01-25 2001-11-25 Warner Lambert Co Pharmaceutical compositions containing di and tricyclic pyrimidine derivatives for inhibiting tyrosine kinases of the epidermal growth factor receptor family and some new such compounds
US6811779B2 (en) 1994-02-10 2004-11-02 Imclone Systems Incorporated Methods for reducing tumor growth with VEGF receptor antibody combined with radiation and chemotherapy
JP3660391B2 (ja) 1994-05-27 2005-06-15 株式会社東芝 半導体装置の製造方法
JPH0848078A (ja) 1994-08-05 1996-02-20 Nippon Paper Ind Co Ltd 感熱記録体
GB9510757D0 (en) 1994-09-19 1995-07-19 Wellcome Found Therapeuticaly active compounds
US5656454A (en) 1994-10-04 1997-08-12 President And Fellows Of Harvard College Endothelial cell-specific enhancer
IL115256A0 (en) 1994-11-14 1995-12-31 Warner Lambert Co 6-Aryl pyrido (2,3-d) pyrimidines and naphthyridines and their use
JPH08176138A (ja) 1994-12-19 1996-07-09 Mercian Corp イソクマリン誘導体
US5948438A (en) 1995-01-09 1999-09-07 Edward Mendell Co., Inc. Pharmaceutical formulations having improved disintegration and/or absorptivity
US5658374A (en) 1995-02-28 1997-08-19 Buckman Laboratories International, Inc. Aqueous lecithin-based release aids and methods of using the same
US5624937A (en) 1995-03-02 1997-04-29 Eli Lilly And Company Chemical compounds as inhibitors of amyloid beta protein production
EP2295415A1 (fr) 1995-03-30 2011-03-16 OSI Pharmaceuticals, Inc. Derives de quinazoline
GB9508538D0 (en) 1995-04-27 1995-06-14 Zeneca Ltd Quinazoline derivatives
DK0831829T3 (da) 1995-06-07 2003-12-15 Pfizer Heterocykliske, ringkondenserede pyrimidinderivater
US5880141A (en) 1995-06-07 1999-03-09 Sugen, Inc. Benzylidene-Z-indoline compounds for the treatment of disease
JPH0923885A (ja) 1995-07-12 1997-01-28 Dai Ichi Seiyaku Co Ltd 遺伝子発現ライブラリー及びその製造法
GB9514265D0 (en) 1995-07-13 1995-09-13 Wellcome Found Hetrocyclic compounds
GB9520822D0 (en) 1995-10-11 1995-12-13 Wellcome Found Therapeutically active compounds
AR004010A1 (es) 1995-10-11 1998-09-30 Glaxo Group Ltd Compuestos heterociclicos
US6346398B1 (en) 1995-10-26 2002-02-12 Ribozyme Pharmaceuticals, Inc. Method and reagent for the treatment of diseases or conditions related to levels of vascular endothelial growth factor receptor
US6143764A (en) 1995-11-07 2000-11-07 Kirin Beer Kabushiki Kaisha Quinoline and quinazoline derivatives inhibiting platelet-derived growth factor receptor autophosphorylation and pharmaceutical compositions containing the same
US5849759A (en) 1995-12-08 1998-12-15 Berlex Laboratories, Inc. Naphthyl-substituted benzimidazole derivatives as anti-coagulants
GB9604361D0 (en) 1996-02-29 1996-05-01 Pharmacia Spa 4-Substituted pyrrolopyrimidine compounds as tyrosine kinase inhibitors
JPH09234074A (ja) 1996-03-04 1997-09-09 Sumitomo Electric Ind Ltd アダプター二本鎖dna及びそれを用いたdna増幅方法
AU2733997A (en) 1996-04-17 1997-11-07 Du Pont Pharmaceuticals Company N-(amidinophenyl)-n'-(subst.)-3h-2,4-benzodiazepin-3-one derivatives as factor xa inhibitors
US6057100A (en) 1996-06-07 2000-05-02 Eos Biotechnology, Inc. Oligonucleotide arrays
WO1998000134A1 (fr) 1996-06-28 1998-01-08 Merck & Co., Inc. Antagonistes du recepteur de fibrinogene
EP0912559B1 (fr) 1996-07-13 2002-11-06 Glaxo Group Limited Composes heterocycliques condenses en tant qu'inhibiteurs de la proteine tyrosine kinase
HRP970371A2 (en) 1996-07-13 1998-08-31 Kathryn Jane Smith Heterocyclic compounds
BR9710362A (pt) 1996-07-13 1999-08-17 Glaxo Group Ltd Composto formula-ao farmaceutica utiliza-ao de um composto processos de tratamento de um ser humano ou animal sofrendo de uma mediada por atividade anormal de cinase de proteina tirosina e para a prepara-ao de um composto
IL128994A (en) 1996-09-25 2004-12-15 Zeneca Ltd History of quinoline and naphthyridine and their salts, processes for their preparation, pharmaceutical preparations containing them and their use as medicines
DE69722019T2 (de) 1996-09-30 2003-11-27 Nihon Nohyaku Co., Ltd. 1,2,3-thiadiazol-derivate und ihre salze, mittel zur kontrolle von krankheiten in landwirtschaft und gartenbau und eine methode zu ihrer anwendung
EP0837063A1 (fr) 1996-10-17 1998-04-22 Pfizer Inc. Dérivés de 4-aminoquinazoline
CN1237177A (zh) 1996-11-27 1999-12-01 辉瑞大药厂 稠合的二环嘧啶衍生物
AU6248798A (en) 1997-01-29 1998-08-18 Eli Lilly And Company Treatment for premenstrual dysphoric disorder
CO4950519A1 (es) 1997-02-13 2000-09-01 Novartis Ag Ftalazinas, preparaciones farmaceuticas que las comprenden y proceso para su preparacion
WO1998037079A1 (fr) 1997-02-19 1998-08-27 Berlex Laboratories, Inc. Derives n-heterocycliques utiles en tant qu'inhibiteurs de la no synthetase
US6090556A (en) 1997-04-07 2000-07-18 Japan Science & Technology Corporation Method for quantitatively determining the expression of a gene
AU7526798A (en) 1997-04-18 1998-11-27 Smithkline Beecham Plc Acetamide and urea derivatives, process for their preparation and their use in the treatment of cns disorders
EP1019040B1 (fr) 1997-05-23 2004-09-29 Bayer Corporation Derives d'aryl urees destines au traitement des maladies inflammatoires ou immunomodulatoires
KR100543614B1 (ko) 1997-06-10 2006-01-20 신톤 비.브이. 4-페닐피페리딘 화합물
US6093742A (en) 1997-06-27 2000-07-25 Vertex Pharmaceuticals, Inc. Inhibitors of p38
AU8283898A (en) 1997-06-30 1999-01-25 University Of Maryland At Baltimore Heparin binding-epidermal growth factor in the diagnosis of interstitial cystitis
HUP0002236A3 (en) 1997-07-01 2003-12-29 Pfizer Prod Inc Solubilized sertraline compositions and process for their preparation
BE1011251A3 (fr) 1997-07-03 1999-06-01 Ucb Sa Compositions pharmaceutiques administrables par voie orale, comprenant une substance active et une cyclodextrine.
CO4940418A1 (es) 1997-07-18 2000-07-24 Novartis Ag Modificacion de cristal de un derivado de n-fenil-2- pirimidinamina, procesos para su fabricacion y su uso
JP3765918B2 (ja) 1997-11-10 2006-04-12 パイオニア株式会社 発光ディスプレイ及びその駆動方法
JP4194678B2 (ja) 1997-11-28 2008-12-10 キリンファーマ株式会社 キノリン誘導体およびそれを含む医薬組成物
JP2001526222A (ja) 1997-12-22 2001-12-18 バイエル コーポレイション アリールおよびヘテロアリール置換複素環尿素を使用するp38キナーゼ活性の阻害
AU2198999A (en) 1997-12-22 1999-07-12 Bayer Corporation Inhibition of raf kinase using substituted heterocyclic ureas
NZ505843A (en) 1997-12-22 2003-06-30 Bayer Ag Diphenyl ureas compounds for treating cancer and raf kinase related diseases
JP4403482B2 (ja) 1997-12-22 2010-01-27 バイエル コーポレイション 置換複素環尿素合成のための中間体およびその製造方法
GB9800569D0 (en) 1998-01-12 1998-03-11 Glaxo Group Ltd Heterocyclic compounds
GB9800575D0 (en) 1998-01-12 1998-03-11 Glaxo Group Ltd Heterocyclic compounds
CN1310706A (zh) 1998-02-25 2001-08-29 遗传研究所有限公司 磷脂酶抑制剂
JPH11322596A (ja) 1998-05-12 1999-11-24 Shionogi & Co Ltd 白金錯体および環状リン酸エステルアミドを含有する抗癌剤
UA60365C2 (uk) 1998-06-04 2003-10-15 Пфайзер Продактс Інк. Похідні ізотіазолу, спосіб їх одержання, фармацевтична композиція та спосіб лікування гіперпроліферативного захворювання у ссавця
US8097648B2 (en) 1998-06-17 2012-01-17 Eisai R&D Management Co., Ltd. Methods and compositions for use in treating cancer
AU762998B2 (en) 1998-06-17 2003-07-10 Eisai R&D Management Co., Ltd. Macrocyclic analogs and methods of their use and preparation
US6653341B1 (en) 1998-06-17 2003-11-25 Eisai Co., Ltd. Methods and compositions for use in treating cancer
EA003786B1 (ru) 1998-11-19 2003-10-30 Варнер Ламберт Компани N-[4-(3-хлор-4-фторфениламино)-7-(3-морфолин-4-илпропокси)хиназолин-6-ил]акриламид - необратимый ингибитор тирозинкиназ
TWI230618B (en) 1998-12-15 2005-04-11 Gilead Sciences Inc Pharmaceutical compositions of 9-[2-[[bis[(pivaloyloxy)methyl]phosphono]methoxy]ethyl]adenine and tablets or capsules containing the same
WO2000042012A1 (fr) 1999-01-13 2000-07-20 Bayer Corporation DIPHENYLUREES A SUBSTITUANTS φ-CARBOXYARYLES, INHIBITRICES DE KINASE RAF
UA73492C2 (en) 1999-01-19 2005-08-15 Aromatic heterocyclic compounds as antiinflammatory agents
ES2208261T3 (es) 1999-01-22 2004-06-16 Kirin Beer Kabushiki Kaisha Derivados de quinolina y derivados de quinazolina.
JP3270834B2 (ja) 1999-01-27 2002-04-02 ファイザー・プロダクツ・インク 抗がん剤として有用なヘテロ芳香族二環式誘導体
UA71945C2 (en) 1999-01-27 2005-01-17 Pfizer Prod Inc Substituted bicyclic derivatives being used as anticancer agents
PL205557B1 (pl) 1999-02-10 2010-05-31 Astrazeneca Ab Pochodne indolu
GB9904103D0 (en) 1999-02-24 1999-04-14 Zeneca Ltd Quinoline derivatives
JP2000328080A (ja) 1999-03-12 2000-11-28 Shin Etsu Chem Co Ltd シートベルト用低摩擦化処理剤
RS49836B (sr) 1999-03-31 2008-08-07 Pfizer Products Inc., Postupci i intermedijeri za dobijanje anti-kancernih jedinjenja
US6887468B1 (en) 1999-04-28 2005-05-03 Board Of Regents, The University Of Texas System Antibody kits for selectively inhibiting VEGF
AU4778500A (en) 1999-05-20 2000-12-12 Takeda Chemical Industries Ltd. Composition containing ascorbic acid salt
JP4304357B2 (ja) 1999-05-24 2009-07-29 独立行政法人理化学研究所 完全長cDNAライブラリーの作成法
PE20010306A1 (es) 1999-07-02 2001-03-29 Agouron Pharma Compuestos de indazol y composiciones farmaceuticas que los contienen utiles para la inhibicion de proteina kinasa
WO2001012600A1 (fr) 1999-08-12 2001-02-22 Cor Therapeutics, Inc. INHIBITEURS DU FACTEUR Xa
AR025752A1 (es) 1999-09-28 2002-12-11 Bayer Corp Piridinas y piridacinas sustituidas con actividad de inhibicion de angiogenesis
UA75054C2 (uk) 1999-10-13 2006-03-15 Бьорінгер Інгельхайм Фарма Гмбх & Ко. Кг Заміщені в положенні 6 індолінони, їх одержання та їх застосування як лікарського засобу
JP2001131071A (ja) 1999-10-29 2001-05-15 Meiji Seika Kaisha Ltd 非晶質および非晶質を含有する医薬組成物
WO2001032926A2 (fr) 1999-11-01 2001-05-10 Curagen Corporation Genes exprimes de maniere differentielle impliques dans l'angiogenese, polypeptides codes par lesdits genes, et techniques d'utilisation de ces genes
WO2001036403A1 (fr) 1999-11-16 2001-05-25 Boehringer Ingelheim Pharmaceuticals, Inc. Derives d'uree utilises comme agents anti-inflammatoires
UA75055C2 (uk) 1999-11-30 2006-03-15 Пфайзер Продактс Інк. Похідні бензоімідазолу, що використовуються як антипроліферативний засіб, фармацевтична композиція на їх основі
EP1255536B1 (fr) 1999-12-22 2006-06-28 Sugen, Inc. DERIVES D'INDOLINONE DESTINES A LA MODULATION DE LA TYROSINE PROTEINE KINASE DE TYPE c-KIT
WO2001047890A1 (fr) 1999-12-24 2001-07-05 Kirin Beer Kabushiki Kaisha Quinoline, derives de la quinazoline et medicaments contenant ces substances
ES2238335T3 (es) 1999-12-24 2005-09-01 Kyowa Hakko Kogyo Co., Ltd. Derivados de purina condensados.
MY130363A (en) 2000-02-15 2007-06-29 Sugen Inc "pyrrole substituted 2-indolinone protein kinase inhibitors"
JP3657203B2 (ja) 2000-04-21 2005-06-08 エーザイ株式会社 銅クロロフィリン塩含有液剤組成物
EP1287029A2 (fr) 2000-06-09 2003-03-05 Corixa Corporation Compositions et procedes pour la therapie et le diagnostic du cancer du colon
AU2001277621A1 (en) 2000-08-09 2002-03-04 Astrazeneca Ab Antiangiogenic bicyclic derivatives
ATE419239T1 (de) * 2000-10-20 2009-01-15 Eisai R&D Man Co Ltd Verfahren zur herstellung von 4-phenoxy chinolin derivaten
TWI283575B (en) 2000-10-31 2007-07-11 Eisai Co Ltd Medicinal compositions for concomitant use as anticancer agent
WO2002041882A2 (fr) 2000-11-22 2002-05-30 Novartis Ag Combinaison comprenant un agent diminuant l'activite du facteur de croissance endotelial vasculaire et un agent diminuant l'activite du facteur de croissance de l'epiderme
JP2004517080A (ja) 2000-11-29 2004-06-10 グラクソ グループ リミテッド Tie−2および/またはvegfr−2の阻害剤として有用なベンゾイミダゾール誘導体
US7101663B2 (en) 2001-03-02 2006-09-05 University of Pittsburgh—of the Commonwealth System of Higher Education PCR method
EP1490362A2 (fr) 2001-03-08 2004-12-29 Millennium Pharmaceuticals, Inc. Composes de quinoline heterocycliques contenant de l'azote
ATE406892T1 (de) 2001-04-06 2008-09-15 Wyeth Corp Antineoplastische kombinationspräparate enthaltend cci-779 (rapamycin derivat) zusammen mit gemcitabin oder fluoro-uracil
US20040171068A1 (en) 2001-04-19 2004-09-02 Juergen Wehland Method for producing stable, regeneratable antibody arrays
JP3602513B2 (ja) 2001-04-27 2004-12-15 麒麟麦酒株式会社 アゾリル基を有するキノリン誘導体およびキナゾリン誘導体
ES2256466T3 (es) 2001-04-27 2006-07-16 Kirin Beer Kabushiki Kaisha Derivado de quinolina que tienen grupo azolilo y derivados de quinazolina.
JP2003026576A (ja) 2001-05-09 2003-01-29 Eisai Co Ltd 味覚改善製剤
US6812341B1 (en) 2001-05-11 2004-11-02 Ambion, Inc. High efficiency mRNA isolation methods and compositions
MXPA03010401A (es) 2001-05-16 2004-03-09 Novartis Ag Combinacion que comprende n-[5-[4- (4-metil- piperazino-metil) -benzoilamido] -2-metilfenil] -4-(3-piridil)-2 -pirimidin-amina, y un agente quimioterapeutico.
CA2454538A1 (fr) 2001-06-22 2003-01-03 Kirin Beer Kabushiki Kaisha Derives de la quinoleine et de la quinozoline pouvant inhiber l'auto- phosphorylation des recepteurs du facteur de croissance des hepatocytes, et composition pharmaceutique ainsi constituee
GB0117144D0 (en) 2001-07-13 2001-09-05 Glaxo Group Ltd Process
US20030013208A1 (en) 2001-07-13 2003-01-16 Milagen, Inc. Information enhanced antibody arrays
JP4824213B2 (ja) 2001-07-16 2011-11-30 日本メナード化粧品株式会社 キトサン含有錠剤
GB0119467D0 (en) 2001-08-09 2001-10-03 Smithkline Beecham Plc Novel compound
AU2002341621A1 (en) 2001-09-10 2003-03-24 Meso Scale Technologies, Llc Methods, reagents, kits and apparatus for protein function analysis
EP1427379B1 (fr) 2001-09-20 2008-08-13 AB Science Utilisation d'inhibiteurs c-kit puissants, selectifs et non toxiques pour le traitement de la cystopathie interstitielle
EP1432422A2 (fr) 2001-09-27 2004-06-30 Novartis AG Utilisation d'inhibiteurs de c-kit pour traiter un myelome
JP2005508336A (ja) 2001-09-27 2005-03-31 アラーガン、インコーポレイテッド キナーゼ阻害物質としての3−(アリールアミノ)メチレン−1,3−ジヒドロ−2h−インドール−2−オン類
EP1435959A2 (fr) 2001-10-09 2004-07-14 University of Cincinnati Methode de traitement du cancer thyroidien
US7521053B2 (en) 2001-10-11 2009-04-21 Amgen Inc. Angiopoietin-2 specific binding agents
US7658924B2 (en) 2001-10-11 2010-02-09 Amgen Inc. Angiopoietin-2 specific binding agents
EP1447405A4 (fr) 2001-10-17 2005-01-12 Kirin Brewery Derives de quinoline ou de quinazoline inhibant l'autophosphorylation de recepteurs du facteur de croissance des fibroblastes
AU2002359489B2 (en) 2001-11-27 2008-10-30 Wyeth Holdings Corporation 3-cyanoquinolines as inhibitors of EGF-R and Her2 kinases
GB0201508D0 (en) 2002-01-23 2002-03-13 Novartis Ag Organic compounds
JP4542783B2 (ja) 2002-03-05 2010-09-15 エーザイ・アール・アンド・ディー・マネジメント株式会社 スルホンアミド含有複素環化合物及び血管新生抑制剤とを組み合わせてなる抗腫瘍剤
BR0308343A (pt) 2002-03-12 2006-06-06 Bristol Myers Squibb Co composições farmacêuticas na forma de pó, método para preparar uma suspensão oral de uma droga, método para mascarar o sabor amargo ou outro sabor de uma droga e suspensão oral de des-quinolona
AU2003226676A1 (en) 2002-03-20 2003-09-29 Dana-Farber Cancer Institute Inc. Methods and compositions for the identification, assessment, and therapy of small cell lung cancer
US7598258B2 (en) 2002-05-01 2009-10-06 Kirin Beer Kabushiki Kaisha Quinoline derivatives and quinazoline derivatives inhibiting autophosphorylation of macrophage colony stimulating factor receptor
UA77303C2 (en) 2002-06-14 2006-11-15 Pfizer Derivatives of thienopyridines substituted by benzocondensed heteroarylamide useful as therapeutic agents, pharmaceutical compositions and methods for their use
WO2004006862A2 (fr) 2002-07-16 2004-01-22 Children's Medical Center Corporation Methode de modulation de l'angiogenese
US7169936B2 (en) 2002-07-23 2007-01-30 Boehringer Ingelheim Pharma Gmbh & Co. Kg Indolinone derivatives substituted in the 6-position, their preparation and their use as medicaments
US7252976B2 (en) 2002-08-28 2007-08-07 Board Of Regents The University Of Texas System Quantitative RT-PCR to AC133 to diagnose cancer and monitor angiogenic activity in a cell sample
CN100339376C (zh) 2002-08-30 2007-09-26 卫材R&D管理有限公司 含氮芳环衍生物
RU2005114018A (ru) 2002-10-09 2006-01-20 Козан Байосайенсиз, Инк. (Us) Эпотилон d+фторурацил/гемцитабин
GB0223380D0 (en) 2002-10-09 2002-11-13 Astrazeneca Ab Combination therapy
EP1552833B1 (fr) * 2002-10-16 2016-12-28 Takeda Pharmaceutical Company Limited Procédé de préparation d'un iosmère optiquement actif du lansoprazole
JP4749660B2 (ja) * 2002-10-16 2011-08-17 武田薬品工業株式会社 安定な固形製剤
EP1556356B1 (fr) 2002-10-21 2006-05-31 Warner-Lambert Company LLC Derives de tetrahydroquinoline antagonistes de crth2
EP1566379A4 (fr) 2002-10-29 2005-11-09 Kirin Brewery DERIVES DE QUINOLINE ET DE QUINAZOLINE INHIBANT L'AUTOPHOSPHORYLATION DE Flt3 ET COMPOSITIONS MEDICALES LES CONTENANT
DE10250711A1 (de) 2002-10-31 2004-05-19 Degussa Ag Pharmazeutische und kosmetische Zubereitungen
WO2004041308A1 (fr) 2002-11-06 2004-05-21 Cyclacel Limited Composition pharmaceutique a base de gemcitabine et d'un inhibiteur de cdk
GB0226434D0 (en) 2002-11-13 2002-12-18 Astrazeneca Ab Combination product
ITSV20020056A1 (it) 2002-11-14 2004-05-15 Alstom Transp Spa Dispositivo e metodo di verifica di motori software logici di comando di impianti ferroviari, in particolare di impianti di stazione
AR042042A1 (es) 2002-11-15 2005-06-08 Sugen Inc Administracion combinada de una indolinona con un agente quimioterapeutico para trastornos de proliferacion celular
ES2387909T3 (es) 2003-01-14 2012-10-03 Cytokinetics, Inc. Compuestos, composiciones y procedimientos de tratamiento de la insuficiencia cardiaca
JP3581361B1 (ja) 2003-02-17 2004-10-27 株式会社脳機能研究所 脳活動測定装置
ZA200507321B (en) 2003-03-05 2007-03-28 Celgene Corp Diphenylethylene compounds and uses thereof
EP1604665B1 (fr) 2003-03-10 2011-05-11 Eisai R&D Management Co., Ltd. Inhibiteur de kinase c-kit
AU2004220156B2 (en) 2003-03-14 2007-04-19 Taisho Pharmaceutical Co., Ltd. Monoclonal antibody and hybridoma producing the same
RU2366655C2 (ru) 2003-03-14 2009-09-10 Оно Фармасьютикал Ко., Лтд. Азотсодержащие гетероциклические производные и лекарственные средства, содержащие их в качестве активного ингредиента
WO2004087096A1 (fr) 2003-04-02 2004-10-14 Pliva-Istrazivanje I Razvoj D.O.O. Compositions pharmaceutiques ayant un gout amer reduit
US20070117842A1 (en) 2003-04-22 2007-05-24 Itaru Arimoto Polymorph of 4-[3-chloro-4-(cyclopropylaminocarbonyl)aminophenoxy]-7-methoxy-6- quinolinecarboxamide and a process for the preparation of the same
KR100503949B1 (ko) 2003-04-28 2005-07-26 주식회사유한양행 염산 온단세트론의 쓴맛을 효과적으로 은폐한 경구용 구강속붕해정 조성물
US7107104B2 (en) 2003-05-30 2006-09-12 Medtronic, Inc. Implantable cortical neural lead and method
JP2005008534A (ja) 2003-06-17 2005-01-13 Soc De Conseils De Recherches & D'applications Scientifiques (Scras) 抗癌剤及び癌の治療方法
US20060167027A1 (en) 2003-07-10 2006-07-27 Wedge Stephen R Use of the quinazoline derivative zd6474 combined with platinum compounds and optionally ionising radiation in the treatment of diseases associated with angiogenesis and/or increased vascular permeability
HUE037508T2 (hu) 2003-07-24 2018-09-28 Glaxosmithkline Llc Szájban oldódó filmek
US20070032521A1 (en) 2003-08-15 2007-02-08 Ab Science Use of c-kit inhibitors for treating type II diabetes
KR20060121818A (ko) 2003-08-21 2006-11-29 오에스아이 파마슈티컬스, 인코포레이티드 N-치환된 벤즈이미다졸릴 c-kit 억제제
US7485658B2 (en) 2003-08-21 2009-02-03 Osi Pharmaceuticals, Inc. N-substituted pyrazolyl-amidyl-benzimidazolyl c-Kit inhibitors
MXPA06002017A (es) 2003-08-21 2006-05-31 Osi Pharm Inc Pirazolil-amidil-bencimidazolilo n-sustituidos, ibnhibidores de c-kit.
US7312243B1 (en) 2003-08-29 2007-12-25 Jay Pravda Materials and methods for treatment of gastrointestinal disorders
US20080085902A1 (en) 2003-09-23 2008-04-10 Guido Bold Combination Of A Vegf Receptor Inhibitor Or With A Chemotherapeutic Agent
PT2213661E (pt) 2003-09-26 2011-12-15 Exelixis Inc Moduladores de c-met e métodos de uso
CN101337930B (zh) 2003-11-11 2010-09-08 卫材R&D管理有限公司 脲衍生物的制备方法
EP1689376A2 (fr) 2003-11-28 2006-08-16 Novartis AG Derives de diaryluree utilises en traitement de maladies dependant de proteines kinases
US6984403B2 (en) 2003-12-04 2006-01-10 Pfizer Inc. Azithromycin dosage forms with reduced side effects
MXPA06006406A (es) 2003-12-05 2007-03-21 Adnexus Therapeutics Inc Inhibidores de receptores de factor de crecimiento endotelial vascular tipo 2.
CN101337933B (zh) * 2003-12-25 2011-03-02 卫材R&D管理有限公司 喹啉羧酰胺的甲磺酸盐的结晶(a)及其制备方法
EP1713484A2 (fr) 2004-01-23 2006-10-25 Amgen Inc. Composes et leurs procedes d'utilisation
CN1906166A (zh) 2004-02-27 2007-01-31 卫材株式会社 新型吡啶衍生物及嘧啶衍生物(1)
KR20050091462A (ko) 2004-03-12 2005-09-15 한국과학기술연구원 푸로피리미딘 화합물 및 이를 포함하는 ddr2 티로신키나아제 활성 저해제
US20050244493A1 (en) 2004-04-30 2005-11-03 Withiam Michael C Rapidly disintegrating tablets comprising calcium carbonate
WO2005113507A1 (fr) 2004-05-21 2005-12-01 Novartis Vaccines And Diagnostics Inc. Dérivés de quinolinone substituée en tant qu’inhibiteurs de kinésine mitotique
CA2567836A1 (fr) 2004-06-03 2005-12-15 F. Hoffmann-La Roche Ag Traitement a base de gemcitabine et d'un inhibiteur de egfr
US20080214606A1 (en) 2004-06-18 2008-09-04 The Government of the United States of America as represented by The Secretary of the Dept. of ..... Methods for the Identification and Use of Compounds Suitable for the Treatment of Drug Resistant Cancer Cells
US20050288521A1 (en) 2004-06-29 2005-12-29 Phytogen Life Sciences Inc. Semi-synthetic conversion of paclitaxel to docetaxel
US7306807B2 (en) 2004-09-13 2007-12-11 Wyeth Hemorrhagic feline calicivirus, calicivirus vaccine and method for preventing calicivirus infection or disease
US8772269B2 (en) 2004-09-13 2014-07-08 Eisai R&D Management Co., Ltd. Use of sulfonamide-including compounds in combination with angiogenesis inhibitors
WO2006030947A1 (fr) 2004-09-13 2006-03-23 Eisai R & D Management Co., Ltd. Utilisation conjointe d’un compose a base de sulfonamide et d'un inhibiteur d’angiogenese
EP1797881B1 (fr) 2004-09-17 2009-04-15 Eisai R&D Management Co., Ltd. Composition medicamenteuse avec une stabilite amelioree et une tendence de gelification reduite
JP2008514635A (ja) 2004-09-27 2008-05-08 コーザン バイオサイエンシス インコーポレイテッド 特異的キナーゼ阻害剤
MX2007004247A (es) 2004-10-19 2007-06-12 Amgen Inc Agentes de aglutinacion especifica a angiopoyetina-2.
WO2007040565A2 (fr) 2004-11-22 2007-04-12 King Pharmaceuticals Research & Development, Inc. Amelioration du traitement du cancer et de troubles medies par hif-1 au moyen d'antagonistes des recepteurs de l'adenosine a3
DE602005017118D1 (de) 2004-11-23 2009-11-26 Dong Wha Pharm Co Ltd N-HYDROXY-4-ä5-Ä4-(5-ISOPROPYL-2-METHYL-1,3-THIAZOL-4-YL)PHENOXYÜPENTOXYüBENZAMIDIN 2 METHANSULFONSAURESALZ
CA2589274A1 (fr) 2004-12-07 2006-06-15 Locus Pharmaceuticals, Inc. Inhibiteurs de proteines kinases
ZA200705695B (en) 2004-12-21 2009-02-25 Astrazeneca Ab Antibodies directed to angiopoietin-2 and uses thereof
US20060198885A1 (en) 2005-02-22 2006-09-07 Sun Pharmaceutical Industries Ltd. Oral pharmaceutical composition
DE602006021401D1 (de) 2005-02-28 2011-06-01 Eisai R&D Man Co Ltd Neue kombinierte anwendung einer sulfonamid-verbindung zur behandlung von krebs
WO2006090931A1 (fr) 2005-02-28 2006-08-31 Eisai R & D Management Co., Ltd. Nouvelle utilisation concomitante d'un compose de sulfonamide avec un agent anti-cancer
EP2439273B1 (fr) 2005-05-09 2019-02-27 Ono Pharmaceutical Co., Ltd. Anticorps monoclonaux humains pour mort programmée 1 (PD-1) et procédés de traitement du cancer à l'aide d'anticorps anti-PD-1 seuls ou combinés à d'autres formulations immunothérapeutiques
WO2007013896A2 (fr) 2005-05-17 2007-02-01 Plexxikon, Inc. Composes modulant l'activite de c-kit et c-fms et utilisations
AU2006248593B2 (en) 2005-05-17 2011-03-17 Actelion Pharmaceuticals Ltd. Dispersible bosertan tablet
MY153898A (en) 2005-06-22 2015-04-15 Plexxikon Inc Compounds and methods for kinase modulation, and indications therefor
US7550483B2 (en) * 2005-06-23 2009-06-23 Eisai R&D Management Co., Ltd. Amorphous salt of 4-(3-chloro-4-(cyclopropylaminocarbonyl)aminophenoxy)-7-methoxy-6-quinolinecarboxamide and process for preparing the same
CA2606719C (fr) 2005-06-23 2010-08-10 Eisai R & D Management Co., Ltd. Sel amorphe du 4-(3-chloro-4-(cyclopropylaminocarbonyl)aminophenoxy)-7-methoxy-6-quinolinecarboxamide et procede de synthese dudit sel
JP2008546821A (ja) 2005-06-29 2008-12-25 ロゼリ、 パトリツィア Vegf受容体を制御する化合物、およびその使用
EA015535B1 (ru) 2005-07-11 2011-08-30 Никомед Данмарк Апс Формуляция бензимидазола
US8101799B2 (en) 2005-07-21 2012-01-24 Ardea Biosciences Derivatives of N-(arylamino) sulfonamides as inhibitors of MEK
US20080219977A1 (en) 2005-07-27 2008-09-11 Isaiah Josh Fidler Combinations Comprising Gemcitabine and Tyrosine Kinase Inhibitors for the Treatment of Pancreatic Cancer
WO2007015569A1 (fr) 2005-08-01 2007-02-08 Eisai R & D Management Co., Ltd. Procédé de prédiction de l’efficacité d’un inhibiteur de vascularisation
US9006240B2 (en) 2005-08-02 2015-04-14 Eisai R&D Management Co., Ltd. Method for assay on the effect of vascularization inhibitor
JP4077028B2 (ja) 2005-08-24 2008-04-16 エーザイ・アール・アンド・ディー・マネジメント株式会社 新規ピリジン誘導体およびピリミジン誘導体(3)
AU2006285673B2 (en) 2005-09-01 2010-12-02 Eisai R&D Management Co., Ltd. Method for preparation of pharmaceutical composition having improved disintegratability
KR101353763B1 (ko) 2005-11-07 2014-01-21 에자이 알앤드디 매니지먼트 가부시키가이샤 혈관 신생 저해 물질과 c―kit 키나아제 저해 물질의병용
WO2007061127A1 (fr) 2005-11-22 2007-05-31 Eisai R & D Management Co., Ltd. Agent antitumeur pour myelomes multiples
AR059066A1 (es) * 2006-01-27 2008-03-12 Amgen Inc Combinaciones del inhibidor de la angiopoyetina -2 (ang2) y el inhibidor del factor de crecimiento endotelial vascular (vegf)
WO2007097386A1 (fr) 2006-02-22 2007-08-30 Eisai R & D Management Co., Ltd. Composition pharmaceutique stabilisee
AU2007227614B2 (en) 2006-03-16 2011-01-06 Gsk Consumer Healthcare Sarl Solid dosage form containing a taste masked active agent
KR100728926B1 (ko) 2006-03-20 2007-06-15 삼성전자주식회사 3축 힌지 구조를 갖는 휴대용 전자기기
CA2652442C (fr) 2006-05-18 2014-12-09 Eisai R & D Management Co., Ltd. Agent antitumoral destine au cancer de la thyroide
EA200970045A1 (ru) 2006-06-22 2009-06-30 Солвей Фармасьютикалс Б.В. Фармацевтическая композиция для перорального введения плохо растворимого в воде активного вещества
AU2007288793B2 (en) 2006-08-23 2012-04-19 Eisai R & D Management Co., Ltd. Salt of phenoxypyridine derivative or crystal thereof and process for producing the same
CN101511793B (zh) 2006-08-28 2011-08-03 卫材R&D管理有限公司 针对未分化型胃癌的抗肿瘤剂
JP2010502209A (ja) 2006-09-07 2010-01-28 アストラゼネカ アクチボラグ Retレセプターチロシンキナーゼを標的とする薬剤による治療のために患者を評価する方法
RU2462247C2 (ru) 2006-10-12 2012-09-27 ПиТиСи ТЕРАПЬЮТИКС, ИНК. Способы дозирования перорально активного 1,2,4-оксадиазола для терапии, подавляющей нонсенс-мутацию
JP2009184925A (ja) 2006-11-02 2009-08-20 Dai Ichi Seiyaku Co Ltd 5−(1h−1,2,3−トリアゾール−4−イル)−1h−ピラゾール誘導体
EP2116246A1 (fr) 2007-01-19 2009-11-11 Eisai R&D Management Co., Ltd. Composition destinée au traitement du cancer pancréatique
JP5491199B2 (ja) 2007-01-19 2014-05-14 アルデア バイオサイエンシズ,インコーポレイティド Mekのインヒビター
US8962655B2 (en) 2007-01-29 2015-02-24 Eisai R&D Management Co., Ltd. Composition for treatment of undifferentiated gastric cancer
JP2008214249A (ja) 2007-03-02 2008-09-18 Takeda Chem Ind Ltd 製剤における溶出改善方法および溶出性の改善された製剤
KR20090116794A (ko) 2007-03-05 2009-11-11 교와 핫꼬 기린 가부시키가이샤 의약 조성물
KR20090115866A (ko) 2007-03-05 2009-11-09 교와 핫꼬 기린 가부시키가이샤 의약 조성물
US7807172B2 (en) 2007-06-13 2010-10-05 University Of Washington Methods and compositions for detecting thyroglobulin in a biological sample
PE20090368A1 (es) 2007-06-19 2009-04-28 Boehringer Ingelheim Int Anticuerpos anti-igf
EP2175885B1 (fr) 2007-07-30 2016-10-12 Ardea Biosciences, Inc. Combinaisons d'inhibiteurs de mek et d'inhibiteurs de raf kinase et leurs utilisations
EP2218712B1 (fr) 2007-11-09 2015-07-01 Eisai R&D Management Co., Ltd. Combinaison d'une substance antiangiogénique et d'un complexe de platine antitumoral
JP2009132660A (ja) 2007-11-30 2009-06-18 Eisai R & D Management Co Ltd 食道癌治療用組成物
MX2010008187A (es) 2008-01-29 2010-08-10 Eisai R&D Man Co Ltd Uso combinado de inhibidor de angiogenesis y taxano.
GB2456907A (en) 2008-01-30 2009-08-05 Astrazeneca Ab Method for determining subsequent VEGFR2 inhibitor therapy comprising measuring baseline VEGF level.
CA2753844A1 (fr) * 2008-03-05 2009-09-11 Vicus Therapeutics, Llc Compositions et procedes pour des therapies de la mucosite et d'oncologie
US8044240B2 (en) 2008-03-06 2011-10-25 Ardea Biosciences Inc. Polymorphic form of N-(S)-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)-6-methoxyphenyl)-1-(2,3-dihydroxypropyl)cyclopropane-1-sulfonamide and uses thereof
US8168757B2 (en) 2008-03-12 2012-05-01 Merck Sharp & Dohme Corp. PD-1 binding proteins
CN102131771A (zh) 2008-04-14 2011-07-20 阿迪生物科学公司 组合物及其制备和使用方法
JP2009263298A (ja) 2008-04-28 2009-11-12 Ss Pharmaceut Co Ltd 不快な味を隠ぺいした経口組成物
WO2009137649A2 (fr) 2008-05-07 2009-11-12 The Trustees Of The University Of Pennsylvania Procédés de traitement du cancer de la thyroïde
EP2288383A1 (fr) 2008-05-14 2011-03-02 Amgen, Inc Combinaisons d'inhibiteurs de vegf(r) et d'inhibiteurs du facteur de croissance d'hépatocyte (c-met) pour le traitement du cancer
WO2009150256A1 (fr) 2008-06-13 2009-12-17 Institut National De La Sante Et De La Recherche Medicale (Inserm) Marqueurs permettant de prévoir la réponse et la survie chez des patients subissant un traitement anti-egfr
KR20110028651A (ko) 2008-07-11 2011-03-21 노파르티스 아게 (a) 포스포이노시타이드 3-키나제 억제제 및 (b) ras/raf/mek 경로의 조절제의 조합물
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
WO2010086964A1 (fr) 2009-01-28 2010-08-05 株式会社 静岡カフェイン工業所 Thérapie de combinaison pour traitement d'un cancer
US20120164148A1 (en) 2009-08-07 2012-06-28 The Wistar Institute Compositions Containing JARID1B Inhibitors and Methods for Treating Cancer
CA2771403C (fr) 2009-08-19 2015-02-24 Eisai R&D Management Co. Ltd. Composition pharmaceutique contenant un derive de quinoleine
CA2771606A1 (fr) 2009-08-21 2011-02-24 Mount Sinai School Of Medicine Of New York University Procedes d'utilisation de proteines de fusion de cd44 pour traiter le cancer
EP2293071A1 (fr) 2009-09-07 2011-03-09 Universität Zu Köln Biomarkers pour le cancer colorectal
BR112012032462A2 (pt) 2010-06-25 2016-11-08 Eisai R&D Man Co Ltd agente antitumoral empregando compostos que, em combinação, têm efeito inibidor de quinase.
CN103003262A (zh) 2010-07-16 2013-03-27 协和发酵麒麟株式会社 含氮芳香族杂环衍生物
WO2012010550A1 (fr) 2010-07-19 2012-01-26 F. Hoffmann-La Roche Ag Méthode d'identification d'un patient présentant une probabilité accrue de répondre à un traitement anticancéreux
AU2011281700B2 (en) 2010-07-19 2017-02-09 F. Hoffmann-La Roche Ag Blood plasma biomarkers for bevacizumab combination therapies for treatment of pancreatic cancer
JP6055764B2 (ja) 2010-07-19 2016-12-27 エフ・ホフマン−ラ・ロシュ・アクチェンゲゼルシャフト 乳癌の治療のためのベバシズマブ組合せ療法のための血漿バイオマーカー
KR20130126576A (ko) 2010-07-19 2013-11-20 에프. 호프만-라 로슈 아게 항암요법에 반응할 가능성이 증가된 환자를 확인하는 방법
WO2012019300A1 (fr) 2010-08-10 2012-02-16 Siu K W Michael Marqueurs biologiques d'un cancer endométrial et procédés pour les identifier et les utiliser
WO2012029913A1 (fr) 2010-09-01 2012-03-08 興和株式会社 Préparation orale
US20120077837A1 (en) 2010-09-24 2012-03-29 Eisai R&D Management Co., Ltd. Anti-tumor agent
BR112013014708B1 (pt) 2011-02-28 2021-10-19 Sunshine Lake Pharma Co., Ltd. Composto, composição farmacêutica, e, uso de um composto ou composição farmacêutica
US20120244209A1 (en) 2011-03-02 2012-09-27 Roth Jack A Tusc2 therapies
JP6322413B2 (ja) 2011-03-10 2018-05-09 プロヴェクタス ファーマテック,インク. 改善されたがん治療のための局所および全身性免疫修飾療法の組み合わせ
SI2691112T1 (en) 2011-03-31 2018-07-31 Merck Sharp & Dohme Corp. STABILITY FORMULATION PROTITELES FOR HUMAN PROGRAMMED DEPRESSOR RECEPTOR PD-1 AND RELATED HEALTH
MX2013009931A (es) 2011-04-18 2013-10-01 Eisai R&D Man Co Ltd Agentes terapeuticos contra tumores.
WO2012154935A1 (fr) 2011-05-12 2012-11-15 Eisai R&D Management Co., Ltd. Biomarqueurs prédictifs d'une réactivité ou d'une absence de réactivité à un traitement au lenvatinib ou à son sel pharmaceutiquement acceptable
WO2012157672A1 (fr) 2011-05-17 2012-11-22 エーザイ・アール・アンド・ディー・マネジメント株式会社 Méthode de prédiction de l'efficacité d'un inhibiteur de l'angiogenèse
EP2714937B1 (fr) 2011-06-03 2018-11-14 Eisai R&D Management Co., Ltd. Biomarqueurs pour la prédiction et l'estimation de la sensibilité de sujets atteints d'un cancer de la thyroïde et du rein vis-à-vis de composés lenvatinib
BR112014002353B1 (pt) 2011-08-01 2022-09-27 Genentech, Inc Usos de antagonistas de ligação do eixo pd-1 e inibidores de mek, composições farmacêuticas, e kit
WO2013043569A1 (fr) 2011-09-20 2013-03-28 Vical Incorporated Immunothérapie combinée à action antitumorale synergique faisant appel à des alloantigènes
JP5941558B2 (ja) 2012-02-28 2016-06-29 株式会社ソウル製薬Seoul Pharma. Co., Ltd. シルデナフィルを有効成分として含有し、且つ、苦味の隠蔽された高含量速溶フィルム
AR090263A1 (es) 2012-03-08 2014-10-29 Hoffmann La Roche Terapia combinada de anticuerpos contra el csf-1r humano y las utilizaciones de la misma
EA037351B8 (ru) 2012-05-15 2021-04-29 Бристол-Майерс Сквибб Компани Способ лечения злокачественных опухолей с использованием комбинации антител против pd-1 и ctla-4
WO2013171287A1 (fr) 2012-05-16 2013-11-21 Boehringer Ingelheim International Gmbh Combinaison d'anticorps anti-cd37 avec ice (ifosmamide, carboplatine, etoposide)
PL2904011T3 (pl) 2012-10-02 2018-01-31 Bristol Myers Squibb Co Połączenie przeciwciał anty-kir i przeciwciał anty-pd-1 w leczeniu raka
WO2014087230A1 (fr) 2012-12-04 2014-06-12 Eisai R&D Management Co., Ltd. Utilisation d'éribuline dans le traitement de cancer du sein
EP3939614A1 (fr) 2013-01-18 2022-01-19 Foundation Medicine, Inc. Méthodes de traitement du cholangiocarcinome
KR20230070054A (ko) 2013-03-15 2023-05-19 제넨테크, 인크. Pd-1 및 pd-l1 관련 상태를 치료하기 위한 바이오마커 및 방법
CN105264380B (zh) 2013-05-14 2017-09-05 卫材R&D管理有限公司 用于预测和评价子宫内膜癌受试者对乐伐替尼化合物响应性的生物标志
WO2014208774A1 (fr) 2013-06-26 2014-12-31 Eisai R&D Management Co., Ltd. Utilisation d'éribuline et de lenvatinib en tant que polythérapie pour le traitement du cancer
US9174998B2 (en) 2013-12-25 2015-11-03 Eisai R&D Management Co., Ltd. (6S,9aS)-N-benzyl-6-[(4-hydroxyphenyl)methyl]-4,7-dioxo-8-({6-[3-(piperazin-1-yl)azetidin-1-yl]pyridin-2-yl}methyl)-2-(prop-2-en-1-yl)-octahydro-1H-pyrazino[2,1-c][1,2,4]triazine-1-carboxamide compound
JOP20200094A1 (ar) 2014-01-24 2017-06-16 Dana Farber Cancer Inst Inc جزيئات جسم مضاد لـ pd-1 واستخداماتها
KR20160108568A (ko) 2014-02-04 2016-09-19 인사이트 코포레이션 암을 치료하기 위한 pd-1 길항제 및 ido1 억제제의 조합
JP2017509671A (ja) 2014-03-28 2017-04-06 ウニベルシタ デリィ ストゥディ ディ ジェノバ カロリー摂取量減少と協同したがん治療方法で使用されるチロシンキナーゼ阻害剤
LT3524595T (lt) 2014-08-28 2022-09-26 Eisai R&D Management Co., Ltd. Aukšto grynumo chinolino darinys ir jo gamybos būdas
WO2016140717A1 (fr) 2015-03-04 2016-09-09 Merck Sharp & Dohme Corp. Association d'un antagoniste de pd-1 et d'un inhibiteur des tyrosines kinases vegfr/fgfr/ret pour traiter le cancer
WO2016184436A1 (fr) 2015-05-21 2016-11-24 苏州晶云药物科技有限公司 Nouvelle forme cristalline de sel de méthanesulfonate de lenvatinib et son procédé de préparation
WO2016196389A1 (fr) 2015-05-29 2016-12-08 Bristol-Myers Squibb Company Traitement du néphrocarcinome
MX373231B (es) 2015-06-16 2020-05-08 Eisai R&D Man Co Ltd Agente anticancerigeno.
KR102559211B1 (ko) 2015-06-23 2023-07-25 에자이 알앤드디 매니지먼트 가부시키가이샤 (6S,9aS)-N-벤질-8-({6-[3-(4-에틸피페라진-1-일)아제티딘-1-일]피리딘-2-일}메틸)-6-(2-플루오로-4-하이드록시벤질)-4,7-디옥소-2-(프로프-2-엔-1-일)헥사하이드로-2H-피라지노[2,1-c][1,2,4]트리아진-1(6H)-카복사마이드의 결정
US20200375975A1 (en) 2016-04-15 2020-12-03 Eisai R&D Management Co., Ltd. Treatment of Renal Cell Carcinoma with Lenvatinib and Everolimus
CN107305202B (zh) 2016-04-22 2020-04-17 北京睿创康泰医药研究院有限公司 分析甲磺酸乐伐替尼及其制剂杂质的hplc方法及杂质作参比标准的用途
JP6581320B2 (ja) 2017-02-08 2019-09-25 エーザイ・アール・アンド・ディー・マネジメント株式会社 腫瘍治療用医薬組成物
HUE069392T2 (hu) 2017-04-04 2025-03-28 Synthon Bv Lenvatinib-mezilátot tartalmazó gyógyszerkészítmény
WO2018196687A1 (fr) 2017-04-25 2018-11-01 苏州科睿思制药有限公司 Nouvelle forme cristalline de méthanesulfonate de lenvatinib et procédé de préparation correspondant
CN109988112A (zh) 2017-12-29 2019-07-09 四川科伦药物研究院有限公司 仑伐替尼甲磺酸盐的晶型及其制备方法
US10583133B2 (en) 2018-03-12 2020-03-10 Shilpa Medicare Limited Pharmaceutical compositions of lenvatinib
WO2019228485A1 (fr) 2018-06-01 2019-12-05 成都苑东生物制药股份有限公司 Nouvelle forme cristalline de mésylate de lenvatinib et procédé de préparation correspondant
CN110818634B (zh) 2018-08-13 2021-11-30 上海新礼泰药业有限公司 甲磺酸乐伐替尼的精制方法
CN110903239A (zh) 2018-09-18 2020-03-24 苏州科睿思制药有限公司 乐伐替尼甲磺酸盐的新晶型及其制备方法
CN110563644A (zh) 2019-10-30 2019-12-13 北京赛思源生物医药技术有限公司 一种仑伐替尼甲磺酸盐的新晶型
EP4147689A1 (fr) 2021-09-13 2023-03-15 Lotus Pharmaceutical Co., Ltd. Formulation de lenvatinib

Also Published As

Publication number Publication date
CY1117481T1 (el) 2017-04-26
EP2468281B1 (fr) 2016-01-27
UA105671C2 (uk) 2014-06-10
ES2564797T3 (es) 2016-03-29
CL2012000412A1 (es) 2012-08-31
AU2010285740C1 (en) 2016-03-17
HK1169599A1 (en) 2013-02-01
HUE026957T2 (en) 2016-07-28
EP2468281A4 (fr) 2013-01-23
US20130296365A1 (en) 2013-11-07
TH121482A (th) 2013-02-28
BR112012003592A2 (pt) 2016-03-15
KR20120055559A (ko) 2012-05-31
CA2771403C (fr) 2015-02-24
SG178009A1 (en) 2012-03-29
US20210228722A1 (en) 2021-07-29
SI2468281T1 (sl) 2016-05-31
BR112012003592B1 (pt) 2020-11-03
RU2548673C2 (ru) 2015-04-20
NZ598291A (en) 2013-02-22
ZA201108697B (en) 2012-07-25
RU2012103471A (ru) 2013-09-27
IL217197A0 (en) 2012-02-29
IL217197A (en) 2016-08-31
HRP20160283T1 (hr) 2016-05-06
CO6440512A2 (es) 2012-05-15
AU2010285740B2 (en) 2014-12-04
JP5048871B2 (ja) 2012-10-17
PE20121030A1 (es) 2012-08-18
SMT201600077B (it) 2016-04-29
JPWO2011021597A1 (ja) 2013-01-24
HK1167607A1 (en) 2012-12-07
EP2468281A1 (fr) 2012-06-27
DK2468281T3 (en) 2016-03-21
MY162940A (en) 2017-07-31
BR112012003592B8 (pt) 2021-05-25
MX2012002011A (es) 2012-03-26
ME02359B (fr) 2016-06-20
KR101496395B1 (ko) 2015-02-26
AU2010285740A1 (en) 2011-12-15
CA2771403A1 (fr) 2011-02-24
CN102470133B (zh) 2013-08-28
RS54686B1 (sr) 2016-08-31
RU2548673C3 (ru) 2018-07-20
US12508313B2 (en) 2025-12-30
US20120077842A1 (en) 2012-03-29
CN102470133A (zh) 2012-05-23
PL2468281T3 (pl) 2016-06-30
MX344927B (es) 2017-01-11
WO2011021597A1 (fr) 2011-02-24

Similar Documents

Publication Publication Date Title
MA33581B1 (fr) Composition pharmaceutique contenant un dérivé de quinoléine
MA33072B1 (fr) Composes pyridazinone
RU2018121834A (ru) Новое соединение бифенила или его соль
AR051780A1 (es) Compuestos en anillo fusionados que contienen nitrogeno y utilizacion de los mismos
MA30890B1 (fr) Compose indole
TW200607504A (en) Cinnamide compound
MA33836B1 (fr) Compositions pharmaceutiques contenant des ligands des récepteurs sigma
MA32171B1 (fr) Compose heterocyclique
AR054560A1 (es) Espiropiperidina como inhibidores de beta-secretasa para el tratamiento de la enfermedad de alzheimer
MA31574B1 (fr) Dérivés de pyrazole et leur utilisation comme inhibiteurs de raf
BRPI0707491B8 (pt) compostos úteis como agentes moduladores de receptores de mineralocorticóides, os referidos agentes compreendendo os mesmos e composições farmacêuticas
CO6190582A2 (es) Derivados de heteroarilamida
BRPI0713253A2 (pt) método de inibição de pde4, método de tratamento de um doença mediada por pde4, composto e composição farmacêutica
EA200401613A1 (ru) Лекарственное средство для лечения рака
MA45782B1 (fr) Modulateurs du récepteur de cxcr7 pipéridine
MA38935B1 (fr) Dérivés de diazacarbazole à titre de ligands tau-pet
MA32642B1 (fr) Amides utiles en therapie
RU2007103815A (ru) Производное тиенопиразола, имеющее ингибирующую фосфодиэстеразу 7(pde 7) активность
MA49127B1 (fr) Dérivés d'indole n-substitués
AR094123A1 (es) Compuesto triciclicos
MA33352B1 (fr) Derives de cyclopenta[c]pyrrolylalkylcarbamates d'heterocycles a 5 chainons, leur preparation et leur application en therapeutique
MA38679B1 (fr) Modulateurs du récepteur de cxcr7
NO20054854L (no) Femrings heterocykliske derivater
MA31784B1 (fr) Nouveaux dérivés d'imidazole
EA200970779A1 (ru) Новое сульфированное соединение сахара и его применение в качестве лекарственного средства