MA29543B1 - Procedes pour traiter un cancer pharmacoresistant - Google Patents
Procedes pour traiter un cancer pharmacoresistantInfo
- Publication number
- MA29543B1 MA29543B1 MA30468A MA30468A MA29543B1 MA 29543 B1 MA29543 B1 MA 29543B1 MA 30468 A MA30468 A MA 30468A MA 30468 A MA30468 A MA 30468A MA 29543 B1 MA29543 B1 MA 29543B1
- Authority
- MA
- Morocco
- Prior art keywords
- resistant cancer
- methods
- compound
- treating drug
- salt
- Prior art date
Links
- 208000016691 refractory malignant neoplasm Diseases 0.000 title abstract 3
- 150000001875 compounds Chemical class 0.000 abstract 5
- 150000003839 salts Chemical class 0.000 abstract 4
- 239000000203 mixture Substances 0.000 abstract 2
- 239000003814 drug Substances 0.000 abstract 1
- 229940079593 drug Drugs 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/496—Non-condensed piperazines containing further heterocyclic rings, e.g. rifampin, thiothixene or sparfloxacin
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/4425—Pyridinium derivatives, e.g. pralidoxime, pyridostigmine
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/4164—1,3-Diazoles
- A61K31/4184—1,3-Diazoles condensed with carbocyclic rings, e.g. benzimidazoles
-
- 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
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/4965—Non-condensed pyrazines
- A61K31/497—Non-condensed pyrazines containing further heterocyclic rings
-
- 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
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Pharmacology & Pharmacy (AREA)
- Chemical & Material Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Epidemiology (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Hematology (AREA)
- Oncology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
Abstract
LA PRÉSENTE INVENTION CONCERNE UN PROCÉDÉ POUR TRAITER UN CANCER PHARMACORÉSISTANT, QUI CONSISTE À ADMINISTRER À UN PATIENT QUI LE NÉCESSITE UN COMPOSÉ DE FORMULE (I), UN TAUTOMÈRE DE CE COMPOSÉ, UN SEL DE CE COMPOSÉ, UN SEL DUDIT TAUTOMÈRE OU UN MÉLANGE DE CEUX-CI OU UNE COMPOSITION PHARMACEUTIQUE COMPRENANT LEDIT COMPOSÉ, LEDIT TAUTOMÈRE, LEDIT SEL DU COMPOSÉ, LEDIT SEL DU TAUTOMÈRE OU LEDIT MÉLANGE. LE PATIENT EST UN PATIENT ATTEINT D'UN CANCER PHARMACORÉSISTANT ET LE COMPOSÉ DE FORMULE (I) EST TEL QUE DÉFINI DANS LA DEMANDE.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US68072205P | 2005-05-13 | 2005-05-13 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| MA29543B1 true MA29543B1 (fr) | 2008-06-02 |
Family
ID=37431829
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MA30468A MA29543B1 (fr) | 2005-05-13 | 2007-12-10 | Procedes pour traiter un cancer pharmacoresistant |
Country Status (22)
| Country | Link |
|---|---|
| US (1) | US8299081B2 (fr) |
| EP (1) | EP1885187B1 (fr) |
| JP (2) | JP5344910B2 (fr) |
| KR (1) | KR101319122B1 (fr) |
| CN (1) | CN101222850B (fr) |
| AU (1) | AU2006247803B2 (fr) |
| BR (1) | BRPI0610360A2 (fr) |
| CA (1) | CA2608171C (fr) |
| DK (1) | DK1885187T3 (fr) |
| ES (1) | ES2440799T3 (fr) |
| IL (1) | IL187327A (fr) |
| MA (1) | MA29543B1 (fr) |
| MX (1) | MX2007014206A (fr) |
| NO (1) | NO20076425L (fr) |
| NZ (1) | NZ564144A (fr) |
| PL (1) | PL1885187T3 (fr) |
| PT (1) | PT1885187E (fr) |
| RU (1) | RU2426539C2 (fr) |
| SI (1) | SI1885187T1 (fr) |
| TN (1) | TNSN07419A1 (fr) |
| WO (1) | WO2006124413A2 (fr) |
| ZA (1) | ZA200709620B (fr) |
Families Citing this family (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101423513B (zh) * | 2007-10-29 | 2013-03-27 | 中国医学科学院药物研究所 | 胺基嘧啶衍生物、及其制法和药物组合物与用途 |
| PT2149372E (pt) * | 2008-07-31 | 2014-07-25 | Universität Ulm | Utilização de opióides do grupo da metadona para o tratamento de pacientes com cancros resistentes |
| US9095592B2 (en) * | 2008-11-07 | 2015-08-04 | The Research Foundation For The State University Of New York | Bruton's tyrosine kinase as anti-cancer drug target |
| US9519613B2 (en) * | 2009-02-02 | 2016-12-13 | Asurion, Llc | Method for integrating applications in an electronic address book |
| TWI410418B (zh) | 2009-04-29 | 2013-10-01 | Ind Tech Res Inst | 氮雜薁化合物、藥學組合物與抑制一細胞中蛋白質激酶之活性的方法 |
| PH12012501977A1 (en) * | 2010-04-16 | 2013-01-07 | Novartis Ag | Combination of organic compounds |
| MX2013013437A (es) * | 2011-05-19 | 2013-12-06 | Novartis Ag | 4-amino-5-fluoro-3- [6- (4-metil-piperazin-1-il) -1h-bencimidazol-2-il] -1h-quinolin-2-ona parea usarse en el tratamiento de un carcinoma adenoide quistico. |
| WO2013063003A1 (fr) | 2011-10-28 | 2013-05-02 | Novartis Ag | Méthode de traitement des tumeurs stromales gastro-intestinales |
| MX2014009303A (es) * | 2012-01-31 | 2014-10-14 | Novartis Ag | Combinacion de un inhibidor de rtk con un anti-estrogeno y uso del mismo para el tratamiento de cancer. |
| EP2872142A1 (fr) * | 2012-07-11 | 2015-05-20 | Novartis AG | Méthode de traitement de tumeurs stromales gastro-intestinales |
| WO2014058785A1 (fr) | 2012-10-10 | 2014-04-17 | Novartis Ag | Polythérapie |
| RU2547999C1 (ru) * | 2013-10-28 | 2015-04-10 | Государственное бюджетное учреждение здравоохранения Московской области "Московский областной научно-исследовательский клинический институт им. М.Ф. Владимирского" (ГБУЗ МО МОНИКИ им. М.Ф. Владимирского) | Способ лечения аденогенного местно-распространенного рака нижнеампулярного отдела прямой кишки |
| WO2016123054A2 (fr) * | 2015-01-26 | 2016-08-04 | The University Of North Carolina At Chapel Hill | Combinaisons de médicaments à base de kinase et leurs procédés d'utilisation |
| WO2018057618A1 (fr) * | 2016-09-20 | 2018-03-29 | Dana-Farber Cancer Institute, Inc. | Compositions et méthodes pour l'identification, l'évaluation, la prévention et le traitement de la lma au moyen de biomarqueurs usp10 et de modulateurs |
Family Cites Families (79)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US580883A (en) * | 1897-04-20 | Logging-sled | ||
| US3663606A (en) | 1966-06-21 | 1972-05-16 | Mitsui Toatsu Chemicals | Organic imino-compounds |
| DE2363459A1 (de) | 1973-12-20 | 1975-06-26 | Basf Ag | Neue fluoreszierende chinolinverbindungen |
| US4659657A (en) | 1982-12-24 | 1987-04-21 | Bayer Aktiengesellschaft | Chromogenic and fluorogenic esters for photometric or fluorimetric determination of phosphatases or sulphatases |
| DE3248043A1 (de) | 1982-12-24 | 1984-06-28 | Bayer Ag, 5090 Leverkusen | Fluorogene phosphorsaeureester, verfahren zu deren herstellung sowie verfahren und mittel zum nachweis und zur fluorometrischen bestimmung von phosphaten |
| DE3634066A1 (de) | 1986-10-07 | 1988-04-21 | Boehringer Mannheim Gmbh | Neue 5-alkylbenzimidazole, verfahren zu ihrer herstellung sowie arzneimittel |
| US5073492A (en) | 1987-01-09 | 1991-12-17 | The Johns Hopkins University | Synergistic composition for endothelial cell growth |
| JPH07121937B2 (ja) | 1987-03-18 | 1995-12-25 | 大塚製薬株式会社 | カルボスチリル誘導体 |
| JPH0699497B2 (ja) | 1987-04-16 | 1994-12-07 | 富士写真フイルム株式会社 | 光重合性組成物 |
| GB8709448D0 (en) | 1987-04-21 | 1987-05-28 | Pfizer Ltd | Heterobicyclic quinoline derivatives |
| JPH02229165A (ja) | 1989-03-02 | 1990-09-11 | Otsuka Pharmaceut Co Ltd | カルボスチリル誘導体 |
| DE3932953A1 (de) | 1989-10-03 | 1991-04-11 | Boehringer Mannheim Gmbh | Neue 2-bicyclo-benzimidazole, verfahren zu ihrer herstellung und diese verbindungen enthaltende arzneimittel |
| US5151360A (en) | 1990-12-31 | 1992-09-29 | Biomembrane Institute | Effect of n,n,n-trimethylsphingosine on protein kinase-c activity, melanoma cell growth in vitro, metastatic potential in vivo and human platelet aggregation |
| GB9107742D0 (en) | 1991-04-11 | 1991-05-29 | Rhone Poulenc Agriculture | New compositions of matter |
| GB9108369D0 (en) | 1991-04-18 | 1991-06-05 | Rhone Poulenc Agriculture | Compositions of matter |
| GB9108547D0 (en) | 1991-04-22 | 1991-06-05 | Fujisawa Pharmaceutical Co | Quinoline derivatives |
| 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 |
| US5480883A (en) | 1991-05-10 | 1996-01-02 | Rhone-Poulenc Rorer Pharmaceuticals Inc. | Bis mono- and bicyclic aryl and heteroaryl compounds which inhibit EGF and/or PDGF receptor tyrosine kinase |
| ES2108120T3 (es) | 1991-05-10 | 1997-12-16 | Rhone Poulenc Rorer Int | Compuestos bis arilicos y heteroarilicos mono- y biciclicos que inhiben tirosina quinasa receptora de egf y/o pdgf. |
| USRE37650E1 (en) | 1991-05-10 | 2002-04-09 | Aventis Pharmacetical Products, Inc. | Aryl and heteroaryl quinazoline compounds which inhibit CSF-1R receptor tyrosine kinase |
| US5856115A (en) | 1991-05-24 | 1999-01-05 | Fred Hutchinson Cancer Research Center | Assay for identification therapeutic agents |
| US6004554A (en) | 1992-03-05 | 1999-12-21 | Board Of Regents, The University Of Texas System | Methods for targeting the vasculature of solid tumors |
| JP3142378B2 (ja) | 1992-06-22 | 2001-03-07 | ティーディーケイ株式会社 | 有機el素子 |
| AU673193B2 (en) | 1992-09-02 | 1996-10-31 | Isis Pharmaceuticals, Inc. | Oligonucleotide modulation of cell adhesion |
| US5330992A (en) * | 1992-10-23 | 1994-07-19 | Sterling Winthrop Inc. | 1-cyclopropyl-4-pyridyl-quinolinones |
| SE9203318D0 (sv) | 1992-11-06 | 1992-11-06 | Kabi Pharmacia Ab | Novel 3,3-diphenylpropylamines, their use and preparation |
| US5792771A (en) | 1992-11-13 | 1998-08-11 | Sugen, Inc. | Quinazoline compounds and compositions thereof for the treatment of disease |
| US5981569A (en) | 1992-11-13 | 1999-11-09 | Yissum Research Development Company Of The Hebrew University Of Jerusalem | Substituted phenylacrylonitrile compounds and compositions thereof for the treatment of disease |
| US5763441A (en) | 1992-11-13 | 1998-06-09 | Sugen, Inc. | Compounds for the treatment of disorders related to vasculogenesis and/or angiogenesis |
| JPH0743896A (ja) | 1993-07-28 | 1995-02-14 | Toyobo Co Ltd | 光重合性組成物 |
| US5498608A (en) | 1994-01-07 | 1996-03-12 | Salix Pharmaceuticals | Use of 2-hydroxy-5-phenylazobenzoic acid derivatives as colon cancer chemopreventative and chemotherapeutic agents |
| AU5881394A (en) | 1994-01-08 | 1995-08-01 | Rhone-Poulenc Agriculture Limited | Benzimidazolyl quinoline-3-carboxylate derivatives, intermediates thereto, and their use as herbicides |
| JPH0829973A (ja) | 1994-07-11 | 1996-02-02 | Toyobo Co Ltd | 光重合性組成物 |
| GB9508538D0 (en) | 1995-04-27 | 1995-06-14 | Zeneca Ltd | Quinazoline derivatives |
| JP3441246B2 (ja) | 1995-06-07 | 2003-08-25 | 富士写真フイルム株式会社 | 光重合性組成物 |
| GB9514265D0 (en) | 1995-07-13 | 1995-09-13 | Wellcome Found | Hetrocyclic compounds |
| EP0868179A4 (fr) | 1995-12-12 | 2002-01-30 | Merck & Co Inc | Nouvelle utilisation du losartan |
| GB9624482D0 (en) | 1995-12-18 | 1997-01-15 | Zeneca Phaema S A | Chemical compounds |
| US6010711A (en) | 1996-01-26 | 2000-01-04 | University Of Rochester | Methods, articles and compositions for the pharmacologic inhibition of bone resorption with phosphodiesterase inhibitors |
| DE19610723A1 (de) | 1996-03-19 | 1997-09-25 | Bayer Ag | Elektrolumineszierende Anordnungen unter Verwendung von Blendsystemen |
| US5942385A (en) | 1996-03-21 | 1999-08-24 | Sugen, Inc. | Method for molecular diagnosis of tumor angiogenesis and metastasis |
| CA2258728C (fr) | 1996-06-19 | 2011-09-27 | Rhone Poulenc Rorer Limited | Composes azabicycliques substitues et leur utilisation en tant qu'inhibiteurs de la production de tnf et de la photodiesterase cyclique d'amp |
| US6111110A (en) | 1996-10-30 | 2000-08-29 | Eli Lilly And Company | Synthesis of benzo[f]quinolinones |
| US6245760B1 (en) | 1997-05-28 | 2001-06-12 | Aventis Pharmaceuticals Products, Inc | Quinoline and quinoxaline compounds which inhibit platelet-derived growth factor and/or p56lck tyrosine kinases |
| GB9716557D0 (en) | 1997-08-06 | 1997-10-08 | Glaxo Group Ltd | Benzylidene-1,3-dihydro-indol-2-one derivatives having anti-cancer activity |
| DE19756235A1 (de) | 1997-12-17 | 1999-07-01 | Klinge Co Chem Pharm Fab | Neue piperidinylsubstituierte Pyridylalkan- alken- und -alkincarbonsäureamide |
| AU3850299A (en) | 1998-05-20 | 1999-12-06 | Kyowa Hakko Kogyo Co. Ltd. | Vegf activity inhibitors |
| US6174912B1 (en) | 1998-08-21 | 2001-01-16 | Dupont Pharmaceuticals Company | Nitrogen substituted imidazo[4,5-C]pyrazoles as corticotropin releasing hormone antagonists |
| DE19841985A1 (de) | 1998-09-03 | 2000-03-09 | Schering Ag | Dialkylsulfonsäure- und Dialkylcarbonsäure-Derivate |
| US20030087854A1 (en) | 2001-09-10 | 2003-05-08 | Isis Pharmaceuticals Inc. | Antisense modulation of fibroblast growth factor receptor 3 expression |
| JP4707240B2 (ja) | 1999-05-05 | 2011-06-22 | アベンティス・フアーマ・リミテッド | 細胞接着調節剤としての尿素 |
| KR100298572B1 (ko) | 1999-08-19 | 2001-09-22 | 박찬구 | 카바아닐라이드로부터 4-니트로디페닐아민과 4-니트로소디페닐아민의 제조방법 |
| EP1226119B1 (fr) | 1999-10-19 | 2005-03-16 | MERCK & CO. INC. | Inhibiteurs tyrosine kinase |
| ES2234698T3 (es) | 1999-10-19 | 2005-07-01 | MERCK & CO., INC. | Inhibidores de tirosina quinasa. |
| US6420382B2 (en) | 2000-02-25 | 2002-07-16 | Merck & Co., Inc. | Tyrosine kinase inhibitors |
| US6313138B1 (en) | 2000-02-25 | 2001-11-06 | Merck & Co., Inc. | Tyrosine kinase inhibitors |
| WO2001066084A2 (fr) | 2000-03-07 | 2001-09-13 | Rush-Presbyterian-St. Luke's Medical Center | Compositions et procedes permettant de pieger et d'inactiver les microbes pathogenes et les spermatozoides |
| CA2420844A1 (fr) | 2000-08-30 | 2003-02-28 | Sankyo Company, Limited | Compositions medicinales utilisees dans la prevention ou le traitement de l'insuffisance cardiaque |
| US7179912B2 (en) | 2000-09-01 | 2007-02-20 | Icos Corporation | Materials and methods to potentiate cancer treatment |
| PT1313734E (pt) * | 2000-09-01 | 2010-02-09 | Novartis Vaccines & Diagnostic | Derivados aza heterocíclicos e sua utilização terapêutica |
| ATE309996T1 (de) | 2000-09-11 | 2005-12-15 | Chiron Corp | Chinolinonderivate als tyrosin-kinase inhibitoren |
| US20030028018A1 (en) | 2000-09-11 | 2003-02-06 | Chiron Coporation | Quinolinone derivatives |
| EP1401831A1 (fr) | 2001-07-03 | 2004-03-31 | Chiron Corporation | Composes d'indazole benzimidazole utilises comme inhibiteurs de tyrosine et de serine/threonine kinase |
| US6476068B1 (en) * | 2001-12-06 | 2002-11-05 | Pharmacia Italia, S.P.A. | Platinum derivative pharmaceutical formulations |
| US20030159702A1 (en) | 2002-01-21 | 2003-08-28 | Lindell Katarina E.A. | Formulation and use manufacture thereof |
| US7323479B2 (en) * | 2002-05-17 | 2008-01-29 | Celgene Corporation | Methods for treatment and management of brain cancer using 1-oxo-2-(2,6-dioxopiperidin-3-yl)-4-methylisoindoline |
| EP1539754A4 (fr) * | 2002-08-23 | 2009-02-25 | Novartis Vaccines & Diagnostic | Quinolinones de benzimidazole et leurs utilisations |
| US7825132B2 (en) | 2002-08-23 | 2010-11-02 | Novartis Vaccines And Diagnostics, Inc. | Inhibition of FGFR3 and treatment of multiple myeloma |
| US20050256157A1 (en) | 2002-08-23 | 2005-11-17 | Chiron Corporation | Combination therapy with CHK1 inhibitors |
| US7838527B2 (en) | 2002-11-13 | 2010-11-23 | Novartis Vaccines And Diagnostics, Inc. | Methods of treating cancer and related methods |
| WO2004073631A2 (fr) * | 2003-02-14 | 2004-09-02 | Combinatorx, Incorporated | Polytherapie pour le traitement de neoplasmes |
| US6774327B1 (en) | 2003-09-24 | 2004-08-10 | Agilent Technologies, Inc. | Hermetic seals for electronic components |
| CA2542662A1 (fr) * | 2003-10-17 | 2005-04-28 | Novo Nordisk A/S | Combinaisons pharmaceutiques comprenant de l'il-21 |
| WO2005046590A2 (fr) | 2003-11-07 | 2005-05-26 | Chiron Corporation | Methodes de synthese de composes de quinolinone |
| JP5019884B2 (ja) | 2004-02-20 | 2012-09-05 | ノバルティス バクシンズ アンド ダイアグノスティックス,インコーポレーテッド | 炎症プロセスおよび転移プロセスの調節 |
| SG173317A1 (en) * | 2005-01-27 | 2011-08-29 | Novartis Vaccines & Diagnostic | Treatment of metastasized tumors |
| EP1885801A1 (fr) | 2005-05-18 | 2008-02-13 | M & G Polimeri Italia S.P.A. | Composition polyester |
| EP2040738A1 (fr) | 2006-07-13 | 2009-04-01 | Zymogenetics, Inc. | Traitement de combinaison d'interleukine 21 et d'inhibiteur de tyrosine kinase |
| CA2659270A1 (fr) | 2006-07-28 | 2008-01-31 | Novartis Ag | Utilisation d'une proteine d'inhibition de l'activite d'un melanome (mia) en tant qu'indicateur precoce d'une reponse therapeutique dans un melanome |
-
2006
- 2006-05-10 US US11/913,828 patent/US8299081B2/en not_active Expired - Fee Related
- 2006-05-10 MX MX2007014206A patent/MX2007014206A/es active IP Right Grant
- 2006-05-10 SI SI200631674T patent/SI1885187T1/sl unknown
- 2006-05-10 RU RU2007145932/15A patent/RU2426539C2/ru not_active IP Right Cessation
- 2006-05-10 KR KR1020077029071A patent/KR101319122B1/ko not_active Expired - Fee Related
- 2006-05-10 CN CN2006800256454A patent/CN101222850B/zh not_active Expired - Fee Related
- 2006-05-10 DK DK06752445.4T patent/DK1885187T3/da active
- 2006-05-10 JP JP2008511274A patent/JP5344910B2/ja not_active Expired - Fee Related
- 2006-05-10 BR BRPI0610360-0A patent/BRPI0610360A2/pt not_active IP Right Cessation
- 2006-05-10 PL PL06752445T patent/PL1885187T3/pl unknown
- 2006-05-10 AU AU2006247803A patent/AU2006247803B2/en not_active Ceased
- 2006-05-10 PT PT67524454T patent/PT1885187E/pt unknown
- 2006-05-10 ES ES06752445.4T patent/ES2440799T3/es active Active
- 2006-05-10 WO PCT/US2006/017922 patent/WO2006124413A2/fr not_active Ceased
- 2006-05-10 NZ NZ564144A patent/NZ564144A/en not_active IP Right Cessation
- 2006-05-10 CA CA2608171A patent/CA2608171C/fr not_active Expired - Fee Related
- 2006-05-10 EP EP06752445.4A patent/EP1885187B1/fr not_active Not-in-force
-
2007
- 2007-11-08 ZA ZA200709620A patent/ZA200709620B/xx unknown
- 2007-11-12 IL IL187327A patent/IL187327A/en not_active IP Right Cessation
- 2007-11-12 TN TNP2007000419A patent/TNSN07419A1/en unknown
- 2007-12-10 MA MA30468A patent/MA29543B1/fr unknown
- 2007-12-13 NO NO20076425A patent/NO20076425L/no not_active Application Discontinuation
-
2013
- 2013-05-08 JP JP2013098616A patent/JP2013173787A/ja active Pending
Also Published As
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| MA29543B1 (fr) | Procedes pour traiter un cancer pharmacoresistant | |
| MA29378B1 (fr) | Composition pharmaceutique comprenant une diphenyluree substituee par un omega-carboxyaryle pour le traitement du cancer | |
| TNSN07145A1 (fr) | Derives de 2-amido-4-phenylthiazole, leur preparation et leur application en therapeutique | |
| MA27908A1 (fr) | Agents therapeutiques utiles pour le traitement de la douleur | |
| MA28742B1 (fr) | Derives de pyrido-pyrimidine, leur preparation, leur application en therapeutique | |
| EA200700501A1 (ru) | Композиция (варианты) и способ для лечения гиперпролиферативных процессов, способ лечения рака (варианты) и способ получения твёрдой дисперсии вещества | |
| MA30260B1 (fr) | Acides 4-phenyl-thiazole-5-carboxyliques et amides d'acide 4-phenyl-thiazole-5-carboxylique en tant qu'inhibiteurs de plk 1 | |
| TN2009000138A1 (fr) | Biaryl-ether-urees | |
| MA31497B1 (fr) | Nouveaux inhibiteurs peptidiques de la replication du virus de l'hepatite c | |
| TNSN06439A1 (fr) | Derives de 2-carbamide -4-phenylthiazole, leur preparation et leur application en therapeutique | |
| MA30351B1 (fr) | Composes de tetrahydropyridothienopyrimidine et leurs procedes d'utilisation | |
| MA26877A1 (fr) | Derives d'azetidine, leur preparation et les compositions pharmaceutiques les contenant | |
| MA31894B1 (fr) | Composes organiques | |
| MA29692B1 (fr) | Derives de la xanthine en tant qu'agonistes selectifs du hm74a | |
| MA30911B1 (fr) | Nouveaux derives de sulfonamide en tant qu'antagonistes de bradykinine | |
| TNSN08270A1 (fr) | Dérivés pyrimidiques destinés à traiter une croissance cellulaire anormale | |
| WO2006044497A3 (fr) | Composes de spiropiperidine utilises comme inhibiteurs de beta-secretase en vue du traitement de la maladie d'alzheimer | |
| MA35404B1 (fr) | Composés pour le traitement de la toxicomanie | |
| RU2013119129A (ru) | Органические соединения | |
| MA34361B1 (fr) | Dérivés de tétrahydro-pyrido-pyrimidine | |
| MA33836B1 (fr) | Compositions pharmaceutiques contenant des ligands des récepteurs sigma | |
| MA30916B1 (fr) | Nouveaux derives de benzamide en tant qu'antagonistes de bradykinine | |
| MA34308B1 (fr) | Triazolopyridines substituées | |
| EP1864649A3 (fr) | Composé de type bis-urée, composition le comprenant, utilisation et procédé de traitement cosmétique | |
| JP2015536997A5 (fr) |