MX2009004861A - Forma de dosificacion farmaceutica para la administracion oral de inhibidor de tirosina quinasa. - Google Patents
Forma de dosificacion farmaceutica para la administracion oral de inhibidor de tirosina quinasa.Info
- Publication number
- MX2009004861A MX2009004861A MX2009004861A MX2009004861A MX2009004861A MX 2009004861 A MX2009004861 A MX 2009004861A MX 2009004861 A MX2009004861 A MX 2009004861A MX 2009004861 A MX2009004861 A MX 2009004861A MX 2009004861 A MX2009004861 A MX 2009004861A
- Authority
- MX
- Mexico
- Prior art keywords
- dosage form
- tyrosine kinase
- kinase inhibitor
- pharmaceutical dosage
- oral administration
- Prior art date
Links
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/10—Dispersions; Emulsions
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/14—Particulate form, e.g. powders, Processes for size reducing of pure drugs or the resulting products, Pure drug nanoparticles
- A61K9/141—Intimate drug-carrier mixtures characterised by the carrier, e.g. ordered mixtures, adsorbates, solid solutions, eutectica, co-dried, co-solubilised, co-kneaded, co-milled, co-ground products, co-precipitates, co-evaporates, co-extrudates, co-melts; Drug nanoparticles with adsorbed surface modifiers
- A61K9/146—Intimate drug-carrier mixtures characterised by the carrier, e.g. ordered mixtures, adsorbates, solid solutions, eutectica, co-dried, co-solubilised, co-kneaded, co-milled, co-ground products, co-precipitates, co-evaporates, co-extrudates, co-melts; Drug nanoparticles with adsorbed surface modifiers with organic macromolecular compounds
-
- 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
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/20—Pills, tablets, discs, rods
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/20—Pills, tablets, discs, rods
- A61K9/2004—Excipients; Inactive ingredients
- A61K9/2013—Organic compounds, e.g. phospholipids, fats
- A61K9/2018—Sugars, or sugar alcohols, e.g. lactose, mannitol; Derivatives thereof, e.g. polysorbates
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/20—Pills, tablets, discs, rods
- A61K9/2004—Excipients; Inactive ingredients
- A61K9/2022—Organic macromolecular compounds
- A61K9/2027—Organic macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds, e.g. polyvinyl pyrrolidone, poly(meth)acrylates
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P13/00—Drugs for disorders of the urinary system
- A61P13/12—Drugs for disorders of the urinary system of the kidneys
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P27/00—Drugs for disorders of the senses
- A61P27/02—Ophthalmic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
- A61P35/02—Antineoplastic agents specific for leukemia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
Abstract
Se presenta una forma de dosificación farmacéutica que comprende un producto de dispersión de sólidos de por lo menos un inhibidor de tirosina quinasa, por lo menos un polímero farmacéuticamente aceptable, y por lo menos un solubilizador farmacéuticamente aceptable.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP06023367A EP1920767A1 (en) | 2006-11-09 | 2006-11-09 | Melt-processed imatinib dosage form |
US99957907P | 2007-10-19 | 2007-10-19 | |
PCT/EP2007/062101 WO2008055966A1 (en) | 2006-11-09 | 2007-11-08 | Pharmaceutical dosage form for oral administration of tyrosine kinase inhibitor |
Publications (1)
Publication Number | Publication Date |
---|---|
MX2009004861A true MX2009004861A (es) | 2009-05-21 |
Family
ID=38859725
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
MX2009004861A MX2009004861A (es) | 2006-11-09 | 2007-11-08 | Forma de dosificacion farmaceutica para la administracion oral de inhibidor de tirosina quinasa. |
Country Status (8)
Country | Link |
---|---|
US (1) | US20100143459A1 (es) |
EP (1) | EP2089003A1 (es) |
JP (1) | JP2010509289A (es) |
KR (1) | KR20090094815A (es) |
AU (1) | AU2007316558A1 (es) |
CA (1) | CA2667720A1 (es) |
MX (1) | MX2009004861A (es) |
WO (1) | WO2008055966A1 (es) |
Families Citing this family (35)
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EP2298311B1 (en) | 1999-01-13 | 2012-05-09 | Bayer HealthCare LLC | w-Carboxy aryl substituted diphenyl ureas as p38 kinase inhibitors |
US8124630B2 (en) | 1999-01-13 | 2012-02-28 | Bayer Healthcare Llc | ω-carboxyaryl substituted diphenyl ureas as raf kinase inhibitors |
MXPA04007832A (es) | 2002-02-11 | 2005-09-08 | Bayer Pharmaceuticals Corp | Aril-ureas con actividad inhibitoria de angiogenesis. |
CA2526617C (en) | 2003-05-20 | 2015-04-28 | Bayer Pharmaceuticals Corporation | Diaryl ureas with kinase inhibiting activity |
UA84156C2 (ru) | 2003-07-23 | 2008-09-25 | Байер Фармасьютикалс Корпорейшн | Фторозамещённая омега-карбоксиарилдифенилмочевина для лечения и профилактики болезней и состояний |
US7772404B2 (en) * | 2007-10-19 | 2010-08-10 | Abbott Laboratories | Crystalline form 2 of the chemotherapeutic N-[4-(3-amino-1H-indazol-4-yl)phenyl]-N′-(2-fluoro-5-methylphenyl)urea |
CA2699301A1 (en) * | 2007-10-19 | 2009-04-23 | Abbott Gmbh & Co. Kg | Solid dispersion product of n-aryl urea-based drugs |
US7943782B2 (en) * | 2007-10-19 | 2011-05-17 | Abbott Laboratories | Crystalline chemotherapeutic |
US7947843B2 (en) * | 2007-10-19 | 2011-05-24 | Abbott Laboratories | Crystalline chemotherapeutic |
US7960564B2 (en) * | 2007-10-19 | 2011-06-14 | Abbott Laboratories | Crystalline chemotherapeutic |
US7994208B2 (en) * | 2007-10-19 | 2011-08-09 | Abbott Laboratories | Crystalline chemotherapeutic |
US20090203709A1 (en) * | 2008-02-07 | 2009-08-13 | Abbott Laboratories | Pharmaceutical Dosage Form For Oral Administration Of Tyrosine Kinase Inhibitor |
EP2300825A4 (en) * | 2008-06-18 | 2012-04-25 | Abbott Lab | P / GF 1 COMPARATIVE DIAGNOSTIC PROCEDURES AND PRODUCTS |
BRPI1013366A2 (pt) * | 2009-03-06 | 2016-03-29 | Novartis Ag | uso de derivados de pirimidilaminobenzamida para o tratamento de distúrbios mediados pela quinase contendo zíper de leucina e quinase contendo motivo alfa estéril (zak). |
EP2255792A1 (en) * | 2009-05-20 | 2010-12-01 | Ratiopharm GmbH | Pharmaceutical compositions for N-[2-(Diethylamino)ethyl]5-[(fluoro-1,2-dihydro-2-oxo-3H-indole-3-ylidene) methyl]-2,4-dimenthyl-1H-pyrrole-3-carboxamide |
WO2011035540A1 (zh) | 2009-09-28 | 2011-03-31 | 齐鲁制药有限公司 | 作为酪氨酸激酶抑制剂的4-(取代苯胺基)喹唑啉衍生物 |
SG186248A1 (en) * | 2010-06-09 | 2013-01-30 | Abbvie Inc | Solid dispersions containing kinase inhibitors |
UA113500C2 (xx) | 2010-10-29 | 2017-02-10 | Одержані екструзією розплаву тверді дисперсії, що містять індукуючий апоптоз засіб | |
AR086913A1 (es) * | 2011-06-14 | 2014-01-29 | Novartis Ag | 4-metil-3-[[4-(3-piridinil)-2-pirimidinil]-amino]-n-[5-(4-metil-1h-imidazol-1-il)-3-(trifluoro-metil)-fenil]-benzamida amorfa, forma de dosificacion que la contiene y metodo para prepararlas |
CN103764676A (zh) * | 2011-08-04 | 2014-04-30 | 日本国立癌症研究中心 | Kif5b基因和ret基因的融合基因、以及以该融合基因为目标的判断癌症治疗有效性的方法 |
AU2013208323B2 (en) * | 2012-01-13 | 2017-07-06 | Xspray Microparticles Ab | A method for producing stable, amorphous hybrid nanoparticles comprising at least one protein kinase inhibitor and at least one polymeric stabilizing and matrix- forming component. |
DK2802314T3 (da) * | 2012-01-13 | 2021-01-25 | Xspray Microparticles Ab | Fremgangsmåde til fremstilling af stabile, amorfe hybride nanopartikler, der omfatter mindst én proteinkinaseinhibitor og mindst én polymer stabiliserende og matrixdannende bestanddel |
KR101386697B1 (ko) | 2012-06-18 | 2014-04-18 | 아주대학교산학협력단 | 이매티닙 또는 이의 약학적으로 허용되는 염을 유효성분으로 포함하는 혈관 투과성 관련 질환의 치료 또는 예방용 조성물 |
KR101674457B1 (ko) * | 2013-11-04 | 2016-11-09 | 아주대학교산학협력단 | 다사티닙 또는 이의 약학적으로 허용되는 염을 유효성분으로 포함하는 혈관 투과성 관련 질환의 예방 또는 치료용 약학적 조성물 |
KR101796684B1 (ko) * | 2016-05-19 | 2017-11-10 | 건국대학교 산학협력단 | 케라틴 8 인산화 억제제를 포함하는 황반변성 예방 또는 치료용 약학 조성물 및 황반변성 치료제의 스크리닝 방법 |
MA47798A (fr) | 2017-03-15 | 2020-01-22 | Sun Pharma Advanced Res Co Ltd | Nouvelle dispersion amorphe d'acide cyclopropanecarboxylique (5-{5-[ n'-(2-chloro-6-méthylbenzoyl) hydrazinocarbonyl] -2-méthyl-phényléthynyl}-pyridin-2-yl) amide |
CA3056348A1 (en) * | 2017-03-15 | 2018-09-20 | Sun Pharma Advanced Research Company Limited | Novel amorphous dispersion of 4-methyl-3-quinolin-3-ylethynyl-benzoic acid n'-(2-chloro-6-methyl-benzoyl) hydrazide |
KR102184117B1 (ko) * | 2017-10-31 | 2020-11-30 | 주식회사 삼양바이오팜 | 수용해도 및 생체이용율이 개선된 소라페닙 나노입자 경구용 조성물 및 이의 제조 방법 |
EP3806858A4 (en) * | 2018-06-15 | 2022-03-09 | Handa Pharmaceuticals, Inc. | SALTS OF KINASE INHIBITORS AND ASSOCIATED COMPOSITIONS |
CN110801434A (zh) * | 2019-10-31 | 2020-02-18 | 金华职业技术学院 | 一种冻干法制备甲苯磺酸拉帕替尼固体分散体的方法 |
KR102538075B1 (ko) * | 2019-12-17 | 2023-05-30 | 주식회사 삼양홀딩스 | 수니티닙 염산염을 포함하는 경구용 고형제제 및 그 제조 방법 |
EP4093379A1 (en) | 2020-01-24 | 2022-11-30 | Nanocopoeia LLC | Amorphous solid dispersions of dasatinib and uses thereof |
JP2023513045A (ja) | 2020-01-31 | 2023-03-30 | ナノコピーア リミテッド ライアビリティ カンパニー | 非晶質ニロチニブ微粒子及びその使用 |
WO2021222739A1 (en) | 2020-04-30 | 2021-11-04 | Nanocopoeia, Llc | Orally disintegrating tablet comprising amorphous solid dispersion of nilotinib |
CN113876715B (zh) * | 2021-10-28 | 2023-11-21 | 和记黄埔医药(苏州)有限公司 | 一种索凡替尼固体分散体及其片剂以及它们的制备方法 |
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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 |
GB0317663D0 (en) * | 2003-07-29 | 2003-09-03 | Astrazeneca Ab | Pharmaceutical composition |
WO2005063209A1 (en) * | 2003-12-23 | 2005-07-14 | Tibotec Pharmaceuticals Ltd. | Self-microemulsifying drug delivery systems of a hiv protease inhibitor |
EP1796642B1 (en) * | 2004-08-27 | 2008-05-21 | Bayer Pharmaceuticals Corporation | Pharmaceutical compositions in the form of solid dispersions for the treatment of cancer |
MY191349A (en) * | 2004-08-27 | 2022-06-17 | Bayer Pharmaceuticals Corp | New pharmaceutical compositions for the treatment of hyper-proliferative disorders |
CA2578356C (en) * | 2004-09-24 | 2013-05-28 | Boehringer Ingelheim Pharmaceuticals, Inc. | A new class of surfactant-like materials |
US7625911B2 (en) * | 2005-01-12 | 2009-12-01 | Mai De Ltd. | Amorphous form of erlotinib hydrochloride and its solid amorphous dispersion |
AR052660A1 (es) * | 2005-01-21 | 2007-03-28 | Astex Therapeutics Ltd | Derivados de pirazol para inhibir la cdk's y gsk's |
WO2006081985A1 (en) * | 2005-02-04 | 2006-08-10 | F. Hoffmann-La Roche Ag | Combined treatment with an n4-(substituted-oxycarbonyl)-5’-deoxy-5-fluorocytidine derivative and an epidermal growth factor receptor kinase inhibitor |
CN1857204A (zh) * | 2006-03-06 | 2006-11-08 | 济南帅华医药科技有限公司 | 一种同载血管抑制剂及其增效剂的抗癌缓释剂 |
-
2007
- 2007-11-08 MX MX2009004861A patent/MX2009004861A/es not_active Application Discontinuation
- 2007-11-08 EP EP07857203A patent/EP2089003A1/en not_active Withdrawn
- 2007-11-08 US US12/447,488 patent/US20100143459A1/en not_active Abandoned
- 2007-11-08 KR KR1020097009697A patent/KR20090094815A/ko not_active Application Discontinuation
- 2007-11-08 CA CA002667720A patent/CA2667720A1/en not_active Abandoned
- 2007-11-08 JP JP2009535737A patent/JP2010509289A/ja active Pending
- 2007-11-08 WO PCT/EP2007/062101 patent/WO2008055966A1/en active Application Filing
- 2007-11-08 AU AU2007316558A patent/AU2007316558A1/en not_active Abandoned
Also Published As
Publication number | Publication date |
---|---|
CA2667720A1 (en) | 2008-05-15 |
AU2007316558A1 (en) | 2008-05-15 |
KR20090094815A (ko) | 2009-09-08 |
EP2089003A1 (en) | 2009-08-19 |
WO2008055966A1 (en) | 2008-05-15 |
US20100143459A1 (en) | 2010-06-10 |
JP2010509289A (ja) | 2010-03-25 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
FA | Abandonment or withdrawal |