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
- 239000002552 dosage form Substances 0.000 title abstract 2
- 229940121358 tyrosine kinase inhibitor Drugs 0.000 title abstract 2
- 239000005483 tyrosine kinase inhibitor Substances 0.000 title abstract 2
- 150000004917 tyrosine kinase inhibitor derivatives Chemical class 0.000 title abstract 2
- 229920000642 polymer Polymers 0.000 abstract 1
- 239000007962 solid dispersion Substances 0.000 abstract 1
- 239000002904 solvent Substances 0.000 abstract 1
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
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Public Health (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- Epidemiology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Chemistry (AREA)
- Biophysics (AREA)
- Molecular Biology (AREA)
- Oncology (AREA)
- Ophthalmology & Optometry (AREA)
- Hematology (AREA)
- Heart & Thoracic Surgery (AREA)
- Cardiology (AREA)
- Urology & Nephrology (AREA)
- Dispersion Chemistry (AREA)
- Medicinal Preparation (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
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 (40)
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US8124630B2 (en) | 1999-01-13 | 2012-02-28 | Bayer Healthcare Llc | ω-carboxyaryl substituted diphenyl ureas as raf kinase inhibitors |
JP2002534468A (ja) | 1999-01-13 | 2002-10-15 | バイエル コーポレイション | p38キナーゼ阻害剤としてのω−カルボキシアリール置換ジフェニル尿素 |
EP2324825A1 (en) | 2002-02-11 | 2011-05-25 | Bayer Healthcare LLC | Aryl ureas with angiogenesis inhibiting activity |
JP4860474B2 (ja) | 2003-05-20 | 2012-01-25 | バイエル、ファーマシューテイカルズ、コーポレイション | Pdgfrによって仲介される病気のためのジアリール尿素 |
JP4777887B2 (ja) | 2003-07-23 | 2011-09-21 | バイエル、ファーマシューテイカルズ、コーポレイション | 病気および状態の処置および防止のためのフロロ置換オメガカルボキシアリールジフェニル尿素 |
US7947843B2 (en) * | 2007-10-19 | 2011-05-24 | Abbott Laboratories | Crystalline chemotherapeutic |
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 |
US7960564B2 (en) * | 2007-10-19 | 2011-06-14 | Abbott Laboratories | Crystalline chemotherapeutic |
US7943782B2 (en) * | 2007-10-19 | 2011-05-17 | Abbott Laboratories | Crystalline chemotherapeutic |
US7994208B2 (en) * | 2007-10-19 | 2011-08-09 | Abbott Laboratories | Crystalline chemotherapeutic |
PA8800101A1 (es) * | 2007-10-19 | 2009-05-15 | Abbott Gmbh & Co Kg | Producto de dispersion sólida que contiene un compuesto a base de n-aril urea |
US20090203709A1 (en) * | 2008-02-07 | 2009-08-13 | Abbott Laboratories | Pharmaceutical Dosage Form For Oral Administration Of Tyrosine Kinase Inhibitor |
CN102224419A (zh) * | 2008-06-18 | 2011-10-19 | 雅培制药有限公司 | PlGF-1搭配诊断法和产物 |
EP2403492A1 (en) * | 2009-03-06 | 2012-01-11 | Novartis AG | Use of pyrimidylaminobenzamide derivatives for the treatment of disorders mediated by the leucine zipper- and sterile alpha motif-containing kinase (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 |
ES2535176T3 (es) | 2009-09-28 | 2015-05-06 | Qilu Pharmaceutical Co., Ltd | Derivados de 4-(anilino sustituido)quinazolina como inhibidores de la tirosina quinasa |
UA108886C2 (ru) * | 2010-06-09 | 2015-06-25 | Еббві Бахамаз Лтд. | Твердые дисперсии, содержащие ингибиторы киназ |
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 |
IN2014DN01605A (es) | 2011-08-04 | 2015-05-15 | Nat Cancer Ct | |
MX371297B (es) * | 2012-01-13 | 2020-01-24 | Xspray Microparticles Ab | Una composición farmacéutica que comprende nanopartículas híbridas amorfas estables, de al menos un inhibidor de proteína quinasa y al menos un componente estabilizador polimérico y formador de matriz. |
PL3181122T3 (pl) | 2012-01-13 | 2023-07-31 | Xspray Pharma Ab (Publ) | Kompozycja farmaceutyczna dazatynibu |
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 |
JP7234129B2 (ja) * | 2017-03-15 | 2023-03-07 | サン・ファーマ・アドバンスド・リサーチ・カンパニー・リミテッド | 4-メチル-3-キノリン-3-イルエチニル-安息香酸n’-(2-クロロ-6-メチル-ベンゾイル)ヒドラジドの新規非晶質分散体 |
CA3056356A1 (en) | 2017-03-15 | 2018-09-20 | Sun Pharma Advanced Research Company Limited | Amorphous dispersion of cyclopropanecarboxylic acid (5-{5-[n'-(2- chloro-6-methylbenzoyl) hydrazinocarbonyl]-2-methyl-phenylethynyl}-pyridin-2-yl) amide |
KR102184117B1 (ko) * | 2017-10-31 | 2020-11-30 | 주식회사 삼양바이오팜 | 수용해도 및 생체이용율이 개선된 소라페닙 나노입자 경구용 조성물 및 이의 제조 방법 |
US20190175589A1 (en) * | 2017-11-09 | 2019-06-13 | Sunesis Pharmaceuticals, Inc. | Pharmaceutical formulations, processes for preparation, and methods of use |
CA3102381A1 (en) | 2018-06-15 | 2019-12-19 | Handa Oncology, Llc | Kinase inhibitor salts and compositions thereof |
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 |
WO2021125788A1 (ko) * | 2019-12-17 | 2021-06-24 | 주식회사 삼양홀딩스 | 수니티닙 염산염을 포함하는 경구용 고형제제 및 그 제조 방법 |
JP2023513444A (ja) | 2020-01-24 | 2023-03-31 | ナノコピーア リミテッド ライアビリティ カンパニー | ダサチニブの非晶質固体分散体及びその使用 |
EP4096791A1 (en) | 2020-01-31 | 2022-12-07 | Nanocopoeia LLC | Amorphous nilotinib microparticles and uses thereof |
IL297776A (en) | 2020-04-30 | 2022-12-01 | Nanocopoeia Llc | Orally disintegrating tablets containing an amorphous solid dispersion of nalotinib |
CA3203975A1 (en) | 2020-12-03 | 2022-06-09 | Battelle Memorial Institute | Polymer nanoparticle and dna nanostructure compositions and methods for non-viral delivery |
JP7628020B2 (ja) | 2021-01-25 | 2025-02-07 | 日本化薬株式会社 | アキシチニブを有効成分とする医薬錠剤 |
CN117500923A (zh) | 2021-04-07 | 2024-02-02 | 巴特尔纪念研究院 | 用于鉴定和使用非病毒载体的快速设计、构建、测试和学习技术 |
US11980619B2 (en) | 2021-07-28 | 2024-05-14 | Nanocopoeia, Llc | Pharmaceutical compositions and crushable tablets including amorphous solid dispersions of dasatinib and uses |
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 |
Family Cites Families (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
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 |
US20070104740A1 (en) * | 2003-12-23 | 2007-05-10 | Voorspoels Jody Firmin M | Self-microemulsifying drug delivery systems of a hiv protease inhibitor |
MY191349A (en) * | 2004-08-27 | 2022-06-17 | Bayer Pharmaceuticals Corp | New pharmaceutical compositions for the treatment of hyper-proliferative disorders |
ES2306216T3 (es) * | 2004-08-27 | 2008-11-01 | Bayer Pharmaceuticals Corporation | Composiciones farmaceuticas en forma de dispersiones solidas para el tratamiento de cancer. |
ATE533473T1 (de) * | 2004-09-24 | 2011-12-15 | Boehringer Ingelheim Pharma | Neue klasse von surfuctantähnlichen materialien mit vitamin-e-tpgs und wasserlöslichem polymer |
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 CA CA002667720A patent/CA2667720A1/en not_active Abandoned
- 2007-11-08 JP JP2009535737A patent/JP2010509289A/ja active Pending
- 2007-11-08 AU AU2007316558A patent/AU2007316558A1/en not_active Abandoned
- 2007-11-08 KR KR1020097009697A patent/KR20090094815A/ko not_active Application Discontinuation
- 2007-11-08 EP EP07857203A patent/EP2089003A1/en not_active Withdrawn
- 2007-11-08 WO PCT/EP2007/062101 patent/WO2008055966A1/en active Application Filing
- 2007-11-08 MX MX2009004861A patent/MX2009004861A/es not_active Application Discontinuation
- 2007-11-08 US US12/447,488 patent/US20100143459A1/en not_active Abandoned
Also Published As
Publication number | Publication date |
---|---|
KR20090094815A (ko) | 2009-09-08 |
AU2007316558A1 (en) | 2008-05-15 |
JP2010509289A (ja) | 2010-03-25 |
US20100143459A1 (en) | 2010-06-10 |
CA2667720A1 (en) | 2008-05-15 |
EP2089003A1 (en) | 2009-08-19 |
WO2008055966A1 (en) | 2008-05-15 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
FA | Abandonment or withdrawal |