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CL2011002918A1 - Composicion farmaceutica solida que comprende al inhibidor de quinasa aurora acido 4-{[9-cloro-7-(2-fluoro-6-metoxifenil)-5h-pirimido-[5,4-d][2]benzazepin-2-il]amino}-2-metoxibenzoico, una sal o una forma cristalina del mismo; metodo para prepararla que incluye un proceso de granulacion en humedo. - Google Patents

Composicion farmaceutica solida que comprende al inhibidor de quinasa aurora acido 4-{[9-cloro-7-(2-fluoro-6-metoxifenil)-5h-pirimido-[5,4-d][2]benzazepin-2-il]amino}-2-metoxibenzoico, una sal o una forma cristalina del mismo; metodo para prepararla que incluye un proceso de granulacion en humedo.

Info

Publication number
CL2011002918A1
CL2011002918A1 CL2011002918A CL2011002918A CL2011002918A1 CL 2011002918 A1 CL2011002918 A1 CL 2011002918A1 CL 2011002918 A CL2011002918 A CL 2011002918A CL 2011002918 A CL2011002918 A CL 2011002918A CL 2011002918 A1 CL2011002918 A1 CL 2011002918A1
Authority
CL
Chile
Prior art keywords
carbonate
benzazepin
salt
pharmaceutical composition
solid pharmaceutical
Prior art date
Application number
CL2011002918A
Other languages
English (en)
Inventor
Bhavishya Mittal
Original Assignee
Millennium Pharm Inc
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
Application filed by Millennium Pharm Inc filed Critical Millennium Pharm Inc
Publication of CL2011002918A1 publication Critical patent/CL2011002918A1/es

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    • 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
    • A61K9/205—Polysaccharides, e.g. alginate, gums; Cyclodextrin
    • A61K9/2054—Cellulose; Cellulose derivatives, e.g. hydroxypropyl methylcellulose
    • 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
    • A61K9/145—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 compounds
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    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
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    • A61K31/335—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
    • A61K31/337—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having four-membered rings, e.g. taxol
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
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    • 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
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    • 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
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    • A61K31/513—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim having oxo groups directly attached to the heterocyclic ring, e.g. cytosine
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    • A61K47/30—Macromolecular organic or inorganic compounds, e.g. inorganic polyphosphates
    • A61K47/34—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds, e.g. polyesters, polyamino acids, polysiloxanes, polyphosphazines, copolymers of polyalkylene glycol or poloxamers
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  • Health & Medical Sciences (AREA)
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  • Life Sciences & Earth Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Veterinary Medicine (AREA)
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  • Medicinal Chemistry (AREA)
  • Epidemiology (AREA)
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  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Organic Chemistry (AREA)
  • Diabetes (AREA)
  • Rheumatology (AREA)
  • Obesity (AREA)
  • Immunology (AREA)
  • Emergency Medicine (AREA)
  • Endocrinology (AREA)
  • Hematology (AREA)
  • Cardiology (AREA)
  • Ophthalmology & Optometry (AREA)
  • Pain & Pain Management (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Vascular Medicine (AREA)
  • Orthopedic Medicine & Surgery (AREA)
  • Physical Education & Sports Medicine (AREA)
  • Dermatology (AREA)
  • Urology & Nephrology (AREA)
  • Proteomics, Peptides & Aminoacids (AREA)
  • Inorganic Chemistry (AREA)
  • Medicinal Preparation (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

Abstract

LA PRESENTE INVENCIÓN SE REFIERE A UNA COMPOSICIÓN FARMACÉUTICA SÓLIDA QUE EL INGREDIENTE ACTIVO OS EL ÁCIDO 4-{Í9-CLORO-7- (2- FIUORA-6-METOXIFENI)) -5H-PIRIMIDO(5 4-DL (2]BENZAZEPIN-2-ILJAMINO}-2-METOXIBENZOICO O UNO SAL FORRNACÉUTICOMERTE ACEPTABLE DEL MISMO, O UNA FORMA CRISTAHNA DEL MISMO; Y UN AMORTIGUADOR; EN DONDE E) INGREDIENTE ACTIVO ESTÁ EN FORMA GRANULAR, Y EL AMORTIGUADOR ES EXTRAGRANU)AR AL INGREDIENTE ACTIVO, Y DONDE E) AMORTIGUADOR COMPRENDE BICARBONATO DE SODIO, FOSFATO DE MONOSODIO, FOSFATO DE DISODIO, FOSFATO DE MONOPOLASIO, FOSFATO DE DIPOTASIO, BICARBONATO DE POTASIO, CARBONATO DE SODIO O CARBONATO DE POTASIO, EL MÉTODO PARA PREPARARLA QUE INCLUYE UN PROCESO DO GRANULACIÓN EN HÚMEDO.
CL2011002918A 2009-05-18 2011-11-18 Composicion farmaceutica solida que comprende al inhibidor de quinasa aurora acido 4-{[9-cloro-7-(2-fluoro-6-metoxifenil)-5h-pirimido-[5,4-d][2]benzazepin-2-il]amino}-2-metoxibenzoico, una sal o una forma cristalina del mismo; metodo para prepararla que incluye un proceso de granulacion en humedo. CL2011002918A1 (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US21649309P 2009-05-18 2009-05-18
US26843809P 2009-06-12 2009-06-12

Publications (1)

Publication Number Publication Date
CL2011002918A1 true CL2011002918A1 (es) 2012-05-25

Family

ID=42332398

Family Applications (1)

Application Number Title Priority Date Filing Date
CL2011002918A CL2011002918A1 (es) 2009-05-18 2011-11-18 Composicion farmaceutica solida que comprende al inhibidor de quinasa aurora acido 4-{[9-cloro-7-(2-fluoro-6-metoxifenil)-5h-pirimido-[5,4-d][2]benzazepin-2-il]amino}-2-metoxibenzoico, una sal o una forma cristalina del mismo; metodo para prepararla que incluye un proceso de granulacion en humedo.

Country Status (30)

Country Link
US (6) US9173846B2 (es)
EP (1) EP2432456B1 (es)
JP (2) JP5802199B2 (es)
KR (1) KR101809140B1 (es)
CN (2) CN103860512A (es)
AR (1) AR076879A1 (es)
AU (1) AU2010250099B2 (es)
BR (1) BRPI1012875B8 (es)
CA (1) CA2762336C (es)
CL (1) CL2011002918A1 (es)
CO (1) CO6470892A2 (es)
CR (1) CR20110626A (es)
DK (1) DK2432456T3 (es)
DO (1) DOP2011000358A (es)
EA (1) EA024209B1 (es)
EC (1) ECSP11011542A (es)
ES (1) ES2908655T3 (es)
GE (1) GEP20156328B (es)
IL (1) IL216427A (es)
JO (1) JO3635B1 (es)
MA (1) MA33349B1 (es)
MX (1) MX2011012368A (es)
MY (1) MY178082A (es)
NZ (1) NZ596883A (es)
PE (1) PE20120316A1 (es)
SG (1) SG176158A1 (es)
TW (1) TWI597073B (es)
UY (1) UY32647A (es)
WO (1) WO2010134965A1 (es)
ZA (1) ZA201108846B (es)

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WO2010074724A1 (en) 2008-12-22 2010-07-01 Millennium Pharmaceuticals, Inc. Combination of aurora kinase inhibitors and anti-cd20 antibodies
JO3635B1 (ar) 2009-05-18 2020-08-27 Millennium Pharm Inc مركبات صيدلانية صلبة وطرق لانتاجها
JO3434B1 (ar) 2009-07-31 2019-10-20 Millennium Pharm Inc مركبات صيدلانية لمعالجة السرطان وامراض واضطرابات اخري
JP2013520424A (ja) 2010-02-19 2013-06-06 ミレニアム ファーマシューティカルズ， インコーポレイテッド ナトリウム４−｛［９−クロロ−７−（２−フルオロ−６−メトキシフェニル）−５Ｈ−ピリミド［５，４−ｄ］［２］ベンゾアゼピン−２−イル］アミノ｝−２−メトキシベンゾエートの結晶形
TW201316991A (zh) 2011-06-03 2013-05-01 Millennium Pharm Inc Ｍｅｋ抑制劑與奧諾拉（ａｕｒｏｒａ）ａ激酶選擇性抑制劑之組合
ITBO20110461A1 (it) * 2011-07-29 2013-01-30 Alfa Wassermann Spa Composizioni farmaceutiche comprendenti rifaximina, processi per la loro preparazione e loro uso nel trattamento di infezioni vaginali.
US20130303519A1 (en) 2012-03-20 2013-11-14 Millennium Pharmaceuticals, Inc. Methods of treating cancer using aurora kinase inhibitors
US9724354B2 (en) 2013-03-22 2017-08-08 Millennium Pharmaceuticals, Inc. Combination of catalytic mTORC1/2 inhibitors and selective inhibitors of Aurora A kinase
WO2015085289A1 (en) 2013-12-06 2015-06-11 Millennium Pharmaceuticals, Inc. Combination of aurora kinase inhibitors and anti-cd30 antibodies
EA036922B1 (ru) * 2014-05-29 2021-01-15 Новартис Аг Состав церитиниба
AU2015362849B2 (en) * 2014-12-19 2020-05-07 Merck Sharp & Dohme Corp. (S)-N-(3-(6-isopropoxypyridin-3-yl)-1H-indazol-5-yl)-1-(2-(4-(4-(1-methyl-1H-1,2,4-triazol-3-yl)phenyl)-3,6-dihydropyridin-1(2H)-yl)-2-oxoethyl)-3-(methylthio)pyrrolidine-3-carboxamide compositions for pharmaceutical preparations
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