GT201300144A - Composiciones farmaceuticas - Google Patents

Composiciones farmaceuticas

Info

Publication number
GT201300144A
GT201300144A GT201300144A GT201300144A GT201300144A GT 201300144 A GT201300144 A GT 201300144A GT 201300144 A GT201300144 A GT 201300144A GT 201300144 A GT201300144 A GT 201300144A GT 201300144 A GT201300144 A GT 201300144A
Authority
GT
Guatemala
Prior art keywords
quinolin
imidazo
dihydro
approximately
pharmaceutical composition
Prior art date
Application number
GT201300144A
Other languages
English (en)
Inventor
Cao Yu
Hackl Wolfgang
Li Ping
Li Shoufeng
Mirza Tahseen
Zehender Hartmut
Zhu Jiahao
Original Assignee
Novartis Ag
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=45346568&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=GT201300144(A) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Novartis Ag filed Critical Novartis Ag
Publication of GT201300144A publication Critical patent/GT201300144A/es

Links

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
    • 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
    • A61K31/4353—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 ortho- or peri-condensed with heterocyclic ring systems
    • A61K31/437—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 ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a five-membered ring having nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline
    • 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
    • A61K9/16—Agglomerates; Granulates; Microbeadlets ; Microspheres; Pellets; Solid products obtained by spray drying, spray freeze drying, spray congealing,(multiple) emulsion solvent evaporation or extraction
    • 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
    • A61K9/16—Agglomerates; Granulates; Microbeadlets ; Microspheres; Pellets; Solid products obtained by spray drying, spray freeze drying, spray congealing,(multiple) emulsion solvent evaporation or extraction
    • A61K9/1605—Excipients; Inactive ingredients
    • A61K9/1617—Organic compounds, e.g. phospholipids, fats
    • 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
    • A61K9/16—Agglomerates; Granulates; Microbeadlets ; Microspheres; Pellets; Solid products obtained by spray drying, spray freeze drying, spray congealing,(multiple) emulsion solvent evaporation or extraction
    • A61K9/1605—Excipients; Inactive ingredients
    • A61K9/1617—Organic compounds, e.g. phospholipids, fats
    • A61K9/1623—Sugars or sugar alcohols, e.g. lactose; Derivatives thereof; Homeopathic globules
    • 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
    • A61K9/16—Agglomerates; Granulates; Microbeadlets ; Microspheres; Pellets; Solid products obtained by spray drying, spray freeze drying, spray congealing,(multiple) emulsion solvent evaporation or extraction
    • A61K9/1605—Excipients; Inactive ingredients
    • A61K9/1629—Organic macromolecular compounds
    • A61K9/1635—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
    • 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
    • A61K9/16—Agglomerates; Granulates; Microbeadlets ; Microspheres; Pellets; Solid products obtained by spray drying, spray freeze drying, spray congealing,(multiple) emulsion solvent evaporation or extraction
    • A61K9/1605—Excipients; Inactive ingredients
    • A61K9/1629—Organic macromolecular compounds
    • A61K9/1641—Organic macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds, e.g. polyethylene glycol, poloxamers
    • 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
    • A61K9/16—Agglomerates; Granulates; Microbeadlets ; Microspheres; Pellets; Solid products obtained by spray drying, spray freeze drying, spray congealing,(multiple) emulsion solvent evaporation or extraction
    • A61K9/1682—Processes
    • A61K9/1694—Processes resulting in granules or microspheres of the matrix type containing more than 5% of excipient
    • 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
    • A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
    • C07D471/04—Ortho-condensed systems

Landscapes

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

Abstract

LA PRESENTE INVENCIÓN SE REFIERE A UNA COMPOSICIÓN FARMACÉUTICA PARA LA ADMINISTRACIÓN ORAL DE UN COMPUESTO TERAPÉUTICO DE FÓRMULA (I), QUE COMPRENDE GRÁNULOS QUE COMPRENDEN AL MENOS COMPUESTO TERAPÉUTICO DE FÓRMULA (I), EN PARTICULAR 2-METIL-2-[4 - (3-METIL-2-OXO-8-QUINOLIN-3-IL-2 ,3-DIHIDRO-IMIDAZO [4,5-C] QUINOLIN-1-IL)-FENIL] - PROPIONITRILO O 8-( 6-METOXI-PIRIDIN-3-IL)-3-METIL-1-(4-PIPERAZIN-1-IL-3-TRIFL UOROMETHYL-FENIL) -1,3-DIHIDRO-IMIDAZO [4,5-C] QUINOLIN-2-ONA , O UN TAUTÓMERO DEL MISMO, O UNA SAL FARMACÉUTICAMENTE ACEPTABLE, O UN HIDRATO O SOLVATO DE LOS MISMOS AL MENOS UN TENSIOACTIVO NO IÓNICO QUE ES LA VITAMINA E TPGS EN UNA CANTIDAD QUE VARÍA DE APROXIMADAMENTE 15 A APROXIMADAMENTE 80% EN PESO DE LA COMPOSICIÓN Y AL MENOS UN AGENTE MEJORADOR DE LA DISOLUCIÓN SELECCIONADO DE ENTRE POLIETILENGLICOL, ÓXIDO DE POLIETILENO, Y CUALQUIER COMBINACIÓN DE LOS ANTERIORES.LA PRESENTE INVENCIÓN TAMBIÉN SE REFIERE A PROCESOS PARA LA FABRICACIÓN DE TALES COMPOSICIONES FARMACÉUTICAS, UN KIT QUE COMPRENDE DICHA COMPOSICIÓN FARMACÉUTICA Y RELACIONADOS CON LOS USOS Y MÉTODOS DE TRATAMIENTO.
GT201300144A 2010-12-03 2013-06-03 Composiciones farmaceuticas GT201300144A (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US41953810P 2010-12-03 2010-12-03
US201161436324P 2011-01-26 2011-01-26

Publications (1)

Publication Number Publication Date
GT201300144A true GT201300144A (es) 2014-06-09

Family

ID=45346568

Family Applications (1)

Application Number Title Priority Date Filing Date
GT201300144A GT201300144A (es) 2010-12-03 2013-06-03 Composiciones farmaceuticas

Country Status (21)

Country Link
US (1) US20130245061A1 (es)
EP (1) EP2645999A2 (es)
JP (1) JP2013544845A (es)
KR (1) KR20140010009A (es)
CN (1) CN103237544A (es)
AR (1) AR084067A1 (es)
AU (1) AU2011336478A1 (es)
CA (1) CA2817618A1 (es)
CL (1) CL2013001557A1 (es)
CO (1) CO6801722A2 (es)
EC (1) ECSP13012654A (es)
GT (1) GT201300144A (es)
MA (1) MA34806B1 (es)
MX (1) MX2013006187A (es)
NZ (1) NZ610467A (es)
PE (1) PE20140792A1 (es)
RU (1) RU2013130224A (es)
SG (1) SG190210A1 (es)
TW (1) TW201304779A (es)
WO (1) WO2012075253A2 (es)
ZA (1) ZA201303223B (es)

Families Citing this family (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2013192367A1 (en) * 2012-06-22 2013-12-27 Novartis Ag Neuroendocrine tumor treatment
EP2900219B1 (en) * 2012-09-27 2016-07-06 Basf Se A storage-stable dust-free homogeneous particulate formulation comprising at least one water-soluble vitamin e-derivative and at least one hydrophilic polymer
AU2016239270B2 (en) 2015-04-02 2020-03-26 Merck Patent Gmbh Imidazolonyl quinolines and use thereof as ATM kinase inhibitors
CN107847491A (zh) 2015-05-20 2018-03-27 诺华公司 依维莫司(everolimus)与达托里昔布(dactolisib)的医药组合
GB201516504D0 (en) 2015-09-17 2015-11-04 Astrazeneca Ab Imadazo(4,5-c)quinolin-2-one Compounds and their use in treating cancer
CA3044355A1 (en) 2016-11-23 2018-05-31 Novartis Ag Methods of enhancing immune response with everolimus, dactolisib or both
WO2019157516A1 (en) 2018-02-12 2019-08-15 resTORbio, Inc. Combination therapies
US20220313682A1 (en) * 2019-08-07 2022-10-06 Aclipse One Inc. Pharmaceutical Compositions of (6aS)-6-methyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinoline-10,11-diol
US20230070369A1 (en) * 2019-12-20 2023-03-09 Intervet Inc. Pyrazole pharmaceutical composition

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB0211649D0 (en) * 2002-05-21 2002-07-03 Novartis Ag Organic compounds
KR20060117329A (ko) * 2003-11-21 2006-11-16 노파르티스 아게 단백질 키나제 저해제로서의 1ｈ-이미다조퀴놀린 유도체
GB0510390D0 (en) * 2005-05-20 2005-06-29 Novartis Ag Organic compounds
US20080125477A1 (en) * 2006-05-16 2008-05-29 Decode Genetics, Ehf. 7-(acryloyl) indole compositions and methods of making and using same
PE20080766A1 (es) * 2006-08-30 2008-06-15 Novartis Ag Sales de benzimidazolil piridil eteres y formulaciones que las contienen
WO2008079629A2 (en) * 2006-12-21 2008-07-03 Boehringer Ingelheim International Gmbh Formulations with improved bioavailability
EP2129379B1 (en) 2007-02-20 2019-04-10 Novartis AG Imidazoquinolines as dual lipid kinase and mtor inhibitors

Also Published As

Publication number Publication date
CN103237544A (zh) 2013-08-07
JP2013544845A (ja) 2013-12-19
SG190210A1 (en) 2013-06-28
EP2645999A2 (en) 2013-10-09
PE20140792A1 (es) 2014-07-09
TW201304779A (zh) 2013-02-01
NZ610467A (en) 2015-01-30
ECSP13012654A (es) 2013-08-30
US20130245061A1 (en) 2013-09-19
AR084067A1 (es) 2013-04-17
AU2011336478A1 (en) 2013-06-06
CL2013001557A1 (es) 2013-10-25
RU2013130224A (ru) 2015-01-10
ZA201303223B (en) 2014-01-29
WO2012075253A3 (en) 2012-08-09
MX2013006187A (es) 2013-07-15
CA2817618A1 (en) 2012-06-07
KR20140010009A (ko) 2014-01-23
CO6801722A2 (es) 2013-11-29
WO2012075253A2 (en) 2012-06-07
MA34806B1 (fr) 2014-01-02

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