MX2012014982A - Formulacion oral de inhibidores de quinasa. - Google Patents
Formulacion oral de inhibidores de quinasa.Info
- Publication number
- MX2012014982A MX2012014982A MX2012014982A MX2012014982A MX2012014982A MX 2012014982 A MX2012014982 A MX 2012014982A MX 2012014982 A MX2012014982 A MX 2012014982A MX 2012014982 A MX2012014982 A MX 2012014982A MX 2012014982 A MX2012014982 A MX 2012014982A
- Authority
- MX
- Mexico
- Prior art keywords
- patients
- formulations
- fak
- peg
- bioactive compounds
- 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
- A61K9/107—Emulsions ; Emulsion preconcentrates; Micelles
-
- 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
- A61K31/535—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
- A61K31/5375—1,4-Oxazines, e.g. morpholine
- A61K31/5377—1,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
- A61P19/02—Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- 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
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D213/72—Nitrogen atoms
- C07D213/74—Amino or imino radicals substituted by hydrocarbon or substituted hydrocarbon radicals
-
- 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
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Veterinary Medicine (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- Epidemiology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Dispersion Chemistry (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Rheumatology (AREA)
- Engineering & Computer Science (AREA)
- Immunology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Physical Education & Sports Medicine (AREA)
- Pain & Pain Management (AREA)
- Medicinal Preparation (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
La invención se dirige a formulaciones de compuestos bioactivos de solubilidad limitada en agua, los inhibidores de quinasa de adhesión focal (FAK) de la clase 2,4-diaminopiridina, adaptados para administración oral a pacientes. Las formulaciones son autoemulsionantes en el tracto gastrointestinal de los pacientes, proporcionando una absorción y biodispoibilidad mejorada de los compuestos bioactivos como dispersiones o emulsiones en una base oleosa. Por ejemplo, los ésteres de glicerol PEG-ilado se pueden utilizar como el aceite, junto con un tensioactivos tales como lecitina y succinato de TEPG y solubilizantes tales como PEG 400 para proporcionar formulaciones orales útiles para administración a pacientes que tengan una mala condición, en donde la inhibición de FAK está indicada medicamente, tal como cáncer o artritis.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US35969410P | 2010-06-29 | 2010-06-29 | |
PCT/US2011/042162 WO2012006081A1 (en) | 2010-06-29 | 2011-06-28 | Oral formulation of kinase inhibitors |
Publications (2)
Publication Number | Publication Date |
---|---|
MX2012014982A true MX2012014982A (es) | 2013-07-03 |
MX340819B MX340819B (es) | 2016-07-26 |
Family
ID=45441513
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
MX2012014982A MX340819B (es) | 2010-06-29 | 2011-06-28 | Formulacion oral de inhibidores de quinasa. |
Country Status (10)
Country | Link |
---|---|
US (1) | US9375402B2 (es) |
EP (1) | EP2588081A4 (es) |
JP (1) | JP5936609B2 (es) |
CN (1) | CN103313697B (es) |
AU (1) | AU2011276552B2 (es) |
CA (1) | CA2803004A1 (es) |
MX (1) | MX340819B (es) |
NZ (1) | NZ604583A (es) |
WO (1) | WO2012006081A1 (es) |
ZA (1) | ZA201300009B (es) |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CA2827172C (en) | 2011-02-17 | 2019-02-26 | Cancer Therapeutics Crc Pty Limited | Selective fak inhibitors |
JP5937111B2 (ja) | 2011-02-17 | 2016-06-22 | カンサー・セラピューティクス・シーアールシー・プロプライエタリー・リミテッドCancer Therapeutics Crc Pty Limited | Fak阻害剤 |
CA2871820C (en) | 2012-05-10 | 2020-11-03 | Painreform Ltd. | Depot formulations of a hydrophobic active ingredient and methods for preparation thereof |
Family Cites Families (18)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4656182A (en) | 1983-12-06 | 1987-04-07 | Warner-Lambert Company | Substituted trans-1,2-diaminocyclohexyl amide compounds |
US20040006005A1 (en) * | 2002-07-02 | 2004-01-08 | Sanjay Bhanot | Use of integrin-linked kinase inhibitors for treating insulin resistance, hyperglycemia and diabetes |
GB9828511D0 (en) | 1998-12-24 | 1999-02-17 | Zeneca Ltd | Chemical compounds |
GB0004887D0 (en) | 2000-03-01 | 2000-04-19 | Astrazeneca Uk Ltd | Chemical compounds |
ATE417608T1 (de) | 2000-10-11 | 2009-01-15 | Cephalon Inc | Arzneizusammensetzungen enthaltend modafinilverbindungen |
TW200409629A (en) | 2002-06-27 | 2004-06-16 | Bristol Myers Squibb Co | 2,4-disubstituted-pyridine N-oxides useful as HIV reverse transcriptase inhibitors |
US20080119515A1 (en) * | 2003-03-10 | 2008-05-22 | M Arshad Siddiqui | Heterocyclic Kinase Inhibitors: Methods of Use and Synthesis |
GT200500310A (es) * | 2004-11-19 | 2006-06-19 | Compuestos organicos | |
US7935711B2 (en) | 2005-02-18 | 2011-05-03 | Tibotec Pharmaceuticals Ltd. | HIV inhibiting 2-(4-cyanophenylamino) pyrimidine oxide derivatives |
US20070104780A1 (en) * | 2005-10-25 | 2007-05-10 | Lipari John M | Formulation comprising a drug of low water solubility and method of use thereof |
SG172700A1 (en) | 2006-04-28 | 2011-07-28 | Schering Corp | Process for the precipitation and isolation of 6,6-dimethyl-3-aza-bicyclo [3.1.0] hexane-amide compounds by controlled precipitation and pharmaceutical formulations containing same |
DK2046292T3 (da) | 2006-07-21 | 2010-06-07 | Novartis Ag | Formuleringer for benzimidazolylpyridylethere |
DK2134689T3 (da) * | 2007-03-16 | 2014-06-30 | Scripps Research Inst | Inhibitorer af fokal adhæsionskinase |
US20090203709A1 (en) * | 2008-02-07 | 2009-08-13 | Abbott Laboratories | Pharmaceutical Dosage Form For Oral Administration Of Tyrosine Kinase Inhibitor |
WO2009105498A1 (en) | 2008-02-19 | 2009-08-27 | Smithkline Beecham Corporation | Anilinopyridines as inhibitors of fak |
BRPI0914927B8 (pt) | 2008-06-17 | 2021-05-25 | Astrazeneca Ab | composto, composição farmacêutica e uso de um composto |
WO2011019943A1 (en) | 2009-08-12 | 2011-02-17 | Poniard Pharmaceuticals, Inc. | Method of promoting apoptosis and inhibiting metastasis |
WO2011133668A2 (en) | 2010-04-20 | 2011-10-27 | President And Fellows Of Harvard College | Methods and compositions for the treatment of cancer |
-
2011
- 2011-06-28 JP JP2013518572A patent/JP5936609B2/ja not_active Expired - Fee Related
- 2011-06-28 EP EP11804122.7A patent/EP2588081A4/en not_active Withdrawn
- 2011-06-28 WO PCT/US2011/042162 patent/WO2012006081A1/en active Application Filing
- 2011-06-28 AU AU2011276552A patent/AU2011276552B2/en not_active Ceased
- 2011-06-28 NZ NZ604583A patent/NZ604583A/en not_active IP Right Cessation
- 2011-06-28 MX MX2012014982A patent/MX340819B/es active IP Right Grant
- 2011-06-28 CN CN201180042122.1A patent/CN103313697B/zh not_active Expired - Fee Related
- 2011-06-28 CA CA2803004A patent/CA2803004A1/en not_active Abandoned
-
2013
- 2013-01-02 ZA ZA2013/00009A patent/ZA201300009B/en unknown
- 2013-08-14 US US13/967,270 patent/US9375402B2/en not_active Expired - Fee Related
Also Published As
Publication number | Publication date |
---|---|
ZA201300009B (en) | 2013-09-25 |
US20140206692A1 (en) | 2014-07-24 |
AU2011276552B2 (en) | 2015-09-03 |
WO2012006081A1 (en) | 2012-01-12 |
CN103313697B (zh) | 2016-06-01 |
JP5936609B2 (ja) | 2016-06-22 |
JP2013529686A (ja) | 2013-07-22 |
EP2588081A1 (en) | 2013-05-08 |
US9375402B2 (en) | 2016-06-28 |
CA2803004A1 (en) | 2012-01-12 |
MX340819B (es) | 2016-07-26 |
EP2588081A4 (en) | 2014-12-10 |
AU2011276552A1 (en) | 2013-01-10 |
CN103313697A (zh) | 2013-09-18 |
NZ604583A (en) | 2015-04-24 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
FG | Grant or registration |