CO6251277A2 - Inhibidor de la dpp-iv combinado con mas de un agente antidiabetico, comprimidos que comprenden tales formulaciones, su uso y procedimientos para su preparación. - Google Patents

Inhibidor de la dpp-iv combinado con mas de un agente antidiabetico, comprimidos que comprenden tales formulaciones, su uso y procedimientos para su preparación.

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Publication number
CO6251277A2
CO6251277A2 CO10121097A CO10121097A CO6251277A2 CO 6251277 A2 CO6251277 A2 CO 6251277A2 CO 10121097 A CO10121097 A CO 10121097A CO 10121097 A CO10121097 A CO 10121097A CO 6251277 A2 CO6251277 A2 CO 6251277A2
Authority
CO
Colombia
Prior art keywords
pharmaceutical composition
dpp4 inhibitor
composition according
inhibitor
drug
Prior art date
Application number
CO10121097A
Other languages
English (en)
Inventor
Thomas Friedl
Michael Braun
Hikaru Fujita
Takaaki Nishioka
Megumi Maruyama
Kenji Egusa
Original Assignee
Boehringer Ingelheim Int
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=39714040&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=CO6251277(A2) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Boehringer Ingelheim Int filed Critical Boehringer Ingelheim Int
Publication of CO6251277A2 publication Critical patent/CO6251277A2/es

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    • A61K31/13Amines
    • A61K31/155Amidines (), e.g. guanidine (H2N—C(=NH)—NH2), isourea (N=C(OH)—NH2), isothiourea (—N=C(SH)—NH2)
    • AHUMAN NECESSITIES
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    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/40Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
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    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495Heterocyclic 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
    • A61K31/505Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/519Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
    • A61K31/52Purines, e.g. adenine
    • A61K31/522Purines, e.g. adenine having oxo groups directly attached to the heterocyclic ring, e.g. hypoxanthine, guanine, acyclovir
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    • A61K47/06Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite
    • A61K47/16Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite containing nitrogen, e.g. nitro-, nitroso-, azo-compounds, nitriles, cyanates
    • A61K47/18Amines; Amides; Ureas; Quaternary ammonium compounds; Amino acids; Oligopeptides having up to five amino acids
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    • A61K47/16Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite containing nitrogen, e.g. nitro-, nitroso-, azo-compounds, nitriles, cyanates
    • A61K47/18Amines; Amides; Ureas; Quaternary ammonium compounds; Amino acids; Oligopeptides having up to five amino acids
    • A61K47/183Amino acids, e.g. glycine, EDTA or aspartame
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    • A61K9/2077Tablets comprising drug-containing microparticles in a substantial amount of supporting matrix; Multiparticulate tablets
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    • A61K9/2072Pills, tablets, discs, rods characterised by shape, structure or size; Tablets with holes, special break lines or identification marks; Partially coated tablets; Disintegrating flat shaped forms
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    • A61K9/2086Layered tablets, e.g. bilayer tablets; Tablets of the type inert core-active coat
    • A61K9/209Layered tablets, e.g. bilayer tablets; Tablets of the type inert core-active coat containing drug in at least two layers or in the core and in at least one outer layer
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    • A61K9/2095Tabletting processes; Dosage units made by direct compression of powders or specially processed granules, by eliminating solvents, by melt-extrusion, by injection molding, by 3D printing
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    • AHUMAN NECESSITIES
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    • A61K9/2833Organic macromolecular compounds
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    • A61K9/16Agglomerates; Granulates; Microbeadlets ; Microspheres; Pellets; Solid products obtained by spray drying, spray freeze drying, spray congealing,(multiple) emulsion solvent evaporation or extraction
    • A61K9/1605Excipients; Inactive ingredients
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    • A61K9/1605Excipients; Inactive ingredients
    • A61K9/1629Organic macromolecular compounds
    • A61K9/1652Polysaccharides, e.g. alginate, cellulose derivatives; Cyclodextrin

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  • Health & Medical Sciences (AREA)
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  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
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  • Bioinformatics & Cheminformatics (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Organic Chemistry (AREA)
  • Diabetes (AREA)
  • Immunology (AREA)
  • Physical Education & Sports Medicine (AREA)
  • Rheumatology (AREA)
  • Inorganic Chemistry (AREA)
  • Obesity (AREA)
  • Hematology (AREA)
  • Orthopedic Medicine & Surgery (AREA)
  • Biophysics (AREA)
  • Molecular Biology (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Proteomics, Peptides & Aminoacids (AREA)
  • Endocrinology (AREA)
  • Emergency Medicine (AREA)
  • Nutrition Science (AREA)
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  • Pain & Pain Management (AREA)
  • Child & Adolescent Psychology (AREA)
  • Transplantation (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Medicinal Preparation (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)

Abstract

La presente invención se refiere a composiciones farmacéuticas que comprenden combinaciones en dosis fijas de un fármaco inhibidor de la DPP4 y un fármaco acompañante, procedimientos para la preparación de las mismas y su uso para tratar determinadas enfermedades. 1.- Una composición farmacéutica que comprende o está hecha de un inhibidor de la DPP4, un fármaco acompañante y uno o más excipientes farmacéuticos y un agente nucleófilo y/o básico para estabilizar dicho inhibidor de la DPP4 frente a la degradación. 2.- Una composición farmacéutica de acuerdo con la reivindicación 1, que comprende un inhibidor de la DPP4, un fármaco acompañante, uno o más excipientes farmacéuticos y una sustancia tamponante para estabilizar dicho inhibidor de la DPP4 frente a la degradación. 3.- La composición farmacéutica de acuerdo con la reivindicación 1 o 2, en la que dicho inhibidor de la DPP4 está estabilizado frente a la degradación química. 4.- La composición farmacéutica según cualquiera de las reivindicaciones 1, 2 o 3, en la que el fármaco acompañante se selecciona del grupo que consiste en biguanidas que incluyen clorhidrato de metformina, tiazolidinonas que incluyen clorhidrato de pioglitazona, estatinas que incluyen atorvastatina, y BRAs que incluyen telmisartán. 5.- La composición farmacéutica según cualquiera de las reivindicaciones 1 a 4, en la que el agente nucleófilo y/o básico o la sustancia tamponante es un aminoácido básico que tiene un grupo amino intramolecular y características alcalinas, que incluyen Larginina, L-lisina y L-histidina. 6.- La composición farmacéutica según cualquiera de las reivindicaciones 1 a 5, en la que el inhibidor de la DPP4 tiene un grupo amino intramolecular primario o secundario libre. 7.- La composición farmacéutica según cualquiera de las reivindicaciones 1 a 6, en la que el inhibidor de la DPP4 se selecciona entre vildagliptina, saxagliptina y alogliptina. 8.- La composición farmacéutica según cualquiera de las reivindicaciones 1 a 6, en la que el inhibidor de la DPP4 es la base libre de la 1-[(4-metil-quinazolin-2- il)metill-3-metil-7-(2-butin-1-il)-8-(3-(R)-amino-piperidin-1- il)-xantina.
CO10121097A 2008-04-03 2010-09-30 Inhibidor de la dpp-iv combinado con mas de un agente antidiabetico, comprimidos que comprenden tales formulaciones, su uso y procedimientos para su preparación. CO6251277A2 (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
EP08154039 2008-04-03
US8734308P 2008-08-08 2008-08-08

Publications (1)

Publication Number Publication Date
CO6251277A2 true CO6251277A2 (es) 2011-02-21

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CO10121097A CO6251277A2 (es) 2008-04-03 2010-09-30 Inhibidor de la dpp-iv combinado con mas de un agente antidiabetico, comprimidos que comprenden tales formulaciones, su uso y procedimientos para su preparación.

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US (10) US9155705B2 (es)
EP (3) EP2285410B1 (es)
JP (2) JP5588428B2 (es)
KR (3) KR20170056021A (es)
CN (4) CN106215190A (es)
AR (1) AR071175A1 (es)
AU (1) AU2009232043B2 (es)
BR (1) BRPI0911273B8 (es)
CA (1) CA2720450C (es)
CO (1) CO6251277A2 (es)
DK (1) DK2285410T3 (es)
EA (2) EA038435B1 (es)
EC (1) ECSP10010489A (es)
ES (1) ES2696124T3 (es)
HK (1) HK1149485A1 (es)
IL (2) IL207497A0 (es)
MA (1) MA32200B1 (es)
MX (2) MX2010010819A (es)
NZ (1) NZ587747A (es)
PE (2) PE20091730A1 (es)
PL (1) PL2285410T3 (es)
TW (2) TWI527816B (es)
UA (1) UA104136C2 (es)
UY (1) UY31747A (es)
WO (1) WO2009121945A2 (es)
ZA (1) ZA201005664B (es)

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US7501426B2 (en) 2004-02-18 2009-03-10 Boehringer Ingelheim International Gmbh 8-[3-amino-piperidin-1-yl]-xanthines, their preparation and their use as pharmaceutical compositions
DE102004054054A1 (de) 2004-11-05 2006-05-11 Boehringer Ingelheim Pharma Gmbh & Co. Kg Verfahren zur Herstellung chiraler 8-(3-Amino-piperidin-1-yl)-xanthine
US7772191B2 (en) 2005-05-10 2010-08-10 Boehringer Ingelheim International Gmbh Processes for preparing of glucopyranosyl-substituted benzyl-benzene derivatives and intermediates therein
DE102005035891A1 (de) 2005-07-30 2007-02-08 Boehringer Ingelheim Pharma Gmbh & Co. Kg 8-(3-Amino-piperidin-1-yl)-xanthine, deren Herstellung und deren Verwendung als Arzneimittel
PE20080251A1 (es) 2006-05-04 2008-04-25 Boehringer Ingelheim Int Usos de inhibidores de dpp iv
EP1852108A1 (en) * 2006-05-04 2007-11-07 Boehringer Ingelheim Pharma GmbH & Co.KG DPP IV inhibitor formulations
EA015687B1 (ru) 2006-05-04 2011-10-31 Бёрингер Ингельхайм Интернациональ Гмбх Полиморфы
PE20090938A1 (es) 2007-08-16 2009-08-08 Boehringer Ingelheim Int Composicion farmaceutica que comprende un derivado de benceno sustituido con glucopiranosilo
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CN101983073B (zh) 2013-06-26
PE20140960A1 (es) 2014-08-15
US20150366812A1 (en) 2015-12-24
PE20091730A1 (es) 2009-12-10
US20210196722A1 (en) 2021-07-01
IL207497A0 (en) 2010-12-30
WO2009121945A3 (en) 2009-12-03
UA104136C2 (ru) 2014-01-10
HK1149485A1 (en) 2011-10-07
UY31747A (es) 2009-11-10
US20160310435A1 (en) 2016-10-27
KR101611314B1 (ko) 2016-04-11
JP5588428B2 (ja) 2014-09-10
KR20160042174A (ko) 2016-04-18
MA32200B1 (fr) 2011-04-01
CN101983073A (zh) 2011-03-02
EA201300121A1 (ru) 2014-12-30
TW201509941A (zh) 2015-03-16
CN103083672B (zh) 2016-09-07
TW200946534A (en) 2009-11-16
JP2013237707A (ja) 2013-11-28
EP2285410B1 (en) 2018-09-26
EP3453403A1 (en) 2019-03-13
BRPI0911273B1 (pt) 2019-07-16
AU2009232043B2 (en) 2014-09-25
US20170119773A1 (en) 2017-05-04
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US20230338386A1 (en) 2023-10-26
ECSP10010489A (es) 2010-10-30
US20200069693A1 (en) 2020-03-05
US10973827B2 (en) 2021-04-13
CN113648422A (zh) 2021-11-16
IL225637A0 (en) 2013-06-27
EA029395B1 (ru) 2018-03-30
MX351232B (es) 2017-10-06
CA2720450A1 (en) 2009-10-08
US20110206766A1 (en) 2011-08-25
KR20110005690A (ko) 2011-01-18
WO2009121945A2 (en) 2009-10-08
US20180289716A1 (en) 2018-10-11
EA038435B1 (ru) 2021-08-27
CA2720450C (en) 2017-01-03
CN103083672A (zh) 2013-05-08
BRPI0911273A2 (pt) 2015-09-29
BRPI0911273B8 (pt) 2021-05-25
JP2011516456A (ja) 2011-05-26
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MX2010010819A (es) 2010-11-05

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