SG171649A1 - Dpp iv inhibitor formulations - Google Patents

Dpp iv inhibitor formulations

Info

Publication number
SG171649A1
SG171649A1 SG201103141-6A SG2011031416A SG171649A1 SG 171649 A1 SG171649 A1 SG 171649A1 SG 2011031416 A SG2011031416 A SG 2011031416A SG 171649 A1 SG171649 A1 SG 171649A1
Authority
SG
Singapore
Prior art keywords
dpp
inhibitor formulations
formulations
inhibitor
inhibitors
Prior art date
Application number
SG201103141-6A
Other languages
English (en)
Inventor
Anja Kohlrausch
Patrick Romer
Gerd Seiffert
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=36972901&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=SG171649(A1) "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 SG171649A1 publication Critical patent/SG171649A1/en

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • 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
    • A61K31/495Heterocyclic 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K47/00Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
    • A61K47/30Macromolecular organic or inorganic compounds, e.g. inorganic polyphosphates
    • A61K47/36Polysaccharides; Derivatives thereof, e.g. gums, starch, alginate, dextrin, hyaluronic acid, chitosan, inulin, agar or pectin
    • A61K47/38Cellulose; Derivatives thereof
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • 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
    • A61K31/495Heterocyclic 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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    • 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
    • A61K31/495Heterocyclic 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
    • A61K31/517Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with carbocyclic ring systems, e.g. quinazoline, perimidine
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K47/00Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
    • A61K47/30Macromolecular organic or inorganic compounds, e.g. inorganic polyphosphates
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
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    • A61K47/30Macromolecular organic or inorganic compounds, e.g. inorganic polyphosphates
    • A61K47/34Macromolecular 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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    • A61K9/2009Inorganic compounds
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    • A61K9/2013Organic compounds, e.g. phospholipids, fats
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    • A61K9/2022Organic macromolecular compounds
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    • A61K9/2059Starch, including chemically or physically modified derivatives; Amylose; Amylopectin; Dextrin
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    • A61K9/2833Organic macromolecular compounds
    • A61K9/2853Organic macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds, e.g. polyethylene glycol, polyethylene oxide, poloxamers, poly(lactide-co-glycolide)
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    • A61K9/2806Coating materials
    • A61K9/2833Organic macromolecular compounds
    • A61K9/286Polysaccharides, e.g. gums; Cyclodextrin
    • A61K9/2866Cellulose; Cellulose derivatives, e.g. hydroxypropyl methylcellulose
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    • A61K9/48Preparations in capsules, e.g. of gelatin, of chocolate
    • A61K9/4841Filling excipients; Inactive ingredients
    • A61K9/4866Organic macromolecular compounds
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    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/48Preparations in capsules, e.g. of gelatin, of chocolate
    • A61K9/4891Coated capsules; Multilayered drug free capsule shells
    • AHUMAN NECESSITIES
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    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P19/00Drugs for skeletal disorders
    • A61P19/02Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
    • AHUMAN NECESSITIES
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    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P19/00Drugs for skeletal disorders
    • A61P19/08Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease
    • A61P19/10Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease for osteoporosis
    • AHUMAN NECESSITIES
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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
    • A61K9/2077Tablets comprising drug-containing microparticles in a substantial amount of supporting matrix; Multiparticulate tablets

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  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Veterinary Medicine (AREA)
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  • Epidemiology (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • General Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Inorganic Chemistry (AREA)
  • Diabetes (AREA)
  • Obesity (AREA)
  • Hematology (AREA)
  • Immunology (AREA)
  • Physical Education & Sports Medicine (AREA)
  • Rheumatology (AREA)
  • Orthopedic Medicine & Surgery (AREA)
  • Molecular Biology (AREA)
  • Biophysics (AREA)
  • Proteomics, Peptides & Aminoacids (AREA)
  • Transplantation (AREA)
  • Child & Adolescent Psychology (AREA)
  • Endocrinology (AREA)
  • Pain & Pain Management (AREA)
  • Emergency Medicine (AREA)
  • Medicinal Preparation (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Nutrition Science (AREA)
  • Physiology (AREA)
SG201103141-6A 2006-05-04 2007-04-30 Dpp iv inhibitor formulations SG171649A1 (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
EP06009201A EP1852108A1 (en) 2006-05-04 2006-05-04 DPP IV inhibitor formulations

Publications (1)

Publication Number Publication Date
SG171649A1 true SG171649A1 (en) 2011-06-29

Family

ID=36972901

Family Applications (1)

Application Number Title Priority Date Filing Date
SG201103141-6A SG171649A1 (en) 2006-05-04 2007-04-30 Dpp iv inhibitor formulations

Country Status (36)

Country Link
US (9) US20080107731A1 (cg-RX-API-DMAC7.html)
EP (5) EP1852108A1 (cg-RX-API-DMAC7.html)
JP (8) JP5478244B2 (cg-RX-API-DMAC7.html)
KR (5) KR101710881B1 (cg-RX-API-DMAC7.html)
CN (2) CN101437493B (cg-RX-API-DMAC7.html)
AR (2) AR060755A1 (cg-RX-API-DMAC7.html)
AT (1) ATE480228T1 (cg-RX-API-DMAC7.html)
AU (1) AU2007247193B2 (cg-RX-API-DMAC7.html)
BR (2) BRPI0711179B1 (cg-RX-API-DMAC7.html)
CA (1) CA2649922C (cg-RX-API-DMAC7.html)
CL (2) CL2012002522A1 (cg-RX-API-DMAC7.html)
CY (2) CY1111354T1 (cg-RX-API-DMAC7.html)
DE (1) DE602007009091D1 (cg-RX-API-DMAC7.html)
DK (3) DK2277509T5 (cg-RX-API-DMAC7.html)
EA (2) EA016559B1 (cg-RX-API-DMAC7.html)
EC (1) ECSP088800A (cg-RX-API-DMAC7.html)
ES (3) ES2348576T3 (cg-RX-API-DMAC7.html)
HR (2) HRP20100507T1 (cg-RX-API-DMAC7.html)
HU (1) HUE025210T2 (cg-RX-API-DMAC7.html)
IL (2) IL195030A (cg-RX-API-DMAC7.html)
ME (2) ME01170B (cg-RX-API-DMAC7.html)
MX (3) MX358617B (cg-RX-API-DMAC7.html)
MY (2) MY146969A (cg-RX-API-DMAC7.html)
NO (1) NO343067B1 (cg-RX-API-DMAC7.html)
NZ (3) NZ595983A (cg-RX-API-DMAC7.html)
PE (2) PE20110666A1 (cg-RX-API-DMAC7.html)
PL (3) PL2283819T3 (cg-RX-API-DMAC7.html)
PT (2) PT2023902E (cg-RX-API-DMAC7.html)
RS (2) RS51466B (cg-RX-API-DMAC7.html)
SG (1) SG171649A1 (cg-RX-API-DMAC7.html)
SI (2) SI2023902T1 (cg-RX-API-DMAC7.html)
TW (2) TWI474843B (cg-RX-API-DMAC7.html)
UA (1) UA94942C2 (cg-RX-API-DMAC7.html)
UY (1) UY30319A1 (cg-RX-API-DMAC7.html)
WO (1) WO2007128724A1 (cg-RX-API-DMAC7.html)
ZA (1) ZA200808361B (cg-RX-API-DMAC7.html)

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JP2530113B2 (ja) 1994-06-29 1996-09-04 インターナショナル・ビジネス・マシーンズ・コーポレイション デ―タ転送制御用インタ―フェ―ス回路及び磁気ディスク装置
US7407955B2 (en) 2002-08-21 2008-08-05 Boehringer Ingelheim Pharma Gmbh & Co., Kg 8-[3-amino-piperidin-1-yl]-xanthines, the preparation thereof and their use as pharmaceutical compositions
US7495005B2 (en) * 2002-08-22 2009-02-24 Boehringer Ingelheim Pharma Gmbh & Co. Kg Xanthine derivatives, their preparation and their use in pharmaceutical compositions
US7482337B2 (en) * 2002-11-08 2009-01-27 Boehringer Ingelheim Pharma Gmbh & Co. Kg Xanthine derivatives, the preparation thereof and their use as pharmaceutical compositions
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DE102004030502A1 (de) 2004-06-24 2006-01-12 Boehringer Ingelheim Pharma Gmbh & Co. Kg Neue Imidazole und Triazole, deren Herstellung und Verwendung als Arzneimittel
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
EP1852108A1 (en) 2006-05-04 2007-11-07 Boehringer Ingelheim Pharma GmbH & Co.KG DPP IV inhibitor formulations
JP5323684B2 (ja) * 2006-05-04 2013-10-23 ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング 多形体
PE20080251A1 (es) 2006-05-04 2008-04-25 Boehringer Ingelheim Int Usos de inhibidores de dpp iv
US9255099B2 (en) 2006-06-06 2016-02-09 Intra-Cellular Therapies, Inc. Pyrazolo[3,4-D]pyrimidine-4,6(5H,7H)-diones as phosphodiesterase 1 inhibitors
JP2010500326A (ja) 2006-08-08 2010-01-07 ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング 糖尿病の治療のためのdpp−iv阻害剤としてのピロロ[3,2−d]ピリミジン
EP2025674A1 (de) 2007-08-15 2009-02-18 sanofi-aventis Substituierte Tetrahydronaphthaline, Verfahren zu ihrer Herstellung und ihre Verwendung als Arzneimittel
PE20090938A1 (es) 2007-08-16 2009-08-08 Boehringer Ingelheim Int Composicion farmaceutica que comprende un derivado de benceno sustituido con glucopiranosilo
AU2008331833A1 (en) 2007-12-06 2009-06-11 Intra-Cellular Therapies, Inc Organic compounds
PE20091730A1 (es) * 2008-04-03 2009-12-10 Boehringer Ingelheim Int Formulaciones que comprenden un inhibidor de dpp4
BRPI0916997A2 (pt) 2008-08-06 2020-12-15 Boehringer Ingelheim International Gmbh Inibidor de dpp-4 e seu uso
UY32030A (es) 2008-08-06 2010-03-26 Boehringer Ingelheim Int "tratamiento para diabetes en pacientes inapropiados para terapia con metformina"
CA2733778A1 (en) * 2008-08-14 2010-02-18 Hiroshi Uchida Stabilized pharmaceutical composition
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PL2277509T3 (pl) 2015-07-31
AU2007247193B2 (en) 2013-05-16
JP6100998B2 (ja) 2017-03-22
AR079930A2 (es) 2012-02-29
EP2283819A1 (en) 2011-02-16
BRPI0711179B1 (pt) 2022-02-08
US12178819B2 (en) 2024-12-31
KR101855323B1 (ko) 2018-05-09
HRP20100507T1 (hr) 2010-10-31
RS53570B1 (sr) 2015-02-27
HRP20150003T2 (hr) 2015-12-18
HRP20150003T1 (xx) 2015-03-13
TW200812648A (en) 2008-03-16
US20250064818A1 (en) 2025-02-27
SI2023902T1 (sl) 2011-01-31
EA029890B1 (ru) 2018-05-31
CA2649922A1 (en) 2007-11-15
EA201100958A1 (ru) 2012-04-30
DK2023902T3 (da) 2010-11-15
KR101855323B9 (ko) 2025-10-15
CN101437493A (zh) 2009-05-20
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ATE480228T1 (de) 2010-09-15
JP2022075826A (ja) 2022-05-18
IL212841A0 (en) 2011-07-31
US20130122089A1 (en) 2013-05-16
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EP2023902B8 (en) 2010-11-24
NO20084256L (no) 2008-12-02
ES2527409T3 (es) 2015-01-23
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ES2348576T3 (es) 2010-12-09
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US20210260068A1 (en) 2021-08-26
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US20120219622A1 (en) 2012-08-30
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IL195030A0 (en) 2009-08-03
RS51466B (sr) 2011-04-30
EP2277509A1 (en) 2011-01-26
PE20110666A1 (es) 2011-09-23
TW201417844A (zh) 2014-05-16
KR20170141812A (ko) 2017-12-26
JP2024074800A (ja) 2024-05-31
HK1130442A1 (en) 2009-12-31
CL2012002521A1 (es) 2012-12-21
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US20170312287A1 (en) 2017-11-02
ME01941B (me) 2015-05-20
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