EE200200097A - Bensamiididerivaati sisaldav farmatseutiline preparaat - Google Patents

Bensamiididerivaati sisaldav farmatseutiline preparaat

Info

Publication number: EE200200097A
Authority: EE; Estonia
Prior art keywords: pharmaceutical preparation; preparation containing; benzamide derivative; benzamide; derivative
Prior art date: 1999-08-30

Application number

EEP200200097A

Other languages

English (en)

Inventor

Ishibashi Masahiko

Sakabe Masahiro

Sakai Ikuo

Suzuki Tsuneji

Ando Tomoyuki

Original Assignee

Schering Aktiengesellschaft

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.)

1999-08-30

Filing date

2000-08-29

Publication date

2003-04-15

2000-08-29 Application filed by Schering Aktiengesellschaft filed Critical Schering Aktiengesellschaft

2003-04-15 Publication of EE200200097A publication Critical patent/EE200200097A/et

2008-08-15 Publication of EE05063B1 publication Critical patent/EE05063B1/et

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
- 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
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/4406—Non condensed pyridines; Hydrogenated derivatives thereof only substituted in position 3, e.g. zimeldine
- 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
- C07D213/24—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 substituted hydrocarbon radicals attached to ring carbon atoms
- C07D213/28—Radicals substituted by singly-bound oxygen or sulphur atoms
- C07D213/30—Oxygen atoms
- 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
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
- A61P37/06—Immunosuppressants, e.g. drugs for graft rejection
- 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
- C07D213/62—Oxygen or sulfur atoms
- C07D213/63—One oxygen atom
- C07D213/65—One oxygen atom attached in position 3 or 5
- 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
- C07D213/75—Amino or imino radicals, acylated by carboxylic or carbonic acids, or by sulfur or nitrogen analogues thereof, e.g. carbamates

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Health & Medical Sciences (AREA)
General Health & Medical Sciences (AREA)
Veterinary Medicine (AREA)
Public Health (AREA)
Medicinal Chemistry (AREA)
Animal Behavior & Ethology (AREA)
Life Sciences & Earth Sciences (AREA)
Pharmacology & Pharmacy (AREA)
Bioinformatics & Cheminformatics (AREA)
Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
Engineering & Computer Science (AREA)
General Chemical & Material Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
Immunology (AREA)
Transplantation (AREA)
Epidemiology (AREA)
Medicinal Preparation (AREA)
Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Pyridine Compounds (AREA)

EEP200200097A 1999-08-30 2000-08-29 Bensamiididerivaati sisaldav farmatseutiline preparaat EE05063B1 (et)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
JP24244499A JP2001081031A (ja)	1999-08-30	1999-08-30	溶解性および経口吸収性を改善したベンズアミド誘導体含有製剤
PCT/EP2000/008421 WO2001016106A1 (en)	1999-08-30	2000-08-29	Benzamide formulation with histone deacetylase inhibitor activity

Publications (2)

Publication Number	Publication Date
EE200200097A true EE200200097A (et)	2003-04-15
EE05063B1 EE05063B1 (et)	2008-08-15

Family

ID=17089193

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
EEP200200097A EE05063B1 (et)	1999-08-30	2000-08-29	Bensamiididerivaati sisaldav farmatseutiline preparaat

Country Status (32)

Country	Link
US (1)	US6638530B1 (et)
EP (1)	EP1208086B1 (et)
JP (2)	JP2001081031A (et)
KR (1)	KR100712640B1 (et)
CN (1)	CN1147472C (et)
AR (1)	AR025434A1 (et)
AT (1)	ATE318258T1 (et)
AU (1)	AU773617B2 (et)
BG (1)	BG65544B1 (et)
BR (1)	BR0013648A (et)
CA (1)	CA2382886C (et)
CZ (1)	CZ301737B6 (et)
DE (1)	DE60026144T2 (et)
DK (1)	DK1208086T3 (et)
EE (1)	EE05063B1 (et)
ES (1)	ES2259289T3 (et)
HK (1)	HK1046277B (et)
HR (1)	HRP20020182B1 (et)
HU (1)	HUP0203330A3 (et)
IL (2)	IL148357A0 (et)
MX (1)	MXPA02002090A (et)
NO (1)	NO322532B1 (et)
NZ (1)	NZ517520A (et)
PL (1)	PL201274B1 (et)
PT (1)	PT1208086E (et)
RU (1)	RU2260428C2 (et)
SI (1)	SI1208086T1 (et)
SK (1)	SK287252B6 (et)
TW (1)	TWI268778B (et)
UA (1)	UA72541C2 (et)
WO (1)	WO2001016106A1 (et)
ZA (1)	ZA200201424B (et)

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US20070148228A1 (en) *	1999-02-22	2007-06-28	Merrion Research I Limited	Solid oral dosage form containing an enhancer
US7658938B2 (en) *	1999-02-22	2010-02-09	Merrion Reasearch III Limited	Solid oral dosage form containing an enhancer
EP1374855A1 (en) *	2001-03-30	2004-01-02	Takeda Chemical Industries, Ltd.	Medicinal solutions
US7868204B2 (en)	2001-09-14	2011-01-11	Methylgene Inc.	Inhibitors of histone deacetylase
AU2002327627B2 (en) *	2001-09-14	2006-09-14	Methylgene Inc.	Inhibitors of histone deacetylase
US6897220B2 (en)	2001-09-14	2005-05-24	Methylgene, Inc.	Inhibitors of histone deacetylase
AU2006252047B2 (en) *	2001-09-14	2010-02-11	Methylgene Inc.	Inhibitors of histone deacetylase
US6706686B2 (en)	2001-09-27	2004-03-16	The Regents Of The University Of Colorado	Inhibition of histone deacetylase as a treatment for cardiac hypertrophy
EP2269609A3 (en)	2001-10-16	2012-07-11	Sloan-Kettering Institute for Cancer Research	Treatment of neurodegenerative diseases and cancer of the brain with SAHA
JPWO2003070691A1 (ja) *	2002-02-21	2005-06-09	財団法人大阪産業振興機構	Ｎ−ヒドロキシカルボキサミド誘導体
US7456219B2 (en)	2002-03-04	2008-11-25	Merck Hdac Research, Llc	Polymorphs of suberoylanilide hydroxamic acid
PL372239A1 (en)	2002-03-04	2005-07-11	Aton Pharma, Inc.	Methods of inducing terminal differentiation
US7148257B2 (en)	2002-03-04	2006-12-12	Merck Hdac Research, Llc	Methods of treating mesothelioma with suberoylanilide hydroxamic acid
US7566535B2 (en)	2002-03-07	2009-07-28	University Of Delaware	Enhanced oligonucleotide-mediated nucleic acid sequence alteration
GB0209715D0 (en) *	2002-04-27	2002-06-05	Astrazeneca Ab	Chemical compounds
DE10233412A1 (de) *	2002-07-23	2004-02-12	4Sc Ag	Neue Verbindungen als Histondeacetylase-Inhibitoren
US7154002B1 (en)	2002-10-08	2006-12-26	Takeda San Diego, Inc.	Histone deacetylase inhibitors
US7250514B1 (en)	2002-10-21	2007-07-31	Takeda San Diego, Inc.	Histone deacetylase inhibitors
GB0226855D0 (en) *	2002-11-18	2002-12-24	Queen Mary & Westfield College	Histone deacetylase inhibitors
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EP1608628A2 (en)	2003-03-17	2005-12-28	Takeda San Diego, Inc.	Histone deacetylase inhibitors
CN100455564C (zh) *	2003-09-12	2009-01-28	深圳微芯生物科技有限责任公司	组蛋白去乙酰化酶抑制剂及其药用制剂的制备和应用
CN101445469B (zh) *	2003-09-24	2013-02-13	梅特希尔基因公司	组蛋白脱乙酰基酶抑制剂
US7868205B2 (en)	2003-09-24	2011-01-11	Methylgene Inc.	Inhibitors of histone deacetylase
US9115090B2 (en)	2003-12-02	2015-08-25	The Ohio State University Research Foundation	Zn2+-chelating motif-tethered short-chain fatty acids as a novel class of histone deacetylase inhibitors
WO2005059167A1 (en) *	2003-12-18	2005-06-30	Istituto Di Ricerche Di Biologia Molecolare P Angeletti Spa	Method for identifying histone deacetylase inhibitors
US7253204B2 (en)	2004-03-26	2007-08-07	Methylgene Inc.	Inhibitors of histone deacetylase
JP2008524246A (ja)	2004-12-16	2008-07-10	タケダサンディエゴインコーポレイテッド	ヒストンデアセチラーゼ阻害剤
US7604939B2 (en) *	2005-03-01	2009-10-20	The Regents Of The University Of Michigan	Methods of identifying active BRM expression-promoting HDAC inhibitors
US20100087328A1 (en) *	2005-03-01	2010-04-08	The Regents Of The University Of Michigan	Brm expression and related diagnostics
US7642253B2 (en)	2005-05-11	2010-01-05	Takeda San Diego, Inc.	Histone deacetylase inhibitors
TWI365068B (en)	2005-05-20	2012-06-01	Merck Sharp & Dohme	Formulations of suberoylanilide hydroxamic acid and methods for producing same
CA2615105A1 (en)	2005-07-14	2007-01-25	Takeda San Diego, Inc.	Histone deacetylase inhibitors
US20100152188A1 (en) *	2005-08-05	2010-06-17	Akella Satya Surya Visweswara Srinivas	Novel Heterocyclic Compounds
ES2426445T3 (es) *	2006-04-07	2013-10-23	Merrion Research Iii Limited	Forma de dosificación oral sólida que contiene un potenciador
ES2452820T3 (es)	2006-04-07	2014-04-02	Methylgene, Inc.	Derivados de benzamida como inhibidores de histona desacetilasa
WO2007146234A2 (en) *	2006-06-09	2007-12-21	Merrion Research Ii Limited	Solid oral dosage form containing an enhancer
WO2008123395A1 (ja)	2007-03-28	2008-10-16	Santen Pharmaceutical Co., Ltd.	ヒストン脱アセチル化酵素阻害作用を有する化合物を有効成分として含有する眼圧下降剤
WO2009067808A1 (en) *	2007-11-27	2009-06-04	Ottawa Health Research Institute	Amplification of cancer-specific oncolytic viral infection by histone deacetylase inhibitors
CA2725390C (en) *	2008-04-08	2014-09-23	Syndax Pharmaceuticals, Inc.	Use of a hdac inhibitor and a her-2 inhibitor in the treatment of breast cancer
KR20110007614A (ko) *	2008-05-07	2011-01-24	메리온 리서치 Ⅲ 리미티드	ＧｎＲＨ 관련 화합물의 조성물 및 제조 방법
EP2285376A4 (en) *	2008-05-16	2011-07-20	Chipscreen Biosciences Ltd	6-AMINONICOTINAMIDE DERIVATIVES FORMING POWERFUL AND SELECTIVE HISTONE DEACETYLASE INHIBITORS
WO2010011700A2 (en)	2008-07-23	2010-01-28	The Brigham And Women's Hospital, Inc.	Treatment of cancers characterized by chromosomal rearrangement of the nut gene
JP2012518686A (ja) *	2009-02-25	2012-08-16	メリオン・リサーチ・Ｉｉｉ・リミテッド	ビスホスホネート類の組成物および薬物送達
WO2011120033A1 (en)	2010-03-26	2011-09-29	Merrion Research Iii Limited	Pharmaceutical compositions of selective factor xa inhibitors for oral administration
AU2012204213A1 (en)	2011-01-07	2013-06-13	Merrion Research Iii Limited	Pharmaceutical compositions of iron for oral administration
CN103172540B (zh) *	2013-03-18	2015-07-01	潍坊博创国际生物医药研究院	苯甘氨酸类组蛋白去乙酰酶抑制剂及其制备方法和应用
EP3470536A1 (en)	2013-10-01	2019-04-17	The J. David Gladstone Institutes	Compositions, systems and methods for gene expression noise drug screening and uses thereof
ES2975708T3 (es)	2015-01-29	2024-07-12	Novo Nordisk As	Comprimidos que comprenden agonista del GLP-1 y recubrimiento entérico
WO2017002095A1 (en)	2015-07-02	2017-01-05	Acerta Pharma B.V.	Solid forms and formulations of (s)-4-(8-amino-3-(1 -(but-2-ynoyl)pyrrolidin-2-yl)imidazo[1,5-a]pyrazin-1-yl)-n-(pyridin-2-yl)benzamide
TWI808055B (zh)	2016-05-11	2023-07-11	美商滬亞生物國際有限公司	Hdac 抑制劑與 pd-1 抑制劑之組合治療
TWI794171B (zh)	2016-05-11	2023-03-01	美商滬亞生物國際有限公司	Ｈｄａｃ抑制劑與ｐｄ-ｌ１抑制劑之組合治療
MX2019000342A (es) *	2016-07-08	2019-09-04	Ranedis Pharmaceuticals Llc	Composiciones y metodos para tratar y/o prevenir enfermedades de almacenamiento lisosomal y otras enfermedades metabolicas monogeneticas.
WO2018222572A1 (en) *	2017-06-01	2018-12-06	Warner Babcock Institute For Green Chemistry, Llc	Non-covalent derivatives and methods of treatment
WO2018226939A1 (en) *	2017-06-07	2018-12-13	Ranedis Pharmaceuticals, Llc	Compositions and methods of treating and/or preventing cancer
US20220211688A1 (en)	2019-04-25	2022-07-07	Fuji Pharma Co., Ltd.	Pharmaceutical preparation and method for producing the same
CN112294810B (zh) *	2019-07-29	2024-03-01	深圳微芯生物科技股份有限公司	含有西达本胺和表面活性剂的药物组合物
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1999
- 1999-08-30 JP JP24244499A patent/JP2001081031A/ja active Pending
2000
- 2000-08-29 DE DE60026144T patent/DE60026144T2/de not_active Expired - Lifetime
- 2000-08-29 PT PT00956496T patent/PT1208086E/pt unknown
- 2000-08-29 PL PL353063A patent/PL201274B1/pl not_active IP Right Cessation
- 2000-08-29 WO PCT/EP2000/008421 patent/WO2001016106A1/en not_active Ceased
- 2000-08-29 IL IL14835700A patent/IL148357A0/xx active IP Right Grant
- 2000-08-29 UA UA2002032271A patent/UA72541C2/uk unknown
- 2000-08-29 CZ CZ20020724A patent/CZ301737B6/cs not_active IP Right Cessation
- 2000-08-29 AR ARP000104493A patent/AR025434A1/es unknown
- 2000-08-29 AU AU68416/00A patent/AU773617B2/en not_active Ceased
- 2000-08-29 EP EP00956496A patent/EP1208086B1/en not_active Expired - Lifetime
- 2000-08-29 AT AT00956496T patent/ATE318258T1/de active
- 2000-08-29 HR HR20020182A patent/HRP20020182B1/xx not_active IP Right Cessation
- 2000-08-29 HU HU0203330A patent/HUP0203330A3/hu unknown
- 2000-08-29 NZ NZ517520A patent/NZ517520A/en not_active IP Right Cessation
- 2000-08-29 ES ES00956496T patent/ES2259289T3/es not_active Expired - Lifetime
- 2000-08-29 CA CA002382886A patent/CA2382886C/en not_active Expired - Fee Related
- 2000-08-29 KR KR1020027002163A patent/KR100712640B1/ko not_active Expired - Fee Related
- 2000-08-29 TW TW089117485A patent/TWI268778B/zh not_active IP Right Cessation
- 2000-08-29 CN CNB008122849A patent/CN1147472C/zh not_active Expired - Fee Related
- 2000-08-29 EE EEP200200097A patent/EE05063B1/et not_active IP Right Cessation
- 2000-08-29 RU RU2002107992/15A patent/RU2260428C2/ru active IP Right Revival
- 2000-08-29 SI SI200030851T patent/SI1208086T1/sl unknown
- 2000-08-29 MX MXPA02002090A patent/MXPA02002090A/es active IP Right Grant
- 2000-08-29 BR BR0013648-4A patent/BR0013648A/pt not_active Application Discontinuation
- 2000-08-29 US US10/069,582 patent/US6638530B1/en not_active Expired - Fee Related
- 2000-08-29 DK DK00956496T patent/DK1208086T3/da active
- 2000-08-29 HK HK02107642.5A patent/HK1046277B/zh not_active IP Right Cessation
- 2000-08-29 SK SK261-2002A patent/SK287252B6/sk not_active IP Right Cessation
- 2000-08-29 JP JP2001519675A patent/JP2003508386A/ja not_active Withdrawn
2002
- 2002-02-20 ZA ZA200201424A patent/ZA200201424B/en unknown
- 2002-02-25 IL IL148357A patent/IL148357A/en not_active IP Right Cessation
- 2002-02-26 BG BG106439A patent/BG65544B1/bg unknown
- 2002-02-27 NO NO20020952A patent/NO322532B1/no not_active IP Right Cessation

Also Published As

Publication number	Publication date
CZ301737B6 (cs)	2010-06-09
BR0013648A (pt)	2002-05-07
US6638530B1 (en)	2003-10-28
WO2001016106A1 (en)	2001-03-08
DK1208086T3 (da)	2006-06-19
BG65544B1 (bg)	2008-11-28
PL353063A1 (en)	2003-10-06
MXPA02002090A (es)	2003-08-20
PL201274B1 (pl)	2009-03-31
HK1046277B (zh)	2004-11-26
AU773617B2 (en)	2004-05-27
IL148357A0 (en)	2002-09-12
EP1208086A1 (en)	2002-05-29
CZ2002724A3 (cs)	2002-07-17
CA2382886C (en)	2009-06-09
BG106439A (en)	2002-11-29
NZ517520A (en)	2003-05-30
CN1371366A (zh)	2002-09-25
AU6841600A (en)	2001-03-26
DE60026144D1 (de)	2006-04-27
HUP0203330A2 (hu)	2003-02-28
NO322532B1 (no)	2006-10-23
SK2612002A3 (en)	2002-09-10
JP2003508386A (ja)	2003-03-04
HUP0203330A3 (en)	2004-03-01
NO20020952L (no)	2002-03-20
ZA200201424B (en)	2002-11-27
EE05063B1 (et)	2008-08-15
RU2260428C2 (ru)	2005-09-20
ES2259289T3 (es)	2006-10-01
SK287252B6 (sk)	2010-04-07
TWI268778B (en)	2006-12-21
JP2001081031A (ja)	2001-03-27
DE60026144T2 (de)	2006-11-16
PT1208086E (pt)	2006-07-31
UA72541C2 (en)	2005-03-15
SI1208086T1 (sl)	2006-08-31
ATE318258T1 (de)	2006-03-15
AR025434A1 (es)	2002-11-27
HK1046277A1 (en)	2003-01-03
CN1147472C (zh)	2004-04-28
EP1208086B1 (en)	2006-02-22
HRP20020182B1 (en)	2007-08-31
KR100712640B1 (ko)	2007-05-02
NO20020952D0 (no)	2002-02-27
CA2382886A1 (en)	2001-03-08
HRP20020182A2 (en)	2004-02-29
KR20020023424A (ko)	2002-03-28
IL148357A (en)	2006-12-10

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EE200200097A (et)	2003-04-15	Bensamiididerivaati sisaldav farmatseutiline preparaat
DK1207868T3 (da)	2007-09-03	Farmaceutiske tramadolsalte
ITMI20001450A0 (it)	2000-06-28	Nuova composizione farmaceutica
NO20015175D0 (no)	2001-10-23	Farmasöytisk sammensetning
NO20005218L (no)	2000-11-10	Farmasöytisk aerosolpreparat
DK1466615T3 (da)	2009-08-31	Farmaceutisk præparat
NO20015670D0 (no)	2001-11-20	Forbedrede farmasöytiske formuleringer
NO20015149L (no)	2001-12-17	Nytt farmasöytisk preparat
NO20022606L (no)	2002-07-11	Farmasöytiske kombinasjoner
NO20014926L (no)	2001-12-13	Farmasöytiske forbindelser
EE200200073A (et)	2003-04-15	Bensamiididerivaati sisaldav farmatseutiline preparaat
NO20015148L (no)	2001-12-17	Nytt farmasöytisk preparat
EE9900545A (et)	2000-06-15	Farmatseutiline kompositsioon
DK1227817T3 (da)	2004-11-15	Ciclesonid-holdigt vandigt farmaceutisk præparat
FI4488U1 (fi)	2000-07-20	Farmaseuttinen koostumus
NO20015104L (no)	2001-12-19	Nytt farmasöytisk preparat
AR025867A1 (es)	2002-12-18	Formulacion portasdora farmaceutica
NO20015105D0 (no)	2001-10-19	Nytt farmasöytisk preparat
EE200100697A (et)	2003-02-17	Farmatseutiline kompleks
NO20021036L (no)	2002-04-26	Farmasöytisk preparat
SE9904819D0 (sv)	1999-12-28	A new pharmaceutical composition
SE9800251D0 (sv)	1998-01-27	A novel pharmaceutical preparation
DK1060749T3 (da)	2003-06-23	Vandigt farmaceutisk præparat indeholdende Tezosentan
DE50008261D1 (de)	2004-11-18	Retardierte darreichungsform enthaltend tramadolsaccharinat
SE9804128D0 (sv)	1998-11-27	A new pharmaceutical composition

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