SK283348B6 - Farmaceutický prípravok obsahujúci zlúčeninu s antagonickým účinkom na angiotenzín II - Google Patents
Farmaceutický prípravok obsahujúci zlúčeninu s antagonickým účinkom na angiotenzín II Download PDFInfo
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- SK283348B6 SK283348B6 SK1278-98A SK127898A SK283348B6 SK 283348 B6 SK283348 B6 SK 283348B6 SK 127898 A SK127898 A SK 127898A SK 283348 B6 SK283348 B6 SK 283348B6
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- angiotensin
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Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
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JP8391796 | 1996-04-05 | ||
PCT/JP1997/001149 WO1997037688A2 (en) | 1996-04-05 | 1997-04-03 | Pharmaceutical combination containing a compound having angiotensin ii and antagonistic activity |
Publications (2)
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SK127898A3 SK127898A3 (en) | 1999-05-07 |
SK283348B6 true SK283348B6 (sk) | 2003-06-03 |
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SK1278-98A SK283348B6 (sk) | 1996-04-05 | 1997-04-03 | Farmaceutický prípravok obsahujúci zlúčeninu s antagonickým účinkom na angiotenzín II |
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US (2) | US6107323A (cs) |
EP (4) | EP0914158B2 (cs) |
JP (2) | JPH09323940A (cs) |
KR (2) | KR20050047560A (cs) |
CN (1) | CN1215338A (cs) |
AT (1) | ATE220333T1 (cs) |
AU (1) | AU713277B2 (cs) |
BR (1) | BR9708517A (cs) |
CA (3) | CA2241466C (cs) |
CY (1) | CY2300B1 (cs) |
CZ (1) | CZ297941B6 (cs) |
DE (1) | DE69713890T3 (cs) |
DK (1) | DK0914158T4 (cs) |
ES (1) | ES2175385T5 (cs) |
NO (1) | NO321388B1 (cs) |
NZ (1) | NZ330774A (cs) |
PL (2) | PL189066B1 (cs) |
PT (1) | PT914158E (cs) |
RU (1) | RU2188013C2 (cs) |
SI (1) | SI0914158T2 (cs) |
SK (1) | SK283348B6 (cs) |
WO (1) | WO1997037688A2 (cs) |
Families Citing this family (75)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6268392B1 (en) * | 1994-09-13 | 2001-07-31 | G. D. Searle & Co. | Combination therapy employing ileal bile acid transport inhibiting benzothiepines and HMG Co-A reductase inhibitors |
EP0835106A4 (en) * | 1995-06-30 | 1998-09-30 | Merck & Co Inc | METHOD FOR TREATING KIDNEY DISEASES USING AN ACE INHIBITOR AND AII ANTAGONIST |
NZ286920A (en) * | 1995-07-03 | 1997-06-24 | Sankyo Co | Use of combination of hmg-coa reductase inhibitors and of insulin sensitizers for the prevention/treatment of arteriosclerosis or xanthoma |
PT914158E (pt) * | 1996-04-05 | 2002-11-29 | Takeda Chemical Industries Ltd | Combinacao farmaceutica que incorpora um composto que possui actividade antagonista da angiotensina ii e um composto que aumenta a sensibilidade a insulina |
DE69731840T2 (de) | 1996-07-15 | 2005-08-04 | Sankyo Co., Ltd. | Pharmazeutische Zusammensetzungen enthaltend CS-866 und Insulinresistenz verbessernde Mittel und deren Verwendung zur Behandlung von Arteriosklerose und Xanthom |
JP2008094852A (ja) * | 1996-07-15 | 2008-04-24 | Daiichi Sankyo Co Ltd | 医薬 |
CA2300813A1 (en) * | 1997-08-21 | 1999-03-04 | Hiroyuki Odaka | Anti-inflammatory agent |
US7105552B2 (en) * | 1998-05-08 | 2006-09-12 | Theracos, Inc. | Heterocyclic analogs of diphenylethylene compounds |
CA2355293C (en) | 1998-12-23 | 2005-08-16 | Orphan Medical, Inc. | Microbiologically sound and stable solutions of gamma-hydroxybutyrate salt for the treatment of narcolepsy |
US6756360B1 (en) | 1998-12-24 | 2004-06-29 | Metabasis Therapeutics, Inc. | Combination of FBPase inhibitors and insulin sensitizers for the treatment of diabetes |
AU3073700A (en) * | 1999-01-19 | 2000-08-07 | Sankyo Company Limited | Troglitazone-containing medicinal compositions for inhibiting apoptosis |
GB0001662D0 (en) | 1999-02-06 | 2000-03-15 | Zeneca Ltd | Pharmaceutical compositions |
US7407978B2 (en) * | 1999-04-06 | 2008-08-05 | Theracos, Inc. | Heterocyclic analogs of diphenylethylene compounds |
EP1197223B1 (en) | 1999-04-28 | 2005-02-16 | Takeda Pharmaceutical Company Limited | Preventives / remedies / progression inhibitors for simplex retinopathy or preproliferating retinopathy |
DE60037192T2 (de) * | 1999-07-21 | 2008-05-15 | Takeda Pharmaceutical Co. Ltd. | Mittel zur verbesserung der erkrankungen nach zerebralen durchblutungsstörungen sowie zur verhinderung deren fortschreitens |
TWI290470B (en) | 1999-12-01 | 2007-12-01 | Sankyo Co | The composition for treating glaucoma |
HUP0301057A3 (en) * | 2000-02-18 | 2004-01-28 | Takeda Pharmaceutical | Angiotenzin ii antagonist heterocyclic compound an their use for preparation of tnf-alpha inhibitors |
US7563774B2 (en) | 2000-06-29 | 2009-07-21 | Metabasis Therapeutics, Inc. | Combination of FBPase inhibitors and antidiabetic agents useful for the treatment of diabetes |
US20060089389A1 (en) | 2000-08-22 | 2006-04-27 | Malcolm Allison | Combination |
AR033390A1 (es) * | 2000-08-22 | 2003-12-17 | Novartis Ag | Una composicion farmaceutica que comprende un antagonista del receptor at1 y un potenciador de la secrecion de insulina, el uso de dicha composicion para la fabricacion de un medicamento y un kit de partes |
EP1314425A4 (en) * | 2000-08-30 | 2004-06-02 | Sankyo Co | MEDICINAL COMPOSITIONS FOR THE PREVENTION OR TREATMENT OF HEART FAILURE |
EP1370210A4 (en) * | 2001-02-07 | 2004-08-18 | Mclean Hospital Corp | HYPOCHOLESTEROLEMIANTS USED TO TREAT PSYCHOLOGICAL AND COGNITIVE DISORDERS |
US20030078190A1 (en) * | 2001-05-25 | 2003-04-24 | Weinberg Marc S. | Methods for tissue protection using highly effective inhibition of the renin-angiotensin system |
GB0113570D0 (en) | 2001-06-04 | 2001-07-25 | Hewlett Packard Co | Audio-form presentation of text messages |
EP1413315A4 (en) * | 2001-08-03 | 2006-08-16 | Takeda Pharmaceutical | DRUGS WITH CONTINUOUS RELEASE |
JP4484427B2 (ja) * | 2001-12-03 | 2010-06-16 | 武田薬品工業株式会社 | インスリン抵抗性改善剤 |
US20050032854A1 (en) * | 2001-12-03 | 2005-02-10 | Kiminori Kawahara | Insulin resistance improving agents |
MY131170A (en) | 2002-03-28 | 2007-07-31 | Nissan Chemical Ind Ltd | Therapeutic agent for glomerular disease |
US20030229007A1 (en) * | 2002-05-30 | 2003-12-11 | Roberto Levi | Form of human renin and its use as a target in treatments for cardiac ischemia and arrhythmia |
US7776314B2 (en) | 2002-06-17 | 2010-08-17 | Grunenthal Gmbh | Abuse-proofed dosage system |
US7232828B2 (en) | 2002-08-10 | 2007-06-19 | Bethesda Pharmaceuticals, Inc. | PPAR Ligands that do not cause fluid retention, edema or congestive heart failure |
EP1545540A2 (en) * | 2002-08-21 | 2005-06-29 | Merck & Co., Inc. | Combination therapy using a dual ppar alpha/gamma agonist and an angiotensin ii type i receptor antagonist |
US7582662B2 (en) * | 2002-12-27 | 2009-09-01 | Takeda Pharmaceutical Company Limited | Body weight gain inhibitor |
DE10301371A1 (de) * | 2003-01-16 | 2004-08-05 | Boehringer Ingelheim Pharma Gmbh & Co. Kg | Pharmazeutische Kombination zur Prophylaxe oder Therapie von kardiovaskulären, kardiopulmonalen, pulmonalen oder renalen Krankheiten |
KR20050092119A (ko) * | 2003-01-16 | 2005-09-20 | 베링거 인겔하임 인터내셔날 게엠베하 | 심혈관 질환, 심폐 질환, 폐 질환 또는 신장 질환을예방하거나 치료하기 위한 약제학적 배합물 |
JPWO2005011736A1 (ja) * | 2003-07-30 | 2006-09-14 | 株式会社 東北テクノアーチ | アルツハイマー病の予防および/または治療剤 |
DE10361596A1 (de) | 2003-12-24 | 2005-09-29 | Grünenthal GmbH | Verfahren zur Herstellung einer gegen Missbrauch gesicherten Darreichungsform |
US20070048228A1 (en) | 2003-08-06 | 2007-03-01 | Elisabeth Arkenau-Maric | Abuse-proofed dosage form |
DE102005005446A1 (de) | 2005-02-04 | 2006-08-10 | Grünenthal GmbH | Bruchfeste Darreichungsformen mit retardierter Freisetzung |
DE10336400A1 (de) | 2003-08-06 | 2005-03-24 | Grünenthal GmbH | Gegen Missbrauch gesicherte Darreichungsform |
GB0322552D0 (en) | 2003-09-26 | 2003-10-29 | Astrazeneca Uk Ltd | Therapeutic treatment |
US20050250734A1 (en) * | 2003-11-07 | 2005-11-10 | The Procter & Gamble Company | Compositions, kits, and methods for the treatment of conditions associated with elevated cholesterol levels |
WO2005070398A2 (en) * | 2004-01-23 | 2005-08-04 | Ranbaxy Laboratories Limited | Pharmaceutical compositions of candesartan cilexetil stabilized with co-solvents |
DE102004032049A1 (de) | 2004-07-01 | 2006-01-19 | Grünenthal GmbH | Gegen Missbrauch gesicherte, orale Darreichungsform |
US20060039890A1 (en) * | 2004-08-20 | 2006-02-23 | Renshaw Perry F | Treatment of psychological and cognitive disorders using a cholesterol -lowering agent in combination with an antidepressant |
CA2583768A1 (en) * | 2004-10-07 | 2006-04-13 | Takeda Pharmaceutical Company Limited | Agent for prophylaxis or treatment of metabolic syndrome |
ATE518526T1 (de) * | 2005-01-26 | 2011-08-15 | Lek Pharmaceuticals | Neue pharmazeutische zusammensetzung mit candesartan-cilexetil als lipophile kristalline substanz |
DE102005005449A1 (de) | 2005-02-04 | 2006-08-10 | Grünenthal GmbH | Verfahren zur Herstellung einer gegen Missbrauch gesicherten Darreichungsform |
JP4795362B2 (ja) * | 2005-03-30 | 2011-10-19 | 武田薬品工業株式会社 | ベンズイミダゾール誘導体およびその用途 |
CA2677661A1 (en) | 2007-02-07 | 2008-08-14 | Kyowa Hakko Kirin Co., Ltd. | Tricyclic compounds |
DE102007011485A1 (de) | 2007-03-07 | 2008-09-11 | Grünenthal GmbH | Darreichungsform mit erschwertem Missbrauch |
JP5283632B2 (ja) * | 2007-03-28 | 2013-09-04 | 武田薬品工業株式会社 | ベンズイミダゾール−7−カルボキシレート誘導体およびpH調整剤を含有する固形医薬組成物 |
US20090074831A1 (en) * | 2007-09-18 | 2009-03-19 | Robert Falotico | LOCAL VASCULAR DELIVERY OF mTOR INHIBITORS IN COMBINATION WITH PEROXISOME PROLIFERATORS-ACTIVATED RECEPTOR STIMULATORS |
WO2009088006A1 (ja) * | 2008-01-10 | 2009-07-16 | Daiichi Sankyo Company, Limited | 併用医薬 |
AU2009207796B2 (en) | 2008-01-25 | 2014-03-27 | Grunenthal Gmbh | Pharmaceutical dosage form |
WO2009134057A2 (ko) | 2008-04-29 | 2009-11-05 | 한올제약주식회사 | 안지오텐신-ⅱ-수용체 차단제를 포함하는 약제학적 제제 |
RU2508092C2 (ru) | 2008-05-09 | 2014-02-27 | Грюненталь Гмбх | Способ получения твердой лекарственной формы, в частности таблетки для фармацевтического применения, и способ получения прекурсора твердой лекарственной формы, в частности таблетки |
MX2012000644A (es) | 2009-07-22 | 2012-02-08 | Gruenenthal Gmbh | Forma de dosificacion de oxidacion estabilizada resistente a la manipulacion. |
MX2012000317A (es) | 2009-07-22 | 2012-02-08 | Gruenenthal Gmbh | Forma de dosificacion de liberacion controlada extruida por fusion en caliente. |
AU2011297901B2 (en) | 2010-09-02 | 2014-07-31 | Grunenthal Gmbh | Tamper resistant dosage form comprising inorganic salt |
EP2611425B1 (en) | 2010-09-02 | 2014-07-02 | Grünenthal GmbH | Tamper resistant dosage form comprising an anionic polymer |
WO2013017242A1 (en) | 2011-07-29 | 2013-02-07 | Grünenthal GmbH | Tamper-resistant tablet providing immediate drug release |
KR20140053159A (ko) | 2011-07-29 | 2014-05-07 | 그뤼넨탈 게엠베하 | 즉시 약물 방출을 제공하는 탬퍼-저항성 정제 |
CA2864949A1 (en) | 2012-02-28 | 2013-09-06 | Grunenthal Gmbh | Tamper-resistant dosage form comprising pharmacologically active compound and anionic polymer |
LT2838512T (lt) | 2012-04-18 | 2018-11-12 | Grünenthal GmbH | Pažeidimui atspari ir dozės atpalaidavimo nuokrypiui atspari farmacinė vaisto forma |
US10064945B2 (en) | 2012-05-11 | 2018-09-04 | Gruenenthal Gmbh | Thermoformed, tamper-resistant pharmaceutical dosage form containing zinc |
EP2873422A4 (en) * | 2012-07-10 | 2015-12-30 | Takeda Pharmaceutical | PHARMACEUTICAL PREPARATION FOR INJECTION |
AR096438A1 (es) | 2013-05-29 | 2015-12-30 | Gruenenthal Gmbh | Forma de dosificación resistente al uso indebido con perfil de liberación bimodal, proceso |
JP6445537B2 (ja) | 2013-05-29 | 2018-12-26 | グリュネンタール・ゲゼルシャフト・ミト・ベシュレンクテル・ハフツング | 1個または複数の粒子を含有する改変防止(tamper−resistant)剤形 |
US10624862B2 (en) | 2013-07-12 | 2020-04-21 | Grünenthal GmbH | Tamper-resistant dosage form containing ethylene-vinyl acetate polymer |
HK1224189A1 (zh) | 2013-11-26 | 2017-08-18 | Grünenthal GmbH | 通过低温研磨制备粉状药物组合物 |
US20150320690A1 (en) | 2014-05-12 | 2015-11-12 | Grünenthal GmbH | Tamper resistant immediate release capsule formulation comprising tapentadol |
MX2016015417A (es) | 2014-05-26 | 2017-02-22 | Gruenenthal Gmbh | Multiparticulas protegidas contra vertido de dosis etanolico. |
CA2983642A1 (en) | 2015-04-24 | 2016-10-27 | Grunenthal Gmbh | Tamper-resistant dosage form with immediate release and resistance against solvent extraction |
JP2018526414A (ja) | 2015-09-10 | 2018-09-13 | グリュネンタール・ゲゼルシャフト・ミト・ベシュレンクテル・ハフツング | 乱用抑止性の即放性製剤を用いた経口過剰摂取に対する保護 |
Family Cites Families (28)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0238580B2 (ja) * | 1981-06-02 | 1990-08-31 | Takeda Chemical Industries Ltd | Bariooruaminnonnchikanjudotai*sonoseizohooyobyoto |
CA2016710A1 (en) * | 1989-05-15 | 1990-11-15 | Prasun K. Chakravarty | Substituted benzimidazoles as angiotensin ii antagonists |
ES2059121T5 (es) * | 1990-02-09 | 2000-12-01 | Upjohn Co | Uso de agentes sensibilizantes de la insulina para tratar la hipertension. |
US5196444A (en) * | 1990-04-27 | 1993-03-23 | Takeda Chemical Industries, Ltd. | 1-(cyclohexyloxycarbonyloxy)ethyl 2-ethoxy-1-[[2'-(1H-tetrazol-5-yl)biphenyl-4-yl]methyl]benzimidazole-7-carboxylate and compositions and methods of pharmaceutical use thereof |
DK0527879T3 (da) * | 1990-05-11 | 1997-07-14 | Pfizer | Synergistiske terapeutiske præparater og fremgangsmåder. |
US5298497A (en) * | 1990-05-15 | 1994-03-29 | E. R. Squibb & Sons, Inc. | Method for preventing onset of hypertension employing a cholesterol lowering drug |
CA2040865C (en) * | 1990-05-15 | 2002-07-23 | James L. Bergey | Method for preventing, stabilizing or causing regression of atherosclerosis employing a combination of a cholesterol lowering drug and an ace inhibitor |
ATE177634T1 (de) * | 1990-12-14 | 1999-04-15 | Smithkline Beecham Corp | Angiotensin-ii-rezeptor blockierende zusammensetzungen |
AU1256692A (en) * | 1991-02-06 | 1992-09-07 | Schering Corporation | Combination of an angiotensin II antagonist or renin inhibitor with a neutral endopeptidase inhibitor |
EP0503838A3 (en) * | 1991-03-08 | 1992-10-07 | Merck & Co. Inc. | Heterocyclic compounds bearing acidic functional groups as angiotensin ii antagonists |
US5162340A (en) * | 1991-05-10 | 1992-11-10 | Merck & Co., Inc. | Substituted 1-(2h)-isoquinolinones bearing acidic functional groups as angiotensin ii antagonists |
HU9203780D0 (en) * | 1991-12-12 | 1993-03-29 | Sandoz Ag | Stabilized pharmaceutical products of hmg-coa reductase inhibitor and method for producing them |
JPH07505646A (ja) * | 1992-04-13 | 1995-06-22 | ゼネカ・リミテッド | 神経伝達速度の減損を伴う障害,特に糖尿病性ニューロパシーに対するアンギオテンシンiiアンタゴニスト |
US5266583A (en) * | 1992-09-01 | 1993-11-30 | Merck & Co., Inc. | Angitotensin II antagonist |
DE4315349A1 (de) * | 1992-10-06 | 1994-11-10 | Thomae Gmbh Dr K | Benzimidazole, diese Verbindungen enthaltende Arzneimittel und Verfahren zu ihrer Herstellung |
US5300668A (en) * | 1993-03-10 | 1994-04-05 | Pfizer Inc. | Certain esters of 1-(4-X-methylphenyl)cyclopent-3-ene-1-carboxylic acid, wherein X is a trialkylsilyloxy, bromo or hydroxy group, as intermediates |
JP3057471B2 (ja) * | 1993-06-07 | 2000-06-26 | 武田薬品工業株式会社 | アンジオテンシンii介在性諸疾患の予防または治療剤 |
CA2125251C (en) * | 1993-06-07 | 2005-04-26 | Yoshiyuki Inada | A pharmaceutical composition for angiotensin ii-mediated diseases |
EP0629408A1 (en) * | 1993-06-16 | 1994-12-21 | LABORATOIRES MERCK, SHARP & DOHME-CHIBRET | Combination of angiotensin converting enzyme inhibitors and AII antagonists |
EP0635263A3 (en) * | 1993-06-28 | 1995-09-27 | American Cyanamid Co | Angiotensin II antagonists (AII) as inhibitors of the growth of adipose tissue. |
CA2186606A1 (en) * | 1994-03-29 | 1995-10-05 | Edward B. Nelson | Treatment of atherosclerosis with angiotensin ii receptor blocking imidazoles |
GB9406573D0 (en) * | 1994-03-31 | 1994-05-25 | Merck Sharp & Dohme | Medicaments |
FR2733911B1 (fr) * | 1995-05-09 | 1998-05-29 | Takeda Chemical Industries Ltd | Composition pharmaceutique pour maladies renales ou cardio-vasculaires |
FR2735365B1 (fr) * | 1995-06-14 | 1997-09-05 | Sanofi Sa | Utilisation d'un antagoniste de l'angiotensine ii et d'un derive du benzofurane pour la preparation d'un medicament utile dans le traitement des affections cardiovasculaires |
TWI238064B (en) * | 1995-06-20 | 2005-08-21 | Takeda Chemical Industries Ltd | A pharmaceutical composition for prophylaxis and treatment of diabetes |
EP0835106A4 (en) * | 1995-06-30 | 1998-09-30 | Merck & Co Inc | METHOD FOR TREATING KIDNEY DISEASES USING AN ACE INHIBITOR AND AII ANTAGONIST |
NZ286920A (en) * | 1995-07-03 | 1997-06-24 | Sankyo Co | Use of combination of hmg-coa reductase inhibitors and of insulin sensitizers for the prevention/treatment of arteriosclerosis or xanthoma |
PT914158E (pt) * | 1996-04-05 | 2002-11-29 | Takeda Chemical Industries Ltd | Combinacao farmaceutica que incorpora um composto que possui actividade antagonista da angiotensina ii e um composto que aumenta a sensibilidade a insulina |
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1997
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- 1997-04-03 DE DE69713890T patent/DE69713890T3/de not_active Expired - Lifetime
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- 1997-04-03 KR KR1019980706462A patent/KR19990087076A/ko not_active Ceased
- 1997-04-03 CN CN97193515A patent/CN1215338A/zh active Pending
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- 1997-04-03 CA CA002650637A patent/CA2650637A1/en not_active Abandoned
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MM4A | Patent lapsed due to non-payment of maintenance fees |
Effective date: 20130403 |