JP2007277267A5 - - Google Patents

Download PDF

Info

Publication number
JP2007277267A5
JP2007277267A5 JP2007195798A JP2007195798A JP2007277267A5 JP 2007277267 A5 JP2007277267 A5 JP 2007277267A5 JP 2007195798 A JP2007195798 A JP 2007195798A JP 2007195798 A JP2007195798 A JP 2007195798A JP 2007277267 A5 JP2007277267 A5 JP 2007277267A5
Authority
JP
Japan
Prior art keywords
interacting
drug combination
fibrate
combination according
drug
Prior art date
Legal status (The legal status 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 status listed.)
Pending
Application number
JP2007195798A
Other languages
English (en)
Japanese (ja)
Other versions
JP2007277267A (ja
Filing date
Publication date
Priority claimed from GBGB9902593.4A external-priority patent/GB9902593D0/en
Priority claimed from GBGB9921063.5A external-priority patent/GB9921063D0/en
Priority claimed from GBGB9921064.3A external-priority patent/GB9921064D0/en
Application filed filed Critical
Publication of JP2007277267A publication Critical patent/JP2007277267A/ja
Publication of JP2007277267A5 publication Critical patent/JP2007277267A5/ja
Pending legal-status Critical Current

Links

JP2007195798A 1999-02-06 2007-07-27 (e)−7−[4−(4−フルオロフェニル)−6−イソプロピル−2−[メチル(メチルスルホニル)アミノ]ピリミジン−5−イル](3r,5s)−3,5−ジヒドロキシヘプツ−6−エン酸と、p450アイソザイム3a4の阻害剤、誘導剤又は基質を含んでなる薬物の組み合わせ Pending JP2007277267A (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
GBGB9902593.4A GB9902593D0 (en) 1999-02-06 1999-02-06 Drug combinations
GBGB9921063.5A GB9921063D0 (en) 1999-09-08 1999-09-08 Therapy
GBGB9921064.3A GB9921064D0 (en) 1999-09-08 1999-09-08 Drug combination

Related Parent Applications (1)

Application Number Title Priority Date Filing Date
JP2000596937A Division JP2002536331A (ja) 1999-02-06 2000-02-01 (e)−7−[4−(4−フルオロフェニル)−6−イソプロピル−2−[メチル(メチルスルホニル)アミノ]ピリミジン−5−イル](3r,5s)−3,5−ジヒドロキシヘプツ−6−エン酸と、p450アイソザイム3a4の阻害剤、誘導剤又は基質を含んでなる薬物の組み合わせ

Publications (2)

Publication Number Publication Date
JP2007277267A JP2007277267A (ja) 2007-10-25
JP2007277267A5 true JP2007277267A5 (cg-RX-API-DMAC7.html) 2008-05-15

Family

ID=27269637

Family Applications (2)

Application Number Title Priority Date Filing Date
JP2000596937A Pending JP2002536331A (ja) 1999-02-06 2000-02-01 (e)−7−[4−(4−フルオロフェニル)−6−イソプロピル−2−[メチル(メチルスルホニル)アミノ]ピリミジン−5−イル](3r,5s)−3,5−ジヒドロキシヘプツ−6−エン酸と、p450アイソザイム3a4の阻害剤、誘導剤又は基質を含んでなる薬物の組み合わせ
JP2007195798A Pending JP2007277267A (ja) 1999-02-06 2007-07-27 (e)−7−[4−(4−フルオロフェニル)−6−イソプロピル−2−[メチル(メチルスルホニル)アミノ]ピリミジン−5−イル](3r,5s)−3,5−ジヒドロキシヘプツ−6−エン酸と、p450アイソザイム3a4の阻害剤、誘導剤又は基質を含んでなる薬物の組み合わせ

Family Applications Before (1)

Application Number Title Priority Date Filing Date
JP2000596937A Pending JP2002536331A (ja) 1999-02-06 2000-02-01 (e)−7−[4−(4−フルオロフェニル)−6−イソプロピル−2−[メチル(メチルスルホニル)アミノ]ピリミジン−5−イル](3r,5s)−3,5−ジヒドロキシヘプツ−6−エン酸と、p450アイソザイム3a4の阻害剤、誘導剤又は基質を含んでなる薬物の組み合わせ

Country Status (28)

Country Link
US (3) US6982157B1 (cg-RX-API-DMAC7.html)
EP (1) EP1185274B1 (cg-RX-API-DMAC7.html)
JP (2) JP2002536331A (cg-RX-API-DMAC7.html)
KR (2) KR20010101790A (cg-RX-API-DMAC7.html)
CN (1) CN1165310C (cg-RX-API-DMAC7.html)
AR (1) AR029333A1 (cg-RX-API-DMAC7.html)
AT (1) ATE282415T1 (cg-RX-API-DMAC7.html)
AU (1) AU767304B2 (cg-RX-API-DMAC7.html)
BR (1) BR0007999A (cg-RX-API-DMAC7.html)
CA (1) CA2358632C (cg-RX-API-DMAC7.html)
CZ (1) CZ301296B6 (cg-RX-API-DMAC7.html)
DE (1) DE60015965T2 (cg-RX-API-DMAC7.html)
EE (1) EE04929B1 (cg-RX-API-DMAC7.html)
EG (1) EG23858A (cg-RX-API-DMAC7.html)
ES (1) ES2232418T3 (cg-RX-API-DMAC7.html)
GB (1) GB0000710D0 (cg-RX-API-DMAC7.html)
ID (1) ID30485A (cg-RX-API-DMAC7.html)
IL (1) IL144715A0 (cg-RX-API-DMAC7.html)
IS (1) IS2337B (cg-RX-API-DMAC7.html)
MX (1) MXPA01007905A (cg-RX-API-DMAC7.html)
MY (1) MY130606A (cg-RX-API-DMAC7.html)
NO (1) NO320745B1 (cg-RX-API-DMAC7.html)
NZ (1) NZ512982A (cg-RX-API-DMAC7.html)
PL (1) PL198034B1 (cg-RX-API-DMAC7.html)
PT (1) PT1185274E (cg-RX-API-DMAC7.html)
TR (1) TR200102228T2 (cg-RX-API-DMAC7.html)
TW (1) TWI282738B (cg-RX-API-DMAC7.html)
WO (1) WO2000045817A1 (cg-RX-API-DMAC7.html)

Families Citing this family (30)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6489346B1 (en) 1996-01-04 2002-12-03 The Curators Of The University Of Missouri Substituted benzimidazole dosage forms and method of using same
US5840737A (en) 1996-01-04 1998-11-24 The Curators Of The University Of Missouri Omeprazole solution and method for using same
DE19944803A1 (de) * 1999-09-20 2001-03-29 Bayer Ag Kombination von Dihydropyridinverbindungen und HMG-CoA-Reduktase-Inhibitoren und ihre Verwendung in Arzneimitteln
GB0001621D0 (en) * 2000-01-26 2000-03-15 Astrazeneca Ab Pharmaceutical compositions
GB0003305D0 (en) 2000-02-15 2000-04-05 Zeneca Ltd Pyrimidine derivatives
US6982251B2 (en) 2000-12-20 2006-01-03 Schering Corporation Substituted 2-azetidinones useful as hypocholesterolemic agents
US7071181B2 (en) 2001-01-26 2006-07-04 Schering Corporation Methods and therapeutic combinations for the treatment of diabetes using sterol absorption inhibitors
IL156422A0 (en) 2001-01-26 2004-01-04 Schering Corp The use of substituted azetidinone compounds for the treatment of sitosterolemia
SI1413331T1 (sl) 2001-01-26 2008-02-29 Schering Corp Kombinacije fenofibrata peroksisomskega proliferator aktivirajocega receptorja (PPAR) z ezetimib zaviralcem absorpcije sterola za vaskularne indikacije
JP2005504091A (ja) 2001-09-21 2005-02-10 シェーリング コーポレイション ステロール吸収阻害剤としてアゼチジノンを用いる黄色腫の処置
US7056906B2 (en) 2001-09-21 2006-06-06 Schering Corporation Combinations of hormone replacement therapy composition(s) and sterol absorption inhibitor(s) and treatments for vascular conditions in post-menopausal women
US7053080B2 (en) 2001-09-21 2006-05-30 Schering Corporation Methods and therapeutic combinations for the treatment of obesity using sterol absorption inhibitors
EP1562582A1 (en) 2002-11-06 2005-08-17 Schering Corporation Cholesterol absorption inhibitors for the treatment of demyelination
JP2006519869A (ja) 2003-03-07 2006-08-31 シェーリング コーポレイション 置換アゼチジノン化合物、置換アゼチジノン化合物を調製するためのプロセス、それらの処方物および使用
US7459442B2 (en) 2003-03-07 2008-12-02 Schering Corporation Substituted azetidinone compounds, processes for preparing the same, formulations and uses thereof
WO2004081002A1 (en) 2003-03-07 2004-09-23 Schering Corporation Substituted azetidinone compounds, formulations and uses thereof for the treatment of hypercholesterolemia
CN1756756A (zh) 2003-03-07 2006-04-05 先灵公司 取代的2-吖丁啶酮化合物、其制剂及其治疗高胆甾醇血症的用途
US8993599B2 (en) 2003-07-18 2015-03-31 Santarus, Inc. Pharmaceutical formulations useful for inhibiting acid secretion and methods for making and using them
GB0322552D0 (en) 2003-09-26 2003-10-29 Astrazeneca Uk Ltd Therapeutic treatment
US9173847B2 (en) 2003-10-10 2015-11-03 Veloxis Pharmaceuticals A/S Tablet comprising a fibrate
JP5069001B2 (ja) 2003-10-10 2012-11-07 ベロクシス ファーマシューティカルズ エー/エス フィブラートを含む固体投与形態
US8906940B2 (en) 2004-05-25 2014-12-09 Santarus, Inc. Pharmaceutical formulations useful for inhibiting acid secretion and methods for making and using them
MX2007001553A (es) 2004-08-06 2008-03-07 Transform Pharmaceuticals Inc Nuevas composiciones farmaceuticas de estatina y metodos de tratamiento relacionados.
EP1948600B1 (en) * 2005-07-05 2014-04-16 The President & Fellows Of Harvard College Liver targeted conjugates
EA015682B1 (ru) 2005-12-20 2011-10-31 Лек Фармасьютиклз Д.Д. Фармацевтическая композиция
US20080109252A1 (en) * 2006-11-08 2008-05-08 Lafountain Andrea Predicting patient compliance with medical treatment
US20120130202A1 (en) * 2010-11-24 2012-05-24 Fujitsu Limited Diagnosis and Monitoring of Musculoskeletal Pathologies
WO2019241519A1 (en) * 2018-06-14 2019-12-19 Astrazeneca Uk Limited Methods for lowering blood pressure with a dihydropyridine-type calcium channel blocker pharmaceutical composition
MX2022001178A (es) * 2019-07-31 2022-02-22 Intas Pharmaceuticals Ltd Composicion farmaceutica que comprende inhibidores de la hmg-coa reductasa y fenofibrato.
WO2024223797A1 (en) 2023-04-28 2024-10-31 Institut National de la Santé et de la Recherche Médicale Use of cyp3a4 inhibitors for the treatment of hepatitis d virus (hdv) infections

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2627696B1 (fr) * 1988-02-26 1991-09-13 Fournier Innovation Synergie Nouvelle forme galenique du fenofibrate
JP2648897B2 (ja) * 1991-07-01 1997-09-03 塩野義製薬株式会社 ピリミジン誘導体
DK0521417T3 (da) * 1991-07-02 1995-03-27 Benckiser Gmbh Joh A Sammenklappelig forrådsflaske
JP3852621B2 (ja) * 1992-01-21 2006-12-06 あすか製薬株式会社 血管内皮細胞機能改善剤
FR2730231B1 (fr) * 1995-02-02 1997-04-04 Fournier Sca Lab Association de fenofibrate et de vitamine e, utilisation en therapeutique
AU1289899A (en) * 1997-10-31 1999-05-24 Arch Development Corporation Methods and compositions for regulation of 5-alpha reductase activity

Similar Documents

Publication Publication Date Title
JP2007277267A5 (cg-RX-API-DMAC7.html)
HRP20241674T1 (hr) 6'-[[(1s,3s)-3-[[5-(difluormetoksi)-2-pirimidinil]amino]ciklopentil]amino][1(2h),3'-bipiridin]-2-on kao inhibitor pcsk9 i postupci njegove upotrebe
HRP20080525A2 (en) PHARMACEUTICAL COMPOSITIONS COMPRISING A HMG CoA REDUCTASE INHIBITOR
JP2013543896A5 (cg-RX-API-DMAC7.html)
SI1682536T1 (sl) Postopek izdelave kalcijeve soli rosuvastatin-(E)-7-(4-(4-fluorofenil) -6-izopropil-2-(metil(metilsulfonil)amino)pirimidin-5-il) (3r,5s)-3,5- dihidroksihept-6-enojske kisline in njenih kristalnih vmesnih spojin
EA200901442A1 (ru) Комбинированная терапия соединением, проявляющим активность ингибитора рецептора адф на тромбоцитах
JP2017504611A5 (cg-RX-API-DMAC7.html)
LTC1562603I2 (lt) Nauji vaistai, skirti lėtinių obstrukcinių plaučių ligų gydymui
WO2010078486A3 (en) Opioid-containing oral pharmaceutical compositions and methods
EA200702541A1 (ru) Полиморфы этилового эфира 3-[(2-{[4-(гексилоксикарбониламиноиминометил)фениламино]метил}-1-метил-1н-бензимидазол-5-карбонил)пиридин-2-иламино]пропионовой кислоты
JP2015511621A5 (cg-RX-API-DMAC7.html)
JO3021B1 (ar) احادي هيدرات 4-[ 4-{[4- كلورو - 3- (ثلاثي فلورو ميثيل) فينيل ] كربامويل} امينو] -3- فلورو فينوكسي] -n- ميثيل بيريدين -2- كربوكساميد
EA201070598A1 (ru) Терапевтическое применение соединений, обладающих комбинированной активностью в отношении sert, 5-htи 5-ht
TWI370817B (en) Novel crystalline form of bis[(e)-7-[4-(4-fluorophenyl)-6-isopropyl-2-[ methyl(methylsulfonyl)amino]pyrimidin-5-yl](3r,5s)-3,5-dihydroxyhept-6-enoic acid] calcium salt,and relevant manufacture process, pharmaceutical composition, and use
JP2016521279A5 (cg-RX-API-DMAC7.html)
WO2009157014A3 (en) A process for preparing hmg-coa reductase inhibitors and intermediates
NZ594369A (en) Combination of HMG-CoA reductase inhibitors with phosphodiesterase 4 inhibitors for the treatment of inflammatory pulmonary diseases
EP3255043A3 (en) N-(6-((2r,3s)-3,4-dihydroxybutan-2-yloxy)-2-(4-fluorobenzylthio)pyrimidin-4-yl)-3- methylazetidine-1-sulfonamide as chemokine receptor modulator
EA200501058A1 (ru) Фармацевтическая комбинация из телмисартана и аторвастатина для профилактики или терапевтического лечения сердечно-сосудистых, сердечно-легочных, легочных или почечных заболеваний
WO2008020314A3 (en) Statin stabilizing dosage formulations
WO2010030201A3 (en) Stable oral pharmaceutical composition containing a pharmaceutically acceptable salt of [(e)-7-[4-(4-fluorophenyl)-6-isopropyl-2- [methyl(methylsulfonyl)amino]pyrimidine-5-yl] (3r, 5s) - 3,5 dihydroxyhept-6- enoic acid
PL1704144T3 (pl) Sposób wytwarzania soli wapniowej kwasu (E)-7-[4-(4-fluorofenylo)-6-izopropylo-2-[metylo(metylosulfonylo)amino]pirymidyn-5-ylo](3R,5S)-3,5-dihydroksy-6-heptenowego
EP2636677A4 (en) CDK-HEMMENDES PYRROLOPYRIMIDINONCARBOXAMID DERIVATIVE OR PHARMACEUTICAL ACCEPTABLE SALT AND THE PHARMACEUTICAL COMPOSITION CONTAINING THEREOF FOR THE PREVENTION OR TREATMENT OF LIVER CELL CARCINOMA
WO2007071357A3 (en) Pharmaceutical composition comprising (e) -7- [4- (4-fluorophenyl) -6-isopropyl-2- [methyl (methylsulfonyl) amino] pyrimidin-5 -yl- (3r, 5s) -3, 5-dihydr0xyhept-6-en0ic acid
BR112013012699A2 (pt) "método para preparação de sais de rosuvastatina".