JP2009519985A5 - - Google Patents

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Publication number
JP2009519985A5
JP2009519985A5 JP2008546216A JP2008546216A JP2009519985A5 JP 2009519985 A5 JP2009519985 A5 JP 2009519985A5 JP 2008546216 A JP2008546216 A JP 2008546216A JP 2008546216 A JP2008546216 A JP 2008546216A JP 2009519985 A5 JP2009519985 A5 JP 2009519985A5
Authority
JP
Japan
Prior art keywords
pharmaceutical composition
pyrimidin
isopropyl
methyl
methylsulfonyl
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.)
Granted
Application number
JP2008546216A
Other languages
English (en)
Japanese (ja)
Other versions
JP2009519985A (ja
JP5235676B2 (ja
Filing date
Publication date
Application filed filed Critical
Priority claimed from PCT/EP2006/012180 external-priority patent/WO2007071357A2/en
Publication of JP2009519985A publication Critical patent/JP2009519985A/ja
Publication of JP2009519985A5 publication Critical patent/JP2009519985A5/ja
Application granted granted Critical
Publication of JP5235676B2 publication Critical patent/JP5235676B2/ja
Expired - Fee Related legal-status Critical Current
Anticipated expiration legal-status Critical

Links

JP2008546216A 2005-12-20 2006-12-18 (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−ジヒドロキシヘプタ−6−エン酸を含む医薬組成物 Expired - Fee Related JP5235676B2 (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
SI200500344 2005-12-20
SIP200500344 2005-12-20
PCT/EP2006/012180 WO2007071357A2 (en) 2005-12-20 2006-12-18 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

Publications (3)

Publication Number Publication Date
JP2009519985A JP2009519985A (ja) 2009-05-21
JP2009519985A5 true JP2009519985A5 (enExample) 2013-03-28
JP5235676B2 JP5235676B2 (ja) 2013-07-10

Family

ID=37866173

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2008546216A Expired - Fee Related JP5235676B2 (ja) 2005-12-20 2006-12-18 (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−ジヒドロキシヘプタ−6−エン酸を含む医薬組成物

Country Status (9)

Country Link
US (1) US20090093499A1 (enExample)
EP (1) EP1968593B1 (enExample)
JP (1) JP5235676B2 (enExample)
CN (1) CN101330919B (enExample)
AU (1) AU2006329006B2 (enExample)
BR (1) BRPI0620629B8 (enExample)
CA (1) CA2630704C (enExample)
EA (1) EA015682B1 (enExample)
WO (1) WO2007071357A2 (enExample)

Families Citing this family (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2008036286A1 (en) 2006-09-18 2008-03-27 Teva Pharmaceutical Industries Ltd. Crystalline rosuvastatin calcium
EP2285353A1 (en) * 2008-01-30 2011-02-23 Lupin Limited Modified release formulations of hmg coa reductase inhibitors
EP2138165A1 (en) 2008-06-27 2009-12-30 KRKA, tovarna zdravil, d.d., Novo mesto Pharmaceutical composition comprising a statin
HRP20180077T1 (hr) * 2008-06-27 2018-02-23 Krka, Tovarna Zdravil D.D., Novo Mesto Farmaceutski sastav koji sadrži statin
PL386051A1 (pl) * 2008-09-09 2010-03-15 Zakłady Farmaceutyczne POLPHARMA Spółka Akcyjna Stabilna doustna kompozycja farmaceutyczna zawierająca farmaceutycznie dopuszczalną sól kwsu [(E)-7-[4-(4-fluorofenylo)-6-izopropylo-2-[metylo(metylosulfonylo)amino]pirymidyn-5-ylo] (3R,5S)-3,5-dihydroksyhept-6-enowego
TR200902077A2 (tr) 2009-03-17 2010-01-21 Sanovel İlaç San.Veti̇c.A.Ş. Stabil rosuvastatin kompozisyonları
RU2606592C1 (ru) * 2015-10-07 2017-01-10 Открытое Акционерное Общество "Татхимфармпрепараты" Фармацевтическая композиция, содержащая кальциевую соль розувастатина (варианты)
AU2020417043A1 (en) * 2019-12-31 2022-06-09 Pfizer Inc. Stable immediate release tablet and capsule formulations of 1-((2S,5R)-5-((7H-pyrrolo[2,3-d]pyrimidin-4-yl)amino)-2-methylpiperidin-1-yl)prop-2-en-1-one

Family Cites Families (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
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
GB0000710D0 (en) * 1999-02-06 2000-03-08 Zeneca Ltd Drug combination
GB0001621D0 (en) * 2000-01-26 2000-03-15 Astrazeneca Ab Pharmaceutical compositions
US6399101B1 (en) * 2000-03-30 2002-06-04 Mova Pharmaceutical Corp. Stable thyroid hormone preparations and method of making same
EP1368000A4 (en) * 2001-03-13 2004-12-01 Penwest Pharmaceuticals Co CHRONOTHERAPEUTIC PHARMACEUTICAL FORMS CONTAINING A GLUCOCORTICOSTEROID
SE0101329D0 (sv) * 2001-04-12 2001-04-12 Astrazeneca Ab Pharmaceutical formulation
GB0111077D0 (en) * 2001-05-04 2001-06-27 Biochemie Gmbh Organic compounds
US20030215502A1 (en) * 2002-03-20 2003-11-20 Elan Pharma International Limited Fast dissolving dosage forms having reduced friability
WO2003090723A1 (en) * 2002-04-23 2003-11-06 Bristol-Myers Squibb Company Modified-release vasopeptidase inhibitor formulation, combinations and method
CA2483099A1 (en) * 2002-05-03 2003-11-13 Hexal Ag Stable pharmaceutical formulation for a combination of a statin and an ace inhibitor
SI21402A (sl) * 2003-02-12 2004-08-31 LEK farmacevtska dru�ba d.d. Obloženi delci in farmacevtske oblike
WO2005040134A1 (en) * 2003-10-22 2005-05-06 Ranbaxy Laboratories Limited Process for the preparation of amorphous rosuvastatin calcium
US8987322B2 (en) * 2003-11-04 2015-03-24 Circ Pharma Research And Development Limited Pharmaceutical formulations for carrier-mediated transport statins and uses thereof
CA2546894C (en) * 2003-12-02 2009-09-08 Teva Pharmaceutical Industries Ltd. Reference standard for characterization of rosuvastatin
EP1737828A1 (en) * 2004-01-19 2007-01-03 Ranbaxy Laboratories Limited Amorphous magnesium salts of rosuvastatin
EP1709008A1 (en) * 2004-01-19 2006-10-11 Ranbaxy Laboratories Limited Salts of hmg-coa reductase inhibitors and use thereof

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JP2009519985A5 (enExample)
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MX2008008192A (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