ATE417827T1 - Fluvastatin-natrium in der kristallform xiv, verfahren zu deren herstellung, diese enthaltende zusammensetzungen und enstprechende anwendungsverfahren - Google Patents

Fluvastatin-natrium in der kristallform xiv, verfahren zu deren herstellung, diese enthaltende zusammensetzungen und enstprechende anwendungsverfahren

Info

Publication number
ATE417827T1
ATE417827T1 AT04755797T AT04755797T ATE417827T1 AT E417827 T1 ATE417827 T1 AT E417827T1 AT 04755797 T AT04755797 T AT 04755797T AT 04755797 T AT04755797 T AT 04755797T AT E417827 T1 ATE417827 T1 AT E417827T1
Authority
AT
Austria
Prior art keywords
crystal form
fluvastatin sodium
fluvastatin
sodium
processes
Prior art date
Application number
AT04755797T
Other languages
English (en)
Inventor
Revital Lifshitz-Liron
Tamas Koltai
Judith Aronhime
Nurit Perlman
Original Assignee
Teva Pharma
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
Application filed by Teva Pharma filed Critical Teva Pharma
Application granted granted Critical
Publication of ATE417827T1 publication Critical patent/ATE417827T1/de

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
    • C07D209/04—Indoles; Hydrogenated indoles
    • C07D209/10—Indoles; Hydrogenated indoles with substituted hydrocarbon radicals attached to carbon atoms of the hetero ring
    • C07D209/12—Radicals substituted by oxygen atoms
    • 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
    • A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
    • A61K31/403—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil condensed with carbocyclic rings, e.g. carbazole
    • A61K31/404—Indoles, e.g. pindolol
    • 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
    • A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
    • A61K31/403—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil condensed with carbocyclic rings, e.g. carbazole
    • A61K31/404—Indoles, e.g. pindolol
    • A61K31/405—Indole-alkanecarboxylic acids; Derivatives thereof, e.g. tryptophan, indomethacin
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00—Drugs for disorders of the metabolism
    • A61P3/06—Antihyperlipidemics
    • 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
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system
    • A61P9/04—Inotropic agents, i.e. stimulants of cardiac contraction; Drugs for heart failure
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system
    • A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
    • C07D209/04—Indoles; Hydrogenated indoles
    • C07D209/10—Indoles; Hydrogenated indoles with substituted hydrocarbon radicals attached to carbon atoms of the hetero ring
    • C07D209/18—Radicals substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
    • C07D209/24—Radicals substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals with an alkyl or cycloalkyl radical attached to the ring nitrogen atom
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
    • C07B2200/00—Indexing scheme relating to specific properties of organic compounds
    • C07B2200/13—Crystalline forms, e.g. polymorphs

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Cardiology (AREA)
  • Epidemiology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Hospice & Palliative Care (AREA)
  • Urology & Nephrology (AREA)
  • Diabetes (AREA)
  • Hematology (AREA)
  • Obesity (AREA)
  • Vascular Medicine (AREA)
  • Indole Compounds (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
AT04755797T 2003-06-18 2004-06-18 Fluvastatin-natrium in der kristallform xiv, verfahren zu deren herstellung, diese enthaltende zusammensetzungen und enstprechende anwendungsverfahren ATE417827T1 (de)

Applications Claiming Priority (6)

Application Number Priority Date Filing Date Title
US47918203P 2003-06-18 2003-06-18
US48309903P 2003-06-30 2003-06-30
US48574803P 2003-07-10 2003-07-10
US49379303P 2003-08-11 2003-08-11
US50795403P 2003-10-03 2003-10-03
US54546604P 2004-02-19 2004-02-19

Publications (1)

Publication Number Publication Date
ATE417827T1 true ATE417827T1 (de) 2009-01-15

Family

ID=33545688

Family Applications (1)

Application Number Title Priority Date Filing Date
AT04755797T ATE417827T1 (de) 2003-06-18 2004-06-18 Fluvastatin-natrium in der kristallform xiv, verfahren zu deren herstellung, diese enthaltende zusammensetzungen und enstprechende anwendungsverfahren

Country Status (14)

Country Link
US (4) US7414140B2 (de)
EP (9) EP1636184A2 (de)
JP (3) JP2007524619A (de)
KR (6) KR20070094805A (de)
CN (1) CN1849304A (de)
AT (1) ATE417827T1 (de)
CA (6) CA2610635A1 (de)
DE (1) DE602004018494D1 (de)
ES (1) ES2317012T3 (de)
IL (2) IL172514A0 (de)
MX (2) MXPA05013895A (de)
PL (1) PL1638937T3 (de)
PT (1) PT1638937E (de)
WO (2) WO2004113291A2 (de)

Families Citing this family (28)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR100871621B1 (ko) * 2003-06-02 2008-12-02 테바 파마슈티컬 인더스트리즈 리미티드 발라시클로비르 히드로클로라이드의 신규한 결정질 형태
JP2007524619A (ja) * 2003-06-18 2007-08-30 テバ ファーマシューティカル インダストリーズ リミティド フルバスタチンナトリウム結晶型、その調製方法、これを含有する組成物、およびその使用法
US7368581B2 (en) * 2003-06-18 2008-05-06 Teva Pharmaceutical Industries Ltd. Process for the preparation of fluvastatin sodium crystal from XIV
US7368468B2 (en) * 2003-06-18 2008-05-06 Teva Pharmaceutical Industries Ltd. Fluvastatin sodium crystal forms XIV, LXXIII, LXXIX, LXXX and LXXXVII, processes for preparing them, compositions containing them and methods of using them
WO2005037787A1 (en) * 2003-10-16 2005-04-28 Ciba Specialty Chemicals Holding Inc. Crystalline form of fluvastatin sodium
US20070179166A1 (en) * 2003-12-24 2007-08-02 Valerie Niddam-Hildesheim Process for preparation of statins with high syn to anti ratio
US7851624B2 (en) * 2003-12-24 2010-12-14 Teva Pharamaceutical Industries Ltd. Triol form of rosuvastatin and synthesis of rosuvastatin
WO2005080332A1 (en) * 2004-01-14 2005-09-01 Cadila Healthcare Limited Novel form of fluvastatin sodium
WO2006030304A2 (en) * 2004-09-17 2006-03-23 Ranbaxy Laboratories Limited Novel forms of fluvastatin sodium, processes for preparation and pharmaceutical compositions thereof
US8115013B2 (en) * 2004-10-05 2012-02-14 Biocon Limited Process for the preparation of amorphous fluvastatin sodium
WO2006085338A2 (en) * 2005-02-11 2006-08-17 Jubilant Organosys Limited Novel polymorphic forms of fluvastatin sodium and process for preparing the same
CA2601401A1 (en) * 2005-03-22 2006-09-28 Usv Limited Novel polymorph form g of fluvastatin sodium and process for the preparation thereof
WO2006109147A1 (en) * 2005-04-12 2006-10-19 Glenmark Pharmaceuticals Limited Substantially pure amorphous fluvastatin, processes for its preparation and pharmaceutical compositions containing same
DE07752084T1 (de) * 2006-02-27 2008-06-05 Teva Pharmaceutical Industries Ltd. Neuartige formen von fluvastatin-natrium und herstellung davon
EP1847529B1 (de) 2006-04-20 2009-05-20 F.I.S. Fabbrica Italiana Sintetici S.P.A. Verfahren zur Herstellung von Fluvastatin-Natrium
US20110052688A1 (en) * 2006-11-21 2011-03-03 San-Laung Chow Solid dispersion composition
ES2321571B1 (es) * 2007-07-18 2010-03-11 Ercros Industrial, S.A. Solvatos de fluvastatina sodica y su utilizacion como intermedios en la obtencion de fluvastatina sodica amorfa.
CN101250153B (zh) * 2008-02-26 2013-09-18 深圳信立泰药业股份有限公司 一种制备氟伐他汀钠晶型的工艺
US20120035374A1 (en) * 2009-04-15 2012-02-09 Pharmathen S.A. Process for the preparation of fluvastatin and salts thereof
WO2011117875A1 (en) * 2010-03-26 2011-09-29 Hetero Research Foundation Salts of fluvastatin and process for the preparation of substantially amorphous fluvastatin sodium
KR101220266B1 (ko) * 2012-04-19 2013-01-09 홍종옥 수치지도 이미지 제작을 위한 항공영상 이미지 기반 정밀 영상도화 시스템
KR101308745B1 (ko) * 2012-07-04 2013-09-16 주식회사 동운 지리공간정보가 적용된 멀티 기능 기반의 수치지도 시스템
KR101220271B1 (ko) * 2012-07-05 2013-01-10 대한항업(주) 지피에스 기반 실사 지상물의 게시를 위한 수치지도 제작 시스템
KR101273416B1 (ko) * 2012-07-25 2013-06-11 주식회사 동운 좌표정보 및 지형정보 합성을 통한 정밀 수치지도 제작 시스템
KR101217854B1 (ko) * 2012-09-14 2013-01-02 (주)아세아항측 정밀 디에스엠 및 디티엠 정보와 지상 기준점 정보의 정밀해석을 통한 수치지도 높이오차 확인시스템
KR102495018B1 (ko) 2013-11-15 2023-02-06 아케비아 테라퓨틱스 인코포레이티드 ｛[5-(3-클로로페닐)-3-하이드록시피리딘-2-카보닐]아미노｝아세트산의 고체형, 이의 조성물 및 용도
KR20180086508A (ko) * 2015-12-17 2018-07-31 아르퀼 인코포레이티드 치환된 5,6-디하이드로-6-페닐벤조[f]이소퀴놀린-2-아민 화합물의 고체 형태
EP4434967A1 (de) 2023-03-21 2024-09-25 F.I.S.- Fabbrica Italiana Sintetici S.p.A. Verfahren zur herstellung einer kristallinen form von fluvastatin-natriumsalz

Family Cites Families (34)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4231938A (en) 1979-06-15 1980-11-04 Merck & Co., Inc. Hypocholesteremic fermentation products and process of preparation
US4444784A (en) 1980-08-05 1984-04-24 Merck & Co., Inc. Antihypercholesterolemic compounds
DK149080C (da) 1980-06-06 1986-07-28 Sankyo Co Fremgangsmaade til fremstilling af derivater af ml-236b-carboxylsyre
US5354772A (en) 1982-11-22 1994-10-11 Sandoz Pharm. Corp. Indole analogs of mevalonolactone and derivatives thereof
US4739073A (en) 1983-11-04 1988-04-19 Sandoz Pharmaceuticals Corp. Intermediates in the synthesis of indole analogs of mevalonolactone and derivatives thereof
JP2569746B2 (ja) 1987-08-20 1997-01-08 日産化学工業株式会社 キノリン系メバロノラクトン類
NO177005C (no) 1988-01-20 1995-07-05 Bayer Ag Analogifremgangsmåte for fremstilling av substituerte pyridiner, samt mellomprodukter til bruk ved fremstillingen
US5003080A (en) 1988-02-22 1991-03-26 Warner-Lambert Company Process for trans-6-(2-(substituted-pyrrol-1-yl)alkyl)pryan-2-one inhibitors of cholesterol synthesis
DE68911834T2 (de) 1988-10-13 1994-06-23 Sandoz Ag Verfahren zur Herstellung von 7-substituierten Hept-6-en- und Heptansäuren und Derivaten davon.
US5189164A (en) 1989-05-22 1993-02-23 Sandoz Ltd. Processes for the synthesis of syn-(E)-3,5-dihydroxy-7-substituted hept-6-enoic and heptanoic acids and derivatives and intermediates thereof
FR2655047A1 (fr) * 1989-11-24 1991-05-31 Pf Medicament Derives d'etoposide, leur preparation et leur application comme intermediaires de synthese.
EP0463553A1 (de) * 1990-06-29 1992-01-02 Biochemie Gesellschaft M.B.H. Cephalosporin-Derivat
US5177080A (en) 1990-12-14 1993-01-05 Bayer Aktiengesellschaft Substituted pyridyl-dihydroxy-heptenoic acid and its salts
US5202029A (en) 1991-03-13 1993-04-13 Caron Kabushiki Kaisha Process for purification of hmg-coa reductase inhibitors
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
HU217629B (hu) * 1991-12-12 2000-03-28 Novartis Ag. Eljárás fluvasztatint tartalmazó stabilizált gyógyszerkészítmények előállítására
JPH1067795A (ja) * 1996-03-01 1998-03-10 Takeda Chem Ind Ltd エリスロマイシン誘導体の製造法
PT907639E (pt) * 1996-06-24 2003-06-30 Novartis Ag Compostos polimorficos
HRP980037B1 (en) * 1997-01-27 2002-04-30 Warner Lambert Co Method of making (1s, 4r)-1-azabicyclo/2.2.1/heptan-3-one and (1r, 4s), 1-azabicyclo/2.2.1/heptan-3-one
JP2002539108A (ja) 1999-03-08 2002-11-19 メルク エンド カムパニー インコーポレーテッド 結晶質水和ジヒドロキシオープンアシッドシンバスタチンカルシウム塩
US6387925B1 (en) * 1999-06-01 2002-05-14 Pfizer Inc. Polymorphs of a crystalline azo-bicyclo (2.2.2) oct-3-yl amine citrate and their pharmaceutical compositions
ATE263767T1 (de) * 1999-06-03 2004-04-15 Eisai Co Ltd Kristalline cabapenemderivate und pharmazeutische zubereitungen zur injektion
DE60112956T2 (de) * 2000-10-31 2006-06-14 Ciba Sc Holding Ag Kristalline formen von fluvastatin sodium
US7317123B2 (en) 2001-07-06 2008-01-08 Teva Pharmaceutical Industries, Ltd Process for preparation of 7-amino syn 3,5-dihydroxy heptanoic acid derivatives, intermediates thereof and methods for their preparation
IL159861A0 (en) * 2001-08-03 2004-06-20 Ciba Sc Holding Ag Crystalline forms of fluvastatin sodium
CA2486557A1 (en) * 2002-06-13 2003-12-24 Novartis Ag Calcium salts of indole derived statins
JP2007524619A (ja) 2003-06-18 2007-08-30 テバ ファーマシューティカル インダストリーズ リミティド フルバスタチンナトリウム結晶型、その調製方法、これを含有する組成物、およびその使用法
US7368468B2 (en) 2003-06-18 2008-05-06 Teva Pharmaceutical Industries Ltd. Fluvastatin sodium crystal forms XIV, LXXIII, LXXIX, LXXX and LXXXVII, processes for preparing them, compositions containing them and methods of using them
WO2005037787A1 (en) * 2003-10-16 2005-04-28 Ciba Specialty Chemicals Holding Inc. Crystalline form of fluvastatin sodium
US7241800B2 (en) * 2004-03-17 2007-07-10 Mai De Ltd. Anhydrous amorphous form of fluvastatin sodium
WO2006030304A2 (en) 2004-09-17 2006-03-23 Ranbaxy Laboratories Limited Novel forms of fluvastatin sodium, processes for preparation and pharmaceutical compositions thereof
US8115013B2 (en) 2004-10-05 2012-02-14 Biocon Limited Process for the preparation of amorphous fluvastatin sodium
WO2006109147A1 (en) 2005-04-12 2006-10-19 Glenmark Pharmaceuticals Limited Substantially pure amorphous fluvastatin, processes for its preparation and pharmaceutical compositions containing same
US7432980B2 (en) * 2005-08-05 2008-10-07 Terawins, Inc. Method for reducing analog PLL jitter in video application

Also Published As

Publication number Publication date
CA2529859A1 (en) 2004-12-29
EP1790635A2 (de) 2007-05-30
KR20070094805A (ko) 2007-09-21
JP2007525469A (ja) 2007-09-06
EP1636184A2 (de) 2006-03-22
MXPA05013895A (es) 2006-03-09
KR20070092993A (ko) 2007-09-14
WO2004113292A2 (en) 2004-12-29
CA2610635A1 (en) 2004-12-29
KR20070092994A (ko) 2007-09-14
EP1790634A2 (de) 2007-05-30
WO2004113291A3 (en) 2005-04-14
JP4037898B2 (ja) 2008-01-23
EP1638937B1 (de) 2008-12-17
KR20060024426A (ko) 2006-03-16
WO2004113291A2 (en) 2004-12-29
EP1719760A3 (de) 2007-03-21
MXPA05013896A (es) 2006-03-09
EP1752448A2 (de) 2007-02-14
EP1790634A3 (de) 2007-06-13
WO2004113292B1 (en) 2005-11-10
CA2613013A1 (en) 2004-12-29
EP1719759A3 (de) 2007-03-21
EP1719760A2 (de) 2006-11-08
US20090209611A1 (en) 2009-08-20
US7414140B2 (en) 2008-08-19
PL1638937T3 (pl) 2009-06-30
WO2004113292A3 (en) 2005-10-20
PT1638937E (pt) 2009-01-27
IL172514A0 (en) 2006-04-10
KR20060024428A (ko) 2006-03-16
JP2007302693A (ja) 2007-11-22
IL172512A0 (en) 2006-04-10
US20080146817A1 (en) 2008-06-19
CA2610633A1 (en) 2004-12-29
EP1790635A3 (de) 2007-06-13
CA2613021A1 (en) 2004-12-29
EP1726583A3 (de) 2007-05-09
US20050032884A1 (en) 2005-02-10
EP1638937A2 (de) 2006-03-29
EP1719759A2 (de) 2006-11-08
CN1849304A (zh) 2006-10-18
ES2317012T3 (es) 2009-04-16
EP1752448A3 (de) 2007-03-14
CA2529820A1 (en) 2004-12-29
KR20070092995A (ko) 2007-09-14
EP1726583A2 (de) 2006-11-29
US20090118518A1 (en) 2009-05-07
EP1780200A1 (de) 2007-05-02
DE602004018494D1 (de) 2009-01-29
US7687642B2 (en) 2010-03-30
JP2007524619A (ja) 2007-08-30

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