WO2007001065A3 - Methode pour preparer un produit medicamenteux se presentant sous forme de granules humides - Google Patents
Methode pour preparer un produit medicamenteux se presentant sous forme de granules humides Download PDFInfo
- Publication number
- WO2007001065A3 WO2007001065A3 PCT/JP2006/313174 JP2006313174W WO2007001065A3 WO 2007001065 A3 WO2007001065 A3 WO 2007001065A3 JP 2006313174 W JP2006313174 W JP 2006313174W WO 2007001065 A3 WO2007001065 A3 WO 2007001065A3
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- preparation
- drug product
- wet granulated
- granulated drug
- angiotensin
- Prior art date
Links
- 238000000034 method Methods 0.000 title abstract 4
- 238000002360 preparation method Methods 0.000 title abstract 2
- 229940126534 drug product Drugs 0.000 title 1
- 239000000825 pharmaceutical preparation Substances 0.000 title 1
- 229940127291 Calcium channel antagonist Drugs 0.000 abstract 2
- 239000002333 angiotensin II receptor antagonist Substances 0.000 abstract 2
- 229940126317 angiotensin II receptor antagonist Drugs 0.000 abstract 2
- 239000000480 calcium channel blocker Substances 0.000 abstract 2
- 239000007909 solid dosage form Substances 0.000 abstract 2
- 238000004090 dissolution Methods 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- 238000005550 wet granulation Methods 0.000 abstract 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/20—Pills, tablets, discs, rods
- A61K9/2004—Excipients; Inactive ingredients
- A61K9/2022—Organic macromolecular compounds
- A61K9/205—Polysaccharides, e.g. alginate, gums; Cyclodextrin
- A61K9/2054—Cellulose; Cellulose derivatives, e.g. hydroxypropyl methylcellulose
-
- 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
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/4164—1,3-Diazoles
- A61K31/4178—1,3-Diazoles not condensed 1,3-diazoles and containing further heterocyclic rings, e.g. pilocarpine, nitrofurantoin
-
- 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
- A61K31/4422—1,4-Dihydropyridines, e.g. nifedipine, nicardipine
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P13/00—Drugs for disorders of the urinary system
- A61P13/12—Drugs for disorders of the urinary system of the kidneys
-
- 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
-
- 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
- A61P9/06—Antiarrhythmics
-
- 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
-
- 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
- A61P9/12—Antihypertensives
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/14—Particulate form, e.g. powders, Processes for size reducing of pure drugs or the resulting products, Pure drug nanoparticles
- A61K9/16—Agglomerates; Granulates; Microbeadlets ; Microspheres; Pellets; Solid products obtained by spray drying, spray freeze drying, spray congealing,(multiple) emulsion solvent evaporation or extraction
- A61K9/1682—Processes
- A61K9/1694—Processes resulting in granules or microspheres of the matrix type containing more than 5% of excipient
Landscapes
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Veterinary Medicine (AREA)
- Pharmacology & Pharmacy (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Life Sciences & Earth Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Epidemiology (AREA)
- Urology & Nephrology (AREA)
- Hospice & Palliative Care (AREA)
- Vascular Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Medicinal Preparation (AREA)
Abstract
L'invention concerne une méthode pour préparer une forme dosifiée solide comprenant un antagoniste du récepteur II d'angiotensine et un bloqueur de canal de calcium. Cette méthode comprend une étape consistant à préparer, par granulation humide, une composition comprenant l'antagoniste du récepteur II d'angiotensine susmentionné et le bloqueur de canal de calcium susmentionné. La forme dosifiée solide de l'invention obtenue par la méthode de l'invention présente des propriétés de dissolution accrues.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2007558254A JP5063370B2 (ja) | 2005-06-27 | 2006-06-26 | 湿式造粒製薬の調製方法 |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2005-187212 | 2005-06-27 | ||
JP2005187212 | 2005-06-27 |
Publications (2)
Publication Number | Publication Date |
---|---|
WO2007001065A2 WO2007001065A2 (fr) | 2007-01-04 |
WO2007001065A3 true WO2007001065A3 (fr) | 2007-05-03 |
Family
ID=37114405
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/JP2006/313174 WO2007001065A2 (fr) | 2005-06-27 | 2006-06-26 | Methode pour preparer un produit medicamenteux se presentant sous forme de granules humides |
Country Status (3)
Country | Link |
---|---|
JP (1) | JP5063370B2 (fr) |
TW (1) | TWI407978B (fr) |
WO (1) | WO2007001065A2 (fr) |
Families Citing this family (29)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP5769362B2 (ja) * | 2006-06-27 | 2015-08-26 | 第一三共株式会社 | 圧縮製剤 |
TWI399223B (zh) * | 2006-09-15 | 2013-06-21 | Daiichi Sankyo Co Ltd | 奧美沙坦酯及氨氯地平之固體劑型 |
TWI414310B (zh) * | 2006-12-26 | 2013-11-11 | Daiichi Sankyo Co Ltd | 溶出性改善之醫藥品組成物 |
TWI488658B (zh) * | 2006-12-26 | 2015-06-21 | Daiichi Sankyo Co Ltd | 溶出性之改善方法 |
TWI402083B (zh) * | 2006-12-26 | 2013-07-21 | Daiichi Sankyo Co Ltd | 固形製劑及其安定化方法 |
CN101416966B (zh) * | 2007-10-22 | 2010-11-10 | 鲁南制药集团股份有限公司 | 一种治疗高血压的药物组合物 |
EP2253318B1 (fr) * | 2008-03-13 | 2014-08-06 | Daiichi Sankyo Company, Limited | Amélioration de la solubilité d'une préparation contenant de l'olmésartan médoxomil |
JP5296456B2 (ja) * | 2008-08-26 | 2013-09-25 | 大日本住友製薬株式会社 | 溶出が良好なイルベサルタン含有医薬組成物および口腔内崩壊錠 |
CN102292085B (zh) | 2009-01-23 | 2017-01-18 | 韩美科学株式会社 | 包含氨氯地平和氯沙坦的固体药物组合物及其制备方法 |
GEP20135940B (en) * | 2009-04-30 | 2013-10-10 | Takeda Pharmaceuticals Co | Solid preparations |
CN101596195B (zh) * | 2009-05-15 | 2011-09-28 | 迪沙药业集团有限公司 | 降低血压的口服药物组合物 |
PT2448561E (pt) * | 2009-06-30 | 2013-11-21 | Sanofi Sa | Composições farmacêuticas sólidas de dose fixa compreendendo irbesartan e amlodipina, sua preparação e seu aplicação terapêutica |
JP5421945B2 (ja) * | 2010-03-10 | 2014-02-19 | 大日本住友製薬株式会社 | イルベサルタンとアムロジピンまたはその塩を含有する医薬組成物 |
EP2425859A1 (fr) * | 2010-08-08 | 2012-03-07 | Abdi Ibrahim Ilac Sanayi ve Ticaret Anonim Sirketi | Formulations de l'olmesartane |
KR101931489B1 (ko) * | 2012-10-12 | 2018-12-24 | 이에이 파마 가부시키가이샤 | 칼슘 길항약/안지오텐신 ii 수용체 길항약 함유 의약 제제의 제조 방법 |
MX2013001277A (es) * | 2013-01-31 | 2014-07-30 | Miguel Ángel García Pérez | Composicion farmaceutica con un antagonista de los receptores de la angiotensina ii y un bloqueador de los canales de calcio para el tratamiento de la hipertension arterial. |
CN103127110A (zh) * | 2013-03-18 | 2013-06-05 | 吉林省博大伟业制药有限公司 | 含有血管紧张素ⅱ受体拮抗剂和钙通道阻断剂的复方制剂 |
JP5714652B2 (ja) * | 2013-06-13 | 2015-05-07 | 大日本住友製薬株式会社 | 溶出が良好なイルベサルタン含有医薬組成物および口腔内崩壊錠 |
CN104434823A (zh) * | 2013-09-17 | 2015-03-25 | 许昌恒生制药有限公司 | 一种盐酸马尼地平片剂及其制备方法 |
EP2883539A1 (fr) | 2013-12-12 | 2015-06-17 | Sanovel Ilac Sanayi ve Ticaret A.S. | Combinaisons pharmaceutiques d'olmésartan et d'amlodipine |
JP5978335B2 (ja) * | 2015-03-11 | 2016-08-24 | 大日本住友製薬株式会社 | 溶出が良好なイルベサルタン含有医薬組成物および口腔内崩壊錠 |
JP6445923B2 (ja) * | 2015-04-22 | 2018-12-26 | ダイト株式会社 | イルベサルタン含有錠剤の調製方法 |
CN104997778A (zh) * | 2015-07-08 | 2015-10-28 | 南京正大天晴制药有限公司 | 一种奥美沙坦酯氨氯地平药物组合物 |
JP2017210435A (ja) * | 2016-05-25 | 2017-11-30 | ダイト株式会社 | イルベサルタン及びアムロジピンベシル酸塩配合錠の製造方法 |
JP6151413B2 (ja) * | 2016-07-25 | 2017-06-21 | 大日本住友製薬株式会社 | 溶出が良好なイルベサルタン含有医薬組成物および口腔内崩壊錠 |
CN106580992A (zh) * | 2016-11-10 | 2017-04-26 | 许昌恒生制药有限公司 | 一种用于治疗高血压的盐酸马尼地平和厄贝沙坦复合片剂及制备方法 |
JP2017141299A (ja) * | 2017-05-24 | 2017-08-17 | 大日本住友製薬株式会社 | 溶出が良好なイルベサルタン含有医薬組成物および口腔内崩壊錠 |
JP2018168185A (ja) * | 2018-07-05 | 2018-11-01 | 大日本住友製薬株式会社 | 溶出が良好なイルベサルタン含有医薬組成物および口腔内崩壊錠 |
JP2019203031A (ja) * | 2019-09-06 | 2019-11-28 | 大日本住友製薬株式会社 | 溶出が良好なイルベサルタン含有医薬組成物および口腔内崩壊錠 |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20010049384A1 (en) * | 1999-07-08 | 2001-12-06 | Webb Randy Lee | Method of treatment and pharmaceutical composition |
WO2003097045A1 (fr) * | 2002-05-17 | 2003-11-27 | Novartis Ag | Combinaison de composes organiques |
US20040198789A1 (en) * | 2003-02-28 | 2004-10-07 | Recordati Ireland Limited | Lercanidipine/ARB/diuretic therapeutic combinations |
WO2006079496A1 (fr) * | 2005-01-26 | 2006-08-03 | Lek Pharmaceuticals D.D. | Nouvelle composition pharmaceutique contenant candesartan cilexetil en tant que substance cristalline lipophile |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2003034655A (ja) * | 2001-05-15 | 2003-02-07 | Takeda Chem Ind Ltd | 速崩壊性固形製剤 |
JP2003104888A (ja) * | 2001-09-28 | 2003-04-09 | Taiyo Yakuhin Kogyo Kk | ジヒドロピリジン誘導体の錠剤 |
-
2006
- 2006-06-26 WO PCT/JP2006/313174 patent/WO2007001065A2/fr active Application Filing
- 2006-06-26 TW TW095122891A patent/TWI407978B/zh active
- 2006-06-26 JP JP2007558254A patent/JP5063370B2/ja active Active
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20010049384A1 (en) * | 1999-07-08 | 2001-12-06 | Webb Randy Lee | Method of treatment and pharmaceutical composition |
WO2003097045A1 (fr) * | 2002-05-17 | 2003-11-27 | Novartis Ag | Combinaison de composes organiques |
US20040198789A1 (en) * | 2003-02-28 | 2004-10-07 | Recordati Ireland Limited | Lercanidipine/ARB/diuretic therapeutic combinations |
WO2006079496A1 (fr) * | 2005-01-26 | 2006-08-03 | Lek Pharmaceuticals D.D. | Nouvelle composition pharmaceutique contenant candesartan cilexetil en tant que substance cristalline lipophile |
Non-Patent Citations (2)
Title |
---|
BAUER, FRÖMMING, FÜHRER: "Pharmazeutische Technologie", 1997, GUSTAV FISCHER, XP002414403 * |
RUMP L C ET AL: "COMBINATION OF THE ANGIOTENSIN II-RECEPTOR ANTAGONIST OLMESARTAN MEDOXOMIL WITH AMLODIPINE: PHARMACOKINETICS, SAFETY AND TOLERABILITY IN HEALTHY MALE SUBJECTS", JOURNAL OF HYPERTENSION, CURRENT SCIENCE, PHILADELPHIA, PA, US, vol. 22, no. SUPPL 1, 18 February 2004 (2004-02-18), pages 145S, XP008058906, ISSN: 0263-6352 * |
Also Published As
Publication number | Publication date |
---|---|
TWI407978B (zh) | 2013-09-11 |
WO2007001065A2 (fr) | 2007-01-04 |
JP5063370B2 (ja) | 2012-10-31 |
TW200730200A (en) | 2007-08-16 |
JP2008543727A (ja) | 2008-12-04 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
WO2007001065A3 (fr) | Methode pour preparer un produit medicamenteux se presentant sous forme de granules humides | |
WO2007001067A3 (fr) | Forme posologique solide | |
TW200740459A (en) | Pharmaceutical preparation containing an angiotensin II receptor antagonist and a calcium channel blocker | |
WO2008037716A3 (fr) | Compositions pharmaceutiques | |
WO2007052289A3 (fr) | Nouvelle composition de comprime dispersible | |
WO2009022354A3 (fr) | Formes pharmaceutiques modifiées de tacrolimus | |
WO2008051942A3 (fr) | Agonistes du récepteur farnésoïde x | |
WO2006082523A3 (fr) | Compositions pharmaceutiques de metformine | |
AP2303A (en) | d-Crystalline form of ivabradine hydrochloride, a process for its preparation and pharmaceutical compositions containing it. | |
WO2007050802A3 (fr) | Nouveaux antagonistes opioides | |
AP2006003522A0 (en) | Yd-crystalline form of ivabradine hydrochloride, a process for its preparation adn pharmaceutical compositions containing it. | |
WO2007076260A3 (fr) | Agonistes de recepteur de farnesoide x | |
AP2006003521A0 (en) | Y-crystalline form of ivabradine hydrochloride, a process for its preparation and pharmaceutical compositions containing it. | |
PL2054411T3 (pl) | Nowe związki, ich izomery lub ich farmaceutycznie dopuszczalne sole jako antagoniści receptora waniloidowego oraz zawierające je kompozycje farmaceutyczne | |
IL195514A (en) | Converted Pyridyl Compounds | |
WO2007044796A3 (fr) | Composes de pyridazinone servant de calcilytiques | |
WO2010146179A3 (fr) | Composition pharmaceutique solide comprenant du rivaroxaban | |
WO2007097770A8 (fr) | Comprimés de succinate de métoprolol er et méthodes pour leur préparation | |
UA99136C2 (ru) | Улучшенная фармацевтическая композиция, содержащая антагонист кальциевых каналов - лерканидипин, способ ее получения | |
WO2011062437A3 (fr) | Antagonistes des récepteurs de l'hormone de libération des gonadotrophines, leurs procédés de production et composition pharmaceutique les contenant | |
WO2010049449A3 (fr) | Nouveaux sels de sunitinib | |
WO2006123243A3 (fr) | Formes galeniques pharmaceutiques d'un antidepresseur | |
EP2238105A4 (fr) | Nouveaux composés, isomère ou sels pharmaceutiquement acceptables de ces derniers, utilisés comme antagonistes du récepteur vanilloïde, et compositions pharmaceutiques les contenant | |
WO2010012459A3 (fr) | Procédé de préparation de sels de solifénacine et inclusion de ces derniers dans des formes pharmaceutiques | |
WO2010026467A3 (fr) | Forme pharmaceutique à libération prolongée de principe actif hautement soluble |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
121 | Ep: the epo has been informed by wipo that ep was designated in this application | ||
ENP | Entry into the national phase |
Ref document number: 2007558254 Country of ref document: JP Kind code of ref document: A |
|
NENP | Non-entry into the national phase |
Ref country code: DE |
|
122 | Ep: pct application non-entry in european phase |
Ref document number: 06767752 Country of ref document: EP Kind code of ref document: A2 |