WO2010056059A3 - Novel crystalline dexlansoprazole and pharmaceutical composition comprising same - Google Patents
Novel crystalline dexlansoprazole and pharmaceutical composition comprising same Download PDFInfo
- Publication number
- WO2010056059A3 WO2010056059A3 PCT/KR2009/006678 KR2009006678W WO2010056059A3 WO 2010056059 A3 WO2010056059 A3 WO 2010056059A3 KR 2009006678 W KR2009006678 W KR 2009006678W WO 2010056059 A3 WO2010056059 A3 WO 2010056059A3
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- pharmaceutical composition
- same
- novel crystalline
- crystalline dexlansoprazole
- dexlansoprazole
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- 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
- A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
- A61K31/4439—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/04—Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
A crystalline (+)-lansoprazole, whose X-ray diffraction spectrum comprises a major peak having a relative intensity of at least 20 % at an interplanar distance (d value) of 17.4 A, is homogeneous, non-hygroscopic, and stable, and a pharmaceutical composition comprising said crystal is effective for treating or preventing gastric acid-related diseases.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
KR1020117013635A KR101321055B1 (en) | 2008-11-14 | 2009-11-13 | Novel crystalline dexlansoprazole and pharmaceutical composition comprising same |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
KR20080113507 | 2008-11-14 | ||
KR10-2008-0113507 | 2008-11-14 |
Publications (2)
Publication Number | Publication Date |
---|---|
WO2010056059A2 WO2010056059A2 (en) | 2010-05-20 |
WO2010056059A3 true WO2010056059A3 (en) | 2010-07-29 |
Family
ID=42170531
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/KR2009/006678 WO2010056059A2 (en) | 2008-11-14 | 2009-11-13 | Novel crystalline dexlansoprazole and pharmaceutical composition comprising same |
Country Status (2)
Country | Link |
---|---|
KR (1) | KR101321055B1 (en) |
WO (1) | WO2010056059A2 (en) |
Families Citing this family (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2012095859A1 (en) * | 2011-01-12 | 2012-07-19 | Hetero Research Foundation | Polymorphs of dexlansoprazole salts |
WO2012176140A1 (en) * | 2011-06-21 | 2012-12-27 | Ranbaxy Laboratories Limited | Process for the preparation of dexlansoprazole |
WO2013140120A1 (en) | 2012-03-22 | 2013-09-26 | Cipla Limited | Glycerol solvate forms of (r) - 2 - [ [ [3 -methyl -4 (2,2, 2 - trifluoroethoxy) pyridin- 2 - yl] methyl] sulphinyl] - 1h - ben zimidazole |
WO2016174664A1 (en) | 2015-04-29 | 2016-11-03 | Dexcel Pharma Technologies Ltd. | Orally disintegrating compositions |
US10076494B2 (en) | 2016-06-16 | 2018-09-18 | Dexcel Pharma Technologies Ltd. | Stable orally disintegrating pharmaceutical compositions |
CN106279107A (en) * | 2016-08-10 | 2017-01-04 | 成都尚药科技有限公司 | A kind of preparation method of Dexlansoprazole crystal formation |
CN106749182A (en) * | 2016-11-08 | 2017-05-31 | 山东裕欣药业有限公司 | A kind of Dexlansoprazole crystal-form compound and preparation method thereof |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6462058B1 (en) * | 1999-06-17 | 2002-10-08 | Takeda Chemical Industries, Ltd. | Benzimidazole compound crystal |
US6608092B1 (en) * | 1999-06-30 | 2003-08-19 | Takeda Chemical Industries, Ltd. | Crystals of benzimidazole compounds |
US7285668B2 (en) * | 2000-12-01 | 2007-10-23 | Takeda Pharmaceutical Company Limited | Process for the crystallization of (R)- or (S)-lansoprazole |
EP1889841A1 (en) * | 2005-06-07 | 2008-02-20 | Takeda Pharmaceutical Company Limited | Crystal of salt of benzimidazole compound |
-
2009
- 2009-11-13 WO PCT/KR2009/006678 patent/WO2010056059A2/en active Application Filing
- 2009-11-13 KR KR1020117013635A patent/KR101321055B1/en not_active IP Right Cessation
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6462058B1 (en) * | 1999-06-17 | 2002-10-08 | Takeda Chemical Industries, Ltd. | Benzimidazole compound crystal |
US6608092B1 (en) * | 1999-06-30 | 2003-08-19 | Takeda Chemical Industries, Ltd. | Crystals of benzimidazole compounds |
US7285668B2 (en) * | 2000-12-01 | 2007-10-23 | Takeda Pharmaceutical Company Limited | Process for the crystallization of (R)- or (S)-lansoprazole |
EP1889841A1 (en) * | 2005-06-07 | 2008-02-20 | Takeda Pharmaceutical Company Limited | Crystal of salt of benzimidazole compound |
Also Published As
Publication number | Publication date |
---|---|
KR20110086607A (en) | 2011-07-28 |
KR101321055B1 (en) | 2013-10-23 |
WO2010056059A2 (en) | 2010-05-20 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
WO2010056059A3 (en) | Novel crystalline dexlansoprazole and pharmaceutical composition comprising same | |
WO2006123113A3 (en) | Pyrazolylaminopyrimidine derivatives useful as tyrosine kinase inhibitors | |
MY149512A (en) | Pyrazolylaminopyridine derivatives useful as kinase inhibitors | |
WO2008079339A3 (en) | Tetracycline derivatives for the treatment of bacterial, viral and parasitic infections | |
WO2007117778A3 (en) | Quinolones useful as inducible nitric oxide synthase inhibitors | |
WO2010022055A3 (en) | 1, 3, 5 -triaz ine derivatives useful in the treatment of chronic pain disorders | |
WO2005075425A3 (en) | Substituted bisarylurea derivatives as kinase inhibitors | |
EA200601273A1 (en) | NEW CRYSTAL FORM V AGOMELATIN, THE METHOD OF ITS OBTAINING AND PHARMACEUTICAL COMPOSITIONS THAT HERE CONTAINS | |
WO2006104668A3 (en) | Composition and methods for the treatment of proliferative diseases | |
WO2007101864A3 (en) | Compounds that modulate ppar activity, their preparation and use | |
WO2005117867A3 (en) | Monocyclic heterocycles as kinase inhibitors | |
WO2007096151A3 (en) | Inhibitors of p38-kinase for treatment of pulmonary hypertension | |
WO2007059230A3 (en) | Substituted 1h-benzimidazole-4-carboxamides are potent parp inhibitors | |
WO2009010139A3 (en) | Quinazolinamide derivatives | |
EA200802119A1 (en) | NEW CRYSTAL FORM VI OF AGOMELATIN, THE METHOD OF ITS OBTAINING AND PHARMACEUTICAL COMPOSITIONS THAT HERE CONTAINS | |
IL196543A (en) | Pyridazinone derivatives and pharmaceutical compositions comprising them for use in the treatment of disorders | |
MX2009006630A (en) | 4-imidazolyl-1,2,3,4-tetrahydroquinoline derivatives and their use as aldosterone/11-beta-hydroxylase inhibitors. | |
WO2005110994A8 (en) | Substituted pyrazolyl urea derivatives useful in the treatment of cancer | |
WO2008135826A3 (en) | 2 -pyridine carboxamide derivatives as sodium channel modulators | |
WO2006102610A3 (en) | Bicycloheteroaryl compounds as p2x7 modulators and uses thereof | |
WO2010002655A3 (en) | Pyrimidine derivatives as kinase inhibitors | |
EA200601271A1 (en) | NEW CRYSTAL FORM IV OF AGOMELATIN, THE METHOD OF ITS OBTAINING AND PHARMACEUTICAL COMPOSITIONS THAT HERE CONTAINS | |
WO2005080352A3 (en) | Quinazoline derivatives and therapeutic use thereof | |
WO2008073452A8 (en) | Compositions, synthesis, and methods of using indanone based cholinesterase inhibitors | |
WO2009158431A3 (en) | Pyrimidine derivatives as kinase inhibitors |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
121 | Ep: the epo has been informed by wipo that ep was designated in this application |
Ref document number: 09826291 Country of ref document: EP Kind code of ref document: A2 |
|
NENP | Non-entry into the national phase |
Ref country code: DE |
|
ENP | Entry into the national phase |
Ref document number: 20117013635 Country of ref document: KR Kind code of ref document: A |
|
122 | Ep: pct application non-entry in european phase |
Ref document number: 09826291 Country of ref document: EP Kind code of ref document: A2 |