KR20120117986A - 활성 약학적 성분 및 고도불포화지방산 에스테르로 이루어진 심혈관 질환 치료용 캡슐 - Google Patents
활성 약학적 성분 및 고도불포화지방산 에스테르로 이루어진 심혈관 질환 치료용 캡슐 Download PDFInfo
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- KR20120117986A KR20120117986A KR1020127015768A KR20127015768A KR20120117986A KR 20120117986 A KR20120117986 A KR 20120117986A KR 1020127015768 A KR1020127015768 A KR 1020127015768A KR 20127015768 A KR20127015768 A KR 20127015768A KR 20120117986 A KR20120117986 A KR 20120117986A
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- polyunsaturated fatty
- fatty acid
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Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2014142607A1 (fr) * | 2013-03-14 | 2014-09-18 | 보령제약 주식회사 | Médicament combiné pharmaceutique |
Families Citing this family (63)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
ES2385240B1 (es) * | 2010-07-26 | 2013-09-23 | Gp-Pharm, S.A. | Cápsulas de principios activos farmacéuticos y ácidos grasos poliinsaturados para el tratamiento de enfermedades de la próstata. |
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WO2013167990A1 (fr) | 2012-05-07 | 2013-11-14 | Mahesh Kandula | Compositions et méthodes de traitement de la dépression |
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US9266823B2 (en) | 2012-05-08 | 2016-02-23 | Cellix Bio Private Limited | Compositions and methods for the treatment of parkinson's disease |
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US9273061B2 (en) | 2012-05-10 | 2016-03-01 | Cellix Bio Private Limited | Compositions and methods for the treatment of chronic pain |
WO2013168012A1 (fr) | 2012-05-10 | 2013-11-14 | Mahesh Kandula | Compositions et méthodes de traitement de troubles respiratoires |
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US9315461B2 (en) | 2012-05-10 | 2016-04-19 | Cellix Bio Private Limited | Compositions and methods for the treatment of neurologic diseases |
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WO2013168016A1 (fr) | 2012-05-10 | 2013-11-14 | Mahesh Kandula | Compositions et méthodes de traitement du syndrome métabolique |
US9346742B2 (en) | 2012-05-10 | 2016-05-24 | Cellix Bio Private Limited | Compositions and methods for the treatment of fibromyalgia pain |
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CN104603100A (zh) | 2012-05-23 | 2015-05-06 | 塞利克斯比奥私人有限公司 | 用于治疗炎症性肠病的组合物和方法 |
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SG11201407326XA (en) | 2012-05-23 | 2014-12-30 | Cellix Bio Private Ltd | Compositions and methods for treatment of mucositis |
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WO2014041445A2 (fr) * | 2012-09-13 | 2014-03-20 | Mahesh Kandula | Compositions et procédés pour le traitement de l'hypertension et la gestion de la néphropathie diabétique |
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FR3002736B1 (fr) | 2013-03-04 | 2015-06-26 | Virbac | Composition orale nutritionnelle et medicamenteuse a usage veterinaire |
FR3002735B1 (fr) * | 2013-03-04 | 2015-07-03 | Virbac | Composition orale nutritionnelle et medicamenteuse a usage veterinaire |
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WO2016046835A1 (fr) | 2014-09-26 | 2016-03-31 | Cellix Bio Private Limited | Compositions et méthodes de traitement de l'épilepsie et de troubles neurologiques |
WO2016051420A1 (fr) | 2014-09-29 | 2016-04-07 | Cellix Bio Private Limited | Compositions et méthodes pour le traitement de la sclérose en plaques |
RU2605848C2 (ru) * | 2014-10-10 | 2016-12-27 | Александр Александрович Кролевец | Способ получения нанокапсул лекарственных препаратов группы цефалоспоринов в интерфероне |
EP3212626B1 (fr) | 2014-10-27 | 2018-11-07 | Cellix Bio Private Limited | Séls á trois composants du ester monométhylique du acid fumarique avec pipérazine ou ethylene diamine pour le traitement de sclérose en plaques |
US9290486B1 (en) | 2014-11-05 | 2016-03-22 | Cellix Bio Private Limited | Compositions and methods for the treatment of epilepsy |
US10208014B2 (en) | 2014-11-05 | 2019-02-19 | Cellix Bio Private Limited | Compositions and methods for the treatment of neurological disorders |
US9321716B1 (en) | 2014-11-05 | 2016-04-26 | Cellix Bio Private Limited | Compositions and methods for the treatment of metabolic syndrome |
US9284287B1 (en) | 2014-11-05 | 2016-03-15 | Cellix Bio Private Limited | Compositions and methods for the suppression of carbonic anhydrase activity |
US9173877B1 (en) | 2014-11-05 | 2015-11-03 | Cellix Bio Private Limited | Compositions and methods for the treatment of local pain |
US9175008B1 (en) | 2014-11-05 | 2015-11-03 | Cellix Bio Private Limited | Prodrugs of anti-platelet agents |
US9150557B1 (en) | 2014-11-05 | 2015-10-06 | Cellix Bio Private Limited | Compositions and methods for the treatment of hyperglycemia |
US9932294B2 (en) | 2014-12-01 | 2018-04-03 | Cellix Bio Private Limited | Compositions and methods for the treatment of multiple sclerosis |
US9206111B1 (en) | 2014-12-17 | 2015-12-08 | Cellix Bio Private Limited | Compositions and methods for the treatment of neurological diseases |
RU2596476C1 (ru) * | 2015-04-27 | 2016-09-10 | Александр Александрович Кролевец | Способ получения нанокапсул лекарственных растений, обладающих спазмолитическим действием |
JP6298435B2 (ja) * | 2015-10-28 | 2018-03-20 | 大原薬品工業株式会社 | アンジオテンシンii受容体拮抗薬を含有する口腔内崩壊錠 |
CN106074542A (zh) * | 2016-08-30 | 2016-11-09 | 佛山市弘泰药物研发有限公司 | 一种阿齐沙坦酯钾盐软胶囊的制备方法 |
KR101914051B1 (ko) * | 2018-07-13 | 2018-12-28 | (주)바이오제닉스 | 숯이 함유된 이중 캡슐 및 이의 제조방법 |
CN114617264A (zh) * | 2020-12-14 | 2022-06-14 | 深圳市前海小藻科技有限公司 | 具有高含量epa的植物胶囊制剂 |
WO2022145443A1 (fr) * | 2020-12-28 | 2022-07-07 | 株式会社Cured | Composition pharmaceutique pour le traitement d'une maladie rénale chronique |
Family Cites Families (47)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5312473B1 (fr) | 1971-05-24 | 1978-05-01 | ||
PH19942A (en) | 1980-11-18 | 1986-08-14 | Sintex Inc | Microencapsulation of water soluble polypeptides |
JPS60100516A (ja) | 1983-11-04 | 1985-06-04 | Takeda Chem Ind Ltd | 徐放型マイクロカプセルの製造法 |
US4830853A (en) | 1986-10-20 | 1989-05-16 | Warner-Lambert Company | Drug compositions stabilized against oxidation |
US4793998A (en) | 1986-10-20 | 1988-12-27 | Warner-Lambert Company | Stabilized drug compositions |
US4743450A (en) | 1987-02-24 | 1988-05-10 | Warner-Lambert Company | Stabilized compositions |
GB2209937B (en) | 1987-09-21 | 1991-07-03 | Depiopharm S A | Water insoluble polypeptides |
DE3739690A1 (de) | 1987-11-24 | 1989-06-08 | Hoechst Ag | Stabilisierte arzneistoffe, verfahren zu ihrer herstellung sowie stabile arzneizubereitungen |
US5035896A (en) | 1988-06-15 | 1991-07-30 | Warner-Lambert Company | Water insoluble drugs coated by coacervated fish gelatin |
HU222489B1 (hu) | 1990-07-25 | 2003-07-28 | Novartis Ag. | Stabilizált gyógyszerkészítmények és eljárás az előállításukra |
CH683149A5 (fr) | 1991-07-22 | 1994-01-31 | Debio Rech Pharma Sa | Procédé pour la préparation de microsphères en matériau polymère biodégradable. |
TW284688B (fr) | 1991-11-20 | 1996-09-01 | Takeda Pharm Industry Co Ltd | |
US5447729A (en) | 1994-04-07 | 1995-09-05 | Pharmavene, Inc. | Multilamellar drug delivery systems |
GB2290965A (en) | 1994-07-11 | 1996-01-17 | Therapicon Srl | Multiple layer capsules for drugs |
TW442301B (en) | 1995-06-07 | 2001-06-23 | Sanofi Synthelabo | Pharmaceutical compositions containing irbesartan |
GB9613470D0 (en) | 1996-06-27 | 1996-08-28 | Ciba Geigy Ag | Small solid oral dosage form |
US6417196B1 (en) | 1998-06-05 | 2002-07-09 | Warner-Lambert Company | Stabilization of quinapril using magnesium oxide |
US20040157911A1 (en) | 1999-08-31 | 2004-08-12 | Spiridon Spireas | Storage-stable and bio-stable formulations of ace inhibitors, and methods for preparation thereof |
HU226950B1 (en) | 1999-11-03 | 2010-03-29 | Richter Gedeon Nyrt | The magnesium salt of enalapril and antihypertensive pharmaceutical composition containing it |
US20030180352A1 (en) * | 1999-11-23 | 2003-09-25 | Patel Mahesh V. | Solid carriers for improved delivery of active ingredients in pharmaceutical compositions |
CA2357982A1 (fr) | 2001-09-28 | 2003-03-28 | Bernard Charles Sherman | Compositions solides contenant du ramipril |
BR0306928A (pt) | 2002-01-15 | 2004-11-09 | Ranbaxy Lab Ltd | Composições farmacêuticas estáveis compreendendo inibidores de enzimas conversoras de angiotensina (ace) |
ITMI20020731A1 (it) * | 2002-04-08 | 2003-10-08 | Ibsa Inst Biochimique Sa | Composizioni farmaceutiche per acido acetilsalicilico e oli omega-3 |
WO2004064834A1 (fr) | 2003-01-21 | 2004-08-05 | Ranbaxy Laboratories Limited | Losartan amorphe co-precipite et posologies comprenant celui-ci |
EP1653929A1 (fr) | 2003-01-22 | 2006-05-10 | Sandoz AG | Composition pharmaceutique solide comprenant du ramipril |
US20060188568A1 (en) | 2003-10-30 | 2006-08-24 | Lupin Limited | Stable formulations of ace inhibitors and methods for preparation thereof |
WO2005070398A2 (fr) | 2004-01-23 | 2005-08-04 | Ranbaxy Laboratories Limited | Compositions pharmaceutiques de candesartan cilexetil stabilisees par des co-solvants |
WO2005079751A2 (fr) | 2004-01-23 | 2005-09-01 | Ranbaxy Laboratories Limited | Compositions pharmaceutiques orales de candesartan cilexetil |
WO2005084648A1 (fr) | 2004-02-27 | 2005-09-15 | Ranbaxy Laboratories Limited | Compositions pharmaceutiques comprenant du candesartan cilexetil |
WO2006135415A2 (fr) | 2004-09-08 | 2006-12-21 | University Of Florida Research Foundation, Inc. | Micelles et nanoemulsions pour le traitement prophylactique et reactif de l'atherosclerose |
ES2255426B1 (es) * | 2004-10-19 | 2007-08-16 | Gp Pharm, S.A. | Formulacion farmaceutica que comprende microcapsulas de estatinas suspendidas en ester alquilicos de acidos grasos poliinsaturados (pufa). |
MX2007005373A (es) | 2004-11-05 | 2007-08-14 | King Pharmaceuticals Res & Dev | Composiciones estabilizadas de ramipril y metodos para elaborarlas. |
WO2006076097A2 (fr) | 2004-12-07 | 2006-07-20 | Nektar Therapeutics | Preparation non cristalline stable contenant du losartan |
EP1674080A1 (fr) | 2004-12-24 | 2006-06-28 | KRKA, D.D., Novo Mesto | Composition pharmaceutique comprenant du valsartan |
WO2006081518A2 (fr) | 2005-01-28 | 2006-08-03 | Collegium Pharmaceutical, Inc. | Excipients non aqueux non ioniques pour administration topique et par voie orale d'agents actifs lies a un support |
CA2646131C (fr) * | 2005-03-21 | 2018-09-04 | Vicus Therapeutics Spe 1, Llc | Compositions et procedes permettant d'ameliorer la cachexie |
GR1006875B (el) | 2005-06-30 | 2010-07-12 | "Φαρματεν" Φαρμακευτικη Βιομηχανικη Εμπορικη Α.Ε., | Βελτιωμενες φαρμακευτικες συνθεσεις περιεχουσες αναστολεις του μετατρεπτικου ενζυμου αγγειοτενσινης και μεθοδοι παρασκευης αυτων. |
US20070166372A1 (en) | 2006-01-19 | 2007-07-19 | Mai De Ltd. | Preparation of solid coprecipitates of amorphous valsartan |
EP2081550B2 (fr) * | 2006-03-09 | 2021-05-26 | Reliant Pharmaceuticals, Inc. | Revêtement de capsules avec des ingrédients pharmaceutiques actifs |
US20070281000A1 (en) | 2006-06-02 | 2007-12-06 | Michael Fox | Stable formulation comprising moisture sensitive drug/s and manufacturing procedure thereof |
WO2008001184A2 (fr) | 2006-06-26 | 2008-01-03 | Emcure Pharmaceuticals Limited | Composition solide |
WO2008000040A1 (fr) | 2006-06-30 | 2008-01-03 | Alphapharm Pty Ltd | Composition stabilisée comprenant des inhibiteurs de l'eca |
WO2008012371A1 (fr) | 2006-07-28 | 2008-01-31 | Krka, Tovarna Zdravil, D.D., Novo Mesto | Procédé de préparation de formes amorphes et cristallines de candésartan cilexétil par chromatographie sur colonne |
US20080152717A1 (en) | 2006-12-14 | 2008-06-26 | Isp Investments, Inc. | Amorphous valsartan and the production thereof |
EP1952806A1 (fr) | 2007-02-01 | 2008-08-06 | Helm AG | Procédé de préparation des produits d'absorption de candesartan |
EP1997479A1 (fr) | 2007-05-31 | 2008-12-03 | Helm AG | Formulations stabilisées contentant du candesartan cilexetil amorphe pour l'administration orale |
KR20100111292A (ko) * | 2008-01-10 | 2010-10-14 | 다케다 야쿠힌 고교 가부시키가이샤 | 캡슐 제제 |
-
2009
- 2009-11-20 ES ES200931024A patent/ES2364011B1/es not_active Expired - Fee Related
-
2010
- 2010-11-18 AR ARP100104270A patent/AR079428A1/es unknown
- 2010-11-19 CN CN201080052613XA patent/CN102711735A/zh active Pending
- 2010-11-19 AU AU2010321248A patent/AU2010321248A1/en not_active Abandoned
- 2010-11-19 CA CA2781434A patent/CA2781434A1/fr not_active Abandoned
- 2010-11-19 MX MX2012005744A patent/MX2012005744A/es not_active Application Discontinuation
- 2010-11-19 RU RU2012122886/15A patent/RU2012122886A/ru unknown
- 2010-11-19 WO PCT/EP2010/007025 patent/WO2011060945A2/fr active Application Filing
- 2010-11-19 TW TW099139975A patent/TW201141469A/zh unknown
- 2010-11-19 EP EP10781842A patent/EP2501365A2/fr not_active Withdrawn
- 2010-11-19 BR BR112012011902A patent/BR112012011902A2/pt not_active IP Right Cessation
- 2010-11-19 KR KR1020127015768A patent/KR20120117986A/ko not_active Application Discontinuation
- 2010-11-19 JP JP2012539231A patent/JP2013511480A/ja active Pending
-
2012
- 2012-05-17 IL IL219874A patent/IL219874A0/en unknown
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2014142607A1 (fr) * | 2013-03-14 | 2014-09-18 | 보령제약 주식회사 | Médicament combiné pharmaceutique |
US9592233B2 (en) | 2013-03-14 | 2017-03-14 | Boryung Pharmaceutical Co., Ltd. | Pharmaceutical combination drug |
Also Published As
Publication number | Publication date |
---|---|
CA2781434A1 (fr) | 2011-05-26 |
WO2011060945A3 (fr) | 2012-01-19 |
TW201141469A (en) | 2011-12-01 |
ES2364011A1 (es) | 2011-08-23 |
BR112012011902A2 (pt) | 2017-10-10 |
AU2010321248A1 (en) | 2012-06-07 |
IL219874A0 (en) | 2012-07-31 |
RU2012122886A (ru) | 2013-12-27 |
EP2501365A2 (fr) | 2012-09-26 |
ES2364011B1 (es) | 2013-01-24 |
AR079428A1 (es) | 2012-01-25 |
WO2011060945A2 (fr) | 2011-05-26 |
CN102711735A (zh) | 2012-10-03 |
MX2012005744A (es) | 2012-12-05 |
JP2013511480A (ja) | 2013-04-04 |
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