MA31797B1 - Compositions pharmaceutiques - Google Patents
Compositions pharmaceutiquesInfo
- Publication number
- MA31797B1 MA31797B1 MA32803A MA32803A MA31797B1 MA 31797 B1 MA31797 B1 MA 31797B1 MA 32803 A MA32803 A MA 32803A MA 32803 A MA32803 A MA 32803A MA 31797 B1 MA31797 B1 MA 31797B1
- Authority
- MA
- Morocco
- Prior art keywords
- methyl
- biphenyl
- oral dosage
- solid oral
- dosage forms
- Prior art date
Links
- 239000008194 pharmaceutical composition Substances 0.000 title abstract 2
- 238000000034 method Methods 0.000 abstract 2
- 239000006186 oral dosage form Substances 0.000 abstract 2
- 239000007787 solid Substances 0.000 abstract 2
- -1 (1s, 3r) -1-biphenyl-4-yl-methyl-3-ethoxycarbonyl-1-butylcarbamoyl Chemical group 0.000 abstract 1
- FERIUCNNQQJTOY-UHFFFAOYSA-M Butyrate Chemical compound CCCC([O-])=O FERIUCNNQQJTOY-UHFFFAOYSA-M 0.000 abstract 1
- FERIUCNNQQJTOY-UHFFFAOYSA-N Butyric acid Natural products CCCC(O)=O FERIUCNNQQJTOY-UHFFFAOYSA-N 0.000 abstract 1
- 238000005056 compaction Methods 0.000 abstract 1
- 238000007907 direct compression Methods 0.000 abstract 1
- 239000003814 drug Substances 0.000 abstract 1
- 239000012729 immediate-release (IR) formulation Substances 0.000 abstract 1
- 238000009490 roller compaction Methods 0.000 abstract 1
- 229940124597 therapeutic agent Drugs 0.000 abstract 1
- SOBHUZYZLFQYFK-UHFFFAOYSA-K trisodium;hydroxy-[[phosphonatomethyl(phosphonomethyl)amino]methyl]phosphinate Chemical group [Na+].[Na+].[Na+].OP(O)(=O)CN(CP(O)([O-])=O)CP([O-])([O-])=O SOBHUZYZLFQYFK-UHFFFAOYSA-K 0.000 abstract 1
- 125000003774 valeryl group Chemical group O=C([*])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 abstract 1
Classifications
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- 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
- A61K31/21—Esters, e.g. nitroglycerine, selenocyanates
- A61K31/215—Esters, e.g. nitroglycerine, selenocyanates of carboxylic acids
- A61K31/216—Esters, e.g. nitroglycerine, selenocyanates of carboxylic acids of acids having aromatic rings, e.g. benactizyne, clofibrate
-
- 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
-
- 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
- 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
- A61P9/10—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
Landscapes
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Public Health (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Epidemiology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Organic Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Emergency Medicine (AREA)
- Urology & Nephrology (AREA)
- Vascular Medicine (AREA)
- Hospice & Palliative Care (AREA)
- Medicinal Preparation (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Abstract
L'invention concerne des formes de dosage orales solides, en particulier des comprimés, d'une composition pharmaceutique comprenant un complexe supramoléculaire, lesquelles formes peuvent être formées par un procédé de compression directe ou un procédé de compactage, comme un compactage par rouleaux. De telles formes de dosage orales solides présentent un profil de libération immédiate qui permet une libération rapide de l'agent thérapeutique. Un complexe supramoléculaire particulièrement utile est le trisodium [3-((1s,3r) -1-biphényl-4-yl-méthyl-3-éthoxycarbonyl-1- butylcarbamoyl) propionate-(s)-3'-méthyl-2'- (pentanoyl{2'-(tétrazol-5-ylate)biphényl-4'-yl-méthyl}amino)butyrate] hémipentahydrate.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US98566807P | 2007-11-06 | 2007-11-06 | |
| PCT/US2008/082324 WO2009061713A1 (fr) | 2007-11-06 | 2008-11-04 | Compositions pharmaceutiques |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| MA31797B1 true MA31797B1 (fr) | 2010-10-01 |
Family
ID=40451030
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MA32803A MA31797B1 (fr) | 2007-11-06 | 2010-04-30 | Compositions pharmaceutiques |
Country Status (33)
| Country | Link |
|---|---|
| US (3) | US20100267786A1 (fr) |
| EP (4) | EP2295035B1 (fr) |
| JP (2) | JP5653218B2 (fr) |
| KR (2) | KR101589317B1 (fr) |
| CN (2) | CN101848700A (fr) |
| AR (1) | AR069184A1 (fr) |
| AU (1) | AU2008324878B2 (fr) |
| BR (1) | BRPI0823505A2 (fr) |
| CA (1) | CA2703598C (fr) |
| CL (1) | CL2008003298A1 (fr) |
| CY (2) | CY1116280T1 (fr) |
| DK (3) | DK2217205T3 (fr) |
| EC (1) | ECSP10010160A (fr) |
| ES (3) | ES2587336T3 (fr) |
| FI (1) | FI3067043T3 (fr) |
| GT (1) | GT201000131A (fr) |
| HR (3) | HRP20150459T1 (fr) |
| HU (2) | HUE028866T2 (fr) |
| IL (3) | IL262990B2 (fr) |
| JO (1) | JOP20080499B1 (fr) |
| MA (1) | MA31797B1 (fr) |
| MX (1) | MX2010004930A (fr) |
| MY (1) | MY153730A (fr) |
| NZ (1) | NZ584686A (fr) |
| PE (2) | PE20141072A1 (fr) |
| PL (3) | PL2295035T3 (fr) |
| PT (3) | PT2295035T (fr) |
| RU (1) | RU2493844C3 (fr) |
| SG (1) | SG185951A1 (fr) |
| SI (3) | SI2295035T1 (fr) |
| TN (1) | TN2010000200A1 (fr) |
| TW (1) | TWI484982B (fr) |
| WO (1) | WO2009061713A1 (fr) |
Families Citing this family (58)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101848700A (zh) | 2007-11-06 | 2010-09-29 | 诺瓦提斯公司 | 基于血管紧张素受体拮抗剂/阻断剂(arb)和中性内肽酶(nep)抑制剂的超结构的双重作用的药物组合物 |
| JP5420761B2 (ja) | 2009-05-28 | 2014-02-19 | ノバルティス アーゲー | ネプリリシン阻害剤としての置換アミノプロピオン酸誘導体 |
| SG176010A1 (en) | 2009-05-28 | 2011-12-29 | Novartis Ag | Substituted aminobutyric derivatives as neprilysin inhibitors |
| JO2967B1 (en) | 2009-11-20 | 2016-03-15 | نوفارتس ايه جي | Acetic acid derivatives of carbamoyl methyl amino are substituted as new NEP inhibitors |
| PH12013500231A1 (en) * | 2010-08-24 | 2017-08-09 | Novartis Ag | Treatment of hypertension and/or prevention or treatment of heart failure in a mammal receiving anti-coagulant therapy |
| US8673974B2 (en) | 2010-11-16 | 2014-03-18 | Novartis Ag | Substituted amino bisphenyl pentanoic acid derivatives as NEP inhibitors |
| SI2887961T1 (sl) * | 2012-08-24 | 2021-08-31 | Novartis Ag | Zaviralci NEP za zdravljenje bolezni, značilnih po atrialni širitvi ali preoblikovanju |
| NZ710574A (en) | 2013-02-14 | 2017-11-24 | Novartis Ag | Substituted bisphenyl butanoic phosphonic acid derivatives as nep (neutral endopeptidase) inhibitors |
| WO2014126972A1 (fr) | 2013-02-14 | 2014-08-21 | Novartis Ag | Dérivés de l'acide butanoïque bisphényle substitué utiles en tant qu'inhibiteurs de nep présentant une meilleure efficacité in vivo |
| EP3038653A1 (fr) * | 2013-08-26 | 2016-07-06 | Novartis AG | Nouvelle utilisation |
| RS65037B1 (sr) | 2013-08-26 | 2024-02-29 | Novartis Ag | Lečenje kardiovaskularnih oboljenja |
| WO2015154673A1 (fr) * | 2014-04-10 | 2015-10-15 | Zhaoyin Wang | Nouveaux pro-médicaments et combinaisons pour le traitement de l'hypertension et de maladies cardiovasculaires |
| CN105461647B (zh) * | 2014-09-28 | 2018-06-29 | 四川海思科制药有限公司 | 缬沙坦沙库比曲三钠盐复合物的固态形式及其制备方法和用途 |
| PL3229799T3 (pl) | 2014-12-08 | 2019-05-31 | Crystal Pharmatech Co Ltd | Krystaliczne postacie supramolekularnego kompleksu trisodowego zawierającego walsartan i AHU-377 i ich sposoby |
| CN104473938B (zh) * | 2014-12-30 | 2017-06-09 | 北京瑞都医药科技有限公司 | 一种治疗慢性心衰药物及其制备方法 |
| CN104826115A (zh) * | 2015-04-19 | 2015-08-12 | 浙江巨泰药业有限公司 | 一种抗心衰药物组合物及其制备方法 |
| HUE071910T2 (hu) | 2015-05-11 | 2025-10-28 | Novartis Ag | Szakubitril-valzartán adagolási rend krónikus szisztolés szívelégtelenség kezelésére |
| EP3302460A1 (fr) | 2015-05-29 | 2018-04-11 | Novartis AG | Sacubitril et valsartan pour le traitement d'une maladie métabolique |
| CN106309388A (zh) * | 2015-06-30 | 2017-01-11 | 深圳信立泰药业股份有限公司 | 一种用于心衰治疗的药物组合物及其制备方法 |
| WO2017006254A1 (fr) | 2015-07-08 | 2017-01-12 | Novartis Ag | Combinaison de médicaments comprenant un antagoniste du récepteur de l'angiotensine ii, un inhibiteur d'endopeptidase neutre et un antagoniste du récepteur de minéralocorticoïdes |
| CN106074421A (zh) * | 2015-07-11 | 2016-11-09 | 凌莉 | 一种提高稳定性的药物组合物 |
| CN106176725A (zh) * | 2015-07-11 | 2016-12-07 | 凌莉 | 一种提高稳定性的药物组合物及其制备方法和用途 |
| CN106176723A (zh) * | 2015-07-11 | 2016-12-07 | 凌莉 | 一种固体药物组合物及其制备方法 |
| CN105997993B (zh) * | 2015-07-11 | 2018-03-30 | 麦丽芳 | 一种用于心血管疾病治疗的固体口服型制剂及其制备方法 |
| CN105997994A (zh) * | 2015-07-11 | 2016-10-12 | 凌莉 | 一种固体口服型制剂及其制备方法 |
| CN106176724A (zh) * | 2015-07-11 | 2016-12-07 | 凌莉 | 一种稳定的固体药物组合物及其制备方法 |
| WO2017012600A1 (fr) | 2015-07-20 | 2017-01-26 | Zentiva, K.S. | Composition pharmaceutique contenant du valsartan et du sacubitril et procédés de préparation et de stabilisation correspondants |
| CN106397249A (zh) * | 2015-08-03 | 2017-02-15 | 深圳信立泰药业股份有限公司 | 一种高稳定性lcz696结晶粉末及其制备方法 |
| WO2017037596A1 (fr) * | 2015-08-28 | 2017-03-09 | Dr. Reddy's Laboratories Limited | Dispersion solide amorphe de lcz-696 |
| JP6598985B2 (ja) | 2015-08-28 | 2019-10-30 | ノバルティス アーゲー | 新規の使用 |
| WO2017063581A1 (fr) * | 2015-10-16 | 2017-04-20 | 深圳信立泰药业股份有限公司 | Préparation orale pour le traitement de maladies cardiovasculaires et son procédé de préparation |
| CN105669581B (zh) * | 2015-11-09 | 2017-03-22 | 成都苑东生物制药股份有限公司 | 一种血管紧张受体拮抗剂和中性内肽酶抑制剂复合物 |
| WO2017085573A1 (fr) * | 2015-11-20 | 2017-05-26 | Lupin Limited | Complexe de sacubitril-valsartan amorphe et son procédé de préparation |
| CN105330609B (zh) * | 2015-12-07 | 2017-12-22 | 南京正大天晴制药有限公司 | 一种制备lcz696的方法 |
| CN105935358B (zh) * | 2015-12-18 | 2019-06-07 | 重庆两江药物研发中心有限公司 | 一种沙库比曲缬沙坦缓释剂及其制备方法 |
| CN105929031B (zh) * | 2015-12-18 | 2018-08-21 | 重庆两江药物研发中心有限公司 | 一种血管紧张素受体拮抗剂和nep抑制剂的复合物中杂质的分离方法 |
| CN106905253B (zh) * | 2015-12-23 | 2020-01-03 | 正大天晴药业集团股份有限公司 | 一种超分子复合物的结晶 |
| US10722471B2 (en) | 2016-02-03 | 2020-07-28 | Novartis Ag | Galenic formulations of organic compounds |
| HRP20250913T1 (hr) * | 2016-02-03 | 2025-09-26 | Novartis Ag | Nova upotreba kombinacije sakubitrila i valsartana |
| CN105748420B (zh) * | 2016-03-04 | 2018-11-06 | 山东省药学科学院 | 一种治疗心力衰竭的lcz696缓释骨架片的制备方法 |
| CN105902506A (zh) * | 2016-06-12 | 2016-08-31 | 佛山市腾瑞医药科技有限公司 | 一种沙卡布曲缬沙坦制剂及其应用 |
| WO2018069937A1 (fr) | 2016-10-13 | 2018-04-19 | Mylan Laboratories Limited | Dispersions solides de sacubitril/valsartan trisodique et procédé de leur préparation |
| EP3600255B1 (fr) * | 2017-03-31 | 2021-07-07 | Alfred E. Tiefenbacher (GmbH & Co. KG) | Extrudat thermofusible stable contenant du valsartan et du sacubitril |
| WO2018178295A1 (fr) | 2017-03-31 | 2018-10-04 | Alfred E. Tiefenbacher (Gmbh & Co. Kg) | Extrudat thermofusible stable contenant du valsartan et du sacubitril |
| WO2018211479A1 (fr) * | 2017-05-19 | 2018-11-22 | Lupin Limited | Compositions stabilisées d'inhibiteurs de l'angiotensine ii et d'inhibiteurs de l'endopeptidase neutre, et leur procédé de préparation |
| US11382866B2 (en) | 2017-07-06 | 2022-07-12 | Mankind Pharma Ltd. | Fixed dose pharmaceutical composition of valsartan and sacubitril |
| WO2019020706A1 (fr) | 2017-07-28 | 2019-01-31 | Synthon B.V. | Composition pharmaceutique comprenant du sacubitril et du valsartan |
| US20200276129A1 (en) | 2017-10-13 | 2020-09-03 | Alfred E. Tiefenbacher (Gmbh & Co. Kg) | Tablet containing valsartan and sacubitril |
| WO2019180735A1 (fr) * | 2018-03-19 | 2019-09-26 | Natco Pharma Limited | Compositions pharmaceutiques stables comprenant un complexe de sacubitril-valsartan |
| US11877576B2 (en) | 2018-06-22 | 2024-01-23 | Ideaz, Llc | Diphenyl tablets and methods of preparing the same |
| US20210177803A1 (en) | 2018-08-23 | 2021-06-17 | Novartis Ag | New pharmaceutical use for the treatment of heart failure |
| WO2020039394A1 (fr) | 2018-08-24 | 2020-02-27 | Novartis Ag | Nouvelles combinaisons de médicaments |
| EP3766484B1 (fr) | 2019-07-19 | 2021-08-25 | Zentiva, K.S. | Forme posologique pharmaceutique solide comprenant du valsartan et du sacubitril |
| KR102545274B1 (ko) | 2020-02-26 | 2023-06-20 | 에리슨제약(주) | 사쿠비트릴 및 발사르탄을 포함하는 심부전 치료용 서방성 제제, 및 이를 포함하는 다중방출 복합제제와 이의 제조방법 |
| KR20210120560A (ko) | 2020-03-27 | 2021-10-07 | 주식회사 유영제약 | 고함량의 주성분을 포함하는 정제 및 그 제조방법 |
| KR20210138510A (ko) | 2020-05-12 | 2021-11-19 | 에리슨제약(주) | 사쿠비트릴, 발사르탄 및 네비보롤을 포함하는 심부전 및 허혈성 심질환의 예방 또는 치료용 약제학적 조성물 및 이를 포함하는 약제학적 복합제제 |
| KR20220091767A (ko) | 2020-12-24 | 2022-07-01 | 주식회사 보령 | 사쿠비트릴 발사르탄 하이브리드 화합물 또는 그 약제학적으로 허용되는 염을 유효성분으로 포함하는 약제학적 조성물 |
| KR102486815B1 (ko) | 2021-01-20 | 2023-01-10 | 주식회사 대웅제약 | Nep 저해제 및 arb를 포함하는 약학 조성물 및 이의 제조 방법 |
Family Cites Families (26)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US607893A (en) | 1898-07-26 | Automatic switch-operating machine | ||
| US607355A (en) | 1898-07-12 | Carrier for bicycles | ||
| US608220A (en) | 1898-08-02 | Mechanical movement | ||
| US735093A (en) | 1903-01-31 | 1903-08-04 | Oscar Greenwald | Elevator-cable guard. |
| GB9613470D0 (en) | 1996-06-27 | 1996-08-28 | Ciba Geigy Ag | Small solid oral dosage form |
| US6558699B2 (en) * | 1997-11-17 | 2003-05-06 | Smithkline Beecham Corporation | High drug load immediate and modified release oral dosage formulations and processes for their manufacture |
| PL340587A1 (en) * | 1997-11-17 | 2001-02-12 | Smithkline Beecham Corp | Oral preparations of high therapeutic substance content with instantaneous or modifiable release of such substance and methods of obtaining them |
| WO1999065500A1 (fr) * | 1998-06-17 | 1999-12-23 | Bristol-Myers Squibb Company | Prevention de l'infarctus cerebral par administration d'une combinaison d'un anti-agregant plaquettaire bloquant les recepteurs d'adp et d'un medicament antihypertenseur |
| KR100646716B1 (ko) | 1998-12-23 | 2006-11-17 | 노파르티스 아게 | At-1 또는 at-2 수용체의 증가와 관련된 질환의치료에 있어서 at-1 수용체 길항제 또는 at-2 수용체조절제의 용도 |
| BR0112665A (pt) | 2000-07-19 | 2003-06-24 | Novartis Ag | Sais |
| PT1467728E (pt) | 2002-01-17 | 2007-11-14 | Novartis Ag | Composições farmacêuticas compreendendo valsartan e inibidores da nep |
| US7468390B2 (en) * | 2002-01-17 | 2008-12-23 | Novartis Ag | Methods of treatment and pharmaceutical composition |
| JP3751287B2 (ja) * | 2002-03-27 | 2006-03-01 | バイエル薬品株式会社 | 小型化されたニフェジピン有核錠剤 |
| WO2003089417A1 (fr) | 2002-04-15 | 2003-10-30 | Dr. Reddy's Laboratories Limited | Nouvelles formes cristallines de (s)-n-(1-carboxy-2-methyl-prop-1-yl) -n-pentanoyl-n- [2'-(1h-tetrazol-5-yl-)- biphenyl-4-yl methyl] amine (valsartan) |
| GB0209265D0 (en) | 2002-04-23 | 2002-06-05 | Novartis Ag | Organic compounds |
| EP1511739B1 (fr) | 2003-03-17 | 2008-04-30 | Teva Pharmaceutical Industries Ltd. | Formes polymorphes de valsartan |
| EP1648515B1 (fr) * | 2003-07-16 | 2012-11-21 | Boehringer Ingelheim International GmbH | Combinaisons de chlorthalidone |
| GB0402262D0 (en) * | 2004-02-02 | 2004-03-10 | Novartis Ag | Process for the manufacture of organic compounds |
| GT200600371A (es) | 2005-08-17 | 2007-03-21 | Formas de dosis sólidas de valsartan y amlodipina y método para hacer las mismas | |
| JP2009513622A (ja) * | 2005-10-27 | 2009-04-02 | ルピン・リミテッド | ロサルタンの医薬製剤 |
| WO2007052307A2 (fr) | 2005-10-31 | 2007-05-10 | Lupin Limited | Formes posologiques solides orales stables de valsartan |
| EP1951111B1 (fr) | 2005-11-07 | 2010-08-11 | Stryker Corporation | Appareil de manipulation de patients comprenant une signalisation locale, un ajustement de l'angle de fowler à l'aide d'une seule touche et une configuration d'alarme d'alimentation |
| CA2626682A1 (fr) | 2005-11-08 | 2007-05-18 | Novartis Ag | Combinaison de composes organiques pour le traitement des maladies cardiovasculaires |
| AR057882A1 (es) | 2005-11-09 | 2007-12-26 | Novartis Ag | Compuestos de accion doble de bloqueadores del receptor de angiotensina e inhibidores de endopeptidasa neutra |
| EP1897537A1 (fr) * | 2006-09-04 | 2008-03-12 | Novartis AG | Composition contenant un antagoniste des récepteurs de l'angiotensine II |
| CN101848700A (zh) | 2007-11-06 | 2010-09-29 | 诺瓦提斯公司 | 基于血管紧张素受体拮抗剂/阻断剂(arb)和中性内肽酶(nep)抑制剂的超结构的双重作用的药物组合物 |
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2008
- 2008-11-04 CN CN200880114940A patent/CN101848700A/zh active Pending
- 2008-11-04 CA CA2703598A patent/CA2703598C/fr active Active
- 2008-11-04 PL PL10173506.6T patent/PL2295035T3/pl unknown
- 2008-11-04 EP EP10173506.6A patent/EP2295035B1/fr not_active Revoked
- 2008-11-04 PL PL16157767.1T patent/PL3067043T3/pl unknown
- 2008-11-04 PT PT101735066T patent/PT2295035T/pt unknown
- 2008-11-04 KR KR1020107009852A patent/KR101589317B1/ko not_active Ceased
- 2008-11-04 EP EP16157767.1A patent/EP3067043B1/fr active Active
- 2008-11-04 PT PT161577671T patent/PT3067043T/pt unknown
- 2008-11-04 SG SG2012081394A patent/SG185951A1/en unknown
- 2008-11-04 ES ES10173506.6T patent/ES2587336T3/es active Active
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- 2008-11-04 DK DK08848154.4T patent/DK2217205T3/en active
- 2008-11-04 EP EP22200982.1A patent/EP4186491A1/fr active Pending
- 2008-11-04 ES ES16157767T patent/ES2939163T3/es active Active
- 2008-11-04 MY MYPI2010001722A patent/MY153730A/en unknown
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- 2008-11-04 CN CN2013101540642A patent/CN103251587A/zh active Pending
- 2008-11-04 PE PE2013002393A patent/PE20141072A1/es active IP Right Grant
- 2008-11-04 HU HUE10173506A patent/HUE028866T2/en unknown
- 2008-11-04 RU RU2010123027A patent/RU2493844C3/ru active
- 2008-11-04 SI SI200832204T patent/SI3067043T1/sl unknown
- 2008-11-04 NZ NZ584686A patent/NZ584686A/xx unknown
- 2008-11-04 SI SI200831427T patent/SI2217205T1/sl unknown
- 2008-11-04 DK DK16157767.1T patent/DK3067043T3/da active
- 2008-11-04 HU HUE16157767A patent/HUE061321T2/hu unknown
- 2008-11-04 DK DK10173506.6T patent/DK2295035T3/en active
- 2008-11-04 EP EP08848154.4A patent/EP2217205B1/fr not_active Revoked
- 2008-11-04 AR ARP080104826A patent/AR069184A1/es not_active Application Discontinuation
- 2008-11-04 PE PE2008001886A patent/PE20091390A1/es not_active Application Discontinuation
- 2008-11-04 MX MX2010004930A patent/MX2010004930A/es active IP Right Grant
- 2008-11-04 BR BRPI0823505-8A patent/BRPI0823505A2/pt not_active Application Discontinuation
- 2008-11-04 ES ES08848154.4T patent/ES2536514T3/es active Active
- 2008-11-04 JO JOP/2008/0499A patent/JOP20080499B1/ar active
- 2008-11-04 FI FIEP16157767.1T patent/FI3067043T3/fi active
- 2008-11-04 US US12/741,251 patent/US20100267786A1/en not_active Abandoned
- 2008-11-04 KR KR1020157033633A patent/KR101700062B1/ko not_active Ceased
- 2008-11-04 WO PCT/US2008/082324 patent/WO2009061713A1/fr not_active Ceased
- 2008-11-05 TW TW097142724A patent/TWI484982B/zh active
- 2008-11-05 CL CL2008003298A patent/CL2008003298A1/es unknown
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2010
- 2010-04-19 IL IL205208A patent/IL205208A/en active IP Right Grant
- 2010-04-30 MA MA32803A patent/MA31797B1/fr unknown
- 2010-04-30 TN TN2010000200A patent/TN2010000200A1/fr unknown
- 2010-05-05 GT GT201000131A patent/GT201000131A/es unknown
- 2010-05-06 EC EC2010010160A patent/ECSP10010160A/es unknown
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2014
- 2014-08-12 JP JP2014164022A patent/JP2015038069A/ja not_active Withdrawn
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2015
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2016
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2017
- 2017-01-03 IL IL249922A patent/IL249922A0/en unknown
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2020
- 2020-12-02 US US17/109,716 patent/US20210085631A1/en not_active Abandoned
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2023
- 2023-05-09 US US18/314,745 patent/US20240115536A1/en not_active Abandoned
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