MA26692A1 - Compositions pharmaceutiques contenant un complexe stable insoluble, procede de preparation et complexe stable insoluble obtenu - Google Patents
Compositions pharmaceutiques contenant un complexe stable insoluble, procede de preparation et complexe stable insoluble obtenuInfo
- Publication number
- MA26692A1 MA26692A1 MA25778A MA25778A MA26692A1 MA 26692 A1 MA26692 A1 MA 26692A1 MA 25778 A MA25778 A MA 25778A MA 25778 A MA25778 A MA 25778A MA 26692 A1 MA26692 A1 MA 26692A1
- Authority
- MA
- Morocco
- Prior art keywords
- stable complex
- insoluble
- insoluble stable
- preparation
- pharmaceutical compositions
- Prior art date
Links
- 239000008194 pharmaceutical composition Substances 0.000 title 1
- 238000002360 preparation method Methods 0.000 title 1
- 150000001875 compounds Chemical class 0.000 abstract 3
- 229920000831 ionic polymer Polymers 0.000 abstract 2
- 230000009477 glass transition Effects 0.000 abstract 1
- 229920003176 water-insoluble polymer Polymers 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
- A61K9/14—Particulate form, e.g. powders, Processes for size reducing of pure drugs or the resulting products, Pure drug nanoparticles
- A61K9/141—Intimate drug-carrier mixtures characterised by the carrier, e.g. ordered mixtures, adsorbates, solid solutions, eutectica, co-dried, co-solubilised, co-kneaded, co-milled, co-ground products, co-precipitates, co-evaporates, co-extrudates, co-melts; Drug nanoparticles with adsorbed surface modifiers
- A61K9/146—Intimate drug-carrier mixtures characterised by the carrier, e.g. ordered mixtures, adsorbates, solid solutions, eutectica, co-dried, co-solubilised, co-kneaded, co-milled, co-ground products, co-precipitates, co-evaporates, co-extrudates, co-melts; Drug nanoparticles with adsorbed surface modifiers with organic macromolecular compounds
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
- A61K47/50—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
- A61K47/50—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates
- A61K47/51—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent
- A61K47/56—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an organic macromolecular compound, e.g. an oligomeric, polymeric or dendrimeric molecule
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P7/00—Drugs for disorders of the blood or the extracellular fluid
- A61P7/02—Antithrombotic agents; Anticoagulants; Platelet aggregation inhibitors
Landscapes
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Epidemiology (AREA)
- General Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Hematology (AREA)
- Virology (AREA)
- Communicable Diseases (AREA)
- Oncology (AREA)
- Diabetes (AREA)
- Dermatology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicinal Preparation (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Plural Heterocyclic Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Des complexes stables et insolubles dans l'eau de composés faiblement solubles et dispersés moléculairement dans des polymères ioniques insolubles dans l'eau sont décrits. Les polymères ioniques insolubles utiles possèdent une masse moléculaire supérieure à environ 80 000 D et une température de transition vitreuse égale ou supérieure à environ 50o.C. Les composés sont microprécipités dans les polymères ioniques sous forme amorphe. Les complexes selon la présente invention augmentent de manière significative la biodisponibilité des composés thérapeutiquement actifs faiblement solubies.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US10133698P | 1998-09-22 | 1998-09-22 | |
| US13653199P | 1999-05-28 | 1999-05-28 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| MA26692A1 true MA26692A1 (fr) | 2004-12-20 |
Family
ID=26798138
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MA25778A MA26692A1 (fr) | 1998-09-22 | 1999-09-21 | Compositions pharmaceutiques contenant un complexe stable insoluble, procede de preparation et complexe stable insoluble obtenu |
Country Status (32)
| Country | Link |
|---|---|
| US (1) | US6350786B1 (fr) |
| EP (1) | EP0988863B2 (fr) |
| JP (5) | JP2000095708A (fr) |
| KR (1) | KR100362019B1 (fr) |
| CN (1) | CN1201821C (fr) |
| AR (2) | AR022096A1 (fr) |
| AT (1) | ATE265232T1 (fr) |
| AU (1) | AU770745B2 (fr) |
| BR (1) | BR9904283A (fr) |
| CA (1) | CA2282906C (fr) |
| CO (1) | CO5140077A1 (fr) |
| CZ (1) | CZ300215B6 (fr) |
| DE (1) | DE69916733T3 (fr) |
| DK (1) | DK0988863T4 (fr) |
| ES (1) | ES2218918T5 (fr) |
| HR (1) | HRP990287B1 (fr) |
| HU (1) | HU228341B1 (fr) |
| ID (1) | ID24034A (fr) |
| IL (1) | IL131957A (fr) |
| MA (1) | MA26692A1 (fr) |
| MY (1) | MY124377A (fr) |
| NO (1) | NO326928B1 (fr) |
| NZ (1) | NZ337884A (fr) |
| PE (1) | PE20001049A1 (fr) |
| PL (1) | PL202757B1 (fr) |
| PT (1) | PT988863E (fr) |
| RS (1) | RS50193B (fr) |
| RU (1) | RU2240827C2 (fr) |
| SG (1) | SG97131A1 (fr) |
| SI (1) | SI0988863T2 (fr) |
| TR (1) | TR199902324A2 (fr) |
| TW (1) | TWI234465B (fr) |
Families Citing this family (94)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE60039379D1 (de) | 1999-02-10 | 2008-08-21 | Pfizer Prod Inc | Pharmazeutische feste Dispersionen |
| US6440959B1 (en) | 1999-04-21 | 2002-08-27 | Hoffman-La Roche Inc. | Pyrazolobenzodiazepines |
| AR033651A1 (es) * | 1999-10-01 | 2004-01-07 | Hoffmann La Roche | Derivados de pirimidina-2,4,6-triona, composiciones farmaceuticas que contienen dichos compuestos y el empleo de los mismos para la manufactura de un medicamento |
| US6313143B1 (en) * | 1999-12-16 | 2001-11-06 | Hoffmann-La Roche Inc. | Substituted pyrroles |
| CA2409003C (fr) * | 2000-05-16 | 2010-10-19 | Ortho-Mcneil Pharmaceutical, Inc. | Procede de revetement de dispositifs medicaux par du dioxyde de carbone hypercritique |
| US6482847B2 (en) * | 2000-10-03 | 2002-11-19 | Hoffmann-La Roche Inc. | Amorphous form of cell cycle inhibitor having improved solubility and bioavailability |
| US6469179B1 (en) | 2000-10-03 | 2002-10-22 | Hoffmann-La Roche Inc. | Amorphous form of cell cycle inhibitor having improved solubility and bioavailability |
| US6951656B2 (en) | 2000-12-22 | 2005-10-04 | Baxter International Inc. | Microprecipitation method for preparing submicron suspensions |
| US7193084B2 (en) | 2000-12-22 | 2007-03-20 | Baxter International Inc. | Polymorphic form of itraconazole |
| US7037528B2 (en) | 2000-12-22 | 2006-05-02 | Baxter International Inc. | Microprecipitation method for preparing submicron suspensions |
| US8067032B2 (en) | 2000-12-22 | 2011-11-29 | Baxter International Inc. | Method for preparing submicron particles of antineoplastic agents |
| US20050048126A1 (en) | 2000-12-22 | 2005-03-03 | Barrett Rabinow | Formulation to render an antimicrobial drug potent against organisms normally considered to be resistant to the drug |
| US6884436B2 (en) | 2000-12-22 | 2005-04-26 | Baxter International Inc. | Method for preparing submicron particle suspensions |
| US6977085B2 (en) | 2000-12-22 | 2005-12-20 | Baxter International Inc. | Method for preparing submicron suspensions with polymorph control |
| US9700866B2 (en) | 2000-12-22 | 2017-07-11 | Baxter International Inc. | Surfactant systems for delivery of organic compounds |
| US6548531B2 (en) | 2001-02-09 | 2003-04-15 | Hoffmann-La Roche Inc. | Method for cancer therapy |
| US6716845B2 (en) * | 2001-03-30 | 2004-04-06 | Hoffmann-La Roche Inc. | Barbituric acid derivatives |
| CH695418A5 (de) * | 2001-05-30 | 2006-05-15 | Csir | Verfahren zur Einkapselung eines Wirkstoffs. |
| US20030044514A1 (en) * | 2001-06-13 | 2003-03-06 | Richard Robert E. | Using supercritical fluids to infuse therapeutic on a medical device |
| WO2002102373A1 (fr) * | 2001-06-15 | 2002-12-27 | F. Hoffmann-La Roche Ag | Procede d'administration d'un agent destine a la therapie du cancer |
| CA2450957A1 (fr) | 2001-06-22 | 2003-01-03 | Pfizer Products Inc. | Compositions pharmaceutiques de dispersions de medicaments et de polymeres neutres |
| ATE480226T1 (de) | 2001-06-22 | 2010-09-15 | Bend Res Inc | Pharmazeutische zusammensetzung enthaltend schwer lösliche und säureempfindliche arzneistoffe und neutralisierte anionische polymere |
| US20060003012A9 (en) | 2001-09-26 | 2006-01-05 | Sean Brynjelsen | Preparation of submicron solid particle suspensions by sonication of multiphase systems |
| BR0212833A (pt) | 2001-09-26 | 2004-10-13 | Baxter Int | Preparação de nanopartìculas de tamanho submìcron através de dispersão e de remoção de solvente ou de fase lìquida |
| US7112340B2 (en) | 2001-10-19 | 2006-09-26 | Baxter International Inc. | Compositions of and method for preparing stable particles in a frozen aqueous matrix |
| US20030139373A1 (en) * | 2001-11-20 | 2003-07-24 | Breimer Lars Holger | Method for cancer therapy |
| WO2003063822A2 (fr) * | 2002-02-01 | 2003-08-07 | Pfizer Products Inc. | Procede de fabrication de dispersions medicamenteuses amorphes solides homogenes sechees par pulverisation au moyen d'un appareil de sechage par pulverisation modifie |
| WO2004014342A1 (fr) | 2002-08-12 | 2004-02-19 | Pfizer Products Inc. | Compositions pharmaceutiques de medicaments partiellement ordonnes et de polymeres |
| DE10351087A1 (de) * | 2003-10-31 | 2005-05-25 | Bayer Technology Services Gmbh | Feste Wirkstoff-Formulierung |
| WO2005046696A1 (fr) | 2003-11-14 | 2005-05-26 | Ajinomoto Co., Inc. | Dispersion solide ou preparation de dispersion solide medicinale d'un derive de phenylalanine |
| EP3216449A1 (fr) * | 2003-11-14 | 2017-09-13 | EA Pharma Co., Ltd. | Préparation d'administration orale de dérivés de phénylalanine |
| US20070191404A1 (en) * | 2004-04-01 | 2007-08-16 | Pierre Bartsch | Pharmaceutical compositions of pyrimidine-2,4,6-triones |
| AR049915A1 (es) * | 2004-06-14 | 2006-09-13 | Anacor Pharmaceuticals Inc | Compuestos con contenido de boro y metodos de uso de los mismos |
| WO2006062980A2 (fr) * | 2004-12-07 | 2006-06-15 | Nektar Therapeutics | Formulation non cristalline stable comprenant de la tiagabine |
| JP5209876B2 (ja) * | 2004-12-28 | 2013-06-12 | エーザイ・アール・アンド・ディー・マネジメント株式会社 | 速崩壊性錠剤及びその製造方法 |
| WO2006073973A2 (fr) * | 2004-12-31 | 2006-07-13 | Reddy Us Therapeutics, Inc. | Nouveaux dérivés de benzylamine en tant qu'inhibiteurs de cetp |
| US8604055B2 (en) | 2004-12-31 | 2013-12-10 | Dr. Reddy's Laboratories Ltd. | Substituted benzylamino quinolines as cholesterol ester-transfer protein inhibitors |
| WO2006081497A2 (fr) * | 2005-01-27 | 2006-08-03 | Corium International, Inc. | Formulations et utilisations d'adhesifs hydrophiles biocompatibles |
| EP1690528A1 (fr) * | 2005-02-11 | 2006-08-16 | Abbott GmbH & Co. KG | Procedé pour la préparation des formes de dosage comprenant une dispersion solide d'un agent active microcristalline |
| WO2006123223A1 (fr) * | 2005-05-19 | 2006-11-23 | Pfizer Inc. | Compositions pharmaceutiques comprenant une forme d'un inhibiteur vegf-r |
| EP1767194A1 (fr) * | 2005-06-09 | 2007-03-28 | Helm AG | Procédé pour la préparation d'adsorbats de drospirenone |
| MY153898A (en) * | 2005-06-22 | 2015-04-15 | Plexxikon Inc | Compounds and methods for kinase modulation, and indications therefor |
| US20080031944A1 (en) * | 2006-08-04 | 2008-02-07 | Cima Labs Inc. | Stabilization of lorazepam |
| CA2660374A1 (fr) * | 2006-08-10 | 2008-02-14 | Cipla Limited | Composition orale solide antiretrovirale |
| US20080107725A1 (en) * | 2006-10-13 | 2008-05-08 | Albano Antonio A | Pharmaceutical Solid Dosage Forms Comprising Amorphous Compounds Micro-Embedded in Ionic Water-Insoluble Polymers |
| WO2008063888A2 (fr) | 2006-11-22 | 2008-05-29 | Plexxikon, Inc. | Composés modulant l'activité de c-fms et/ou de c-kit et utilisations associées |
| PE20121126A1 (es) * | 2006-12-21 | 2012-08-24 | Plexxikon Inc | Compuestos pirrolo [2,3-b] piridinas como moduladores de quinasa |
| WO2008079909A1 (fr) * | 2006-12-21 | 2008-07-03 | Plexxikon, Inc. | Composés et méthodes de modulation des kinases, et indications connexes |
| US20080221047A1 (en) | 2006-12-27 | 2008-09-11 | Astellas Pharma Inc., | Aminoakyl methacrylate copolymer E for maintaining solubility of poorly-soluble drug |
| CN101702878B (zh) * | 2007-05-11 | 2012-11-28 | 弗·哈夫曼-拉罗切有限公司 | 可溶性差的药物的药物组合物 |
| US8722736B2 (en) | 2007-05-22 | 2014-05-13 | Baxter International Inc. | Multi-dose concentrate esmolol with benzyl alcohol |
| US8426467B2 (en) | 2007-05-22 | 2013-04-23 | Baxter International Inc. | Colored esmolol concentrate |
| EP1997479A1 (fr) * | 2007-05-31 | 2008-12-03 | Helm AG | Formulations stabilisées contentant du candesartan cilexetil amorphe pour l'administration orale |
| MX2010000617A (es) | 2007-07-17 | 2010-05-17 | Plexxikon Inc | Compuestos y metodos para modulacion de cinasa, e indicaciones de estos. |
| JP2011500724A (ja) * | 2007-10-19 | 2011-01-06 | パーデュ リサーチ ファンデーション | 結晶性化合物の固体製剤 |
| US8632805B2 (en) * | 2008-06-20 | 2014-01-21 | Mutual Pharmaceutical Company, Inc. | Controlled-release formulations, method of manufacture, and use thereof |
| US7794750B2 (en) * | 2008-06-20 | 2010-09-14 | Mutual Pharmaceutical Company, Inc. | Controlled-release formulations, method of manufacture, and use thereof |
| US20100099696A1 (en) * | 2008-10-16 | 2010-04-22 | Anthony Edward Soscia | Tamper resistant oral dosage forms containing an embolizing agent |
| KR20100073454A (ko) * | 2008-12-23 | 2010-07-01 | 국립암센터 | 트란스글루타미나제 억제제로 사용되는 신규한 피라졸로디아제핀계 화합물, 이의 제조방법 및 이를 포함하는 조성물 |
| EA022924B1 (ru) | 2009-04-03 | 2016-03-31 | Ф.Хоффманн-Ля Рош Аг | ТВЁРДАЯ ФОРМА {3-[5-(4-ХЛОРФЕНИЛ)-1Н-ПИРРОЛО[2,3-b]ПИРИДИН-3-КАРБОНИЛ]-2,4-ДИФТОРФЕНИЛ}АМИДА ПРОПАН-1-СУЛЬФОНОВОЙ КИСЛОТЫ И ЕЁ ПРИМЕНЕНИЕ |
| US8329724B2 (en) | 2009-08-03 | 2012-12-11 | Hoffmann-La Roche Inc. | Process for the manufacture of pharmaceutically active compounds |
| NZ629615A (en) | 2009-11-06 | 2016-01-29 | Plexxikon Inc | Compounds and methods for kinase modulation, and indications therefor |
| EP2581084A4 (fr) * | 2010-05-31 | 2014-06-25 | Astellas Pharma Inc | Dispersion solide comprenant un composé de triazole |
| SI2672967T1 (sl) | 2011-02-07 | 2018-12-31 | Plexxikon Inc. | Spojine in postopki za kinazno modulacijo in indikacije zanjo |
| KR20140006879A (ko) | 2011-02-17 | 2014-01-16 | 에프. 호프만-라 로슈 아게 | 고온 용융 압출에 의해 활성 약학 성분을 과냉된 액체 상태로부터 제어되는 방식으로 결정화시키는 방법 |
| AR085279A1 (es) | 2011-02-21 | 2013-09-18 | Plexxikon Inc | Formas solidas de {3-[5-(4-cloro-fenil)-1h-pirrolo[2,3-b]piridina-3-carbonil]-2,4-difluor-fenil}-amida del acido propano-1-sulfonico |
| SMT201900179T1 (it) | 2011-06-20 | 2019-05-10 | H Lundbeck As | 1–piperazino–3–fenil indani deuterati per il trattamento della schizofrenia |
| CA2845284C (fr) | 2011-08-18 | 2018-03-06 | Dr. Reddy's Laboratories Ltd. | Composes amines heterocycliques substitues comme inhibiteurs de la proteine de transfert d'ester cholesterylique (cetp) |
| WO2013037396A1 (fr) * | 2011-09-12 | 2013-03-21 | Bioneer A/S | Solution de polymère dans un principe actif pour forme posologique solide |
| AU2012313971B2 (en) | 2011-09-27 | 2016-09-29 | Dr. Reddy's Laboratories, Ltd. | 5 - benzylaminomethyl - 6 - aminopyrazolo [3, 4 -b] pyridine derivatives as cholesteryl ester -transfer protein (CETP) inhibitors useful for the treatment of atherosclerosis |
| LT2765990T (lt) | 2011-10-14 | 2018-01-25 | Array Biopharma, Inc. | Solidinė dispersija |
| RS57140B1 (sr) | 2012-03-23 | 2018-07-31 | Array Biopharma Inc | Amorfna čvrsta disperzija za korišćenje u lečenju raka mozga |
| US20140128431A1 (en) | 2012-04-03 | 2014-05-08 | Hoffmann-Laroche Inc. | Pharmaceutical composition with improved bioavailability, safety and tolerability |
| EP2649989B1 (fr) | 2012-04-13 | 2017-10-18 | King Saud University | Procédé de préparation d'une dispersion solide, dispersion solide ainsi obtenue et son utilisation |
| US9150570B2 (en) | 2012-05-31 | 2015-10-06 | Plexxikon Inc. | Synthesis of heterocyclic compounds |
| JO3339B1 (ar) * | 2012-09-11 | 2019-03-13 | Shanghai Inst Pharmaceutical Ind | شكل مستقر غير متبلور من الأغوميلاتين وعملية تحضيره والتركيبات الدوائية التي تحتوي عليه |
| CA2891502A1 (fr) | 2012-11-19 | 2014-05-22 | Dr. Reddy's Laboratories Ltd. | Compositions pharmaceutiques d'inhibiteurs de cetp |
| CA3053189A1 (fr) | 2012-12-20 | 2014-06-26 | Kashiv Biosciences, Llc | Formulation de comprime a desintegration orale pour une meilleure biodisponibilite |
| HK1211217A1 (en) | 2013-01-22 | 2016-05-20 | 霍夫曼-拉罗奇有限公司 | Pharmaceutical composition with improved bioavailability |
| TWI615157B (zh) | 2013-02-06 | 2018-02-21 | 大塚製藥股份有限公司 | 包括不定形西洛他唑的固體分散劑 |
| WO2015038376A1 (fr) * | 2013-09-11 | 2015-03-19 | 3M Innovative Properties Company | Compositions de revêtement, structures dentaires les utilisant et procédés permettant de générer un contraste |
| WO2015082562A1 (fr) * | 2013-12-05 | 2015-06-11 | Alrise Biosystems Gmbh | Procédé de production de formulations médicamenteuses pour une administration par voie orale |
| PT107846B (pt) * | 2014-08-01 | 2019-03-22 | Hovione Farm S A | Produção de nano- partículas de dispersões sólidas amorfas por co-precipitação controlada |
| MX2017015322A (es) * | 2015-05-29 | 2018-03-28 | Sun Pharmaceutical Ind Ltd | Composicion farmaceutica oral de isotretinoin. |
| CN108218868B (zh) * | 2016-12-13 | 2019-02-19 | 南京药捷安康生物科技有限公司 | 多激酶抑制剂化合物、其晶型及用途 |
| EA201992573A1 (ru) | 2017-04-28 | 2020-04-06 | Сиэтл Дженетикс, Инк. | Лечение her2-положительных злокачественных новообразований |
| KR102082775B1 (ko) * | 2017-05-02 | 2020-02-28 | 주식회사 삼양바이오팜 | 수용해도 및 생체이용율이 개선된 조성물 |
| RU2725879C2 (ru) * | 2018-07-26 | 2020-07-07 | Федеральное государственное бюджетное образовательное учреждение высшего образования "Казанский Государственный медицинский университет" Министерства здравоохранения Российской Федерации | Интерполимерный носитель для пероральных систем контролируемой доставки активных фармацевтических ингредиентов |
| EP3891134A1 (fr) | 2018-12-03 | 2021-10-13 | H. Lundbeck A/S | Promédicaments de 4-((1r,3s)-6-chloro-3-phényl-2,3-dihydro-1h-inden-1-yl)-1,2,2-triméthylpipérazine et 4-((1/r,3s)-6-chloro-3-(phényl-d5)-2,3-dihydro-1h-inden-1-yl)-2,2-diméthy-1-(méthyl-d3)pipérazine |
| CA3168667A1 (fr) | 2020-01-24 | 2021-07-29 | Nanocopoeia, Llc | Dispersions solides amorphes de dasatinib et leurs utilisations |
| EP4096791A1 (fr) | 2020-01-31 | 2022-12-07 | Nanocopoeia LLC | Microparticules de nilotinib amorphe et leurs utilisations |
| JP7705715B2 (ja) | 2020-03-03 | 2025-07-10 | デクセリアルズ株式会社 | 画像表示装置の製造方法 |
| WO2021222739A1 (fr) | 2020-04-30 | 2021-11-04 | Nanocopoeia, Llc | Comprimé à désintégration orale comprenant une dispersion solide amorphe de nilotinib |
| US11980619B2 (en) | 2021-07-28 | 2024-05-14 | Nanocopoeia, Llc | Pharmaceutical compositions and crushable tablets including amorphous solid dispersions of dasatinib and uses |
Family Cites Families (23)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS51118816A (en) * | 1975-04-08 | 1976-10-19 | Meiji Seika Kaisha Ltd | A process for stabilizing non-crystalloidal solid |
| US4344934A (en) * | 1978-11-20 | 1982-08-17 | American Home Products Corporation | Therapeutic compositions with enhanced bioavailability |
| ZA868963B (en) * | 1985-11-27 | 1988-07-27 | Syntex Inc | Amorphous anthelmintic benzimidazole derivatives |
| GB8608080D0 (en) * | 1986-04-02 | 1986-05-08 | Fujisawa Pharmaceutical Co | Solid dispersion composition |
| CZ280738B6 (cs) * | 1988-02-10 | 1996-04-17 | F. Hoffmann - La Roche And Co., Aktiengesellschaft | Substituované pyrroly, jejich použití pro výrobu léčiv a léčiva na jejich bázi |
| JP2528706B2 (ja) † | 1988-05-30 | 1996-08-28 | ゼリア新薬工業株式会社 | ジヒドロピリジン化合物の製剤組成物 |
| USRE36736E (en) | 1989-02-06 | 2000-06-13 | Hoffman-La Roche Inc. | Substituted pyrroles |
| JPH0729926B2 (ja) † | 1989-07-25 | 1995-04-05 | 大塚製薬株式会社 | 易吸収性製剤用組成物 |
| US5399363A (en) | 1991-01-25 | 1995-03-21 | Eastman Kodak Company | Surface modified anticancer nanoparticles |
| ES2111065T5 (es) † | 1991-04-16 | 2005-06-16 | Nippon Shinyaku Company, Limited | Procedimiento para producir una dispersion solida. |
| US5281420A (en) | 1992-05-19 | 1994-01-25 | The Procter & Gamble Company | Solid dispersion compositions of tebufelone |
| TW493991B (en) | 1995-05-08 | 2002-07-11 | Novartis Ag | Pharmaceutical composition for oral administration of active agent having low water solubility and process for preparation of the same |
| GB9511220D0 (en) † | 1995-06-02 | 1995-07-26 | Glaxo Group Ltd | Solid dispersions |
| FR2736550B1 (fr) * | 1995-07-14 | 1998-07-24 | Sandoz Sa | Composition pharmaceutique sous la forme d'une dispersion solide comprenant un macrolide et un vehicule |
| EP0784974B1 (fr) * | 1995-07-26 | 2003-05-21 | Kyowa Hakko Kogyo Co., Ltd. | dispersion solide de derives xanthine |
| EP0952770A4 (fr) † | 1995-09-07 | 1999-12-22 | Fuisz Technologies Ltd | Systeme permettant de rendre biodisponibles des agents bioalterants sensiblement non solubles |
| DE19548624A1 (de) | 1995-12-23 | 1997-06-26 | Boehringer Mannheim Gmbh | Neue Barbitursäure-Derivate, Verfahren zu deren Herstellung und diese Verbindungen enthaltende Arzneimittel |
| JPH09208459A (ja) * | 1996-02-07 | 1997-08-12 | Eisai Co Ltd | 溶解性を改良した製剤 |
| IL126179A (en) | 1996-03-12 | 2003-04-10 | Pg Txl Co Lp | Pharmaceutical compositions containing anti-tumor drug conjugates |
| DE69730241T2 (de) * | 1996-06-28 | 2005-08-11 | Schering Corp. | Feste lösung eines fungizids mit erhöhter bioverfügbarkeit |
| PE91598A1 (es) | 1996-07-29 | 1998-12-24 | Hoffmann La Roche | Pirroles sustituidos |
| US6229011B1 (en) | 1997-08-22 | 2001-05-08 | Hoffman-La Roche Inc. | N-aroylphenylalanine derivative VCAM-1 inhibitors |
| EP1064279B1 (fr) | 1998-03-17 | 2003-06-25 | F.Hoffmann-La Roche Ag | Bisindolymaleimides substitues destines a l'inhibition de la proliferation cellulaire |
-
1999
- 1999-09-07 US US09/391,060 patent/US6350786B1/en not_active Expired - Lifetime
- 1999-09-13 ES ES99117908T patent/ES2218918T5/es not_active Expired - Lifetime
- 1999-09-13 SI SI9930573T patent/SI0988863T2/sl unknown
- 1999-09-13 AT AT99117908T patent/ATE265232T1/de active
- 1999-09-13 DE DE69916733T patent/DE69916733T3/de not_active Expired - Lifetime
- 1999-09-13 PT PT99117908T patent/PT988863E/pt unknown
- 1999-09-13 EP EP99117908A patent/EP0988863B2/fr not_active Expired - Lifetime
- 1999-09-13 DK DK99117908T patent/DK0988863T4/da active
- 1999-09-16 IL IL13195799A patent/IL131957A/xx not_active IP Right Cessation
- 1999-09-17 PE PE1999000947A patent/PE20001049A1/es not_active IP Right Cessation
- 1999-09-17 CO CO99059117A patent/CO5140077A1/es unknown
- 1999-09-17 SG SG9904570A patent/SG97131A1/en unknown
- 1999-09-17 NZ NZ337884A patent/NZ337884A/xx not_active IP Right Cessation
- 1999-09-17 CZ CZ0330499A patent/CZ300215B6/cs not_active IP Right Cessation
- 1999-09-20 AR ARP990104725A patent/AR022096A1/es not_active Application Discontinuation
- 1999-09-20 ID IDP990878D patent/ID24034A/id unknown
- 1999-09-20 HR HR990287 patent/HRP990287B1/xx not_active IP Right Cessation
- 1999-09-20 MY MYPI99004065A patent/MY124377A/en unknown
- 1999-09-20 AU AU48807/99A patent/AU770745B2/en not_active Expired
- 1999-09-20 CA CA2282906A patent/CA2282906C/fr not_active Expired - Lifetime
- 1999-09-20 TW TW088116184A patent/TWI234465B/zh not_active IP Right Cessation
- 1999-09-20 HU HU9903189A patent/HU228341B1/hu unknown
- 1999-09-21 JP JP11267142A patent/JP2000095708A/ja not_active Withdrawn
- 1999-09-21 CN CNB991194063A patent/CN1201821C/zh not_active Expired - Lifetime
- 1999-09-21 TR TR1999/02324A patent/TR199902324A2/xx unknown
- 1999-09-21 RU RU99120377/15A patent/RU2240827C2/ru active
- 1999-09-21 BR BR9904283-5A patent/BR9904283A/pt not_active Application Discontinuation
- 1999-09-21 RS YUP-473/99A patent/RS50193B/sr unknown
- 1999-09-21 NO NO19994583A patent/NO326928B1/no not_active IP Right Cessation
- 1999-09-21 MA MA25778A patent/MA26692A1/fr unknown
- 1999-09-22 PL PL335592A patent/PL202757B1/pl unknown
- 1999-09-22 KR KR1019990041130A patent/KR100362019B1/ko not_active Expired - Lifetime
-
2007
- 2007-06-06 JP JP2007150911A patent/JP2007224048A/ja active Pending
-
2011
- 2011-04-13 AR ARP110101253A patent/AR080892A2/es not_active Application Discontinuation
-
2012
- 2012-10-18 JP JP2012230446A patent/JP6253135B2/ja not_active Expired - Lifetime
-
2015
- 2015-07-16 JP JP2015141952A patent/JP2015187170A/ja active Pending
-
2016
- 2016-08-31 JP JP2016169245A patent/JP6534979B2/ja not_active Expired - Lifetime
Also Published As
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| MA26692A1 (fr) | Compositions pharmaceutiques contenant un complexe stable insoluble, procede de preparation et complexe stable insoluble obtenu | |
| KR100622796B1 (ko) | 폴리올-ifn-베타 공액체 | |
| JP5140539B2 (ja) | アルブミンを含有していない新規の第viii因子処方物 | |
| US4409233A (en) | Highly concentrated preparations of dopa compounds | |
| FI951266A0 (fi) | Pieneliöitä tappavat detergentti-jodi-koostumukset, joilla on alentunut detergenttipitoisuus | |
| FR2710840B1 (fr) | Compositions viscoélastiques hautement concentrées en composés fluorés, leur préparation et leurs utilisations dans le domaine médical et en cosmétique. | |
| EA002326B1 (ru) | Способ солюбилизации фармацевтически активных ингредиентов в воде и в водных носителях | |
| GB2217595A (en) | Anti-inflammatory gel | |
| HU197208B (en) | Process for production of medical compositions containing derivatives of oxicame | |
| CA2279277A1 (fr) | Systeme de gel de nimesulide a usage topique | |
| US6214866B1 (en) | Composition comprising mupirocin and chlorhexidine | |
| JPH05502440A (ja) | イブプロフェン摩砕物及びこれを含有する局所用組成物 | |
| CA2347170A1 (fr) | Laxatif osmotique non fermente pour traiter et prevenir les cancers colorectaux | |
| WO1988003799A1 (fr) | Vehicules pharmaceutiques de reduction du flux transdermique | |
| US3728452A (en) | Water-soluble composition comprising sulfadimidine and pyrimethamine | |
| CA2051260A1 (fr) | Systeme anti-oxydant a base d'un acide amine basique en association avec au moins un tocopherol ou un de ses derives et au moins un polypeptide non thiole et compositions contenant un tel systeme anti-oxydant | |
| FR2421173A1 (fr) | 2-(4-ethylpiperazino)-4-phenylquinoleine et ses sels, utiles notamment comme antidepresseurs, et leur procede de preparation | |
| EP0389079A3 (fr) | Polyamides portant des chaínes latérales fonctionnalisées utilisables comme agents hypolipidémiques solubles dans l'eau | |
| JPH08104642A (ja) | ヒアルロン酸ナトリウム注射液用安定化組成物 | |
| FR3134009B1 (fr) | Nécessaire pour le soin des matières kératineuses | |
| MXPA99001136A (en) | Composition comprising mupirocin and chlorhexidine | |
| HUP9903088A2 (hu) | Mupirocint és klórhexidint tartalmazó gyógyszerkészítmény | |
| ECSP993149A (es) | Complejos estables de compuestos escasamente solubles | |
| HK1106705B (en) | Novel albumin-free factor viii formulations |